TY  - JOUR
PY  - 2022//
TI  - Common and distinguishing genetic factors for substance use behavior and disorder: an integrated analysis of genomic and transcriptomic studies from both human and animal studies
JO  - Addiction
A1  - Chang, Xiang-Wen
A1  - Sun, Yan
A1  - Muhai, Jia-Na
A1  - Li, Yang-Yang
A1  - Chen, Yun
A1  - Lu, Lin
A1  - Chang, Su-Hua
A1  - Shi, Jie
SP  - ePub
EP  - ePub
VL  - ePub
IS  - ePub
N2  - BACKGROUND AND AIMS: Genomic and transcriptomic findings greatly broaden the biological knowledge regarding substance use. However, systematic convergence and comparison evidence of genome-wide findings is lacking for substance use. Here, we combined all the genome-wide findings from both substance use behavior and disorder (SUBD) and identified common and distinguishing genetic factors for different SUBDs. <br><br>METHODS: Systemic literature search for genome-wide association (GWAS) and RNA-seq studies of alcohol/nicotine/drug use behavior (partially meets or no-reported diagnostic criteria) and disorder (AUBD, NUBD, DUBD) was performed using PubMed and GWAS Catalog. Drug use was focused on cannabis, opioid, cocaine, methamphetamine use. GWAS studies required case-control or case/cohort samples. RNA-seq studies were based on brain tissues. The genes which contained significant single nucleotide polymorphism (p≤1×10(-6) ) in GWAS and reported as significant in RNA-seq studies were extracted. Pathway enrichment was performed by using Metascape. Gene interaction networks were identified by using the Protein Interaction Network Analysis database. <br><br>RESULTS: Total SUBD-related 2910 genes were extracted from 75 GWAS studies (2,773,889 participants) and 17 RNA-seq studies. By overlapped the genes and pathways of AUBD, NUBD, and DUBD, 4 shared genes (CACNB2, GRIN2B, PLXDC2, and PKNOX2), 4 shared pathways (2 GO terms of 'modulation of chemical synaptic transmission', 'regulation of trans-synaptic signaling', 2 KEGG pathways of 'Dopaminergic synapse', 'Cocaine addiction') were identified (significantly higher than random, p<1×10(-5) ). The top shared KEGG pathways (B-H corrected p-value<0.05) in the pairwise comparison of AUBD vs. DUBD, NUBD vs. DUBD, AUBD vs. NUBD were "Epstein-Barr virus infection", "protein processing in endoplasmic reticulum", and "neuroactive ligand-receptor interaction" respectively. We also identified substance-specific genetic factors: i.e., ADH1B and ALDH2 were unique for AUBD, while CHRNA3 and CHRNA4 for NUBD. <br><br>CONCLUSIONS: This systematic review identifies the shared and unique genes and pathways for alcohol, nicotine, and drug use behaviors and disorders at the genome-wide level and highlights critical biological processes for the common and distinguishing vulnerability of substance use behaviors and disorders.<p />  <p>Language: en</p>
LA  - en
SN  - 0965-2140
UR  - http://dx.doi.org/10.1111/add.15908
ID  - ref1
ER  -