Carey Caitlin E, Agrawal Arpana, Bucholz Kathleen K, Hartz Sarah M, Lynskey Michael T, Nelson Elliot C, Bierut Laura J, Bogdan Ryan
Department of Psychological and Brain Sciences, Washington University in St. Louis St. Louis, MO, USA.
Department of Psychiatry, Washington University School of Medicine St. Louis, MO, USA.
Front Genet. 2016 Aug 15;7:149. doi: 10.3389/fgene.2016.00149. eCollection 2016.
Despite evidence of substantial comorbidity between psychiatric disorders and substance involvement, the extent to which common genetic factors contribute to their co-occurrence remains understudied. In the current study, we tested for associations between polygenic risk for psychiatric disorders and substance involvement (i.e., ranging from ever-use to severe dependence) among 2573 non-Hispanic European-American participants from the Study of Addiction: Genetics and Environment. Polygenic risk scores (PRS) for cross-disorder psychopathology (CROSS) were generated based on the Psychiatric Genomics Consortium's Cross-Disorder meta-analysis and then tested for associations with a factor representing general liability to alcohol, cannabis, cocaine, nicotine, and opioid involvement (GENSUB). Follow-up analyses evaluated specific associations between each of the five psychiatric disorders which comprised CROSS-attention deficit hyperactivity disorder (ADHD), autism spectrum disorder (AUT), bipolar disorder (BIP), major depressive disorder (MDD), and schizophrenia (SCZ)-and involvement with each component substance included in GENSUB. CROSS PRS explained 1.10% of variance in GENSUB in our sample (p < 0.001). After correction for multiple testing in our follow-up analyses of polygenic risk for each individual disorder predicting involvement with each component substance, associations remained between: (A) MDD PRS and non-problem cannabis use, (B) MDD PRS and severe cocaine dependence, (C) SCZ PRS and non-problem cannabis use and severe cannabis dependence, and (D) SCZ PRS and severe cocaine dependence. These results suggest that shared covariance from common genetic variation contributes to psychiatric and substance involvement comorbidity.
尽管有证据表明精神疾病与物质使用之间存在大量共病现象,但共同的遗传因素在多大程度上导致它们同时出现仍未得到充分研究。在当前的研究中,我们在来自成瘾:遗传学与环境研究的2573名非西班牙裔欧美参与者中,测试了精神疾病的多基因风险与物质使用(即从曾经使用到严重依赖)之间的关联。基于精神病基因组学联盟的跨疾病荟萃分析生成了跨疾病精神病理学(CROSS)的多基因风险评分(PRS),然后测试其与代表酒精、大麻、可卡因、尼古丁和阿片类物质使用总体易感性的一个因素(GENSUB)之间的关联。后续分析评估了构成CROSS的五种精神疾病——注意力缺陷多动障碍(ADHD)、自闭症谱系障碍(AUT)、双相情感障碍(BIP)、重度抑郁症(MDD)和精神分裂症(SCZ)——与GENSUB中每种成分物质使用之间的具体关联。在我们的样本中,CROSS PRS解释了GENSUB中1.10%的方差(p < 0.001)。在对每种个体疾病的多基因风险预测每种成分物质使用的后续分析中进行多重检验校正后,以下关联仍然存在:(A)MDD PRS与无问题大麻使用,(B)MDD PRS与严重可卡因依赖,(C)SCZ PRS与无问题大麻使用和严重大麻依赖,以及(D)SCZ PRS与严重可卡因依赖。这些结果表明,常见遗传变异的共享协方差导致了精神疾病与物质使用的共病。