Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, CA.
Schizophr Bull. 2018 Oct 17;44(6):1350-1361. doi: 10.1093/schbul/sbx174.
New methods in genetics research, such as linkage disequilibrium score regression (LDSR), quantify overlap in the common genetic variants that influence diverse phenotypes. It is becoming clear that genetic effects often cut across traditional diagnostic boundaries. Here, we introduce genetic correlation analysis (using LDSR) to a nongeneticist audience and report transdisciplinary discoveries about schizophrenia. This analytical study design used publically available genome wide association study (GWAS) data from approximately 1.5 million individuals. Genetic correlations between schizophrenia and 172 medical, psychiatric, personality, and metabolomic phenotypes were calculated using LDSR, as implemented in LDHub in order to identify known and new genetic correlations. Consistent with previous research, the strongest genetic correlation was with bipolar disorder. Positive genetic correlations were also found between schizophrenia and all other psychiatric phenotypes tested, the personality traits of neuroticism and openness to experience, and cigarette smoking. Novel results were found with medical phenotypes: schizophrenia was negatively genetically correlated with serum citrate, positively correlated with inflammatory bowel disease, and negatively correlated with BMI, hip, and waist circumference. The serum citrate finding provides a potential link between rare cases of schizophrenia (strongly influenced by 22q11.2 deletions) and more typical cases of schizophrenia (with polygenic influences). Overall, these genetic correlation findings match epidemiological findings, suggesting that common variant genetic effects are part of the scaffolding underlying phenotypic comorbidity. The "genetic correlation profile" is a succinct report of shared genetic effects, is easily updated with new information (eg, from future GWAS), and should become part of basic disease knowledge about schizophrenia.
遗传学研究中的新方法,如连锁不平衡评分回归(LDSR),量化了影响多种表型的常见遗传变异的重叠。越来越明显的是,遗传效应通常跨越了传统的诊断界限。在这里,我们向非遗传学家介绍了遗传相关分析(使用 LDSR),并报告了关于精神分裂症的跨学科发现。这项分析性研究设计使用了大约 150 万人的公开全基因组关联研究(GWAS)数据。使用 LDSR 计算了精神分裂症与 172 种医学、精神科、人格和代谢表型之间的遗传相关性,该分析是在 LDHub 中实现的,以便识别已知和新的遗传相关性。与先前的研究一致,与双相情感障碍的最强遗传相关性。还发现精神分裂症与所有其他测试的精神科表型、神经质和开放性人格特质以及吸烟之间存在正遗传相关性。在医学表型方面发现了新的结果:精神分裂症与血清柠檬酸盐呈负遗传相关,与炎症性肠病呈正相关,与 BMI、臀部和腰围呈负相关。血清柠檬酸盐的发现为罕见的精神分裂症病例(受 22q11.2 缺失的强烈影响)和更典型的精神分裂症病例(受多基因影响)之间提供了潜在的联系。总体而言,这些遗传相关性发现与流行病学发现相匹配,表明常见变异的遗传效应是表型共病的基础结构的一部分。“遗传相关性图谱”是共享遗传效应的简洁报告,很容易用新信息(例如,来自未来的 GWAS)进行更新,并且应该成为关于精神分裂症的基本疾病知识的一部分。