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注意缺陷多动障碍的遗传学方面

Genetic aspects in attention-deficit/hyperactivity disorder.

作者信息

Albayrak O, Friedel S, Schimmelmann B G, Hinney A, Hebebrand J

机构信息

Department of Child and Adolescent Psychiatry, Rheinische Kliniken Essen, University of Duisburg-Essen, Essen, Germany.

出版信息

J Neural Transm (Vienna). 2008;115(2):305-15. doi: 10.1007/s00702-007-0839-9. Epub 2008 Jan 16.

DOI:10.1007/s00702-007-0839-9
PMID:18200432
Abstract

Attention-deficit/hyperactivity disorder (ADHD) is a common psychiatric disorder among children and adolescents with high heritability. Molecular genetic findings support the thesis that dopaminergic, serotonergic, and noradrenergic neurotransmission pathways account for the etiology of this complex disease. Genetic research comprises formal genetic studies, candidate gene studies, linkage analyses, and recently large-scale genome wide association studies, gene-environement interaction studies, and pharmacogenetics. This article comprehensively reviews the latest findings on the genetics of ADHD.

摘要

注意缺陷多动障碍(ADHD)是儿童和青少年中一种常见的精神疾病,具有高度遗传性。分子遗传学研究结果支持这样一种观点,即多巴胺能、血清素能和去甲肾上腺素能神经传递途径是这种复杂疾病病因的基础。遗传学研究包括正式遗传学研究、候选基因研究、连锁分析,以及最近的大规模全基因组关联研究、基因-环境相互作用研究和药物遗传学。本文全面综述了ADHD遗传学的最新研究结果。

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本文引用的文献

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Adrenergic alpha2A receptor gene and response to methylphenidate in attention-deficit/hyperactivity disorder-predominantly inattentive type.肾上腺素能α2A受体基因与注意缺陷多动障碍(主要为注意力不集中型)对哌甲酯的反应
J Neural Transm (Vienna). 2008;115(2):341-5. doi: 10.1007/s00702-007-0835-0. Epub 2008 Jan 16.
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Norepinephrine transporter and catecholamine-O-methyltransferase gene variants and attention-deficit/hyperactivity disorder symptoms in adults.去甲肾上腺素转运体和儿茶酚-O-甲基转移酶基因变异与成人注意力缺陷多动障碍症状
J Neural Transm (Vienna). 2008;115(2):323-9. doi: 10.1007/s00702-007-0822-5. Epub 2007 Nov 12.
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注意缺陷多动障碍的诊断与治疗监测潜力:与基因型和自身免疫相互作用的新型表观遗传生物标志物。
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No Evidence for Association Between Norepinephrine Transporter-3081 (A/T) Polymorphism and Attention Deficit Hyperactivity Disorder in Iranian Population.在伊朗人群中,无证据表明去甲肾上腺素转运体-3081(A/T)多态性与注意力缺陷多动障碍之间存在关联。
Iran Red Crescent Med J. 2015 Jul 23;17(7):e22996. doi: 10.5812/ircmj.229961v2. eCollection 2015 Jul.
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Focusing on Cause or Cure?: Priorities and Stakeholder Presence in Childhood Psychiatry Research.关注病因还是治疗?儿童精神病学研究中的优先事项与利益相关者参与情况
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Attention deficit hyperactivity disorder.注意缺陷多动障碍
Curr Top Behav Neurosci. 2014;16:235-66. doi: 10.1007/7854_2013_249.
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Bipolar disorder risk alleles in children with ADHD.双相障碍风险等位基因在 ADHD 儿童中。
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Inattention symptoms predict level of depression in early childhood.注意缺陷症状可预测儿童早期的抑郁水平。
Postgrad Med. 2013 Jan;125(1):154-61. doi: 10.3810/pgm.2013.01.2630.
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A high density linkage disequilibrium mapping in 14 noradrenergic genes: evidence of association between SLC6A2, ADRA1B and ADHD.14 个去甲肾上腺素能基因的高密度连锁不平衡图谱:SLC6A2、ADRA1B 和 ADHD 之间关联的证据。
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Genetic risks and ADHD symptomatology: exploring the effects of parental antisocial behaviors in an adoption-based study.遗传风险与 ADHD 症状:在基于收养的研究中探索父母反社会行为的影响。
Child Psychiatry Hum Dev. 2012 Apr;43(2):293-305. doi: 10.1007/s10578-011-0263-0.
An exploratory study of the relationship between four candidate genes and neurocognitive performance in adult ADHD.
一项关于四种候选基因与成人注意力缺陷多动障碍神经认知表现之间关系的探索性研究。
Am J Med Genet B Neuropsychiatr Genet. 2008 Apr 5;147(3):397-402. doi: 10.1002/ajmg.b.30595.
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Association and linkage of allelic variants of the dopamine transporter gene in ADHD.注意力缺陷多动障碍中多巴胺转运体基因等位变异的关联与连锁
Mol Psychiatry. 2007 Oct;12(10):923-33. doi: 10.1038/sj.mp.4001986. Epub 2007 Apr 10.
5
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.对14000例七种常见疾病患者及3000例共享对照进行全基因组关联研究。
Nature. 2007 Jun 7;447(7145):661-78. doi: 10.1038/nature05911.
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A meta-analysis of association studies between the 10-repeat allele of a VNTR polymorphism in the 3'-UTR of dopamine transporter gene and attention deficit hyperactivity disorder.多巴胺转运体基因3'-UTR区VNTR多态性10重复等位基因与注意缺陷多动障碍关联研究的荟萃分析。
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Investigation of parent-of-origin effects in ADHD candidate genes.注意缺陷多动障碍候选基因的亲本来源效应研究。
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Confirmation that a specific haplotype of the dopamine transporter gene is associated with combined-type ADHD.多巴胺转运体基因的特定单倍型与复合型注意力缺陷多动障碍相关的确认。
Am J Psychiatry. 2007 Apr;164(4):674-7. doi: 10.1176/ajp.2007.164.4.674.
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What genome-wide association studies can do for medicine.全基因组关联研究对医学的作用。
N Engl J Med. 2007 Mar 15;356(11):1094-7. doi: 10.1056/NEJMp068126.