Wellcome Trust Clinical Research Fellow, MRC Centre for Neuropsychiatric Genetics and Genomics,Cardiff University,UK.
PhD Student, MRC Centre for Neuropsychiatric Genetics and Genomics,Cardiff University,UK.
Br J Psychiatry. 2019 May;214(5):297-304. doi: 10.1192/bjp.2018.301. Epub 2019 Feb 15.
Rare copy number variants (CNVs) are associated with risk of neurodevelopmental disorders characterised by varying degrees of cognitive impairment, including schizophrenia, autism spectrum disorder and intellectual disability. However, the effects of many individual CNVs in carriers without neurodevelopmental disorders are not yet fully understood, and little is known about the effects of reciprocal copy number changes of known pathogenic loci.AimsWe aimed to analyse the effect of CNV carrier status on cognitive performance and measures of occupational and social outcomes in unaffected individuals from the UK Biobank.
We called CNVs in the full UK Biobank sample and analysed data from 420 247 individuals who passed CNV quality control, reported White British or Irish ancestry and were not diagnosed with neurodevelopmental disorders. We analysed 33 pathogenic CNVs, including their reciprocal deletions/duplications, for association with seven cognitive tests and four general measures of functioning: academic qualifications, occupation, household income and Townsend Deprivation Index.
Most CNVs (24 out of 33) were associated with reduced performance on at least one cognitive test or measure of functioning. The changes on the cognitive tests were modest (average reduction of 0.13 s.d.) but varied markedly between CNVs. All 12 schizophrenia-associated CNVs were associated with significant impairments on measures of functioning.
CNVs implicated in neurodevelopmental disorders, including schizophrenia, are associated with cognitive deficits, even among unaffected individuals. These deficits may be subtle but CNV carriers have significant disadvantages in educational attainment and ability to earn income in adult life.Declaration of interestNone.
罕见的拷贝数变异(CNVs)与认知障碍程度不同的神经发育障碍的风险相关,包括精神分裂症、自闭症谱系障碍和智力障碍。然而,许多在没有神经发育障碍的携带者中的个体 CNV 的影响尚未完全理解,并且对于已知致病性基因座的相互拷贝数变化的影响知之甚少。
我们旨在分析 CNV 携带者状态对英国生物银行中未受影响个体的认知表现和职业及社会结果测量的影响。
我们在全英国生物银行样本中调用了 CNVs,并分析了通过 CNV 质量控制、报告白种英国或爱尔兰血统且未被诊断为神经发育障碍的 420247 名个体的数据。我们分析了 33 个致病性 CNVs,包括它们的相互缺失/重复,以确定其与七种认知测试和四种一般功能测量之间的关联:学术资格、职业、家庭收入和汤森贫困指数。
大多数 CNVs(33 个中的 24 个)与至少一项认知测试或功能测量的表现降低有关。认知测试的变化幅度不大(平均减少 0.13 个标准差),但在 CNV 之间差异显著。所有 12 个与精神分裂症相关的 CNVs 与功能测量的显著障碍有关。
包括精神分裂症在内的神经发育障碍相关的 CNVs 与认知缺陷有关,即使在未受影响的个体中也是如此。这些缺陷可能很微妙,但 CNV 携带者在受教育程度和成年后赚取收入的能力方面存在显著劣势。
无。