Bigdeli Tim B, Chatzinakos Chris, Bendl Jaroslav, Barr Peter B, Venkatesh Sanan, Gorman Bryan R, Clarence Tereza, Genovese Giulio, Iyegbe Conrad O, Peterson Roseann E, Kolokotronis Sergios-Orestis, Burstein David, Meyers Jacquelyn L, Li Yuli, Rajeevan Nallakkandi, Sayward Frederick, Cheung Kei-Hoi, DeLisi Lynn E, Kosten Thomas R, Zhao Hongyu, Achtyes Eric, Buckley Peter, Malaspina Dolores, Lehrer Douglas, Rapaport Mark H, Braff David L, Pato Michele T, Fanous Ayman H, Pato Carlos N, Huang Grant D, Muralidhar Sumitra, Michael Gaziano J, Pyarajan Saiju, Girdhar Kiran, Lee Donghoon, Hoffman Gabriel E, Aslan Mihaela, Fullard John F, Voloudakis Georgios, Harvey Philip D, Roussos Panos
VA New York Harbor Healthcare System, Brooklyn, NY.
Department of Psychiatry and Behavioral Sciences and SUNY Downstate Health Sciences University, Brooklyn, NY.
medRxiv. 2024 Aug 28:2024.08.27.24312631. doi: 10.1101/2024.08.27.24312631.
Large-scale genome-wide association studies of schizophrenia have uncovered hundreds of associated loci but with extremely limited representation of African diaspora populations. We surveyed electronic health records of 200,000 individuals of African ancestry in the Million Veteran and All of Us Research Programs, and, coupled with genotype-level data from four case-control studies, realized a combined sample size of 13,012 affected and 54,266 unaffected persons. Three genome-wide significant signals - near , , and - are the first to be independently identified in populations of predominantly African ancestry. Joint analyses of African, European, and East Asian ancestries across 86,981 cases and 303,771 controls, yielded 376 distinct autosomal loci, which were refined to 708 putatively causal variants via multi-ancestry fine-mapping. Utilizing single-cell functional genomic data from human brain tissue and two complementary approaches, transcriptome-wide association studies and enhancer-promoter contact mapping, we identified a consensus set of 94 genes across ancestries and pinpointed the specific cell types in which they act. We identified reproducible associations of schizophrenia polygenic risk scores with schizophrenia diagnoses and a range of other mental and physical health problems. Our study addresses a longstanding gap in the generalizability of research findings for schizophrenia across ancestral populations, underlining shared biological underpinnings of schizophrenia across global populations in the presence of broadly divergent risk allele frequencies.
大规模的精神分裂症全基因组关联研究已经发现了数百个相关位点,但非洲散居人群的代表性极其有限。我们在“百万退伍军人计划”和“我们所有人研究计划”中调查了20万名非洲裔个体的电子健康记录,并结合来自四项病例对照研究的基因型水平数据,最终获得了一个由13012名患者和54266名非患者组成的合并样本。三个全基因组显著信号——靠近 、 和 ——是首次在以非洲裔为主的人群中独立鉴定出来的。对86981例病例和303771例对照的非洲、欧洲和东亚血统进行联合分析,产生了376个不同的常染色体位点,通过多血统精细定位将其细化为708个推定的因果变异。利用来自人类脑组织的单细胞功能基因组数据以及两种互补方法——全转录组关联研究和增强子-启动子接触图谱分析,我们确定了一组跨血统的94个基因的共识集,并明确了它们发挥作用的特定细胞类型。我们确定了精神分裂症多基因风险评分与精神分裂症诊断以及一系列其他精神和身体健康问题之间的可重复关联。我们的研究填补了精神分裂症研究结果在不同祖先人群中普遍性方面长期存在的空白,强调了在全球人群中存在广泛不同的风险等位基因频率的情况下,精神分裂症具有共同的生物学基础。