ABCB1 Gene Variants and Antidepressant Treatment Outcomes: A Systematic Review and Meta‐Analysis Including Results from the CAN‐BIND‐1 Study

抗抑郁药 荟萃分析 单核苷酸多态性 重性抑郁障碍 优势比 耐受性 医学 内科学 肿瘤科 置信区间 基因分型 药物遗传学 药理学 生物信息学 精神科 基因型 遗传学 生物 基因 不利影响 扁桃形结构 海马体
作者
Leen Magarbeh,Claudia Hassel,Maximilian Choi,Farhana Islam,Victoria S. Marshe,Clement C. Zai,Rayyan Zuberi,Roseann S. Gammal,Xiaoyu Men,Maike Scherf‐Clavel,Dietmar Enko,Benício N. Frey,Roumen Milev,Cláudio N. Soares,Sagar V. Parikh,Franca Placenza,Stephen C. Strother,Stefanie Hassel,Valerie H. Taylor,Francesco Leri,Pierre Blier,Faranak Farzan,Raymond W. Lam,Gustavo Turecki,Jane A. Foster,Susan Rotzinger,Stefan Kloiber,James L. Kennedy,Sidney H. Kennedy,Chad A. Bousman,Daniel J. Müller
出处
期刊:Clinical Pharmacology & Therapeutics [Wiley]
卷期号:114 (1): 88-117 被引量:4
标识
DOI:10.1002/cpt.2854
摘要

The P-glycoprotein efflux pump, encoded by the ABCB1 gene, has been shown to alter concentrations of various antidepressants in the brain. In this study, we conducted a systematic review and meta-analysis to investigate the association between six ABCB1 single-nucleotide polymorphisms (SNPs; rs1045642, rs2032582, rs1128503, rs2032583, rs2235015, and rs2235040) and antidepressant treatment outcomes in individuals with major depressive disorder (MDD), including new data from the Canadian Biomarker and Integration Network for Depression (CAN-BIND-1) cohort. For the CAN-BIND-1 sample, we applied regression models to investigate the association between ABCB1 SNPs and antidepressant treatment response, remission, tolerability, and antidepressant serum levels. For the meta-analysis, we systematically summarized pharmacogenetic evidence of the association between ABCB1 SNPs and antidepressant treatment outcomes. Studies were included in the meta-analysis if they investigated at least one ABCB1 SNP in individuals with MDD treated with at least one antidepressant. We did not find a significant association between ABCB1 SNPs and antidepressant treatment outcomes in the CAN-BIND-1 sample. A total of 39 studies were included in the systematic review. In the meta-analysis, we observed a significant association between rs1128503 and treatment response (T vs. C-allele, odds ratio = 1.30, 95% confidence interval = 1.15-1.48, P value (adjusted) = 0.024, n = 2,526). We did not find associations among the six SNPs and treatment remission nor tolerability. Our findings provide limited evidence for an association between common ABCB1 SNPs and antidepressant outcomes, which do not support the implementation of ABCB1 genotyping to inform antidepressant treatment at this time. Future research, especially on rs1128503, is recommended.
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