Medical School, University of Tampere, 33014 Tampere, Finland.
Eur Arch Psychiatry Clin Neurosci. 2011 Mar;261(2):95-102. doi: 10.1007/s00406-010-0126-x. Epub 2010 Jul 17.
The role of a functional polymorphism in the transcriptional control region of serotonin transporter gene (5-HTTLPR, SERTPR) has been studied intensively in major depression and in the response to selective serotonin inhibitors (SSRIs) in major depression. The findings have been contradictory, although majority of the studies indicate that the short allele is associated with poor response to SSRIs in major depression. In the present study, we evaluated the association of 5-HTTLPR with treatment response to SSRI medication in Finnish Caucasian MDD patients. A secondary purpose was to study the possible association of this particular polymorphism with major depressive disorder. The aim of the study was to replicate the previous findings in this area. Primary outcomes of the treatment were remission, defined by an exit score of seven or less, and response, defined by a reduction of at least 50% on the MADRS. We had also a control population of 375 healthy blood donors, as a secondary objective was to evaluate the possible association of this particular polymorphism with major depressive disorder. Twenty-nine of the 85 (34.1%) patients reached the remission and 58.8% achieved the predefined response criteria. The l/l genotype of 5-HTTLPR was presented in 51.7% of those patients who achieved remission vs. 25.0% in the non-remitters (P = 0.03). The result remained statistically significant after adjusting for age, gender, medication and MADRS points at the study entry. However, the small sample size limits the reliability of this result.
5-羟色胺转运体基因(5-HTTLPR,SERTPR)转录调控区的功能性多态性在重度抑郁症及选择性 5-羟色胺再摄取抑制剂(SSRIs)治疗重度抑郁症的反应中已被深入研究。尽管多数研究表明短等位基因与 SSRIs 治疗反应不佳有关,但研究结果却相互矛盾。在本研究中,我们评估了 5-HTTLPR 与芬兰白种人 MDD 患者 SSRIs 药物治疗反应的相关性。次要目的是研究该特定多态性与重度抑郁症之间的可能关联。该研究的目的是复制该领域的先前发现。治疗的主要结局是缓解,定义为退出评分≤7,反应定义为 MADRS 评分至少降低 50%。我们还对 375 名健康献血者进行了对照人群研究,因为次要目的是评估该特定多态性与重度抑郁症之间的可能关联。85 名患者中有 29 名(34.1%)达到缓解,58.8%达到了预先设定的反应标准。达到缓解的患者中,5-HTTLPR 的 l/l 基因型占 51.7%,而非缓解者为 25.0%(P=0.03)。在调整年龄、性别、药物和研究入组时 MADRS 评分后,该结果仍具有统计学意义。然而,小样本量限制了该结果的可靠性。