4.1 Article

Common genetic substrates of alcohol and substance use disorder severity revealed by pleiotropy detection against GWAS catalog in two populations

期刊

ADDICTION BIOLOGY
卷 26, 期 1, 页码 -

出版社

WILEY
DOI: 10.1111/adb.12877

关键词

admixed population; alcohol use disorders; comorbidity; genetics; pleiotropy; substance use disorders

资金

  1. National Center on Minority Health and Health Disparities [5R37 AA010201]
  2. National Institute on Alcohol Abuse and Alcoholism [5R37 AA010201, K25 AA025095, R01 AA026248, R01 AA027316]
  3. National Institute on Drug Abuse [R01 DA030976]
  4. NIAAA [5R37 AA010201, R01 AA026248, R01 AA027316]
  5. National Institute on Drug Abuse (NIDA) [R01 DA030976]
  6. National Center on Minority Health and Health Disparities (NCMHD) [5R37 AA010201]
  7. National Institutes of Health (NIH): National Institute on Alcohol Abuse and Alcoholism (NIAAA) [K25 AA025095]

向作者/读者索取更多资源

The study investigates the genetic associations of alcohol and other substance use disorders and identifies potential pleiotropic gene variants using a machine learning approach. Differences in the expression and regulation of pleiotropic genes for different substance use disorders in different populations highlight the complexity of genetic factors involved in these disorders.
Alcohol and other substance use disorders (AUD and SUD) are complex diseases that are postulated to have a polygenic inheritance and are often comorbid with other disorders. The comorbidities may arise partially through genetic pleiotropy. Identification of specific gene variants accounting for large parts of the variance in these disorders has yet to be accomplished. We describe a flexible strategy that takes a variant-trait association database and determines if a subset of disease/straits are potentially pleiotropic with the disorder under study. We demonstrate its usage in a study of use disorders in two independent cohorts: alcohol, stimulants, cannabis (CUD), and multi-substance use disorders (MSUD) in American Indians (AI) and AUD and CUD in Mexican Americans (MA). Using a machine learning method with variants in GWAS catalog, we identified 229 to 246 pleiotropic variants for AI and 153 to 160 for MA for each SUD. Inflammation was the most enriched for MSUD and AUD in AIs. Neurological disorder was the most significantly enriched for CUD in both cohorts, and for AUD and stimulants in AIs. Of the select pleiotropic genes shared among substances-cohorts, multiple biological pathways implicated in SUD and other psychiatric disorders were enriched, including neurotrophic factors, immune responses, extracellular matrix, and circadian regulation. Shared pleiotropic genes were significantly up-regulated in brain regions playing important roles in SUD, down-regulated in esophagus mucosa, and differentially regulated in adrenal gland. This study fills a gap for pleiotropy detection in understudied admixed populations and identifies pleiotropic variants that may be potential targets of interest for SUD.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.1
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据