精神分裂症(面向对象编程)
错误发现率
全基因组关联研究
遗传建筑学
多效性
影像遗传学
脑形态计量学
大脑大小
神经影像学
生物
维加维斯
生命银行
基因组学
遗传学
数量性状位点
心理学
神经科学
医学
基因组
单核苷酸多态性
精神科
基因
表型
基因型
磁共振成像
放射科
作者
Dennis van der Meer,Alexey A. Shadrin,Kevin S. O’Connell,Francesco Bettella,Srdjan Djurovic,Thomas Wolfers,Dag Alnæs,Ingrid Agartz,Olav B. Smeland,Ingrid Melle,Jennifer Sánchez,David Edmund Johannes Linden,Anders M. Dale,Lars T. Westlye,Ole A. Andreassen,Oleksandr Frei,Tobias Kaufmann
标识
DOI:10.1016/j.biopsych.2021.12.007
摘要
Schizophrenia is a complex polygenic disorder with subtle, distributed abnormalities in brain morphology. There are indications of shared genetic architecture between schizophrenia and brain measures despite low genetic correlations. Through the use of analytical methods that allow for mixed directions of effects, this overlap may be leveraged to improve our understanding of underlying mechanisms of schizophrenia and enrich polygenic risk prediction outcome.We ran a multivariate genome-wide analysis of 175 brain morphology measures using data from 33,735 participants of the UK Biobank and analyzed the results in a conditional false discovery rate together with schizophrenia genome-wide association study summary statistics of the Psychiatric Genomics Consortium (PGC) Wave 3. We subsequently created a pleiotropy-enriched polygenic score based on the loci identified through the conditional false discovery rate approach and used this to predict schizophrenia in a nonoverlapping sample of 743 individuals with schizophrenia and 1074 healthy controls.We found that 20% of the loci and 50% of the genes significantly associated with schizophrenia were also associated with brain morphology. The conditional false discovery rate analysis identified 428 loci, including 267 novel loci, significantly associated with brain-linked schizophrenia risk, with functional annotation indicating high relevance for brain tissue. The pleiotropy-enriched polygenic score explained more variance in liability than conventional polygenic scores across several scenarios.Our results indicate strong genetic overlap between schizophrenia and brain morphology with mixed directions of effect. The results also illustrate the potential of exploiting polygenetic overlap between brain morphology and mental disorders to boost discovery of brain tissue-specific genetic variants and its use in polygenic risk frameworks.
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