Association of serotonin transporter gene polymorphism with efficacy of the antidepressant drugs sertraline and mirtazapine in newly diagnosed patients with major depressive disorders

IF 1.8 4区 医学 Q3 CLINICAL NEUROLOGY Human Psychopharmacology: Clinical and Experimental Pub Date : 2022-01-28 DOI:10.1002/hup.2833
Syed Gulfishan, Sumita Halder, Rajarshi Kar, Shruti Srivastava, Rachna Gupta
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Abstract

Objective

We examined the association of serotonin receptor transporter gene polymorphism in patients with MDD with the clinical efficacy of mirtazapine (MZ) and sertraline (ST).

Method

Newly diagnosed, treatment naïve, 80 MDD patients (aged 18–45) diagnosed using DSM-5 criteria and with Beck's depression inventory score (BDI) score ≥21 were included and randomly divided into two groups of 40 participants and were administered MZ 15–45 mg/day or ST 25–200 mg/day respectively. Patients were followed up for 6 weeks for evaluation of BDI scores. Genotypic evaluation was done and three allele variants were identified based on the polymerase chain reaction fragment sizes: short (S; 486 bp), long (L; 529 bp), or extralong (XL; 612 or 654 bp) and classified into five genotypes: S/S,S/L, L/L, S/XL, and L/XL.

Result

We found that 32.5% patients belonged to the S/S genotype, suggesting that individuals with the SS genotype are at higher risk of developing MDD. No statistically significant association was seen with ST or MZ groups on the basis of genotypes. Clinically significant improvement was observed with a more than 50% reduction in BDI scores at 6 weeks of treatment with both drugs.

Conclusion

Identification of risk population can be carried out by genotype testing. Prior genotyping in MDD patients might help to predict a better clinical outcome with antidepressants.

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5 -羟色胺转运体基因多态性与新诊断重度抑郁症患者抗抑郁药物舍曲林、米氮平疗效的关系
目的探讨重度抑郁症患者血清素受体转运体基因多态性与米氮平(MZ)、舍曲林(ST)临床疗效的关系。方法采用DSM-5标准诊断,Beck抑郁量表评分(BDI)≥21分,新诊断、治疗naïve的MDD患者80例(18-45岁),随机分为两组,每组40例,分别给予MZ 15 ~ 45mg /d或ST 25 ~ 200mg /d。随访6周,评估BDI评分。进行基因型评估,根据聚合酶链反应片段大小鉴定出三个等位基因变异:短(S;486 bp),长(L;529bp),或外沿(XL;基因型分别为S/S、S/L、L/L、S/XL和L/XL。结果32.5%的患者属于S/S基因型,提示SS基因型患者发生重度抑郁症的风险较高。在基因型的基础上,未发现与ST或MZ组有统计学意义的关联。两种药物治疗6周后,观察到临床显著改善,BDI评分降低50%以上。结论基因型检测可用于高危人群的识别。重度抑郁症患者先前的基因分型可能有助于预测使用抗抑郁药的更好临床结果。
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来源期刊
CiteScore
4.10
自引率
0.00%
发文量
34
审稿时长
6-12 weeks
期刊介绍: Human Psychopharmacology: Clinical and Experimental provides a forum for the evaluation of clinical and experimental research on both new and established psychotropic medicines. Experimental studies of other centrally active drugs, including herbal products, in clinical, social and psychological contexts, as well as clinical/scientific papers on drugs of abuse and drug dependency will also be considered. While the primary purpose of the Journal is to publish the results of clinical research, the results of animal studies relevant to human psychopharmacology are welcome. The following topics are of special interest to the editors and readers of the Journal: -All aspects of clinical psychopharmacology- Efficacy and safety studies of novel and standard psychotropic drugs- Studies of the adverse effects of psychotropic drugs- Effects of psychotropic drugs on normal physiological processes- Geriatric and paediatric psychopharmacology- Ethical and psychosocial aspects of drug use and misuse- Psychopharmacological aspects of sleep and chronobiology- Neuroimaging and psychoactive drugs- Phytopharmacology and psychoactive substances- Drug treatment of neurological disorders- Mechanisms of action of psychotropic drugs- Ethnopsychopharmacology- Pharmacogenetic aspects of mental illness and drug response- Psychometrics: psychopharmacological methods and experimental design
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