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多基因谱定义了注意缺陷多动障碍临床异质性的各个方面。

Polygenic profiles define aspects of clinical heterogeneity in attention deficit hyperactivity disorder.

机构信息

Institute of Biological Psychiatry, Mental Health Center Sct. Hans, Mental Health Services Copenhagen, Roskilde, Denmark.

The Lundbeck Foundation Initiative for Integrative Psychiatric Research, Copenhagen, Denmark.

出版信息

Nat Genet. 2024 Feb;56(2):234-244. doi: 10.1038/s41588-023-01593-7. Epub 2023 Nov 30.

Abstract

Attention deficit hyperactivity disorder (ADHD) is a complex disorder that manifests variability in long-term outcomes and clinical presentations. The genetic contributions to such heterogeneity are not well understood. Here we show several genetic links to clinical heterogeneity in ADHD in a case-only study of 14,084 diagnosed individuals. First, we identify one genome-wide significant locus by comparing cases with ADHD and autism spectrum disorder (ASD) to cases with ADHD but not ASD. Second, we show that cases with ASD and ADHD, substance use disorder and ADHD, or first diagnosed with ADHD in adulthood have unique polygenic score (PGS) profiles that distinguish them from complementary case subgroups and controls. Finally, a PGS for an ASD diagnosis in ADHD cases predicted cognitive performance in an independent developmental cohort. Our approach uncovered evidence of genetic heterogeneity in ADHD, helping us to understand its etiology and providing a model for studies of other disorders.

摘要

注意缺陷多动障碍(ADHD)是一种复杂的疾病,其长期结果和临床表现存在差异。这种异质性的遗传贡献尚不清楚。在这里,我们通过对 14084 名确诊个体的仅病例研究,显示了 ADHD 临床异质性的几个遗传联系。首先,我们通过比较 ADHD 合并自闭症谱系障碍(ASD)与 ADHD 但不合并 ASD 的病例,确定了一个全基因组显著的位点。其次,我们表明,ASD 合并 ADHD、物质使用障碍合并 ADHD、或首次成年后被诊断为 ADHD 的病例,具有独特的多基因评分(PGS)特征,可将其与互补病例亚组和对照区分开来。最后,ADHD 病例的 ASD 诊断 PGS 可预测独立发展队列中的认知表现。我们的方法揭示了 ADHD 遗传异质性的证据,帮助我们了解其病因,并为其他疾病的研究提供了模型。

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