Nonen Shinpei, Kato Masaki, Takekita Yoshiteru, Wakeno Masataka, Sakai Shiho, Serretti Alessandro, Kinoshita Toshihiko
From the *Department of Pharmacy, School of Pharmacy, Hyogo University of Health Sciences, Hyogo; and †Department of Neuropsychiatry, Kansai Medical University, Osaka, Japan; and ‡Department of Biomedical and Neuro Motor Sciences, University of Bologna, Bologna, Italy.
J Clin Psychopharmacol. 2016 Feb;36(1):27-31. doi: 10.1097/JCP.0000000000000454.
Selective serotonin and serotonin-norepinephrine reuptake inhibitors (SSRI/SNRI) are commonly used for treating major depression. Regretfully, significant heterogeneity exists regarding the benefits of SSRI/SNRI in individual cases. We previously reported that a polymorphism located in the serotonin transporter linked promoter region (5-HTT LPR) is associated with an interindividual difference in SSRI treatment efficacy. However, this explains only a small part of the variation of this complex phenotype. Other 5-HTT variants in the coding regions, 3' untranslated region (3' UTR), and introns adjacent to each exon could also contribute to treatment response. Therefore, we performed a sequencing analysis of the SLC6A4 gene (coding for 5-HTT) and investigated the association between variants detected in this study and the antidepressant response to SSRI/SNRI in 201 Japanese depressive patients. Seventeen novel mutations were identified by sequencing analysis. We found that the polymorphism G2563T (rs3813034) as a tag single-nucleotide polymorphism of IVS9 A-90G (rs140701), G2356T (rs1042173), and A3641C (rs7224199) is associated with interindividual variability of SSRI/SNRI efficacy at week 6, independent from clinical variables and effect of 5-HTT LPR (P < 0.001 by multiple regression analysis). This polymorphism could help determine individualized SSRI/SNRI treatments for depressive patients in combination with 5-HTT LPR.
选择性5-羟色胺及5-羟色胺-去甲肾上腺素再摄取抑制剂(SSRI/SNRI)常用于治疗重度抑郁症。遗憾的是,SSRI/SNRI在个体病例中的疗效存在显著异质性。我们之前报道过,位于5-羟色胺转运体连接启动子区域(5-HTT LPR)的一种多态性与SSRI治疗疗效的个体差异相关。然而,这仅解释了这一复杂表型变异的一小部分。编码区、3'非翻译区(3'UTR)以及每个外显子相邻内含子中的其他5-HTT变体也可能影响治疗反应。因此,我们对SLC6A4基因(编码5-HTT)进行了测序分析,并研究了本研究中检测到的变体与201例日本抑郁症患者对SSRI/SNRI的抗抑郁反应之间的关联。通过测序分析鉴定出17个新突变。我们发现,作为IVS9 A-90G(rs140701)、G2356T(rs1042173)和A3641C(rs7224199)标签单核苷酸多态性的G2563T(rs3813034)多态性与第6周时SSRI/SNRI疗效的个体差异相关,独立于临床变量和5-HTT LPR的影响(多元回归分析P<0.001)。这种多态性有助于结合5-HTT LPR为抑郁症患者确定个体化的SSRI/SNRI治疗方案。