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对精神分裂症与其他精神障碍的常见变异进行两两元分析,揭示了共享和独特的基因和基因集关联。

Pairwise common variant meta-analyses of schizophrenia with other psychiatric disorders reveals shared and distinct gene and gene-set associations.

机构信息

School of Biomedical Sciences and Pharmacy, The University of Newcastle, Callaghan, NSW, Australia.

Centre for Brain and Mental Health Research, Hunter Medical Research Institute, Newcastle, NSW, Australia.

出版信息

Transl Psychiatry. 2020 May 12;10(1):134. doi: 10.1038/s41398-020-0817-7.

Abstract

The complex aetiology of schizophrenia is postulated to share components with other psychiatric disorders. We investigated pleiotropy amongst the common variant genomics of schizophrenia and seven other psychiatric disorders using a multimarker association test. Transcriptomic imputation was then leveraged to investigate the functional significance of variation mapped to these genes, prioritising several interesting functional candidates. Gene-based analysis of common variation revealed 67 schizophrenia-associated genes shared with other psychiatric phenotypes, including bipolar disorder, major depressive disorder, ADHD and autism-spectrum disorder. In addition, we uncovered 78 genes significantly enriched with common variant associations for schizophrenia that were not linked to any of these seven disorders (P > 0.05). Multivariable gene-set association suggested that common variation enrichment within biologically constrained genes observed for schizophrenia also occurs across several psychiatric phenotypes. Pairwise meta-analysis of schizophrenia and each psychiatric phenotype was implemented and identified 330 significantly associated genes (P < 2.7 × 10) that were only nominally associated with each disorder individually (P < 0.05). These analyses consolidate the overlap between the genomic architecture of schizophrenia and other psychiatric disorders, uncovering several candidate pleiotropic genes which warrant further investigation.

摘要

精神分裂症的复杂病因被认为与其他精神障碍有共同的成分。我们使用多标记关联测试研究了精神分裂症和其他七种精神障碍的常见变异基因组学中的多效性。然后利用转录组内插来研究映射到这些基因的变异的功能意义,优先考虑了几个有趣的功能候选基因。常见变异的基因分析揭示了 67 个与其他精神表型(包括双相情感障碍、重度抑郁症、ADHD 和自闭症谱系障碍)相关的精神分裂症相关基因。此外,我们还发现了 78 个与精神分裂症常见变异关联显著相关的基因,这些基因与这七种疾病均无关联(P > 0.05)。多变量基因集关联表明,精神分裂症中观察到的生物约束基因内常见变异的富集也发生在几种精神障碍表型中。对精神分裂症和每种精神障碍进行了成对的荟萃分析,并确定了 330 个显著相关的基因(P < 2.7 × 10),这些基因与每种疾病的单独关联仅具有名义上的相关性(P < 0.05)。这些分析整合了精神分裂症和其他精神障碍的基因组结构之间的重叠,揭示了几个值得进一步研究的候选多效性基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8316/7217970/939fd12d5fb1/41398_2020_817_Fig1_HTML.jpg

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