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DOI 10.18433/j3w31f

Медицинская библиотека · Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques · 2017

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

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

СтатьяПеревод пока не подготовлен

Аннотация

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.

Для цитирования: Firouzabadi Negar, Raeesi Roshanak, Zomorrodian Kamiar, Bahramali Ehsan, Yavarian Ilnaz. Beta Adrenoceptor Polymorphism and Clinical Response to Sertraline in Major Depressive Patients.. Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques. 2017. DOI: 10.18433/j3w31f.

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