Martin Joanna, Hamshere Marian L, Stergiakouli Evangelia, O'Donovan Michael C, Thapar Anita
MRC Centre for Neuropsychiatric Genetics and Genomics, Institute of Psychological Medicine and Clinical Neurosciences, Cardiff University, Cardiff, UK.
MRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.
J Child Psychol Psychiatry. 2015 Jun;56(6):648-56. doi: 10.1111/jcpp.12336. Epub 2014 Oct 3.
The genetic architecture of ADHD is complex, with rare and common variants involved. Common genetic variants (as indexed by a composite risk score) associated with clinical ADHD significantly predict ADHD and autistic-like behavioural traits in children from the general population, suggesting that ADHD lies at the extreme of normal trait variation. ADHD and other neurodevelopmental disorders share neurocognitive difficulties in several domains (e.g. impaired cognitive ability and executive functions). We hypothesised that ADHD composite genetic risk scores derived from clinical ADHD cases would also contribute to variation in neurocognitive abilities in the general population.
Children (N = 6,832) from a UK population cohort, the Avon Longitudinal Study of Parents and Children (ALSPAC), underwent neurocognitive testing. Parent-reported measures of their children's ADHD and autistic-like traits were used to construct a behavioural latent variable of 'neurodevelopmental traits'. Composite genetic risk scores for ADHD were calculated for ALSPAC children based on findings from an independent ADHD case-control genome-wide association study. Structural equation modelling was used to assess associations between ADHD composite genetic risk scores and IQ, working memory, inhibitory control and facial emotion recognition, as well as the latent 'neurodevelopmental trait' measure.
The results confirmed that neurocognitive and neurodevelopmental traits are correlated in children in the general population. Composite genetic risk scores for ADHD were independently associated with lower IQ (β = -.05, p < .001) and working memory performance (β = -.034, p = .013), even after accounting for the relationship with latent neurodevelopmental behavioural trait scores. No associations were found between composite genetic risk scores and inhibitory control or emotion recognition (p > .05).
These findings suggest that common genetic variants relevant to clinically diagnosed ADHD have pleiotropic effects on neurocognitive traits as well as behavioural dimensions in the general population. This further suggests that the well-recognised association between cognition and neurodevelopmental behavioural traits is underpinned at a biological level.
注意力缺陷多动障碍(ADHD)的遗传结构复杂,涉及罕见和常见变异。与临床ADHD相关的常见遗传变异(以综合风险评分表示)能显著预测普通人群中儿童的ADHD及类似自闭症的行为特征,这表明ADHD处于正常特质变异的极端情况。ADHD和其他神经发育障碍在多个领域存在神经认知困难(如认知能力和执行功能受损)。我们假设,从临床ADHD病例得出的ADHD综合遗传风险评分也会导致普通人群神经认知能力的差异。
来自英国人群队列“埃文亲子纵向研究”(ALSPAC)的儿童(N = 6832名)接受了神经认知测试。采用父母报告的其子女ADHD及类似自闭症特征的测量方法,构建“神经发育特征”的行为潜变量。基于一项独立的ADHD病例对照全基因组关联研究结果,为ALSPAC儿童计算ADHD综合遗传风险评分。采用结构方程模型评估ADHD综合遗传风险评分与智商、工作记忆、抑制控制和面部情绪识别之间的关联,以及与潜在“神经发育特征”测量值之间的关联。
结果证实,普通人群中的儿童神经认知和神经发育特征存在相关性。即使在考虑了与潜在神经发育行为特征评分的关系后,ADHD综合遗传风险评分仍与较低的智商(β = -0.05,p < 0.001)和工作记忆表现(β = -0.034,p = 0.013)独立相关。未发现综合遗传风险评分与抑制控制或情绪识别之间存在关联(p > 0.05)。
这些发现表明,与临床诊断的ADHD相关的常见遗传变异对普通人群的神经认知特征以及行为维度具有多效性影响。这进一步表明,认知与神经发育行为特征之间广为人知的关联在生物学层面有其基础。