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早发性强迫症中功能性5-羟色胺3A受体变体C178T的传递不平衡分析。

Transmission disequilibrium analysis of the functional 5-HT3A receptor variant C178T in early-onset obsessive compulsive-disorder.

作者信息

Mössner Rainald, Döring Nicole, Scherag André, Schäfer Helmut, Herpertz-Dahlmann Beate, Remschmidt Helmut, Schulz Eberhard, Renner Tobias, Wewetzer Christoph, Warnke Andreas, Lesch Klaus-Peter, Walitza Susanne

机构信息

Department of Psychiatry and Psychotherapy, University of Würzburg, Würzburg, Germany.

出版信息

J Psychopharmacol. 2007 Nov;21(8):833-6. doi: 10.1177/0269881106073560. Epub 2007 Jan 26.

Abstract

The 5-HT(3) receptor is unique among the serotonin receptors in that it is a ligand-gated ion channel. Dysfunction of the serotonin system is thought to contribute to the pathogenesis of obsessive-compulsive disorder (OCD). Apart from the standard treatment with serotonin reuptake inhibitors and behavioural therapy, a 5-HT(3) receptor antagonist has recently been shown to benefit some OCD patients, suggesting the 5-HT(3) receptor as a serotonergic candidate gene in the polygenic aetiology of OCD. A functional regulatory variant of the 5-HT(3A) receptor influences 5-HT(3) receptor expression, serotonin metabolites in cerebrospinal fluid, and amygdala reactivity. We therefore assessed whether this C178T variant influences the risk of developing OCD. In a family-based approach employing the transmission disequilibrium test, we analysed a unique sample of 75 children and adolescents with OCD, as well as their biological parents. We found no evidence for a preferential transmission of either allele to the patients--the estimated transmission rate for the C allele was 0.51 (95% CI 0.36-0.65). This argues against an involvement of the 5-HT(3A) receptor in the polygenic aetiology of early-onset OCD.

摘要

5-羟色胺(5-HT)3受体在5-羟色胺受体中独具特色,因为它是一种配体门控离子通道。5-羟色胺系统功能失调被认为与强迫症(OCD)的发病机制有关。除了使用5-羟色胺再摄取抑制剂和行为疗法的标准治疗外,最近有研究表明,一种5-HT3受体拮抗剂对一些OCD患者有益,这表明5-HT3受体是OCD多基因病因中一个5-羟色胺能候选基因。5-HT3A受体的一个功能性调控变体影响5-HT3受体表达、脑脊液中的5-羟色胺代谢产物以及杏仁核反应性。因此,我们评估了这种C178T变体是否会影响患OCD的风险。在采用传递不平衡检验的基于家系的研究中,我们分析了75名患有OCD的儿童和青少年及其亲生父母这一独特样本。我们没有发现任何证据表明任何一个等位基因会优先传递给患者——C等位基因的估计传递率为0.51(95%置信区间0.36 - 0.65)。这表明5-HT3A受体不参与早发性OCD的多基因病因。

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