Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.
Department of Pharmacology & Toxicology, University of Toronto, Toronto, Ontario, Canada.
Clin Pharmacol Ther. 2023 Jul;114(1):88-117. doi: 10.1002/cpt.2854. Epub 2023 Mar 6.
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.
P-糖蛋白外排泵由 ABCB1 基因编码,已被证明会改变大脑中各种抗抑郁药的浓度。在这项研究中,我们进行了系统评价和荟萃分析,以调查六种 ABCB1 单核苷酸多态性(SNP;rs1045642、rs2032582、rs1128503、rs2032583、rs2235015 和 rs2235040)与重度抑郁症(MDD)患者抗抑郁治疗结果之间的关联,包括来自加拿大生物标志物和抑郁症综合网络(CAN-BIND-1)队列的新数据。对于 CAN-BIND-1 样本,我们应用回归模型来研究 ABCB1 SNP 与抗抑郁治疗反应、缓解、耐受性和抗抑郁血清水平之间的关系。对于荟萃分析,我们系统地总结了 ABCB1 SNP 与抗抑郁治疗结果之间关联的遗传药理学证据。如果研究调查了至少一个 ABCB1 SNP 与至少一种抗抑郁药治疗的 MDD 患者,这些研究将被纳入荟萃分析。我们没有发现 CAN-BIND-1 样本中 ABCB1 SNP 与抗抑郁治疗结果之间的显著关联。共有 39 项研究被纳入系统评价。在荟萃分析中,我们观察到 rs1128503 与治疗反应(T 与 C-等位基因,比值比=1.30,95%置信区间=1.15-1.48,调整后的 P 值=0.024,n=2526)之间存在显著关联。我们没有发现这六个 SNP 与治疗缓解或耐受性之间的关联。我们的研究结果提供了 ABCB1 常见 SNP 与抗抑郁药结果之间关联的有限证据,这并不支持目前通过 ABCB1 基因分型来指导抗抑郁治疗。建议进行未来的研究,特别是针对 rs1128503 的研究。