3.8 Article

An Update on the Role of Common Genetic Variation Underlying Substance Use Disorders

Journal

CURRENT GENETIC MEDICINE REPORTS
Volume 8, Issue 2, Pages 35-46

Publisher

SPRINGERNATURE
DOI: 10.1007/s40142-020-00184-w

Keywords

Substance use disorders; Addiction genetics; Psychiatric genetics; Genome-wide association studies; Single-nucleotide polymorphism; Statistical genetics

Funding

  1. NIAAA [F32AA027435]
  2. NIMH [MH109532]
  3. NIDA [K02DA32573]
  4. American Foundation for Suicide Prevention [YIG-0-064-18]
  5. Washington University in St. Louis (Division of Biology and Biological Sciences)

Ask authors/readers for more resources

Purpose of the ReviewSample size increases have resulted in novel and replicable loci for substance use disorders (SUDs). We summarize some of the latest insights into SUD genetics and discuss next steps for the field.Recent FindingsGenome-wide association studies have substantiated the role of previously known variants (e.g., rs1229984 in ADH1B for alcohol) and identified several novel loci for alcohol, tobacco, cannabis, opioid, and cocaine use disorders. SUDs are genetically correlated with psychiatric outcomes, while liability to substance use is inconsistently associated with these outcomes and more closely associated with lifestyle factors. Specific variant associations appear to differ somewhat across populations, although similar genes and systems are implicated.SummaryThe next decade of human genetic studies of addiction should focus on expanding to non-European populations, consider pleiotropy across SUDs and with other psychiatric disorders, and leverage human and cross-species functional data to elucidate the biological mechanisms underlying SUDs.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

3.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available