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血清素转运体基因中与启动子相关的(多态性)可能与双相情感障碍中抗抑郁药诱发的躁狂有关。

Serotonin transporter linked promoter (polymorphism) in the serotonin transporter gene may be associated with antidepressant-induced mania in bipolar disorder.

作者信息

Masoliver Elisabet, Menoyo Ana, Pérez Victor, Volpini Victor, Rio Elisabet Del, Pérez Josefina, Alvarez Enric, Baiget Monserrat

机构信息

Department of Psychiatry, Santa Creu i Sant Pau Hospital and ICO I Institut de Recerca Oncologica, Barcelona, Spain.

出版信息

Psychiatr Genet. 2006 Feb;16(1):25-9. doi: 10.1097/01.ypg.0000180684.26288.d7.

Abstract

OBJECTIVE

Several pharmacogenetic studies suggest that response to pharmacotherapy in bipolar disorder may be mediated by genetic factors. The aim of this study was to investigate further the association of the genetic variations of the serotonin transporter (5-HTT) gene with antidepressant-induced mania, already reported in recent studies. We also studied the possible association of these genetic variants with diagnosis expression and treatment response to lithium therapy.

METHODS

The sample consisted of 103 and 85 outpatients with diagnosis of bipolar and unipolar disorder, respectively, and 101 controls. Two described polymorphisms of the 5-HTT, the variable number of tandem repeat (VNTR) and serotonin transporter linked promoter (5-HTTLPR) polymorphisms, were genotyped using standard procedures.

RESULTS

The association analysis performed showed a significantly higher rate of homozygous s/s genotype for 5-HTTLPR among patients with a history of antidepressant-induced mania (60% patients s/s versus 40% l/l, chi, P=0.04). No significant difference in the distribution of genotypes of the two polymorphisms was observed between the three groups. We found no significant association between these polymorphisms and lithium response.

CONCLUSIONS

The 5-HTTLPR polymorphism could be a useful contributor, among other clinical variables, to predict the risk for manic switches when a patient with bipolar disorder is treated with antidepressant drugs. The contribution of these genetic markers in diagnosis expression and treatment response to lithium is likely to be minor.

摘要

目的

多项药物遗传学研究表明,双相情感障碍患者对药物治疗的反应可能由遗传因素介导。本研究的目的是进一步探究血清素转运体(5-HTT)基因的遗传变异与抗抑郁药诱发躁狂之间的关联,近期已有相关研究报道。我们还研究了这些基因变异与锂盐治疗的诊断表达及治疗反应之间可能存在的关联。

方法

样本包括分别诊断为双相情感障碍和单相情感障碍的103例和85例门诊患者,以及101例对照。采用标准程序对5-HTT的两种已描述的多态性,即可变串联重复序列(VNTR)和血清素转运体连锁启动子(5-HTTLPR)多态性进行基因分型。

结果

进行的关联分析显示,有抗抑郁药诱发躁狂病史的患者中,5-HTTLPR的纯合子s/s基因型发生率显著更高(60%的患者为s/s,而l/l为40%,χ²,P = 0.04)。三组之间未观察到这两种多态性基因型分布的显著差异。我们发现这些多态性与锂盐反应之间无显著关联。

结论

在其他临床变量中,5-HTTLPR多态性可能有助于预测双相情感障碍患者接受抗抑郁药治疗时发生躁狂转换的风险。这些遗传标记在锂盐治疗的诊断表达及治疗反应中的作用可能较小。

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