注意缺陷多动障碍
自闭症谱系障碍
病因学
遗传异质性
多基因风险评分
队列
神经发育障碍
自闭症
临床心理学
生物
心理学
精神科
遗传学
医学
表型
基因
内科学
基因型
单核苷酸多态性
作者
Sonja LaBianca,Isabell Brikell,Dorte Helenius,Robert J. Loughnan,Joel Mefford,Clare E. Palmer,Rebecca L. Walker,Jesper R. Gådin,Morten Dybdahl Krebs,Vivek Appadurai,Morteza Vaez,Esben Agerbo,Marianne Giørtz Pedersen,Anders Dupont Børglum,DAVID MICHAEL HOUGAARD,Ole N Mors,Merete Nordentoft,Preben Bo Mortensen,Kenneth S. Kendler,Terry L. Jernigan
出处
期刊:Nature Genetics
[Nature Portfolio]
日期:2023-11-30
卷期号:56 (2): 234-244
被引量:32
标识
DOI:10.1038/s41588-023-01593-7
摘要
Abstract Attention deficit hyperactivity disorder (ADHD) is a complex disorder with heterogeneous clinical presentations that manifest variability in long-term outcomes. The genetic contributions to this clinical heterogeneity, however, are not well understood. Here, we study 14 084 individuals diagnosed with ADHD to identify several genetic factors underlying clinical heterogeneity. One genome-wide significant locus was specifically associated with an autism spectrum disorder (ASD) diagnosis among individuals diagnosed with ADHD and it was not previously associated with ASD nor ADHD, individually. We used a novel approach to compare profiles of polygenic scores for groups of individuals diagnosed with ADHD and uncovered robust evidence that biology is an important factor in on-going clinical debates. Specifically, individuals diagnosed with ASD and ADHD, substance use disorder (SUD) and ADHD, or first diagnosed with ADHD in adulthood had different profiles of polygenic scores for ADHD and multiple other psychiatric, cognitive, and socio-behavioral traits. A polygene overlap between an ASD diagnosis in ADHD and cognitive performance was replicated in an independent, typically developing cohort. Our unique approach uncovered evidence of genetic heterogeneity in a widely studied complex disorder, allowing for timely contributions to the understanding of ADHD etiology and providing a model for similar studies of other disorders.
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