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选择性5-羟色胺再摄取抑制剂相关性性功能障碍的遗传决定因素。

Genetic determinants of selective serotonin reuptake inhibitor related sexual dysfunction.

作者信息

Stevenson James M, Bishop Jeffrey R

机构信息

University of Illinois at Chicago College of Pharmacy, Department of Pharmacy Practice, Chicago, IL, USA.

出版信息

Pharmacogenomics. 2014 Nov;15(14):1791-1806. doi: 10.2217/pgs.14.114.

Abstract

Sexual dysfunction is a troubling obstacle for individuals being treated for depression and can be caused by both depressive symptoms as well as antidepressant drugs. Selective serotonin reuptake inhibitors (SSRIs) represent a class of antidepressants commonly associated with sexual dysfunction, even after symptomatic improvement. Candidate gene studies have identified associations between sexual dysfunction and altered SSRI pharmacokinetics or to the neurotransmitter systems affected by depression and SSRI treatment. The multifactorial nature of this phenotype and study heterogeneity are currently limitations to the translation of these findings to clinical use. Larger, prospective studies of genetic-guided antidepressant selection may help to clarify the clinical utility of pharmacogenetics in minimizing sexual side effects.

摘要

性功能障碍是抑郁症患者治疗过程中一个令人困扰的障碍,它可能由抑郁症状以及抗抑郁药物引起。选择性5-羟色胺再摄取抑制剂(SSRI)是一类常与性功能障碍相关的抗抑郁药,即使在症状改善后也是如此。候选基因研究已经确定性功能障碍与SSRI药代动力学改变或与受抑郁症和SSRI治疗影响的神经递质系统之间存在关联。这种表型的多因素性质和研究异质性目前限制了这些研究结果转化为临床应用。关于基因指导下抗抑郁药选择的更大规模的前瞻性研究可能有助于阐明药物遗传学在最小化性副作用方面的临床效用。

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