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马来族首次发作重度抑郁症患者的血清素能受体基因多态性与对选择性5-羟色胺再摄取抑制剂的反应

Serotonergic receptor gene polymorphism and response to selective serotonin reuptake inhibitors in ethnic Malay patients with first episode of major depressive disorder.

作者信息

Badamasi Ibrahim Mohammed, Lye Munn Sann, Ibrahim Normala, Abdul Razaq Nurul Asyikin, Ling King Hwa, Stanslas Johnson

机构信息

Pharmacotherapeutics Unit, Department of Medicine, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Serdang, Malaysia.

Department of Anatomy, Faculty of Basic Medical Sciences, College of Health Sciences, Bayero University, Kano, Nigeria.

出版信息

Pharmacogenomics J. 2021 Aug;21(4):498-509. doi: 10.1038/s41397-021-00228-6. Epub 2021 Mar 17.

DOI:10.1038/s41397-021-00228-6
PMID:33731884
Abstract

The polymorphisms of the 5HTR1A and 5HTR2A receptor genes (rs6295C/G and rs6311G/A) have been evaluated for association with SSRI treatment outcome in various populations with different results. The present study was carried out to determine the association between genotypes of HTR1A-rs6295 and HTR2A-rs6311 with SSRI treatment outcome among the ethnic Malay patients diagnosed with first-episode major depressive disorder (MDD). The patients were recruited from four tertiary hospitals in the Klang Valley region of Malaysia. Predefined efficacy phenotypes based on 25% (partial early response) and 50% (clinical efficacy response) reduction in Montgomery Asberg Depression Rating Scale-self Rated score (MADRS-S) were adopted for assessment of treatment efficacy in this study. Self-reporting for adverse effects (AE) was documented using the Patient Rated Inventory of Side Effect (PRISE) after treatment with SSRI for up to 6 weeks. Adjusted binary logistic regression between genotypes of the polymorphism obtained using sequencing technique with the treatment outcome phenotypes was performed. The 142 patients recruited were made up of 96 females (67.6%) and 46 males (32.4%). Clinical efficacy and Partial early response phenotypes were not significantly associated with genotypes of HTR1A and HTR2A polymorphism. The GG genotype of HTR2A polymorphism has decreased odds for dizziness (CNS) and increased odds for poor concentration. The GA genotype increases the odd for excessive sweating, diarrhoea, constipation and blurred vision. The CC genotype of HTR1A-rs6295 decreases the odd for nausea/vomiting and increases the odd for anxiety. Thus, some genotypes of HTR1A and HTR2A polymorphism were associated with SSRI treatment outcomes in ethnic Malay MDD patients.

摘要

5羟色胺受体1A(5HTR1A)和5羟色胺受体2A(5HTR2A)基因的多态性(rs6295C/G和rs6311G/A)已在不同人群中进行评估,以探讨其与选择性5-羟色胺再摄取抑制剂(SSRI)治疗效果的关联,结果各异。本研究旨在确定在诊断为首发重度抑郁症(MDD)的马来族患者中,5羟色胺受体1A基因(HTR1A)rs6295和5羟色胺受体2A基因(HTR2A)rs6311的基因型与SSRI治疗效果之间的关联。研究对象来自马来西亚巴生谷地区的四家三级医院。本研究采用基于蒙哥马利-艾斯伯格抑郁评定量表自评分数(MADRS-S)降低25%(部分早期反应)和50%(临床疗效反应)来定义疗效表型,以评估治疗效果。在使用SSRI治疗长达6周后,采用患者副作用评定量表(PRISE)记录副作用的自我报告情况。对使用测序技术获得的多态性基因型与治疗效果表型进行校正二元逻辑回归分析。招募的142例患者中,女性96例(67.6%),男性46例(32.4%)。临床疗效和部分早期反应表型与HTR1A和HTR2A基因多态性的基因型无显著关联。HTR2A基因多态性的GG基因型降低了头晕(中枢神经系统症状)的发生几率,增加了注意力不集中的发生几率。GA基因型增加了多汗、腹泻、便秘和视力模糊的发生几率。HTR1A-rs6295的CC基因型降低了恶心/呕吐的发生几率,增加了焦虑的发生几率。因此,HTR1A和HTR2A基因多态性的某些基因型与马来族MDD患者的SSRI治疗效果相关。

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