Alcohol and Cancer: A Statement of the American Society of Clinical Oncology


Alcohol drinking is an established risk factor for several malignancies, and it is a potentially modifiable risk factor for cancer. The Cancer Prevention Committee of the American Society of Clinical Oncology (ASCO) believes that a proactive stance by the Society to minimize excessive exposure to alcohol has important implications for cancer prevention. In addition, the role of alcohol drinking on outcomes in patients with cancer is in its formative stages, and ASCO can play a key role by generating a research agenda. Also, ASCO could provide needed leadership in the cancer community on this issue. In the issuance of this statement, ASCO joins a growing number of international organizations by establishing a platform to support effective public health strategies in this area. The goals of this statement are to:

• Promote public education about the risks between alcohol abuse and certain types of cancer;

• Support policy efforts to reduce the risk of cancer through evidence-based strategies that prevent excessive use of alcohol;

• Provide education to oncology providers about the influence of excessive alcohol use and cancer risks and treatment complications, including clarification of conflicting evidence; and

• Identify areas of needed research regarding the relationship between alcohol use and cancer risk and outcomes.

INTRODUCTIONChooseTop of pageAbstractINTRODUCTION <<EPIDEMIOLOGY OF ALCOHOL U…DRINKING GUIDELINES AND D…ALCOHOL AND CANCERDISPARITIES IN ALCOHOL US…ALCOHOL AND CANCER: OUTCO…BARRIERS TO ADDRESSING AL…RESEARCH NEEDSPUBLIC HEALTH STRATEGIES …THE ROLE OF THE ONCOLOGIS…REFERENCES

The importance of alcohol drinking as a contributing factor to the overall cancer burden is often underappreciated. In fact, alcohol drinking is an established risk factor for several malignancies. As a potentially modifiable risk factor for cancer, addressing high-risk alcohol use is one strategy to reduce the burden of cancer. For example, in 2012, 5.5% of all new cancer occurrences and 5.8% of all cancer deaths worldwide were estimated to be attributable to alcohol.1 In the United States, it has been estimated that 3.5% of all cancer deaths are attributable to drinking alcohol.2 Alcohol is causally associated with oropharyngeal and larynx cancer, esophageal cancer, hepatocellular carcinoma, breast cancer, and colon cancer.3 Even modest use of alcohol may increase cancer risk, but the greatest risks are observed with heavy, long-term use.

Despite the evidence of a strong link between alcohol drinking and certain cancers, ASCO has not previously addressed the topic of alcohol and cancer. In addition, alcohol drinking is a potentially modifiable risk factor that can be targeted with preventive interventions at both the policy and the individual levels. Here, we provide an overview of the evidence of the links between alcohol drinking and cancer risk and cancer outcomes. The areas of greatest need for future research are highlighted. On the basis of this evidence and guidelines adopted by other cancer-focused organizations, ASCO-endorsed strategies for the reduction of high-risk alcohol consumption are presented.

EPIDEMIOLOGY OF ALCOHOL USEChooseTop of pageAbstractINTRODUCTIONEPIDEMIOLOGY OF ALCOHOL U… <<DRINKING GUIDELINES AND D…ALCOHOL AND CANCERDISPARITIES IN ALCOHOL US…ALCOHOL AND CANCER: OUTCO…BARRIERS TO ADDRESSING AL…RESEARCH NEEDSPUBLIC HEALTH STRATEGIES …THE ROLE OF THE ONCOLOGIS…REFERENCES

Beyond oncology, alcohol use and abuse together pose a significant public health problem. According to the Centers for Disease Control and Prevention, approximately 88,000 deaths were attributed to excessive alcohol use in the United States between 2006 and 2010.4 Approximately 3.3 million deaths worldwide result from the harmful use of alcohol each year.5 Population surveys demonstrate that 12% to 14% of adults have a current alcohol use disorder and that 29% have had such a disorder at some point in their lifetime.6,7 In addition to alcohol use disorder, other measures used to assess the impact of alcohol are excessive drinking, binge drinking, and heavy drinking. Excessive drinking includes binge drinking and is defined as consumption of four or more drinks during a single occasion for women, or five or more drinks during a single occasion for men. Binge drinking is the most common form of excessive drinking compared with heavy drinking, which is defined as eight or more drinks per week or three or more drinks per day for women, and as fifteen or more drinks per week or four or more drinks per day for men.8 Recent work has shown that the prevalence of adults who drink more than four to five drinks per occasion, defined as extreme binge drinking, has been increasing during the past decade.9 This study estimated that 13% of the US adult population engaged in extreme binge drinking on at least one occasion in the previous year. Moderate drinking is defined at up to one drink per day for women and up to two drinks per day for men.1,4 Most individuals who drink excessively do not meet the clinical criteria for alcoholism or alcohol dependence.10

Alcohol use during childhood and adolescence is a predictor of increased risk of alcohol use disorder as an adult.11 College-age and younger people who drink are prone to develop an alcohol use disorder later in life.7 Most adults who engage in high-risk alcohol drinking behavior started drinking before age 21 years. Among US youth age 12 to 20 years, 23% were current drinkers in the past 30 days, 10% were episodic drinkers, 2% were heavy episodic drinkers, and 6% met criteria for alcohol use disorder.11 Among childhood cancer survivors, the prevalence of alcohol use in the past 30 days in adulthood (7.8 mean years since diagnosis of their cancer) was 25%, which was lower than that observed in the general population.12 However, alcohol use among teenage patients with cancer is a common occurrence overall and has been observed to be as high among teens without cancer.1315

DRINKING GUIDELINES AND DEFINITIONSChooseTop of pageAbstractINTRODUCTIONEPIDEMIOLOGY OF ALCOHOL U…DRINKING GUIDELINES AND D… <<ALCOHOL AND CANCERDISPARITIES IN ALCOHOL US…ALCOHOL AND CANCER: OUTCO…BARRIERS TO ADDRESSING AL…RESEARCH NEEDSPUBLIC HEALTH STRATEGIES …THE ROLE OF THE ONCOLOGIS…REFERENCES

Internationally, more than 40 countries have issued alcohol drinking guidelines; however, these vary substantially.16 The American Heart Association, American Cancer Society, and US Department of Health and Human Services all recommend that men drink no more than one to two drinks per day and that women drink no more than one drink per day.1719 In addition, it is recommended that drinking alcohol should only be done by adults of legal age. People who do not currently drink alcohol should not start for any reason.

Defining risk-drinking can be challenging, because the amount of ethanol contained in an alcoholic beverage will vary considerably depending on the type of alcohol (eg, beer, wine, or spirits) and the size of the drink consumed. In addition, the definition of a standard drink varies among countries and ranges from 8 g to 14 g.20,21 The National Institute of Alcohol Abuse and Alcoholism (NIAAA) defines a standard drink as one that contains roughly 14 g of pure alcohol, which is the equivalent of 1.5 ounces of distilled spirits (approximately 40% alcohol by volume); 5 ounces of wine (approximately 12% alcohol by volume); or 12 ounces of regular beer (approximately 5% alcohol by volume).22 However, evidence shows that drinkers are often unaware of how standard drinks are defined and that these standard drink sizes are commonly exceeded.20

ALCOHOL AND CANCERChooseTop of pageAbstractINTRODUCTIONEPIDEMIOLOGY OF ALCOHOL U…DRINKING GUIDELINES AND D…ALCOHOL AND CANCER <<DISPARITIES IN ALCOHOL US…ALCOHOL AND CANCER: OUTCO…BARRIERS TO ADDRESSING AL…RESEARCH NEEDSPUBLIC HEALTH STRATEGIES …THE ROLE OF THE ONCOLOGIS…REFERENCES

Evidence to Link Alcohol Consumption to Specific Cancers

The relationship between drinking alcohol and cancer risk has been evaluated extensively in epidemiologic case-control and cohort studies. In a thorough systematic review of the world’s evidence that adhered to prespecified criteria for drawing inferences, a World Cancer Research Fund/American Institute for Cancer Research (AICR) report judged the evidence to be convincing that drinking alcohol was a cause of cancers of the oral cavity, pharynx, larynx, esophagus, breast, and colorectum (in men).23 Also, alcohol was judged to be a probable cause of increased risk of liver cancer and colorectal cancer (in women).23 An updated review of the evidence for liver cancer upgraded the conclusion for an association between alcohol drinking and liver cancer to convincing.24 The International Agency for Research on Cancer (IARC),25 a branch of WHO, has assessed the evidence and come to virtually identical conclusions: that alcohol is a cause of cancers of the oral cavity, pharynx, larynx, esophagus, colorectum, liver (ie, hepatocellular carcinoma), and female breast. For esophageal cancer, the association with alcohol drinking is largely specific to squamous cell carcinoma.25 The more that a person drinks, and the longer the period of time, the greater their risk of development of cancer, especially head and neck cancers.3

A valid question is whether these associations are specific to ethanol per se or whether they vary according to the type of alcoholic beverage (ie, beer, wine, or spirits/liquor). The answer is that the associations between alcohol drinking and cancer risk have been observed consistently regardless of the specific type of alcoholic beverage.25

The full range of cancers for which alcohol drinking represents a risk factor remains to be clarified. For example, the index of suspicion is high that alcohol drinking leads to excess risk of pancreatic cancer25 and gastric cancer.26 For some malignancies, alcohol drinking clearly is statistically associated with increased risk but, because of its strong correlation with other risk factors, it is difficult to discern if alcohol drinking is truly an independent risk factor. For example, alcohol drinking consistently has been statistically strongly associated with increased lung cancer risk.23 However, cigarette smokers also are more likely to be alcohol drinkers, and cigarette smoking is such an overwhelming lung cancer risk factor that confounding by cigarette smoking—rather than a direct association with alcohol drinking—currently cannot be ruled out as a possible explanation.27 As evidence continues to accumulate, the list of alcohol-associated cancers is likely to grow.

Magnitude of the Associations

Characterization of the dose-response relationship between alcohol and cancer is important for causal inference, because, if alcohol increases the risk for a specific cancer, one would expect the magnitude of the cancer risk to increase commensurate with increasing levels of alcohol consumption. Furthermore, the nature of the dose-response relationship provides useful information for communicating with patients about this issue. For alcohol-associated cancers, Table 1 summarizes results from a large-scale meta-analysis28 that show the relative risks of cancer in a comparison of nondrinkers with categories of people with light, moderate, and heavy alcohol consumption. The results summarized in Table 1 illustrate several key points. First, the magnitude of the association between alcohol drinking and cancer risk varied by type of cancer. Compared with nondrinkers, the summary relative risks (sRRs) for those classified as heavy drinkers ranged from 1.44 for colorectal cancer to 5.13 for cancer of the oral cavity and pharynx. The corresponding sRRs were 1.61, 2.07, 2.65, and 4.95 for cancers of the breast, liver, larynx, and esophagus, respectively. The strongest associations were observed for upper aerodigestive tract cancers (ie, larynx, esophagus, and oral cavity/pharynx), which involve tissues that come into direct contact with ingested alcohol. Second, monotonic dose-response relationships are evident for cancers of the oral cavity and pharynx, squamous cell carcinoma of the esophagus, and breast cancer. For liver, laryngeal, and colorectal cancers, the sRRs for the moderate category were intermediate between nondrinkers and heavy drinkers, but there was no evidence of increased risk in the light-drinker category. In a dose-response meta-analysis, the risk of secondary malignancies in patients with upper aerodigestive tract cancers increased incrementally by 9% for every increase in alcohol intake of 10 g/day.29

Table 1. Summary of Relative Risks From a Meta-Analysis for the Association Between Amount of Alcohol Drinking and Risk of Cancer

View larger version (208K)

Clearly, the greatest cancer risks are concentrated in the heavy and moderate drinker categories. Nevertheless, some cancer risk persists even at low levels of consumption. A meta-analysis that focused solely on cancer risks associated with drinking one drink or fewer per day observed that this level of alcohol consumption was still associated with some elevated risk for squamous cell carcinoma of the esophagus (sRR, 1.30; 95% CI, 1.09 to 1.56), oropharyngeal cancer (sRR, 1.17; 95% CI, 1.06 to 1.29), and breast cancer (sRR, 1.05; 95% CI, 1.02 to 1.08), but no discernable associations were seen for cancers of the colorectum, larynx, and liver.30 On the basis of the lesser overall cancer risk at the lower end of the dose-response continuum, the World Cancer Research Fund/AICR made the following recommendation: “If alcoholic drinks are consumed, limit consumption to two drinks a day for men and one drink a day for women.”23 They also recommend that, “for cancer prevention, it’s best not to drink alcohol.” Recent updates to the AICR report estimate a 5% increase in premenopausal breast cancer per 10 grams of ethanol consumed per day (pooled relative risk [RR], 1.05; 95% CI, 1.02 to 1.08). The risk was even greater for postmenopausal breast cancer, which had an RR of 1.09 (95% CI, 1.07 to 1.12) for each 10 grams of ethanol per day.31

Does Cessation of Alcohol Consumption Lead to Lower Cancer Risk?

A key question relevant both to the assessment of causality and the provision of advice and effective interventions to patients is whether the risk of developing an alcohol-associated cancer is reduced after one stops drinking alcohol. The results of meta-analyses and pooled analyses that have focused directly on this question for upper aerodigestive tract cancers indicate that risk of these cancers declines in those who quit drinking alcohol compared with those who remain alcohol drinkers.3235 The evidence from these studies suggests that the risk of cancer may be reduced to that seen in never drinkers after long-term (≥ 20 years) cessation from alcohol drinking. Unfortunately, there are limited existing data on the impact of alcohol cessation on the risk of other alcohol-related cancers. This important topic is in need of more thorough investigation, particularly because those who quit drinking alcohol may differ from current drinkers in important ways that are also associated with cancer risk. For example, similar to smoking cessation, an increased short-term risk of cancer after alcohol cessation may be due to the onset of cancer-related symptoms that contribute to the individual’s decision to stop drinking. Studies that carefully assess the time period between alcohol cessation and cancer diagnosis will help disentangle these complex methodological issues. Another potential bias is introduced by the finding that the category of former drinkers can be overrepresented by former heavy drinkers or alcoholics.36 When present, the risk of cancer after alcohol cessation may be higher than that observed for current drinkers because of the high alcohol exposure doses of those classified as former drinkers. Carefully designed prospective cohort studies will help overcome these bias-based limitations and will lead to a more refined characterization of the impact of cessation of alcohol drinking on cancer risk by longitudinally quantifying the amount of alcohol consumed and the duration of cessation.

Impact of Smoking in Combination With Alcohol Consumption

Some malignancies are causally linked to both alcohol drinking and cigarette smoking; in some cases, an established synergistic interaction between alcohol drinking and cigarette smoking exists. This means that, in cancers for which both alcohol drinking and cigarette smoking are causal factors, the cancer risks in those who are both alcohol drinkers and cigarette smokers are much larger than the risks seen for those who only drink alcohol or only smoke cigarettes. Specific upper aerodigestive tract cancers provide the strongest examples of robust synergistic interactions between alcohol drinking and cigarette smoking. A pooled analysis of 17 case-control studies identified a potent interaction between alcohol drinking and cigarette smoking in cancers of the oral cavity, pharynx, and larynx,37 and a review identified evidence of robust interaction in 22 of 24 published studies on oral, pharyngeal, laryngeal, and esophageal cancers.38 Despite the clear presence of synergistic interaction, the biologic underpinnings of the interaction between alcohol drinking and cigarette smoking are not well understood.

The Mechanistic Role of Alcohol in Carcinogenesis

When the evidence of alcohol’s role in carcinogenesis is considered, a key point is that, in biochemical reactions that are sequentially catalyzed by alcohol dehydrogenase and aldehyde dehydrogenase, ethanol is eliminated from the body by its oxidation first to acetaldehyde and then to acetate. Ethanol per se is not mutagenic, but acetaldehyde is carcinogenic and mutagenic, by binding to DNA and protein.39

The IARC reviewed the potential role of alcohol in carcinogenesis by synthesizing multiple bodies of evidence that included (1) experiments in which ethanol (or aldehyde) is administered to mice and rats in drinking water; (2) the absorption, distribution, metabolism, and excretion of ethanol and its metabolites; and (3) the genotoxicity of alcohol in various experimental systems, including biomarkers in humans.23 One key conclusion of the review was that, in animal models, administration of ethanol or acetaldehyde in drinking water increased the incidence of various tumors in mice and rats; also administration of other known carcinogens with ethanol in drinking water enhanced tumor development more.23 Another key conclusion was that “the role of ethanol metabolism in tumor initiation is implied by the associations observed between different forms of cancer and polymorphisms in genes involved in the oxidation of ethanol.”23 This point about polymorphisms is premised on the fact that genetic predisposition may amplify the toxic and mutagenic effects of alcohol consumption. A specific example of this line of reasoning is that most of the acetaldehyde generated during alcohol metabolism in vivo is eliminated promptly by aldehyde dehydrogenase-2 (ALDH2). However, a genetic variant of ALDH2 exists ([(rs671]*2) that encodes a catalytically inactive protein. Alcohol drinkers with the inactive form of ALDH2 experience excessive accumulation of acetaldehyde, which amplifies its toxic and mutagenic effects, and the amplification would be expected to lead to greater susceptibility to alcohol-induced cancer. Several studies in East Asian populations, who have the highest prevalence of this high-risk genotype, have documented that alcohol drinking is more strongly associated with cancers of the upper aerodigestive tract among those with a high-risk genotype.40 The IARC review also invoked mechanisms that included oxidative stress, sex hormones, folate metabolism, and DNA methylation as well as cirrhosis for hepatocellular carcinoma. Alcohol-induced oxidative stress, via the CYP2E1 pathway, for example, can result in chronic tissue inflammation.23 Alcohol drinking affects circulating concentrations of androgens and estrogens, which is a pathway of particular relevance to breast cancer.23 Consumption of alcohol is associated with lower folate concentrations—a relationship that has been extensively studied in relation to the etiology of colon cancer.41

Classification of Alcohol as a Carcinogen by the WHO

On the basis of the sum total of the evidence from research on mechanistic studies of the carcinogenicity of alcohol and the epidemiologic evidence to link alcohol with increased risk of multiple forms of cancer, the IARC classified alcohol as a group 1 carcinogen, because they found that it causes cancer in humans.41 Specifically, IARC concluded that there is sufficient evidence in humans for the carcinogenicity not only of alcohol consumption but also for the carcinogenicity of acetaldehyde associated with alcoholic beverage consumption.41

DISPARITIES IN ALCOHOL USE AND RELATED CANCERSChooseTop of pageAbstractINTRODUCTIONEPIDEMIOLOGY OF ALCOHOL U…DRINKING GUIDELINES AND D…ALCOHOL AND CANCERDISPARITIES IN ALCOHOL US… <<ALCOHOL AND CANCER: OUTCO…BARRIERS TO ADDRESSING AL…RESEARCH NEEDSPUBLIC HEALTH STRATEGIES …THE ROLE OF THE ONCOLOGIS…REFERENCES

Blacks, Asian Americans, and Hispanic individuals have lower rates of current alcohol use disorder than whites. However, rates among these groups appear to be increasing overall. The NIAAA has accumulated data during two decades by conducting large general-population surveys among US adults age 18 years and older. Their longitudinal surveys from 1991 to 1992 and 2001 to 2002 showed increases in alcohol abuse among men, women, and young black and Hispanic minorities. Rates of dependence also increased among men, young black women, and Asian men, which underscores the need to continue monitoring of prevalence and trends. It is now known that Hispanics and blacks have a higher risk than whites for developing alcohol-related liver disease.42 The longitudinal design of the NIAAA surveys enable the collection of data on cultural variables, such as acculturation. In addition to increasing overall rates, blacks and Hispanics are less likely to use alcohol treatment when it is available.43

All segments of US social strata are affected by alcohol abuse, but the prevalence of alcohol abuse is particularly high within American Indian and Alaska Native (AIAN) populations. AIAN people drink more alcohol and are more highly affected by alcohol-related illness than other populations.44 Among people age 12 years and older, the prevalence of binge drinking was 28% for AIAN people compared with 23% for whites, 22% for blacks, and 14% for Asian Americans. Findings from the 2000 to 2006 Behavioral Risk Factor Surveillance System showed that the rate of binge drinking was a major difference between non-Hispanic white and AIAN people, especially men.45 Similarly, rates of heavy drinking were highest (9%) among AIAN people and lowest (2%) among Asian Americans.44 The Indian Health Service, which provides a large amount of the health care to the AIAN community, addresses alcohol from a disease-model perspective.46 The Indian Health Service identifies alcoholism as a chronic disease with genetic, psychosocial, and environmental factors.47 Individuals with cirrhosis and chronic liver disease are at much higher risk of liver cancer, and the main preventable causes of these conditions are chronic infection with hepatitis B and C, chronic alcohol abuse, and nonalcoholic fatty liver disease. Though viral hepatitis prevention and treatment may be making a significant health difference already, addressing chronic alcohol abuse would be an important cancer prevention strategy.

Differential rates of alcohol use according to socioeconomic status hypothetically could contribute to cancer disparities. In reality, the relationship between alcohol drinking and socioeconomic status is complex, because it depends on how alcohol drinking is measured. When measures of alcohol use are used, those of a higher socioeconomic status are more likely to drink and to drink more heavily.48 However, for reasons that are poorly understood, measures of adverse consequences of alcohol tend to concentrate more among those of a lower socioeconomic status.48 A disproportionate share of the overall burden of cancer occurs in those of a lower socioeconomic status, so alcohol drinking may be a contributing factor to cancer disparities observed across the spectrum of socioeconomic status; however, this remains a relatively unexplored topic.49

Patterns of alcohol use and treatment also vary by sex and sexual orientation; higher rates are seen in sexual and gender minority populations (ie, lesbian, gay, bisexual, transgender, and intersex).50 This population also is known to bear a greater burden of cancer incidence.50 For example, although men have a higher prevalence of heavy drinking, women are less likely to use alcohol treatment services,43 even among those with alcohol dependence.51 Lesbian or bisexual female veterans had higher rates of alcohol misuse than heterosexual female veterans did, which may result at least in part from higher rates of trauma exposure and mental health difficulties experienced by the lesbian/bisexual women.52 Lesbian, gay, and bisexual young adults (ages 17 to 19 years) consume more alcohol both in high school and in college.53 A study of the National Longitudinal Study of Adolescent Health also confirmed significantly increased alcohol use and abuse among lesbian, gay, and bisexual youth.54 A recent ASCO position statement recommended increased cancer prevention education efforts, including reduction in high-risk alcohol use as a target effort.50

ALCOHOL AND CANCER: OUTCOMES AND EFFECT ON TREATMENTChooseTop of pageAbstractINTRODUCTIONEPIDEMIOLOGY OF ALCOHOL U…DRINKING GUIDELINES AND D…ALCOHOL AND CANCERDISPARITIES IN ALCOHOL US…ALCOHOL AND CANCER: OUTCO… <<BARRIERS TO ADDRESSING AL…RESEARCH NEEDSPUBLIC HEALTH STRATEGIES …THE ROLE OF THE ONCOLOGIS…REFERENCES

Compared with the wealth of evidence about the associations between alcohol drinking and the risk of developing cancer, research on the impact of alcohol drinking on outcomes in patients with cancer is still in its nascent stages. For cancers that have known associations with alcohol drinking, it would be expected that alcohol drinking at the time of diagnosis also would be associated with risk of cancer recurrence and/or secondary primary tumors (SPTs). This association has been observed for patients with upper aerodigestive tract cancer when nondrinkers are compared with occasional drinkers. The risk of cancer-specific mortality is increased significantly in moderate drinkers (RR, 1.79; 95% CI, 1.26 to 2.53) and heavy drinkers (RR, 3.63; 95% CI, 2.63 to 5.0).55 Among survivors of upper aerodigestive tract cancer, continued alcohol use after diagnosis is associated with a three-fold increased risk of upper aerodigestive tract second primary tumors,56 and cessation may reduce the increased risk for SPTs in pre-diagnosis drinkers compared with pre-diagnosis nondrinkers.29 In breast cancer survivors, several studies suggest that alcohol drinking is not associated with decreased overall survival,57 whereas other studies indicate that breast cancer–specific mortality may be increased in at least some subgroups of the patient population.5860 The increase in breast cancer–specific mortality or risk of recurrence has been observed with moderate to heavy levels of alcohol drinking.60,61 Li et al showed that, among women with estrogen receptor–positive breast cancer, consumers of seven or more drinks per week versus none had a 90% increased risk of asynchronous contralateral breast cancer,62 which was higher than the 30% increased risk observed in a multicentered case-control study.63 Other SPTs in patients with breast cancer that have been associated with greater alcohol consumption (> 7 drinks per week versus none) include an increased risk of subsequent colorectal cancer (hazard ratio [HR], 1.92; 95% CI, 1.07 to 3.43) and a decreased risk of ovarian cancer (HR, 0.45; 95% CI, 0.21 to 0.98).64 Results of studies to evaluate the relationship between alcohol consumption and colorectal cancer have been mixed; one study observed that heavy drinking was associated with poorer survival,65 whereas the majority of studies have demonstrated either no association between alcohol drinking overall and colorectal cancer outcomes66 or a suggestion of better overall survival with higher levels of wine consumption.67 A recent meta-analysis of cohort studies among 209,597 cancer survivors showed a statistically significant 8% increase in overall mortality and a 17% increased risk for recurrence in the highest versus lowest alcohol consumers.68 More evidence is needed to clarify the impact of both alcohol drinking and cessation on cancer outcomes.

The majority of studies to evaluate the direct effects of alcohol use on cancer treatment have focused on patients with upper aerodigestive tract cancer, because 34% to 57% continue to drink after diagnosis.69 Smoking and alcohol use during and after radiation therapy have been associated with an increased risk of osteoradionecrosis of the jaw in patients with oral and oropharyngeal cancers.7073

Alcohol abuse also complicates treatment outcomes among patients with cancer by contributing to longer hospitalizations, increased surgical procedures, prolonged recovery, higher health care costs,7476 and higher mortality.77 Heavy alcohol use and abuse are important modifiable risk factors for postoperative morbidity.78 Heavy alcohol use79 and alcohol abuse,80 compared with no alcohol use, are associated with higher risks of anastomotic complications after colorectal surgery. Alcohol abuse, compared with no abuse, also has been shown to contribute to low quality-of-life outcomes in patients with head and neck cancer after treatment.81,82 Patients with cancer who abuse alcohol have increased comorbidities that can complicate treatment choices and that are affected by alcohol-related subclinical factors, including nutritional deficiencies, immunosuppression, and cardiovascular insufficiencies that increase treatment morbidity.8385

Light alcohol use among cancer survivors has been perceived as potentially beneficial for treatment-related adverse effects, although there is little evidence to support this concept. A cross-sectional study of patients with head and neck cancer showed that patients who reported drinking at least one serving of alcohol in the past month reported better functional scores and lower levels of symptoms, such as fatigue, pain, dysphagia or dry mouth after treatment than those who reported that they had not used alcohol.86 Given the inability to distinguish the sequence of events in a cross-sectional study design, it is unclear whether light alcohol use promotes treatment recovery and well-being or is the result of improved health-related quality of life among survivors. The consumption of light alcohol for increasing appetite has been regarded as potentially beneficial for patients with cancer,87 because alcohol can stimulate appetite and snacking in cancer-free individuals.88 However, a recent study of patients with advanced cancer who had self-reported loss of appetite and who were randomly assigned to white wine with ≤ 15% alcohol content twice a day for 3 to 4 weeks versus a nutritional supplement showed no improvement in appetite or weight.89

BARRIERS TO ADDRESSING ALCOHOL AND CANCER IN THE ONCOLOGY SETTINGChooseTop of pageAbstractINTRODUCTIONEPIDEMIOLOGY OF ALCOHOL U…DRINKING GUIDELINES AND D…ALCOHOL AND CANCERDISPARITIES IN ALCOHOL US…ALCOHOL AND CANCER: OUTCO…BARRIERS TO ADDRESSING AL… <<RESEARCH NEEDSPUBLIC HEALTH STRATEGIES …THE ROLE OF THE ONCOLOGIS…REFERENCES

In addition to the perception that light alcohol use may have a beneficial effect on appetite and tolerance of cancer treatment, conflicting data about the heart health of alcohol, especially red wine, is one additional barrier to addressing alcohol and cancer risk in the oncology setting. However, subsequent work has revealed multiple confounders to this conclusion about heart health, including frequent classification of former and occasional alcohol drinkers as nondrinkers.90 For example, people who now abstain from alcohol often have underlying health concerns, which explains their reasons to cut down on alcohol and thereby makes the current alcohol drinkers appear healthier than former and occasional drinkers—a so-called abstainer bias.90 In addition, larger studies and meta-analyses have failed to show an all-cause mortality benefit for low-volume alcohol use compared with abstinence or intermittent use, which suggests the lack of a true benefit to daily alcohol use.91,92 Differences in alcohol dehydrogenase variants are associated with nondrinking, and nondrinkers have had lower rates of coronary heart disease and stroke than even light drinkers.93 As such, the benefit of alcohol consumption on cardiovascular health likely has been overstated.94,95 As reviewed in the Magnitude of the Association section, the risk of cancer is increased even with low levels of alcohol consumption,30 so the net effect of alcohol is harmful. Thus, alcohol consumption should not be recommended to prevent cardiovascular disease or all-cause mortality.

Low physician knowledge of alcohol use and cancer risk is another barrier to addressing alcohol use with patients. This lack of knowledge has been demonstrated among general practitioners, who were aware of an association of alcohol with cardiovascular health and obesity and who also felt that preventive health was an important aspect of their work; however, the majority of providers did not ask their patients about alcohol consumption, and most were unaware of alcohol as a carcinogen.96,97 A knowledge deficit was also seen among medical students relative to the role of alcohol as a risk factor in head and neck cancers.98 Knowledge of the association between cancer and alcohol also has been shown to be low among dentists and allied health professionals, who may be evaluating patients for these cancers. For example, dentists and dental hygienists have lower awareness of the association between alcohol use and head and neck cancers than family physician do (40% for dentists v 94% for family physicians), and this lack of knowledge would hamper their ability to counsel patients about alcohol-related cancers.99

In addition to a lack of knowledge of alcohol use as a cancer risk factor, physicians use different approaches to counseling patients about alcohol use. Just as overweight or obese physicians are less likely to counsel their patients about obesity,100 alcohol use among physicians may make them less likely to counsel patients about the risks of alcohol use. In one study of Danish physicians, 18.8% of physicians met criteria for risky alcohol consumption.101 Estimates indicate that up to 14% of American physicians will have an alcohol use disorder in their lifetime, which is a rate similar to the general population.102 Burnout, which is very common among oncology providers, also is strongly associated with high-risk alcohol use.103107

RESEARCH NEEDSChooseTop of pageAbstractINTRODUCTIONEPIDEMIOLOGY OF ALCOHOL U…DRINKING GUIDELINES AND D…ALCOHOL AND CANCERDISPARITIES IN ALCOHOL US…ALCOHOL AND CANCER: OUTCO…BARRIERS TO ADDRESSING AL…RESEARCH NEEDS <<PUBLIC HEALTH STRATEGIES …THE ROLE OF THE ONCOLOGIS…REFERENCES

Although alcohol is a well-established risk factor for the development of certain cancers, very little is known about how current alcohol use affects cancer treatment delivery. Thus, the most compelling and urgent research need for the oncology community with regard to alcohol is better definition of the effect of concurrent alcohol use on cancer treatments, including chemotherapy, radiation, and surgery, as well as on cancer outcomes. Anecdotal stories from providers about the effect of alcohol on cancer treatment are intriguing, but rigorous scientific studies are needed to accurately quantify the effect. Underexplored research areas include the effects of alcohol exposure on postoperative morbidity; on the efficacy of chemotherapy and radiation; and on novel targeted therapies, such as immunotherapy and radiation.

Increased knowledge about the mechanistic effects of alcohol on cancer-related pathways and treatments may improve understanding of its role in disease progression and therapeutic responsiveness and toxicity. For example, a preclinical study demonstrated overlap between alcohol responsive genes and genes that are involved in responsiveness to endocrine therapy in breast cancer cells.108 The insufficient knowledge about the detrimental or potentially beneficial effects of alcohol use overall, as well as effects of its dose and frequency, among patients with cancer creates missed opportunities to intervene to improve overall quality of life and to educate patients about the cancer-specific prognostic role of alcohol.

Systems-based research, including research into successful means for the oncology community to identify patients who are currently using alcohol or who may be at high risk for alcohol relapse, will be critical. How to effectively apply evidence-based clinical interventions to assist patients in reduction of abstention from alcohol use also should be explored.

PUBLIC HEALTH STRATEGIES TO REDUCE HIGH-RISK ALCOHOL CONSUMPTIONChooseTop of pageAbstractINTRODUCTIONEPIDEMIOLOGY OF ALCOHOL U…DRINKING GUIDELINES AND D…ALCOHOL AND CANCERDISPARITIES IN ALCOHOL US…ALCOHOL AND CANCER: OUTCO…BARRIERS TO ADDRESSING AL…RESEARCH NEEDSPUBLIC HEALTH STRATEGIES … <<THE ROLE OF THE ONCOLOGIS…REFERENCES

Policies to reduce excessive alcohol consumption should be evidence based (such as those identified by WHO109 or the Community Preventive Services Task Force110), culturally sensitive, and equitable in their implementation. Recognizing that excessive alcohol use can delay or negatively impact cancer treatment and that reducing high-risk alcohol consumption is cancer prevention, ASCO joins the growing number of cancer care and public health organizations to support strategies designed to prevent high-risk alcohol consumption such as the following and those in Table 2.111129

Table 2. Policy Recommendations of International Cancer Care and Public Health Organizations

View larger version (977K)

  • Clinical strategies of alcohol screening and brief intervention provided in clinical settings: Health care providers can screen adults, including pregnant women, for excessive alcohol use to identify people whose levels or patterns of alcohol use place them at increased risk of alcohol-related harms. Health care providers can then recommend or offer treatment services to those at risk. Brief counseling interventions for adults who drink excessively have been found to positively affect several patterns of excessive drinking, including heavy episodic (binge) drinking and high average weekly intake of alcohol.130
  • Regulate alcohol outlet density: An alcohol outlet is defined as any site where alcohol may be legally sold to an individual to either consume on premises (eg, bars or restaurants) or off premises (eg, liquor stores or other retail settings).131 Using regulatory authority to reduce the number of alcohol outlets in a given area (ie, density) has proven to be an effective strategy for reducing excessive alcohol consumption.131134 This is frequently executed through outlet licensing or zoning processes.
  • Increase alcohol taxes and prices: Taxes are placed on all alcohol beverages by both individual states and the federal government, and a portion of the federal excise tax may or may not be used to support treatment programs. Alcohol taxes vary from state to state and also differ in the amount applied based on the type of alcohol (eg, beer, wine, or spirits/hard liquor). Increasing taxes, and therefore the overall price of alcohol, has been shown to inversely effect levels of excessive consumption and related health harms.135137 Other regulations that may directly or indirectly affect the price of alcoholic beverages, including regulations on wholesale distribution and bans on price-related promotions, may have some impact on excessive consumption, though more research is needed.137,138
  • Maintain limits on days and hours of sale: Limiting the days or hours during which alcoholic beverages can be sold can be applied to both outlets where the alcohol is consumed on premises and retail outlets where the alcohol is consumed off premises. These policies, made at the state and local levels, are intended to prevent excessive consumption by reducing access to the alcohol.139 Evidence from several studies has demonstrated the positive impact that reducing the number of days or hours that alcoholic beverages are sold generally result in a decrease in related harms.140,141
  • Enhance enforcement of laws prohibiting sales to minors: The minimum legal drinking age is 21 years in all US states. Enhanced enforcement of the minimum legal drinking age can reduce sales to minors (younger than 21 years) in retail settings (such as, bars, restaurants, liquor stores), thereby helping to reduce youth access to alcohol.130
  • Restrict youth exposure to advertising of alcoholic beverages: Early onset of drinking has been associated with an increased likelihood of developing dependence on alcohol later in life,142 and studies have demonstrated that youth exposed to more advertisements also show increases in drinking levels.143,144 The alcohol industry has only voluntary advertising codes created by the major trade groups, and are not subjected to federal restrictions. Currently, industry codes require that at least 70% of the audience of the advertisements (including print, radio, television, and internet/digital) consists of adults of legal drinking age.145147 However, the alcohol industry is frequently noncompliant with its own self-regulation guidelines.148
  • Resist further privatization of retail alcohol sales in communities with current government control. Following the end of Prohibition in 1933, all states had wholesale of alcoholic beverages under state control. “License” states allowed retail sales by commercial interests, while some “control” states allowed alcohol to be sold, but only through government-run retail stores that restrict off-premises sales outlets (ie, outlets where alcohol is sold for consumption elsewhere). In the United States, all states and counties that permit the sale of alcohol allow privatized retail sales of beer, and most allow privatized retail sale of all alcoholic beverages. Privatization most often affects wine and spirits (eg, vodka and whiskey) in the control states.149
  • Include alcohol control strategies in comprehensive cancer control plans: State, tribal, and territorial comprehensive alcohol control strategies are not commonly included in comprehensive cancer control plans. Supporting the implementation of evidence-based strategies to prevent the excessive use of alcohol is one tool the cancer control community can use to reduce the risk of cancer.150

In addition to these strategies, ASCO supports efforts to eliminate pinkwashing in the marketing of alcoholic beverages. Pinkwashing is a form of cause marketing in which a company uses the color pink and/or pink ribbons to show a commitment to finding a cure for breast cancer. Given the consistent evidence that shows the link between alcohol consumption and an increased risk of breast cancer,25,151 alcoholic beverage companies should be discouraged from using the symbols of the battle against breast cancer to market their products.

THE ROLE OF THE ONCOLOGISTChooseTop of pageAbstractINTRODUCTIONEPIDEMIOLOGY OF ALCOHOL U…DRINKING GUIDELINES AND D…ALCOHOL AND CANCERDISPARITIES IN ALCOHOL US…ALCOHOL AND CANCER: OUTCO…BARRIERS TO ADDRESSING AL…RESEARCH NEEDSPUBLIC HEALTH STRATEGIES …THE ROLE OF THE ONCOLOGIS… <<REFERENCES

Worldwide, alcohol-related cancers are estimated to be 5.5% of all cancers treated annually, which represents a large number of patients. Oncologists frequently are the ones who manage the treatment of these patients, and they have a direct interest in promotion of the health of patients. Such promotion likely will include helping patients reduce high-risk alcohol use. Oncologists also stand in a position to drive the alcohol-related research agenda as it affects patients with cancer. The most pressing questions include how active alcohol use affects cancer treatments, how alcohol use affects risk of recurrence and overall prognosis, and how alcohol interacts with oral chemotherapy and supportive care medications. As front-line providers for these patients, another need to support is identification of the most effective strategies to help patients reduce their alcohol use. Ways to address racial, ethnic, sex, and sexual orientation disparities that will place these populations at increased rates for cancer also are needed. Oncology providers can serve as community advisors and leaders and can help raise the awareness of alcohol as a cancer risk behavior. Finally, because alcohol use is quite common, an initiative to address alcohol use (particularly high-risk alcohol use) is a potential preventive strategy to decrease the burden of cancer. Policy efforts are likely to be the most effective way to address this need.

Immune Protein May Drive Alcoholism Relapse


Summary: An immune protein called CSF1 may contribute to feelings of anxiety as a result of alcohol withdrawal for those with alcohol use disorder.

Source: Scripps Research Institute

The anxiety that occurs during withdrawal from excessive alcohol use, and contributes to relapse, may be driven in part by the release of an immune protein in the brain, according to a new study from scientists at Scripps Research.

The discovery, reported online June 6, 2022, in Molecular Psychiatry, illuminates the molecular details of the brain’s response to alcohol withdrawal, and suggests that the immune protein, colony stimulating factor 1 (CSF1), could be a target of future treatments for alcohol use disorder (AUD).

“Alcohol withdrawal activates the stress system in the brain, which contributes to relapse, and in this study, we linked this stress response to CSF1, a neuroimmune mediator, opening up new opportunities for therapeutic intervention,” says study senior author Marisa Roberto, PhD, professor and Schimmel Family Chair in the Department of Molecular Medicine at Scripps Research.

The study’s first author, who performed many of the experiments, is Reesha R. Patel, PhD, a former postdoctoral researcher in the Roberto lab.

Alcohol is by far the most used and abused recreational drug. According to the 2019 National Survey on Drug Use and Health, nine million men and more than five million women in the United States have an alcohol use disorder (AUD), which is defined as an inability to control alcohol use despite its negative impact on the user’s health, social life and/or employment.

Drug treatments, talk-therapy and support group-based treatments are available, but relapse is common, mainly due to the limited understanding of the brain-circuit dysfunctions underlying AUD.

Scientists know that relapse-promoting alcohol withdrawal symptoms include rising feelings of anxiety, caused at least in part by the release of stress molecules such as corticotropin-releasing factor (CRF) within the brain. CRF stimulates receptors on neurons in the prefrontal cortex, and in the limbic system, a set of more primitive brain structures that process emotions.

If scientists could fully identify and characterize these CRF-sensitive neuronal populations, they could understand better how anxiety occurs during withdrawal and potentially devise effective treatments to block it.

Toward that end, Roberto and her team, in the new study, identified a population of neurons in the medial prefrontal cortex (mPFC) of mice that are sensitive to CRF because they express a CRF receptor called CRF1. The scientists showed that these neurons are involved in altering mood and behavior during alcohol exposure and withdrawal.

The team’s initial experiments revealed that deletion of these CRF-sensitive neurons makes the mice less anxious, suggesting that the neurons normally mediate anxiety-like behaviors.

The researchers subsequently found that these CRF-sensitive mPFC neurons become less excitable—less likely to fire signals to other neurons when stimulated—in alcohol-dependent mice that experience alcohol withdrawal. In contrast, nearby mPFC neurons lacking CRF receptors become more excitable.

“These CRF-sensitive mPFC neurons appear to constitute a unique neuronal population that undergoes profound neuroadaptations with chronic alcohol exposure,” says study co-author Pauravi Gandhi, PhD, a postdoctoral research associate in the Roberto lab.

Intriguingly, the researchers found that alcohol withdrawal, even as it dialed down the excitability of the CRF-sensitive neurons, also induced large increases in CSF1 gene expression within these neurons. CSF1 is an immune protein best known for its role in stimulating stem cells to mature into large white blood cells called macrophages.

This shows neurons
Scripps Research scientists find the immune protein CSF1 may contribute to anxiety during alcohol withdrawal. Some nuclei (blue) have the corticotropin-releasing factor receptor 1 crhr1 gene (red), as well as the glutamate transporter gene slc17a7 (green), but not the glutamate decarboxylase gene gad2 (yellow), suggesting that they predominantly comprise an excitatory population in the medial prefrontal cortex. Alcohol withdrawal results in increased CSF1 in these neurons, mimicking synaptic changes in glutamate transmission seen following alcohol withdrawal, and leading to heightened anxiety. Credit: Scripps

In the brain, CSF1 is thought to have a similar role in sustaining brain-resident immune cells called microglia. Moreover, prior research in mice has suggested that under conditions of chronic stress, CSF1 production rises in the mPFC, driving microglia to prune connections between neurons, which in turn causes signs of anxiety and depression.

Looking more closely at CSF1’s role in alcohol withdrawal, Roberto and colleagues artificially increased CSF1 production in CRF-sensitive mPFC neurons in mice, and observed that the animals exhibited many of the same neuronal and behavioral changes seen in alcohol withdrawal—suggesting that elevated CSF1 levels in mPFC may be a key driver of alcohol-withdrawal signs and symptoms.

“Targeting CSF1 therefore may be a good strategy for treating AUD, and we’re now eager to test that in our preclinical models,” Patel says.

“Ethanol withdrawal-induced adaptations in prefrontal corticotropin releasing factor receptor 1-expressing neurons regulate anxiety and conditioned rewarding effects of ethanol” was co-authored by Reesha Patel, Sarah Wolfe, Vittoria Borgonetti, Pauravi Gandhi, Larry Rodriguez, Angela Snyder, Shannon D’Ambrosio, Michal Bajo, Alain Domissy, Steven Head, Candice Contet, R. Dayne Mayfield, Amanda Roberts and Marisa Roberto.

Funding: The research was supported by the National Institutes of Health (AA021491, AA017447, AA015566, AA006420, AA013498, AA026685, AA027700, AA029841, K99 AA029180, F32 AA026765, T32 AA007456) and by the Pearson Center for Alcoholism and Addiction Research.


Abstract

Ethanol withdrawal-induced adaptations in prefrontal corticotropin releasing factor receptor 1-expressing neurons regulate anxiety and conditioned rewarding effects of ethanol

Prefrontal circuits are thought to underlie aberrant emotion contributing to relapse in abstinence; however, the discrete cell-types and mechanisms remain largely unknown. Corticotropin-releasing factor and its cognate type-1 receptor, a prominent brain stress system, is implicated in anxiety and alcohol use disorder (AUD).

Here, we tested the hypothesis that medial prefrontal cortex CRF1-expressing (mPFCCRF1+) neurons comprise a distinct population that exhibits neuroadaptations following withdrawal from chronic ethanol underlying AUD-related behavior.

We found that mPFCCRF1+ neurons comprise a glutamatergic population with distinct electrophysiological properties and regulate anxiety and conditioned rewarding effects of ethanol.

Notably, mPFCCRF1+ neurons undergo unique neuroadaptations compared to neighboring neurons including a remarkable decrease in excitability and glutamatergic signaling selectively in withdrawal, which is driven in part by the basolateral amygdala.

To gain mechanistic insight into these electrophysiological adaptations, we sequenced the transcriptome of mPFCCRF1+ neurons and found that withdrawal leads to an increase in colony-stimulating factor 1 (CSF1) in this population.

We found that selective overexpression of CSF1 in mPFCCRF1+ neurons is sufficient to decrease glutamate transmission, heighten anxiety, and abolish ethanol reinforcement, providing mechanistic insight into the observed mPFCCRF1+ synaptic adaptations in withdrawal that drive these behavioral phenotypes.

Together, these findings highlight mPFCCRF1+ neurons as a critical site of enduring adaptations that may contribute to the persistent vulnerability to ethanol misuse in abstinence, and CSF1 as a novel target for therapeutic intervention for withdrawal-related negative affect.

An expanded evaluation of the relationship of four alleles to the level of response to alcohol and the alcoholism risk


Abstract

Background: Alcoholism is a complex, genetically influenced disorder the cause of which may be better understood through the study of genetically influenced phenotypes that mediate the risk. One such intermediate phenotype is the low level of response (LR) to alcohol. This project used a case-control approach to search for genes that may contribute to LR.

Methods: Data were available from alcohol challenges at approximately age 20 and regarding the development of alcohol use disorders over the subsequent 20 years for 85 men, including 40 reported in a previous genetic analysis. LR was evaluated using oral consumption of 0.75 ml/kg of alcohol, after which changes in subjective feelings of intoxication and body sway were measured. Alcohol abuse and dependence were diagnosed by DSM-III-R criteria through structured interviews administered to both the participant and an informant (usually the spouse) 10, 15, and 20 years after initial testing. Four polymorphisms were evaluated, including the serotonin transporter HTTLPR promoter ins/del, GABAAalpha6 Pro385Ser, NPY Leu7Pro, and catalase 262C>T. Two of these, HTTLPR and GABAAalpha6 Pro385Ser, had been previously associated with LR and alcoholism in a preliminary study.

Results: The HTTLPR L allele was significantly related to both the LR and alcoholism in an allele-dosage (stepwise) manner. Furthermore, the association remained when L alleles were subdivided into recently reported functional subtypes: the lowest LR was associated with genotypes correlated with the highest serotonin transporter expression. The GABAAalpha6 Ser385 allele showed a nonsignificant trend for association to a low LR, as had been previously observed, although the Ser385 allele is uncommon, and only 18 heterozygotes were in the current group. However, the six men with both LL and Pro385/Ser385 genotypes had the lowest LR, and each had developed alcoholism during follow-up. Neither NPY nor catalase was associated with either LR or alcoholic outcomes, although the sample did not have sufficient power for definitive conclusions.

Conclusions: This report strengthens the support for a relationship between the HTTLPR L and GABAAalpha6 Ser385 alleles to low alcohol LR and to alcoholism in a prospectively studied cohort evaluated for LR in young adulthood and before the onset of alcohol dependence.

Alcoholic monkeys: New treatment reduces drinking by 50%, could help humans next.


Alcoholic monkeys: New treatment reduces drinking by 50%, could help humans next, Trending News | wionews.com https://www.wionews.com/trending/alcoholic-monkeys-new-treatment-reduces-drinking-by-50-could-help-humans-next-455086?utm_medium=Social&utm_source=Facebook&utm_campaign=FB-M

More older women are drinking hard


New research finds an increase in binge drinking among older women.

More older American women than ever are drinking — and drinking hard, a new study shows.

Most troubling was the finding that the prevalence of binge drinking among older women is increasing dramatically, far faster than it is among older men, the researchers noted.

The difference was striking: Among men, the average prevalence of binge drinking remained stable from 1997 to 2014, while it increased an average of nearly 4 percent per year among women, the researchers found.

Increased drinking and binge drinking can be a serious health problem for women, said study author Rosalind Breslow, an epidemiologist at the U.S. National Institute on Alcohol Abuse and Alcoholism.

Women don’t tolerate alcohol as well as men, and they start to have alcohol-related problems at lower drinking levels than men, Breslow explained.

She pointed out that on average, women weigh less than men, and have less water in their bodies than men do. (Alcohol dissolves in water).

“So, after a man and woman of the same weight drink the same amount of alcohol, the woman’s blood alcohol concentration will tend to be higher, putting her at greater risk for harm,” Breslow said.

For the study, Breslow and her colleagues collected data on more than 65,000 men and women aged 60 and older who were current drinkers. Among these, more than 6,500 men and 1,700 women were binge drinkers.

Older adults, in general, are at greater risk of the effects of alcohol than younger adults, Breslow noted. “They’re more sensitive to the effects of alcohol, which can contribute to falls and other injuries, a major problem in older people,” she said.

As the U.S. population ages, the number of men and women 60 and older who drink will likely increase further, bringing with it more alcohol-related problems.

In the study, said Breslow, “we found that between 1997 and 2014, the proportion of older male drinkers in the U.S. population increased about 1 percent per year, and female drinkers increased nearly 2 percent per year.”

It’s not clear why this is happening, Breslow added.

“We did find that more younger boomers, ages 60 to 64, both men and women, were drinking than people of the same age in past generations,” Breslow added.

Whether drinking is increasing among certain racial or ethnic groups isn’t something the researchers analyzed, she said.

But alcohol can have devastating consequences, particularly for older adults, Breslow said.

“Too much drinking increases your chances of being injured or even killed. Alcohol is a factor, for example, in about 60 percent of fatal burn injuries, drownings and homicides; 50 percent of severe trauma injuries and sexual assaults; and 40 percent of fatal motor vehicle crashes, suicides and fatal falls,” she said.

In addition, heavy drinkers have a greater risk of liver disease, heart disease, sleep disorders, depression, stroke, bleeding from the stomach, sexually transmitted infections from unsafe sex, and several types of cancer, Breslow said. They may also have problems managing diabetes, high blood pressure and other chronic conditions.

“Think before you drink,” she said. Adults over age 65 who are healthy and do not take medications should not have more than three drinks a day or seven drinks in a week, Breslow said.

“Based on your health and how alcohol affects you, you may need to drink less or not at all,” she added.

Another alcohol abuse expert also felt that the rise in binge drinking among older women was the most concerning finding in the study.

“We know that, overall, women are more sensitive to the negative health consequences of alcohol than men,” said Dr. J.C. Garbutt, medical director of the University of North Carolina Alcohol and Substance Abuse Program, in Chapel Hill.

“These consequences include liver disease, high blood pressure, stroke, heart disease and cognitive impairment — serious problems — and addiction to alcohol is possible as well,” he said.

Garbutt said he couldn’t explain the increase in binge drinking among older women.

“One would have to think there are major cultural factors at work, including the greater acceptability for women to drink, family structural changes, and perhaps greater access. But we really don’t know so it would be premature to speculate,” he said.

“Regardless, this speaks to the need to continue to educate the public about the harms of alcohol, including the increased risk to women and older individuals,” he said.

The report was published March 24 in the journal Alcoholism: Clinical and Experimental Research.

A study published last October also found the gap in drinking between men and women is closing.

Women across the globe are now nearly as likely as men to drink and to engage in excessive drinking, according to researchers with the National Drug and Alcohol Research Center at the University of New South Wales in Australia.

Soure:http://www.cbsnews.com

New study points to link between blue eyes, alcoholism.


  • New research out of the United States is pointing to a connection between blue eyes and alcoholism.According to the new study, people with blue eyes have a higher tendency to abuse alcohol than people with darker eyes.
  • The University of Vermont study published in the July issue of theAmerican Journal of Medical Geneticsfound a correlation between European American people with light-coloured eyes like blue, green, grey and light brown – have a higher tendency of alcoholism, with the highest levels of alcoholism found among subjects who had blue eyes.

    It seems simple and Dawei Li, an assistant professor at the school, and one of the study’s authors, admitted that “we still don’t know the reason” why the light colours are associated with heavy drinking.

    But the results do suggest “an intriguing possibility,” he said in a press release.

    Li’s co-author Arvis Sulovari said it does suggest “an intriguing possibility – that eye colour can be useful in the clinic for alcohol dependence diagnosis.”

    The study’s results were borne out of a database of more than 10,000 people who had been diagnosed with at least one form of psychiatric illness, including depression, and schizophrenia, as well as drug and alcohol addiction.

    From that database, the study’s authors filtered out 1,263 alcohol-dependent people and retested three times after noticing the connection to eye colour.

    It’s not the first time scientists have looked at the eye’s association with alcohol. A 2000 study also noted that people with lighter eyes are “more likely than dark-eyed individuals to abuse alcohol.”

    That study suggested the higher consumption was linked with greater alcohol tolerance among people with light eyes.

    Are blue-eyed people more likely to consume large amounts of alcohol? One study says yes.

 

Gabapentin Treatment for Alcohol Dependence.


A Randomized Clinical Trial

Importance  Approved medications for alcohol dependence are prescribed for less than 9% of US alcoholics.

Objective  To determine if gabapentin, a widely prescribed generic calcium channel/γ-aminobutyric acid–modulating medication, increases rates of sustained abstinence and no heavy drinking and decreases alcohol-related insomnia, dysphoria, and craving, in a dose-dependent manner.

Design, Participants and Setting  A 12-week, double-blind, placebo-controlled, randomized dose-ranging trial of 150 men and women older than 18 years with current alcohol dependence, conducted from 2004 through 2010 at a single-site, outpatient clinical research facility adjoining a general medical hospital.

Interventions  Oral gabapentin (dosages of 0 [placebo], 900 mg, or 1800 mg/d) and concomitant manual-guided counseling.

Main Outcomes and Measures  Rates of complete abstinence and no heavy drinking (coprimary) and changes in mood, sleep, and craving (secondary) over the 12-week study.

Results  Gabapentin significantly improved the rates of abstinence and no heavy drinking. The abstinence rate was 4.1% (95% CI, 1.1%-13.7%) in the placebo group, 11.1% (95% CI, 5.2%-22.2%) in the 900-mg group, and 17.0% (95% CI, 8.9%-30.1%) in the 1800-mg group (P = .04 for linear dose effect; number needed to treat [NNT] = 8 for 1800 mg). The no heavy drinking rate was 22.5% (95% CI, 13.6%-37.2%) in the placebo group, 29.6% (95% CI, 19.1%-42.8%) in the 900-mg group, and 44.7% (95% CI, 31.4%-58.8%) in the 1800-mg group (P = .02 for linear dose effect; NNT = 5 for 1800 mg). Similar linear dose effects were obtained with measures of mood (F2 = 7.37; P = .001), sleep (F2 = 136; P < .001), and craving (F2 = 3.56; P = .03). There were no serious drug-related adverse events, and terminations owing to adverse events (9 of 150 participants), time in the study (mean [SD], 9.1 [3.8] weeks), and rate of study completion (85 of 150 participants) did not differ among groups.

Conclusions and Relevance  Gabapentin (particularly the 1800-mg dosage) was effective in treating alcohol dependence and relapse-related symptoms of insomnia, dysphoria, and craving, with a favorable safety profile. Increased implementation of pharmacological treatment of alcohol dependence in primary care may be a major benefit of gabapentin as a treatment option for alcohol dependence.

Soure: JAMA

Anticonvulsant Promising for Alcohol Dependence.


The anticonvulsant gabapentin, a widely prescribed anticonvulsant used to treat epilepsy and neuropathic pain, is showing promise in the treatment of alcohol dependence, new research suggests.

Results from a 12-week, randomized, placebo-controlled trial show that participants taking 1800 mg of gabapentin were twice as likely to refrain from heavy drinking and 4 times as likely to stop drinking altogether compared with participants taking placebo.

“Gabapentin’s effect on drinking outcomes is at least as large or greater than those of existing FDA-approved treatments,” lead researcher Barbara Mason, PhD, Scripps Research Institute, La Jolla, California, said in a statement.

The study was published online November 4 in JAMA Internal Medicine.

Filling a Treatment Gap

According to investigators, gabapentin has the potential to fill a large gap in the treatment of alcohol dependence. They note that of the estimated 8.5 million alcohol-dependent Americans, statistics show that only 720,000 prescriptions were filled for US Food and Drug Administration (FDA)–approved medications for alcohol dependence in 2007, most of them prescribed by psychiatrists.

Previous studies of gabapentin for alcohol-dependent persons have suggested that the drug may be safe and effective, but conclusive results have been hampered by small sample size and methodologic or dosing issues.

To provide a more definitive evaluation of the drug for alcohol dependence, the researchers conducted a 12-week, double-blind, placebo-controlled, randomized, dose-ranging trial of 150 adults with current alcohol dependence who were attending a single outpatient center.

Participants were randomly assigned to receive 900 mg/day, 1800 mg/day, or placebo. All patients received concomitant counseling.

The study’s primary outcomes included sustained abstinence and no heavy drinking, and decreases in alcohol-related insomnia, dysphoria, and craving in a dose-dependent manner.

Results showed that gabapentin significantly improved the rates of abstinence and no heavy drinking with rates of 4.1% (95% confidence interval [CI], 1.1% – 13.7%) in the placebo group, 11.1% (85% CI, 5.2% – 22.2%) in the 900-mg group, and 17.0% (95% CI, 8.9% – 30.1%) in the 1800-mg group.

Further, the investigators report that the no-heavy-drinking rate was 22.5% (95% CI, 13.6% – 37.2%) in the placebo group, 29.6% (95% CI, 19.1% – 42.8%) in the 900-mg group, and 44.7% (95% CI, 31.4% – 58.8%) in the 1800-mg group.

In addition, the results showed that the drug significantly reduced cravings, depression, and sleeplessness. The researchers report that gabapentin had a favorable safety profile with no reports of serious adverse events.

According to Dr. Mason, gabapentin offers several potential advantages over the 3 other FDA-approved medications for alcohol dependence. It is “the only medication shown to improve sleep and mood in people who are quitting or reducing their drinking, and it’s already widely used in primary care ― that’s an appealing combination,” she said.

Broader Access to Treatment

In an accompanying editorial,Edward V. Nunes, MD, writes that the finding that gabapentin prevents relapse in alcohol-dependent patients is “an important development.”

“This well-designed and well-powered trial replicates the positive findings of several previous smaller trials,” Dr. Nunes writes.

He notes that a large proportion of alcohol-dependent patients presenting to family physicians fall into the mild to moderate range of alcohol dependence, which further suggests “the strong potential for gabapentin in the treatment of alcohol dependence in primary care.”

Acting director of the National Institute on Alcohol Abuse and Alcoholism, Kenneth R. Warren, PhD, said, “Gabapentin adds to the list of existing medications that have shown promise in treating alcohol dependence. We will continue to pursue research to expand the menu of treatment options available for alcoholism in the hopes of reaching more people.”

How Exercise Can Moderate Brain Damage Caused by Drinking.


brain-exercise

 

It’s well known that chronic, heavy drinking damages your brain and actually speeds up the brain shrinkage that occurs with age.  This is associated with memory loss, symptoms of dementia and cognitive decline.

Physical exercise is touted as one of the key ways to protect against brain shrinkage and other age-related brain changes, and now it appears it may help protect against some of the brain damage caused by drinking.

Exercise May Help Protect Your Brain From Alcohol-Related Damage

Among 60 long-time drinkers, those who were the most physically active had less damaged white matter in their brains compared to those who were less active.1The white matter is considered the “wiring” of your brain’s communication system, and is known to decline in quality with age and heavy alcohol consumption.

Although the study didn’t prove a cause-and-effect relationship, the researchers concluded that “exercise may protect WM [white matter] integrity from alcohol-related damage,” continuing:2

“We cannot say whether exercise would necessarily improve white matter damage in individuals with a history of heavy drinking.

However, our findings in combination with the many well-established positive physiological and psychological benefits of aerobic exercise suggest that aerobic exercise could be potentially helpful for individuals with history of heavy alcohol use.”

Exercise Protects Your Brain From Shrinkage, Slows Cognitive Decline

One of the effects of chronic heavy drinking is that it speeds the shrinkage of key regions in your brain. Exercise is useful in this area, as research has shown that people who engaged in the most physical exercise showed the least amount of brain shrinkage, a protective effect that was even greater than that offered by mentally stimulating activities.3

Exercise encourages your brain to work at optimum capacity by causing nerve cells to multiply, strengthening their interconnections and protecting them from damage.

During exercise, nerve cells release proteins known as neurotrophic factors, such as brain-derived neurotrophic factor or BDNF, which activates brain stem cells to convert into new neurons. BDNF also triggers numerous other chemicals that promote neural health.

Scientific evidence shows that physical exercise helps you build a brain that not only resists shrinkage, but also increases cognitive abilities.4 In one review of more than 100 studies, both aerobic and resistance training were found to be important for maintaining cognitive and brain health in old age.5

Moderate exercise may even reverse normal brain shrinkage by 2 percent, effectively reversing age-related hippocampus degeneration, which is associated with dementia and poor memory, by one to two years.6 On the other hand, the people in the control group who didn’t exercise saw an average of 1.4 percentdecrease in hippocampus size.

Exercise is a Powerful Tool for Brain Health for Drinkers and Non-Drinkers Alike

The hippocampus region of your brain increases in size as a response to exercise, making this activity a powerful tool to fight the onset of Alzheimer’s disease. The hippocampus, which is considered the memory center of your brain, is the first region of your brain to suffer shrinkage and impairment at the onset of Alzheimer’s disease, leading to memory problems and disorientation.

Other contributing factors to brain disease caused by the normal aging process may also include a decrease in blood flow to your brain, and the accumulation of environmental toxins in your brain. Exercise can help ameliorate both of these conditions by increasing blood flow to your brain, thereby increasing oxygen supply to your brain and encouraging a more vigorous release and removal of accumulated toxins through better blood circulation.

If you’re a regular drinker, this becomes even more important, as alcohol is a neurotoxin that can poison your brain. Increased blood flow may also promote delivery of more of the nutrients necessary to keep your brain cells healthy in the first place.

Brain Exercises are Better than Drugs in Preventing Cognitive Decline

Exercise has been shown to be better than mentally stimulating activities like brain training exercises at protecting your brain, but mental “exercise” is still important. In fact, new research shows it works better than drugs in preventing cognitive decline. The analysis of 32 trials found that mental exercise, such as computer-based brain training programs or memory, reasoning and speed-processing exercises, protected against cognitive decline better than leading dementia drugs like donepezil. Research into brain plasticity has proven that your brain continues to make new neurons throughout life in response to mental activity, which means that cognitive function can be improved, regardless of your age, and cognitive decline can be reversed.

If you’re interested in mental exercises for your brain, Dr. Michael Merzenich, professor emeritus at the University of California, who has pioneered research in brain plasticity for more than 30 years, has been instrumental in the development of a kind of “brain gym” environment — a computer-based brain training program that can help you sharpen a range of skills, from reading and comprehension to improved memorization and more. The program is called Brain HQ.7

“There are some very useful exercises in there that are for free, and you can actually drive improvements, for example, in brain speed, in the accuracy, with which the brain represents information in detail,” he says. “Basically, what you’re doing is reducing the chatter, the noisiness of the process of your brain. That impacts your capacity, for example, to record that information, to remember it. Because when the information is in its degraded form, when it’s fuzzy, when it’s imprecise, all of the uses of it – like your brain makes basically – are degraded.”

In the above-mentioned study, those who used computer-based training programs had significantly better memory and attention skills, improvements that were, in some cases, retained even five years later.

Another Reason for Chronic Heavy Drinkers to Take Up Exercise

There’s little doubt that exercise is one of the most important aspects of optimal health – not only for your brain but also for your entire body. That said, if you or someone you love has been affected by alcohol abuse, you know the great toll it can take on your personal relationships, work life and ability to function normally on a day-to-day basis, let alone fit in regular workouts.

The cravings for alcohol can become all-consuming and eventually an alcoholic does not feel “normal” until they’ve had a drink. The alcohol abuse inevitably throws off your circadian rhythm — the normal times you eat, sleep and wake up — as well, leading to a downward spiral of health and emotional effects. When you drink, it forces your brain to release unnaturally elevated levels of dopamine, a chemical your brain associates with rewarding behaviors. When you exercise, however, this same reward chemical is released, which means you can get the same “buzz” from working out that you can get from a six-pack of beer, with far better outcomes for your health.

This is why, if you know you’re prone to alcohol abuse or have a family history of alcohol addiction, exercising regularly can greatly reduce your risk of becoming dependent.

For those already addicted, exercise is beneficial too, and may actually help to lessen cravings. Research has found, in fact, that hamsters that ran the most consumed less alcohol, while less active hamsters had greater cravings for and consumption of alcohol.8  By replacing drinking with exercise, you may find that the rewarding feeling you get from exercise provides you with a suitable alternative to the rewarding feeling you previously got from alcohol.

What Type of Fitness Program is Best?

Ideally, to truly optimize your health, you’ll want to strive for a varied and well-rounded fitness program that incorporates a variety of exercises. As a general rule, as soon as an exercise becomes easy to complete, you need to increase the intensity and/or try another exercise to keep challenging your body. I recommend incorporating the following types of exercise into your program:

  • High-Intensity Interval (Anaerobic) Training: This is when you alternate short bursts of high-intensity exercise with gentle recovery periods.
  • Strength Training: Rounding out your exercise program with a 1-set strength training routine will ensure that you’re really optimizing the possible health benefits of a regular exercise program. You need enough repetitions to exhaust your muscles. The weight should be heavy enough that this can be done in fewer than 12 repetitions, yet light enough to do a minimum of four repetitions. It is also important NOT to exercise the same muscle groups every day. They need at least two days of rest to recover, repair and rebuild.
  • You can also “up” the intensity by slowing it down. For more information about using super slow weight training as a form of high-intensity interval exercise, please see my interview with Dr. Doug McGuff.
  • Core Exercises: Your body has 29 core muscles located mostly in your back, abdomen and pelvis. This group of muscles provides the foundation for movement throughout your entire body, and strengthening them can help protect and support your back, make your spine and body less prone to injury and help you gain greater balance and stability. Exercise programs like Pilates and yoga are also great for strengthening your core muscles, as are specific exercises you can learn from a personal trainer.
  • Stretching: My favorite type of stretching is active isolated stretching developed by Aaron Mattes. With Active Isolated Stretching (AIS), you hold each stretch for only two seconds, which works with your body’s natural physiological makeup to improve circulation and increase the elasticity of muscle joints. This technique also allows your body to repair itself and prepare for daily activity. You can also use devices like the Power Plate to help you stretch.

Source: .mercola.com

Alcohol calories ‘too often ignored’.


_65018786_red_wine-spl-1

A large glass of wine contains more than 170 calories .

People watching their weight should pay closer attention to how much alcohol they drink since it is second only to fat in terms of calorie content, say experts.

According to the World Cancer Research Fund, alcohol makes up nearly 10% of total calorie intake among drinkers.

Having a large glass of wine will cost you the same 178 calories as eating two chocolate digestive biscuits.

And it will take you more than a half hour’s brisk walk to burn off.

Empty calories

Eating or drinking too many calories on a regular basis can lead to weight gain.

Recent reports have shown that people are unaware of calories in drinks and don’t include them when calculating their daily consumption”

Kate Mendoza World Cancer Research Fund

But unlike food, alcoholic drinks have very little or no nutritional value.

The ’empty calories’ in drinks are often forgotten or ignored by dieters, says the WCRF.

Kate Mendoza, head of health information at WCRF, said: “Recent reports have shown that people are unaware of calories in drinks and don’t include them when calculating their daily consumption.”

Containing 7kcal/g, alcohol is only slightly less calorific than fat, which contains 9kcal/g.

Protein and carbohydrates contain 4kcal/g and fibre 2kcal/g.

Men need around 2,500 calories a day, and women around 2,000.

“Cutting down on drinking can have a big effect on weight loss or maintaining a healthy weight,” said Ms Mendoza.

It can also reduce your risk of cancer, she said.

Alcohol has been linked with breast, bowel, mouth and liver cancer.

If you don’t want to abstain entirely, there are ways that can help you cut down, including opting for smaller glass sizes, diluting alcohol with soda water or a low-calorie soft drink, alternating between alcoholic and non-alcoholic drinks and keeping a few nights each week booze-free.

WCRF has produced an Alcohol Calorie Calculator for different drinks that shows approximately how much exercise you would need to do to burn off the alcohol calories you consume.

Government guidelines recommend men should not regularly drink more than 3-4 units of alcohol a day, and women should limit themselves to 2-3 units a day.

A standard 175ml glass of wine contains about two units and a large 250ml glass contains about three units.

If you have had a heavy drinking session, you should avoid alcohol for at least 48 hours, experts advise.

Source:BBC