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自闭症表型异质性的遗传相关性。

Genetic correlates of phenotypic heterogeneity in autism.

机构信息

Autism Research Centre, Department of Psychiatry, University of Cambridge, Cambridge, UK.

Nic Waals Institute, Lovisenberg Diaconal Hospital, Oslo, Norway.

出版信息

Nat Genet. 2022 Sep;54(9):1293-1304. doi: 10.1038/s41588-022-01072-5. Epub 2022 Jun 2.

Abstract

The substantial phenotypic heterogeneity in autism limits our understanding of its genetic etiology. To address this gap, here we investigated genetic differences between autistic individuals (n = 12,893) based on core and associated features of autism, co-occurring developmental disabilities and sex. We conducted a comprehensive factor analysis of core autism features in autistic individuals and identified six factors. Common genetic variants were associated with the core factors, but de novo variants were not. We found that higher autism polygenic scores (PGS) were associated with lower likelihood of co-occurring developmental disabilities in autistic individuals. Furthermore, in autistic individuals without co-occurring intellectual disability (ID), autism PGS are overinherited by autistic females compared to males. Finally, we observed higher SNP heritability for autistic males and for autistic individuals without ID. Deeper phenotypic characterization will be critical in determining how the complex underlying genetics shape cognition, behavior and co-occurring conditions in autism.

摘要

自闭症表型存在显著异质性,限制了我们对其遗传病因的理解。为了解决这一差距,我们在此基于自闭症的核心和相关特征、共患发育障碍和性别,调查了自闭症个体(n=12893)之间的遗传差异。我们对自闭症个体的核心自闭症特征进行了全面的因子分析,确定了六个因素。常见的遗传变异与核心因素相关,但新生变异则不相关。我们发现,较高的自闭症多基因评分(PGS)与自闭症个体共患发育障碍的可能性降低相关。此外,在没有共患智力障碍(ID)的自闭症个体中,自闭症 PGS 在自闭症女性中比男性更多地被遗传。最后,我们观察到自闭症男性和无 ID 的自闭症个体的 SNP 遗传力更高。更深入的表型特征分析对于确定复杂的潜在遗传学如何影响自闭症患者的认知、行为和共患情况至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/535e/9470531/4eb3bc5a1d70/41588_2022_1072_Fig1_HTML.jpg

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