• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

致病性拷贝数变异携带者的认知表现和功能结局:英国生物库分析。

Cognitive performance and functional outcomes of carriers of pathogenic copy number variants: analysis of the UK Biobank.

机构信息

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.

出版信息

Br J Psychiatry. 2019 May;214(5):297-304. doi: 10.1192/bjp.2018.301. Epub 2019 Feb 15.

DOI:10.1192/bjp.2018.301
PMID:30767844
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6520248/
Abstract

BACKGROUND

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.

METHOD

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

背景

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。

目的

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。

方法

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。

结果

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。

结论

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。

利益声明

无。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2927/6536830/7883ddb097b9/S000712501800301X_fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2927/6536830/d25fe60eb51a/S000712501800301X_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2927/6536830/7e2d36e758fb/S000712501800301X_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2927/6536830/7883ddb097b9/S000712501800301X_fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2927/6536830/d25fe60eb51a/S000712501800301X_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2927/6536830/7e2d36e758fb/S000712501800301X_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2927/6536830/7883ddb097b9/S000712501800301X_fig3.jpg

相似文献

1
Cognitive performance and functional outcomes of carriers of pathogenic copy number variants: analysis of the UK Biobank.致病性拷贝数变异携带者的认知表现和功能结局:英国生物库分析。
Br J Psychiatry. 2019 May;214(5):297-304. doi: 10.1192/bjp.2018.301. Epub 2019 Feb 15.
2
Cognitive Performance Among Carriers of Pathogenic Copy Number Variants: Analysis of 152,000 UK Biobank Subjects.致病性拷贝数变异携带者的认知表现:152000 名英国生物银行参与者的分析。
Biol Psychiatry. 2017 Jul 15;82(2):103-110. doi: 10.1016/j.biopsych.2016.08.014. Epub 2016 Aug 18.
3
Association of Rare Copy Number Variants With Risk of Depression.罕见拷贝数变异与抑郁风险的关联。
JAMA Psychiatry. 2019 Aug 1;76(8):818-825. doi: 10.1001/jamapsychiatry.2019.0566.
4
Genotype-phenotype associations in children with copy number variants associated with high neuropsychiatric risk in the UK (IMAGINE-ID): a case-control cohort study.英国与高神经精神疾病风险相关的拷贝数变异儿童的基因型-表型关联研究(IMAGINE-ID):一项病例对照队列研究
Lancet Psychiatry. 2019 Jun;6(6):493-505. doi: 10.1016/S2215-0366(19)30123-3. Epub 2019 May 2.
5
Clinical Characterization of Copy Number Variants Associated With Neurodevelopmental Disorders in a Large-scale Multiancestry Biobank.大型多血统生物样本库中与神经发育障碍相关的拷贝数变异的临床特征
JAMA Psychiatry. 2022 Mar 1;79(3):250-259. doi: 10.1001/jamapsychiatry.2021.4080.
6
Reciprocal Copy Number Variations at 22q11.2 Produce Distinct and Convergent Neurobehavioral Impairments Relevant for Schizophrenia and Autism Spectrum Disorder.22q11.2 上的相互拷贝数变异导致明显且趋同的神经行为损伤,与精神分裂症和自闭症谱系障碍相关。
Biol Psychiatry. 2020 Aug 1;88(3):260-272. doi: 10.1016/j.biopsych.2019.12.028. Epub 2020 Jan 13.
7
Medical consequences of pathogenic CNVs in adults: analysis of the UK Biobank.成人致病性 CNV 的医学后果:英国生物银行分析。
J Med Genet. 2019 Mar;56(3):131-138. doi: 10.1136/jmedgenet-2018-105477. Epub 2018 Oct 20.
8
Analysis of common genetic variation and rare CNVs in the Australian Autism Biobank.澳大利亚自闭症生物样本库中常见遗传变异与罕见 CNVs 的分析。
Mol Autism. 2021 Feb 10;12(1):12. doi: 10.1186/s13229-020-00407-5.
9
The contribution of copy number variants to psychiatric symptoms and cognitive ability.拷贝数变异对精神症状和认知能力的影响。
Mol Psychiatry. 2023 Apr;28(4):1480-1493. doi: 10.1038/s41380-023-01978-4. Epub 2023 Feb 3.
10
Effects of pathogenic CNVs on physical traits in participants of the UK Biobank.致病性拷贝数变异对英国生物银行参与者身体特征的影响。
BMC Genomics. 2018 Dec 4;19(1):867. doi: 10.1186/s12864-018-5292-7.

引用本文的文献

1
A pattern-learning algorithm associates copy number variations with brain structure and behavioural variables in an adolescent population cohort.一种模式学习算法将青少年群体队列中的拷贝数变异与脑结构和行为变量联系起来。
Nat Biomed Eng. 2025 Jul 18. doi: 10.1038/s41551-025-01454-0.
2
Targeting the Roots of Psychosis: The Role of Aberrant Salience.针对精神病根源:异常突显的作用。
Pediatr Rep. 2025 Jun 4;17(3):63. doi: 10.3390/pediatric17030063.
3
Autism Spectrum Disorder: Genetic Mechanisms and Inheritance Patterns.自闭症谱系障碍:遗传机制与遗传模式

本文引用的文献

1
Medical consequences of pathogenic CNVs in adults: analysis of the UK Biobank.成人致病性 CNV 的医学后果:英国生物银行分析。
J Med Genet. 2019 Mar;56(3):131-138. doi: 10.1136/jmedgenet-2018-105477. Epub 2018 Oct 20.
2
Measuring and Estimating the Effect Sizes of Copy Number Variants on General Intelligence in Community-Based Samples.在社区样本中测量和估计拷贝数变异对一般智力的影响大小。
JAMA Psychiatry. 2018 May 1;75(5):447-457. doi: 10.1001/jamapsychiatry.2018.0039.
3
Comparison of Sociodemographic and Health-Related Characteristics of UK Biobank Participants With Those of the General Population.
Genes (Basel). 2025 Apr 23;16(5):478. doi: 10.3390/genes16050478.
4
The interplay between genomic copy number variants, sleep, and cognition in the general population.普通人群中基因组拷贝数变异、睡眠与认知之间的相互作用。
Res Sq. 2025 Mar 19:rs.3.rs-5200475. doi: 10.21203/rs.3.rs-5200475/v1.
5
Healthy sleep patterns and risk of hospitalization for infection: a large community-based cohort study.健康睡眠模式与感染住院风险:一项基于社区的大型队列研究。
Transl Psychiatry. 2025 Mar 27;15(1):100. doi: 10.1038/s41398-025-03314-6.
6
Large familial chromosomal duplications without apparent disease phenotypes: how to deal with them in prenatal diagnosis?无明显疾病表型的大型家族性染色体重复:产前诊断中如何应对?
Pediatr Res. 2025 Jan 29. doi: 10.1038/s41390-025-03895-4.
7
Effects of gene dosage on cognitive ability: A function-based association study across brain and non-brain processes.基因剂量对认知能力的影响:一项基于功能的跨大脑和非大脑过程的关联研究。
Cell Genom. 2024 Dec 11;4(12):100721. doi: 10.1016/j.xgen.2024.100721.
8
Genome-wide copy number variation association study in anorexia nervosa.神经性厌食症的全基因组拷贝数变异关联研究。
Mol Psychiatry. 2025 May;30(5):2009-2016. doi: 10.1038/s41380-024-02811-2. Epub 2024 Nov 12.
9
Prenatal diagnosis and postnatal follow-up of 15 fetuses with 16p13.11 microduplication syndrome.15例16p13.11微重复综合征胎儿的产前诊断及产后随访
Front Genet. 2024 Oct 15;15:1486974. doi: 10.3389/fgene.2024.1486974. eCollection 2024.
10
A genome-first study of sex chromosome aneuploidies provides evidence of Y chromosome dosage effects on autism risk.一项基于基因组的性染色体非整倍体研究提供了证据,表明 Y 染色体剂量对自闭症风险的影响。
Nat Commun. 2024 Oct 15;15(1):8897. doi: 10.1038/s41467-024-53211-7.
英国生物银行参与者与普通人群的社会人口学特征及健康相关特征比较。
Am J Epidemiol. 2017 Nov 1;186(9):1026-1034. doi: 10.1093/aje/kwx246.
4
Cognitive Performance Among Carriers of Pathogenic Copy Number Variants: Analysis of 152,000 UK Biobank Subjects.致病性拷贝数变异携带者的认知表现:152000 名英国生物银行参与者的分析。
Biol Psychiatry. 2017 Jul 15;82(2):103-110. doi: 10.1016/j.biopsych.2016.08.014. Epub 2016 Aug 18.
5
Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia.智力残疾拷贝数变异与精神分裂症相关性分析
JAMA Psychiatry. 2016 Sep 1;73(9):963-969. doi: 10.1001/jamapsychiatry.2016.1831.
6
Copy number variations and cognitive phenotypes in unselected populations.未选择人群中的拷贝数变异与认知表型
JAMA. 2015 May 26;313(20):2044-54. doi: 10.1001/jama.2015.4845.
7
Refining analyses of copy number variation identifies specific genes associated with developmental delay.对拷贝数变异分析的细化鉴定出与发育迟缓相关的特定基因。
Nat Genet. 2014 Oct;46(10):1063-71. doi: 10.1038/ng.3092. Epub 2014 Sep 14.
8
CNVs conferring risk of autism or schizophrenia affect cognition in controls.CNVs 导致自闭症或精神分裂症的风险会影响对照组的认知能力。
Nature. 2014 Jan 16;505(7483):361-6. doi: 10.1038/nature12818. Epub 2013 Dec 18.
9
Analysis of copy number variations at 15 schizophrenia-associated loci.15个精神分裂症相关基因座的拷贝数变异分析。
Br J Psychiatry. 2014 Feb;204(2):108-14. doi: 10.1192/bjp.bp.113.131052. Epub 2013 Dec 5.
10
The penetrance of copy number variations for schizophrenia and developmental delay.拷贝数变异在精神分裂症和发育迟缓中的外显率。
Biol Psychiatry. 2014 Mar 1;75(5):378-85. doi: 10.1016/j.biopsych.2013.07.022. Epub 2013 Aug 28.