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β肾上腺素能受体多态性与重度抑郁症患者对舍曲林的临床反应

Beta Adrenoceptor Polymorphism and Clinical Response to Sertraline in Major Depressive Patients.

作者信息

Firouzabadi Negar, Raeesi Roshanak, Zomorrodian Kamiar, Bahramali Ehsan, Yavarian Ilnaz

机构信息

Department of Pharmacology & Toxicology, School of Pharmacy, Shiraz University of Medical Sciences, Shiraz, Iran. Non communicable Diseases Research Center, Fasa University of Medical Sciences, Fasa, Iran. Yasuj University of Medical Sciences, Yasuj, Iran.

出版信息

J Pharm Pharm Sci. 2017;20:1-7. doi: 10.18433/J3W31F.

Abstract

PURPOSE

The adrenoceptor family, as one of the main contributors in regulating the noradrenergic system, has been studied in involvement of depression and its treatment. A functional polymorphism of G1165C on beta adrenoceptor (βAR) enhances post receptor signalling and is assumed to be involved in pharmacotherapy of depression. The aim of the present study was to discern the influence of G1165C polymorphism in the β1AR gene on individual differences in response to sertraline.

METHODS

One hundred newly diagnosed patients completed 6 weeks of sertraline treatment. Response to treatment was defined as a 50% decrease in Hamilton Rating Scale for depression (HRSD).

RESULTS

The patients who carried CC genotype responded five times more to sertraline comparing with other variants (P=0.005; OR=5.7; 95%CI=1.4-23.9). Moreover, carriers of C allele responded three times more to sertraline than patients with the G allele (P=0.001; OR= 3.3; 95%CI= 1.72-6.50).

CONCLUSION

In conclusion, our results support the hypothesis that genetic variation of β1AR might influence clinical response to sertraline. This article is open to POST-PUBLICATION REVIEW. Registered readers (see "For Readers") may comment by clicking on ABSTRACT on the issue's contents page.

摘要

目的

肾上腺素能受体家族作为调节去甲肾上腺素能系统的主要因素之一,已被研究与抑郁症及其治疗的关系。β肾上腺素能受体(βAR)上G1165C的功能性多态性增强了受体后信号传导,并被认为与抑郁症的药物治疗有关。本研究的目的是探讨β1AR基因中G1165C多态性对舍曲林反应个体差异的影响。

方法

100名新诊断的患者完成了6周的舍曲林治疗。治疗反应定义为汉密尔顿抑郁量表(HRSD)评分降低50%。

结果

携带CC基因型的患者对舍曲林的反应是其他基因型患者的5倍(P=0.005;OR=5.7;95%CI=1.4-23.9)。此外,携带C等位基因的患者对舍曲林的反应是携带G等位基因患者的3倍(P=0.001;OR=3.3;95%CI=1.72-6.50)。

结论

总之,我们的结果支持β1AR基因变异可能影响对舍曲林临床反应的假设。本文接受发表后审查。注册读者(见“读者须知”)可通过点击本期目录页上的摘要进行评论。

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