• 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

ADHD 的遗传结构及其与其他精神障碍和认知相关表型的重叠。

Genetic architecture of ADHD and overlap with other psychiatric disorders and cognition-related phenotypes.

机构信息

Department of Mental Health, Hospital Universitari Vall d'Hebron, Barcelona, Spain; Psychiatric Genetics Unit, Group of Psychiatry, Mental Health and Addiction, Vall d'Hebron Research Institute (VHIR), Universitat Autònoma de Barcelona, Barcelona, Spain; Biomedical Network Research Centre on Mental Health (CIBERSAM), Barcelona, Spain; Department of Genetics, Microbiology, and Statistics, Faculty of Biology, Universitat de Barcelona, Barcelona, Spain.

Biomedical Network Research Centre on Mental Health (CIBERSAM), Barcelona, Spain; Department of Genetics, Microbiology, and Statistics, Faculty of Biology, Universitat de Barcelona, Barcelona, Spain; Institut de Biomedicina de la Universitat de Barcelona (IBUB), Barcelona, Catalonia, Spain; Institut de Recerca Sant Joan de Déu (IRSJD), Esplugues de Llobregat, Catalonia, Spain.

出版信息

Neurosci Biobehav Rev. 2023 Oct;153:105313. doi: 10.1016/j.neubiorev.2023.105313. Epub 2023 Jul 13.

DOI:10.1016/j.neubiorev.2023.105313
PMID:37451654
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10789879/
Abstract

Attention-deficit/hyperactivity disorder (ADHD) co-occurs with many other psychiatric disorders and traits. In this review, we summarize and interpret the existing literature on the genetic architecture of these comorbidities based on hypothesis-generating approaches. Quantitative genetic studies indicate that genetic factors play a substantial role in the observed co-occurrence of ADHD with many different disorders and traits. Molecular genetic correlations derived from genome-wide association studies and results of studies based on polygenic risk scores confirm the general pattern but provide effect estimates that are smaller than those from twin studies. The identification of the specific genetic variants and biological pathways underlying co-occurrence using genome-wide approaches is still in its infancy. The first analyses of causal inference using genetic data support causal relationships between ADHD and comorbid disorders, although bidirectional effects identified in some instances point to complex relationships. While several issues in the methodology and inferences from the results are still to be overcome, this review shows that the co-occurrence of ADHD with many psychiatric disorders and traits is genetically interpretable.

摘要

注意缺陷多动障碍(ADHD)与许多其他精神疾病和特征共病。在这篇综述中,我们根据产生假设的方法总结和解释了这些共病的遗传结构的现有文献。定量遗传学研究表明,遗传因素在 ADHD 与许多不同的疾病和特征的观察到的共病中起着重要作用。来自全基因组关联研究的分子遗传相关性和基于多基因风险评分的研究结果证实了一般模式,但提供的效应估计值小于来自双胞胎研究的效应估计值。使用全基因组方法确定共病的具体遗传变异和生物学途径仍处于起步阶段。使用遗传数据进行因果推理的首次分析支持 ADHD 与共病障碍之间的因果关系,尽管在某些情况下确定的双向效应表明存在复杂的关系。虽然在方法学和结果推论方面仍有一些问题需要克服,但本综述表明,ADHD 与许多精神疾病和特征的共病在遗传上是可解释的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8224/10789879/962c88c1c345/nihms-1953276-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8224/10789879/6405da649e80/nihms-1953276-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8224/10789879/962c88c1c345/nihms-1953276-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8224/10789879/6405da649e80/nihms-1953276-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8224/10789879/962c88c1c345/nihms-1953276-f0002.jpg

相似文献

1
Genetic architecture of ADHD and overlap with other psychiatric disorders and cognition-related phenotypes.ADHD 的遗传结构及其与其他精神障碍和认知相关表型的重叠。
Neurosci Biobehav Rev. 2023 Oct;153:105313. doi: 10.1016/j.neubiorev.2023.105313. Epub 2023 Jul 13.
2
Association of Polygenic Risk for Attention-Deficit/Hyperactivity Disorder With Co-occurring Traits and Disorders.注意缺陷多动障碍多基因风险与共患特征和障碍的关联。
Biol Psychiatry Cogn Neurosci Neuroimaging. 2018 Jul;3(7):635-643. doi: 10.1016/j.bpsc.2017.11.013. Epub 2017 Dec 14.
3
Insights into attention-deficit/hyperactivity disorder from recent genetic studies.从最近的遗传学研究看注意缺陷多动障碍。
Psychol Med. 2021 Oct;51(13):2274-2286. doi: 10.1017/S0033291721000982. Epub 2021 Apr 5.
4
Genetic risk for attention-deficit/hyperactivity disorder contributes to neurodevelopmental traits in the general population.注意缺陷多动障碍的遗传风险对普通人群的神经发育特征有影响。
Biol Psychiatry. 2014 Oct 15;76(8):664-71. doi: 10.1016/j.biopsych.2014.02.013. Epub 2014 Feb 25.
5
Attention-deficit/hyperactivity disorder polygenic risk scores predict attention problems in a population-based sample of children.注意缺陷多动障碍多基因风险评分可预测基于人群的儿童注意力问题。
J Am Acad Child Adolesc Psychiatry. 2014 Oct;53(10):1123-9.e6. doi: 10.1016/j.jaac.2014.06.014. Epub 2014 Aug 19.
6
[The Genetic Basis of ADHD - An Update].[注意缺陷多动障碍的遗传基础——最新进展]
Z Kinder Jugendpsychiatr Psychother. 2021 May;50(3):203-217. doi: 10.1024/1422-4917/a000868.
7
Novel Loci Associated With Attention-Deficit/Hyperactivity Disorder Are Revealed by Leveraging Polygenic Overlap With Educational Attainment.利用与受教育程度的多基因重叠,揭示了与注意缺陷多动障碍相关的新基因座。
J Am Acad Child Adolesc Psychiatry. 2018 Feb;57(2):86-95. doi: 10.1016/j.jaac.2017.11.013. Epub 2017 Nov 26.
8
Charting the Landscape of Genetic Overlap Between Mental Disorders and Related Traits Beyond Genetic Correlation.绘制精神障碍及相关特征遗传重叠的图谱:超越遗传关联。
Am J Psychiatry. 2022 Nov 1;179(11):833-843. doi: 10.1176/appi.ajp.21101051. Epub 2022 Sep 7.
9
Shared genetic influences between attention-deficit/hyperactivity disorder (ADHD) traits in children and clinical ADHD.儿童注意力缺陷/多动障碍(ADHD)特质与临床ADHD之间的共同遗传影响。
J Am Acad Child Adolesc Psychiatry. 2015 Apr;54(4):322-7. doi: 10.1016/j.jaac.2015.01.010. Epub 2015 Jan 29.
10
Association of Genetic Risk Variants With Attention-Deficit/Hyperactivity Disorder Trajectories in the General Population.普通人群中基因风险变异与注意力缺陷/多动障碍轨迹的关联
JAMA Psychiatry. 2016 Dec 1;73(12):1285-1292. doi: 10.1001/jamapsychiatry.2016.2817.

引用本文的文献

1
Revisiting the Role of Serotonin in Attention-Deficit Hyperactivity Disorder: New Insights from Preclinical and Clinical Studies.重新审视血清素在注意力缺陷多动障碍中的作用:临床前和临床研究的新见解
Clin Drug Investig. 2025 Sep 3. doi: 10.1007/s40261-025-01473-4.
2
Maternal exacerbating and protective factors that shape the prevalence and severity of child attention-deficit hyperactivity disorder: a narrative review.影响儿童注意力缺陷多动障碍患病率和严重程度的母体加重因素和保护因素:一项叙述性综述
Front Psychiatry. 2025 May 29;16:1577707. doi: 10.3389/fpsyt.2025.1577707. eCollection 2025.
3
Umbilical cord length and neurodevelopmental disorders, a national cohort study.

本文引用的文献

1
Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses.利用全基因组分析探讨抑郁症的发病机制、复发风险预测和共患精神障碍。
Nat Med. 2023 Jul;29(7):1832-1844. doi: 10.1038/s41591-023-02352-1. Epub 2023 Jul 18.
2
Anxiety, mood, and substance use disorders in adult men and women with and without attention-deficit/hyperactivity disorder: A substantive and methodological overview.成人注意缺陷多动障碍患者与非注意缺陷多动障碍患者的焦虑、心境及物质使用障碍:实质性与方法学综述。
Neurosci Biobehav Rev. 2023 Aug;151:105209. doi: 10.1016/j.neubiorev.2023.105209. Epub 2023 May 5.
3
脐带长度与神经发育障碍:一项全国队列研究
PLoS One. 2025 Apr 23;20(4):e0322444. doi: 10.1371/journal.pone.0322444. eCollection 2025.
4
Neurobiology of attention-deficit hyperactivity disorder: historical challenges and emerging frontiers.注意缺陷多动障碍的神经生物学:历史挑战与新兴前沿。
Nat Rev Neurosci. 2024 Dec;25(12):759-775. doi: 10.1038/s41583-024-00869-z. Epub 2024 Oct 24.
5
Navigating the Intersection of Technology and Depression Precision Medicine.探索技术与抑郁症精准医学的交汇点。
Adv Exp Med Biol. 2024;1456:401-426. doi: 10.1007/978-981-97-4402-2_20.
6
Increased burden of rare protein-truncating variants in constrained, brain-specific and synaptic genes in extremely impulsively violent males with antisocial personality disorder.具有反社会人格障碍的极度冲动暴力男性中,受约束的、大脑特异性和突触基因中罕见蛋白截断变异的负担增加。
Genes Brain Behav. 2024 Feb;23(1):e12882. doi: 10.1111/gbb.12882.
7
Genetic contribution to the comorbidity between attention-deficit/hyperactivity disorder and substance use disorders.遗传因素对注意缺陷多动障碍与物质使用障碍共病的影响。
Psychiatry Res. 2024 Mar;333:115758. doi: 10.1016/j.psychres.2024.115758. Epub 2024 Feb 3.
Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains.
全基因组分析 ADHD 确定 27 个风险位点,细化遗传结构,并暗示几个认知领域。
Nat Genet. 2023 Feb;55(2):198-208. doi: 10.1038/s41588-022-01285-8. Epub 2023 Jan 26.
4
Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroups.自闭症谱系障碍、注意缺陷多动障碍及亚组病例的共享和差异遗传结构的鉴定。
Nat Genet. 2022 Oct;54(10):1470-1478. doi: 10.1038/s41588-022-01171-3. Epub 2022 Sep 26.
5
Mendelian randomization analysis for attention deficit/hyperactivity disorder: studying a broad range of exposures and outcomes.孟德尔随机化分析注意力缺陷/多动障碍:研究广泛的暴露和结局。
Int J Epidemiol. 2023 Apr 19;52(2):386-402. doi: 10.1093/ije/dyac128.
6
Genetic architecture of 11 major psychiatric disorders at biobehavioral, functional genomic and molecular genetic levels of analysis.分析生物行为、功能基因组和分子遗传学水平上 11 种主要精神疾病的遗传结构。
Nat Genet. 2022 May;54(5):548-559. doi: 10.1038/s41588-022-01057-4. Epub 2022 May 5.
7
An integrated framework for local genetic correlation analysis.用于局部遗传相关性分析的综合框架。
Nat Genet. 2022 Mar;54(3):274-282. doi: 10.1038/s41588-022-01017-y. Epub 2022 Mar 14.
8
Exploring the Contribution to ADHD of Genes Involved in Mendelian Disorders Presenting with Hyperactivity and/or Inattention.探讨孟德尔疾病相关基因对表现为多动和/或注意力不集中的 ADHD 的贡献。
Genes (Basel). 2021 Dec 30;13(1):93. doi: 10.3390/genes13010093.
9
Comprehensive exploration of the genetic contribution of the dopaminergic and serotonergic pathways to psychiatric disorders.全面探索多巴胺能和血清素能通路对精神疾病的遗传贡献。
Transl Psychiatry. 2022 Jan 10;12(1):11. doi: 10.1038/s41398-021-01771-3.
10
Simultaneous estimation of bi-directional causal effects and heritable confounding from GWAS summary statistics.从 GWAS 汇总统计数据中同时估计双向因果效应和可遗传混杂。
Nat Commun. 2021 Dec 14;12(1):7274. doi: 10.1038/s41467-021-26970-w.