Department of Psychiatry, Samsung Medical Center, Sungkyunkwan University School of Medicine, 50 Irwon-dong, Kangnam-gu, Seoul 135-710, Korea.
Psychopharmacology (Berl). 2013 Jan;225(2):283-90. doi: 10.1007/s00213-012-2813-y. Epub 2012 Aug 12.
Serotonin transporter (5-HTT) gene polymorphisms are linked with antidepressant response to selective serotonin reuptake inhibitor drugs (SSRIs), though the favorable allelic variant differs by ethnic group (Caucasian versus Korean or Japanese). In Caucasian patients, response also is linked to measures of platelet 5-HTT function.
Here, we study both 5-HTT gene polymorphisms and 5-HTT function as determinants of antidepressant response to SSRIs in Korean patients.
We enrolled 99 patients with major depression and 48 control subjects. For statistical power, both samples were enriched with the l/l 5-HTTLPR polymorphism, which is uncommon in Koreans. Patients were treated with fluoxetine or sertraline. Response was assessed at 6 weeks. Subjects were genotyped for s/l polymorphism in the 5-HTT promoter region (5-HTTLPR). Platelet 5-HTT activity was determined as maximal uptake rate (Vmax) and affinity constant (Km).
Response was differentially associated with the s allele of 5-HTTLPR, which also was significantly associated with Vmax. These associations are opposite to those reported in Caucasian populations. Responders had significantly higher Vmax and Km than nonresponders. In Koreans as well as Caucasians, high Vmax is related to antidepressant response to SSRIs, though the 5-HTTLPR polymorphism associations with both response and function differ by ethnicity.
Both ethnicity and function must be considered in evaluating candidate gene biomarkers of response to SSRIs in depression.
5-羟色胺转运体(5-HTT)基因多态性与选择性 5-羟色胺再摄取抑制剂(SSRIs)类抗抑郁药的反应相关,然而,有利的等位基因变体因种族(白种人对韩国或日本的白种人)而异。在白种人群中,反应还与血小板 5-HTT 功能的测量相关。
本研究旨在探讨韩国患者中 5-HTT 基因多态性和 5-HTT 功能作为 SSRIs 抗抑郁反应的决定因素。
我们纳入了 99 名患有重度抑郁症的患者和 48 名对照者。为了统计效力,两个样本都富集了 l/l 5-HTTLPR 多态性,这种多态性在韩国人中很少见。患者接受氟西汀或舍曲林治疗。在 6 周时评估反应。对 5-HTT 启动子区域(5-HTTLPR)的 s/l 多态性进行基因分型。通过最大摄取率(Vmax)和亲和常数(Km)来确定血小板 5-HTT 活性。
反应与 5-HTTLPR 的 s 等位基因呈不同相关,该等位基因也与 Vmax 显著相关。这些关联与在白种人群中报道的相反。与非反应者相比,反应者的 Vmax 和 Km 显著更高。在韩国人和白种人中,高 Vmax 与 SSRIs 类抗抑郁药的反应相关,尽管 5-HTTLPR 多态性与反应和功能的关联因种族而异。
在评估 SSRIs 治疗抑郁症的候选基因生物标志物时,必须考虑种族和功能两个因素。