Influence of Genetic Background in Alcohol Dependency

PECRis located within broad linkage peaks for several alcohol-related traits,including alcoholism66,comorbid alcoholism and depression67, level of response to alcohol68, and amplitude of the P3(00)response69, 70. Moreover, aggressive marketing strategies by alcohol brands, offering promotions and discounts, can further entice individuals, especially those with a genetic predisposition to alcoholism, to indulge more than they might have otherwise. It’s crucial for regulatory bodies to monitor and control such influences, ensuring that they don’t exacerbate the substance use disorders already prevalent in society.

As whole exome and whole genome sequencingtechnologies come down in cost, they are being applied to identifying rarevariants. For studies of rare variants, families are quite valuable for sortingout true positives from the background of individual variations that we allharbor. The GI tract is exposed to very high levels of alcohol as it passes throughthe mouth, esophagus, stomach and intestinal tract, and most ethanol passes throughthe liver before entering alcohol definition, formula, and facts the circulation. Alcohol levels in common drinks rangefrom approximately 5% (1.1 M) for beer, 11-15% for wine (∼3M) and 40% for spirits (∼9 M). The oral cavity and esophagus aredirectly exposed to those levels, and the liver is exposed to high levels from theportal circulation. Thus it is not surprising that diseases of the GI system,including cirrhosis, pancreatitis, and cancers of the upper GI tract are affected byalcohol consumption80-86.

Current power and sample size estimates for GWAS with effect sizes of 1.05–1.2 range from 30,000 – 120,000 (Owen et al., 2010; Schizophrenia Working Group of the Psychiatric Genomics, 2014). While the use of a stringent P-value for GWAS avoids the detection of false positive findings, it might also miss ‘true’ variants. Recent attempts to address this issue have used pathway analysis and polygenic risk score approaches (Gelernter et al., 2014) but have not been widely applied to AUD genetic analyses. Alcohol Use Disorder (AUD) is a chronic psychiatric condition characterized by drinking patterns that lead to detrimental emotional, physical, and social outcomes. The Centers for Disease Control and Prevention (CDC) has reported that alcohol use contributes to approximately 88,000 deaths annually in the United States (Stahre et al., 2014), reflecting high morbidity and mortality. To diagnose individuals with AUD, the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (Mizokawa et al., 2013) utilizes 11 criteria pertaining to excessive alcohol use, alcohol abuse, and alcohol dependence.

It is hoped that such information will ultimately lead to improved prevention and treatment efforts. In addition to gene discovery, recent molecular genetics research has focused on modeling the aggregate effects of variants across the genome and leveraging other types of ‘omics’ data to further our understanding of the genetic architecture underlying AUD. Often referred to as “Post-GWAS” approaches, these methods have been used to demonstrate the highly polygenic nature of alcohol-related traits, estimate the heritability and co-heritability of traits, test causal relations between traits, and aid in gene discovery [25,38]. In regions where alcohol is either prohibitively expensive or challenging to procure, there’s a noticeable reduction in alcohol problems and misuse.

Although studies in recent years have identified a plethora of genes that may play a role in determining risk of alcoholism, much work remains to be done. Therefore, it will be critical to confirm these associations in additional studies. A failure to replicate the initial findings may not always disprove the association but may result from differences in the genetic background of the study participants, the environment, or the study design (e.g., differences in the definition of alcohol dependence).

  1. According to the National Institute on Alcohol Abuse and Alcoholism (NIAAA), 5.6% of adults in the United States were living with alcohol use disorder in 2019.
  2. While genetics can play a significant role in your overall AUD risk assessment, it isn’t the only factor that can elevate your chances of developing AUD.
  3. More than 800,000 of the people affected are children between the ages of 12 and 17 years.
  4. Those with a history of alcoholism in their family have the highest risk of becoming alcoholics.
  5. By the same measure, those who choose not to drink alcohol at all during their lives will not develop AUD, even if they are unknowingly at high risk, genetically speaking.

First and perhaps foremost, most studies ofalcohol-related phenotypes have been small – hundreds or a few thousandsamples. Most robust associations that have been reported in common disease haveemployed tens of thousands of samples and are now beginning to combine severalstudies of these magnitude into even larger meta analyses. The alcohol researchcommunity has begun to form larger consortia for meta-analyses and it is anticipatedthat with the resulting increase in sample size the number of robust associationswill increase. A second approach that will likely benefit the alcohol researchcommunity will be greater examination of pathways or gene sets. These approacheshave been quite fruitful for some studies and need to be employed in analyses ofalcohol-related traits and phenotypes. Over the next few years, we anticipate theidentification of additional common and rare variants contributing to the risk ofalcohol dependence.

Research has illuminated that genetics is a significant factor in the risk of developing Alcohol Use Disorder (AUD), but it’s not the only one. A comprehensive review by the University of Cambridge, which analyzed 12 studies involving twins and adopted children, found that genetics accounts for about half of the risk for alcoholism. Recent research from Indiana University has shed light on the significant role genes play in the development of alcohol use disorders (AUDs). The study, led by Feng Zhou, Ph.D., professor emeritus of anatomy, cell biology, and physiology at IU School of Medicine, discovered that altering a group of genes known to influence neuronal plasticity and pain perceptions is linked to AUDs. The National Institute on Alcohol Abuse and Alcoholism (NIAAA), a subset of the government’s health-focused .gov entities, has been at the forefront of alcohol research.

The Role of Environment in Alcoholism

Despite the evidence supporting the prominence of genetic factors in AUD’s etiology, the identification of genetic risk variants has been difficult and labor intensive. With recent advances in technology, the most promising results stem from recent GWAS, which have helped to identify new variants in the genetics of AUD. Among the variants identified, the most significant SNPs remain in the alcohol metabolism enzyme genes, ADH and ALDH. Importantly, the prevalence of the various isoforms of ADH and ALDH differs among ethnicities and populations.

Analysis of social media language using AI models predicts depression severity for white Americans, but not Black Americans

Instead, the awareness should prod you to protect yourself from the damage that alcohol could bring to your life and health. This underscores the importance of early intervention and awareness, especially in homes where family members have a history of alcohol-related issues. Data suggests that individuals hailing from families with an annual household income surpassing $75,000 face a higher susceptibility to becoming an alcoholic in comparison to their counterparts from economically modest backgrounds. Genetic diseases, on the other hand, are illnesses that are caused by mutations in the person’s DNA. Our genes determine our physical traits and, to some extent, our behavioral characteristics. But does that mean your chance of addiction is essentially a coin flip if you have a family history of SUD?

The study highlighted genes with silent mutations affecting alcohol use and emphasized the significance of studying gene groups over individual genes. The world around you also can play a significant role in opening a door that leads to problematic substance use, notes Dr. Anand. Research shows that genetics have somewhere between a 40% and 60% influence on addiction. Recognizing alcoholism as a disease promotes early intervention, access to appropriate healthcare services, and ongoing support for people struggling with AUD. While alcohol addiction isn’t entirely preventable, specific measures can reduce its risk. The environment in which people live and work heavily affects their attitudes and drinking behaviors.

This led to an 85 % decrease in ALDH2 activity in the liver and inhibited voluntary ethanol consumption up to 50 % (Ocaranza et al. 2008). Furthermore, studies with an adenoviral vector containing a multiple expression cassette showed that simultaneous increase of ADH and decrease of ALDH2 activities in the liver dramatically reduced voluntarily ethanol consumption of alcohol-dependent animals (Rivera-Meza et al. 2012). A review of studies from 2020, which looked at a genome-wide analysis of more than 435,000 people, found 29 different genetic variants that increased the risk of problematic drinking. It is now appreciated that a whole spectrum of allele frequencies andeffect sizes may play roles, from common variations with small effects throughrare variants of large effect.

New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders

A changing definition of the heterogeneous phenotype of AUD may also pose a challenge to identifying genetic variants through GWAS. The above studies used the DSM-IV-TR criteria for alcohol dependence in order to define the phenotype. As the field of psychiatry how does alcohol affect blood pressure transitions to the DSM-5 criteria for AUD, there may also be changes in the functional variants identified by GWAS. Future GWAS should focus on the endophenotypes of AUD in order to better understand the genetic connections to specific behavioral symptoms.

Physiological effects of alcohol

We want to give recovering addicts the tools to return to the outside world completely substance-free and successful. Ark Behavioral Health offers 100% confidential substance abuse assessment and treatment placement tailored to your individual needs. By the same measure, those who choose not to drink alcohol at all during their lives will not develop AUD, even if they are unknowingly at high risk, genetically speaking.

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