Washington University in St. Louis, St. Louis, Missouri.
Washington University in St. Louis, St. Louis, Missouri.
Biol Psychiatry. 2017 Nov 15;82(10):709-715. doi: 10.1016/j.biopsych.2017.04.020. Epub 2017 Jun 6.
There are high levels of comorbidity between schizophrenia and substance use disorder, but little is known about the genetic etiology of this comorbidity.
We tested the hypothesis that shared genetic liability contributes to the high rates of comorbidity between schizophrenia and substance use disorder. To do this, polygenic risk scores for schizophrenia derived from a large meta-analysis by the Psychiatric Genomics Consortium were computed in three substance use disorder datasets: the Collaborative Genetic Study of Nicotine Dependence (ascertained for tobacco use disorder; n = 918 cases; 988 control subjects), the Collaborative Study on the Genetics of Alcoholism (ascertained for alcohol use disorder; n = 643 cases; 384 control subjects), and the Family Study of Cocaine Dependence (ascertained for cocaine use disorder; n = 210 cases; 317 control subjects). Phenotypes were harmonized across the three datasets and standardized analyses were performed. Genome-wide genotypes were imputed to the 1000 Genomes reference panel.
In each individual dataset and in the mega-analysis, strong associations were observed between any substance use disorder diagnosis and the polygenic risk score for schizophrenia (mega-analysis pseudo-R range 0.8-3.7%; minimum p = 4 × 10).
These results suggest that comorbidity between schizophrenia and substance use disorder is partially attributable to shared polygenic liability. This shared liability is most consistent with a general risk for substance use disorder rather than specific risks for individual substance use disorders and adds to increasing evidence of a blurred boundary between schizophrenia and substance use disorder.
精神分裂症和物质使用障碍之间存在高度共病,但对于这种共病的遗传病因知之甚少。
我们检验了以下假设:共享遗传易感性导致精神分裂症和物质使用障碍的高共病率。为此,我们计算了来自精神疾病基因组学联盟(Psychiatric Genomics Consortium)的一项大型荟萃分析的精神分裂症多基因风险评分,该分析在三个物质使用障碍数据集进行:合作尼古丁依赖遗传学研究(以确定烟草使用障碍;n=918 例病例;988 名对照)、合作酒精使用障碍遗传学研究(以确定酒精使用障碍;n=643 例病例;384 名对照)和可卡因依赖家庭研究(以确定可卡因使用障碍;n=210 例病例;317 名对照)。三个数据集之间的表型进行了协调,进行了标准化分析。全基因组基因型被内插到 1000 个基因组参考面板。
在每个单独的数据集和荟萃分析中,任何物质使用障碍诊断与精神分裂症的多基因风险评分之间都存在强烈关联(荟萃分析伪 R 范围为 0.8-3.7%;最小 p=4×10)。
这些结果表明,精神分裂症和物质使用障碍之间的共病部分归因于共享的多基因易感性。这种共同的易感性最符合物质使用障碍的一般风险,而不是个体物质使用障碍的特定风险,并增加了越来越多的证据表明精神分裂症和物质使用障碍之间的界限模糊。