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早发性强迫症的遗传学研究。

Genetics of early-onset obsessive-compulsive disorder.

机构信息

Department of Child and Adolescent Psychiatry, University of Zurich, Zurich, Switzerland.

出版信息

Eur Child Adolesc Psychiatry. 2010 Mar;19(3):227-35. doi: 10.1007/s00787-010-0087-7. Epub 2010 Mar 6.

DOI:10.1007/s00787-010-0087-7
PMID:20213231
Abstract

Obsessive-compulsive disorder (OCD) is characterized by recurrent, intrusive and disturbing thoughts as well as by repetitive stereotypic behaviors. Epidemiological data are similar in children and adults, i.e., between 1 and 3% of the general population suffer from OCD. Children with OCD are often seriously impaired in their development. OCD, especially of early onset, has been shown to be familial. Several candidate genes of predominantly neurotransmitter systems have been analyzed and a total of three genome-wide linkage scans have been performed until now. Analyses of candidate genes in linkage regions have not provided evidence for their involvement in OCD, with the exception of the glutamate transporter gene SLC1A1 on 9p24. Genome-wide association analyses are in progress and the results will promote further independent replication studies. The consideration of subtypes regarding age of onset, symptom dimensions and/or comorbid disorders is needed.

摘要

强迫症(OCD)的特征是反复出现、侵入性和令人不安的想法以及重复的刻板行为。儿童和成人的流行病学数据相似,即 1%至 3%的普通人群患有 OCD。患有 OCD 的儿童在发育过程中经常受到严重影响。已经表明 OCD,尤其是早期发病,具有家族性。已经分析了主要涉及神经递质系统的几个候选基因,并且迄今为止已经进行了总共三次全基因组连锁扫描。在连锁区域中对候选基因的分析并未提供其参与 OCD 的证据,谷氨酸转运体基因 SLC1A1 除外,该基因位于 9p24 上。全基因组关联分析正在进行中,结果将促进进一步的独立复制研究。需要考虑亚型,包括发病年龄、症状维度和/或合并症。

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1
Genetics of early-onset obsessive-compulsive disorder.早发性强迫症的遗传学研究。
Eur Child Adolesc Psychiatry. 2010 Mar;19(3):227-35. doi: 10.1007/s00787-010-0087-7. Epub 2010 Mar 6.
2
[Genetic findings in obsessive-compulsive disorder in childhood and adolescence and in adulthood].[儿童期、青少年期及成年期强迫症的遗传学发现]
Z Kinder Jugendpsychiatr Psychother. 2008 Jan;36(1):45-52. doi: 10.1024/1422-4917.36.1.45.
3
Association testing of the positional and functional candidate gene SLC1A1/EAAC1 in early-onset obsessive-compulsive disorder.早发性强迫症中定位和功能候选基因SLC1A1/EAAC1的关联测试。
Arch Gen Psychiatry. 2006 Jul;63(7):778-85. doi: 10.1001/archpsyc.63.7.778.
4
Genetics of obsessive-compulsive disorder: a research update.强迫症的遗传学:研究进展
Expert Rev Neurother. 2007 Aug;7(8):967-80. doi: 10.1586/14737175.7.8.967.
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Glutamate transporter gene SLC1A1 associated with obsessive-compulsive disorder.谷氨酸转运体基因SLC1A1与强迫症相关。
Arch Gen Psychiatry. 2006 Jul;63(7):769-76. doi: 10.1001/archpsyc.63.7.769.
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Association of the SLC1A1 glutamate transporter gene and obsessive-compulsive disorder.溶质载体家族1成员1(SLC1A1)谷氨酸转运体基因与强迫症的关联。
Am J Med Genet B Neuropsychiatr Genet. 2007 Dec 5;144B(8):1027-33. doi: 10.1002/ajmg.b.30533.
7
Genome-wide linkage analysis of obsessive-compulsive disorder implicates chromosome 1p36.全基因组连锁分析提示强迫症与 1p36 染色体有关。
Biol Psychiatry. 2012 Oct 15;72(8):629-36. doi: 10.1016/j.biopsych.2012.03.037. Epub 2012 May 25.
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Replication study supports evidence for linkage to 9p24 in obsessive-compulsive disorder.复制研究支持强迫症与9号染色体短臂24区(9p24)存在连锁关系的证据。
Am J Hum Genet. 2004 Sep;75(3):508-13. doi: 10.1086/423899. Epub 2004 Jul 21.
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A haplotype containing quantitative trait loci for SLC1A1 gene expression and its association with obsessive-compulsive disorder.一个包含SLC1A1基因表达数量性状位点的单倍型及其与强迫症的关联。
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10
The genetics of obsessive-compulsive disorder: a review.强迫症的遗传学:综述
Dialogues Clin Neurosci. 2010;12(2):149-63. doi: 10.31887/DCNS.2010.12.2/dpauls.

引用本文的文献

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Polygenic Heterogeneity Across Obsessive-Compulsive Disorder Subgroups Defined by a Comorbid Diagnosis.由共病诊断定义的强迫症亚组中的多基因异质性
Front Genet. 2021 Aug 31;12:711624. doi: 10.3389/fgene.2021.711624. eCollection 2021.
2
Developmental Considerations in Obsessive Compulsive Disorder: Comparing Pediatric and Adult-Onset Cases.强迫症的发育考量:儿童期起病与成人期起病病例的比较
Front Psychiatry. 2021 Jun 14;12:678538. doi: 10.3389/fpsyt.2021.678538. eCollection 2021.
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On the Development of OCD.强迫症的发展。

本文引用的文献

1
Cluster analysis of obsessive-compulsive symptomatology: identifying obsessive-compulsive disorder subtypes.强迫症状的聚类分析:识别强迫症亚型
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2
A haplotype containing quantitative trait loci for SLC1A1 gene expression and its association with obsessive-compulsive disorder.一个包含SLC1A1基因表达数量性状位点的单倍型及其与强迫症的关联。
Arch Gen Psychiatry. 2009 Apr;66(4):408-16. doi: 10.1001/archgenpsychiatry.2009.6.
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Meta-analysis of the symptom structure of obsessive-compulsive disorder.
Curr Top Behav Neurosci. 2021;49:17-30. doi: 10.1007/7854_2020_195.
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Genetics of OCD and Related Disorders; Searching for Shared Factors.强迫症及相关障碍的遗传学研究:寻找共同因素
Curr Top Behav Neurosci. 2021;49:1-16. doi: 10.1007/7854_2020_194.
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Genetic Association of Epilepsy and Anti-Epileptic Drugs Treatment in Jordanian Patients.约旦患者中癫痫与抗癫痫药物治疗的基因关联
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Impaired Antisaccades in Obsessive-Compulsive Disorder: Evidence From Meta-Analysis and a Large Empirical Study.强迫症中反扫视功能受损:来自荟萃分析和一项大型实证研究的证据
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Assessing Acute Secondary Treatment Outcomes in Early-Onset Obsessive-Compulsive Disorder.评估早发性强迫症的急性二级治疗结果
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Increased decision thresholds enhance information gathering performance in juvenile Obsessive-Compulsive Disorder (OCD).提高决策阈值可增强青少年强迫症(OCD)患者的信息收集能力。
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Cool and Hot Aspects of Executive Function in Childhood Obsessive-Compulsive Disorder.儿童强迫症执行功能的冷热方面
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10
DNA Methylation at the Neonatal State and at the Time of Diagnosis: Preliminary Support for an Association with the Estrogen Receptor 1, Gamma-Aminobutyric Acid B Receptor 1, and Myelin Oligodendrocyte Glycoprotein in Female Adolescent Patients with OCD.新生儿期及诊断时的DNA甲基化:对女性青少年强迫症患者中与雌激素受体1、γ-氨基丁酸B受体1和髓鞘少突胶质细胞糖蛋白关联的初步支持。
Front Psychiatry. 2016 Mar 18;7:35. doi: 10.3389/fpsyt.2016.00035. eCollection 2016.
强迫症症状结构的荟萃分析。
Am J Psychiatry. 2008 Dec;165(12):1532-42. doi: 10.1176/appi.ajp.2008.08020320. Epub 2008 Oct 15.
4
Updated overview of the putative role of the serotoninergic system in obsessive-compulsive disorder.更新的关于 5-羟色胺能系统在强迫症中假设作用的综述。
Neuropsychiatr Dis Treat. 2005 Sep;1(3):231-43.
5
Transmission disequilibrium studies in early onset of obsessive-compulsive disorder for polymorphisms in genes of the dopaminergic system.针对多巴胺能系统基因多态性的强迫症早发的传递不平衡研究。
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The genetics of obsessive compulsive disorder: a review of the evidence.强迫症的遗传学:证据综述
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Evidence for potential relationship between SLC1A1 and a putative genetic linkage region on chromosome 14q to obsessive-compulsive disorder with compulsive hoarding.溶质载体家族1成员1(SLC1A1)与14号染色体q臂上一个假定的与伴有强迫性囤积行为的强迫症相关的遗传连锁区域之间潜在关系的证据。
Am J Med Genet B Neuropsychiatr Genet. 2008 Sep 5;147B(6):1000-2. doi: 10.1002/ajmg.b.30713.
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Targeting the murine serotonin transporter: insights into human neurobiology.靶向小鼠血清素转运体:对人类神经生物学的见解
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9
Association of the SLC1A1 glutamate transporter gene and obsessive-compulsive disorder.溶质载体家族1成员1(SLC1A1)谷氨酸转运体基因与强迫症的关联。
Am J Med Genet B Neuropsychiatr Genet. 2007 Dec 5;144B(8):1027-33. doi: 10.1002/ajmg.b.30533.
10
Extensive genotyping of the BDNF and NTRK2 genes define protective haplotypes against obsessive-compulsive disorder.对脑源性神经营养因子(BDNF)和神经营养酪氨酸激酶2(NTRK2)基因进行广泛的基因分型,确定了针对强迫症的保护性单倍型。
Biol Psychiatry. 2008 Mar 15;63(6):619-28. doi: 10.1016/j.biopsych.2007.06.020. Epub 2007 Sep 19.