Sato Kazuhiro, Yoshida Keizo, Takahashi Hitoshi, Ito Kenichi, Kamata Mitsuhiro, Higuchi Hisashi, Shimizu Tetsuo, Itoh Kunihiko, Inoue Kazuyuki, Tezuka Takehiko, Suzuki Toshio, Ohkubo Taashi, Sugawara Kazunobu, Otani Koichi
Department of Psychiatry, Akita University School of Medicine, Akita, Japan.
Neuropsychobiology. 2002;46(3):136-40. doi: 10.1159/000066394.
Genetic polymorphism of the serotonin 5-HT(2A) receptor seems to be associated with therapeutic response to selective serotonin reuptake inhibitors (SSRIs). The present study investigated whether a novel -1438G/A polymorphism in the promoter region of the 5-HT(2A )receptor gene is associated with therapeutic response to fluvoxamine (an SSRI) in 66 Japanese patients with major depressive disorder. Fluvoxamine (50 to 200 mg) was administered twice daily for 6 weeks. Fifty-four patients completed this study. The genotype distribution and the allele frequencies showed no significant difference between responders and non-responders. The time-course of the Montgomery-Asberg Depression Rating Scale scores showed no significant difference among -1438G/G, -1438G/A, and -1438A/A genotype groups. The results demonstrated that the -1438G/A promoter polymorphism in the 5-HT(2A) receptor gene was unlikely to have a major role in therapeutic response to fluvoxamine in Japanese patients with major depressive disorder.
血清素5-HT(2A)受体的基因多态性似乎与对选择性血清素再摄取抑制剂(SSRI)的治疗反应相关。本研究调查了5-HT(2A)受体基因启动子区域一个新的-1438G/A多态性是否与66名日本重度抑郁症患者对氟伏沙明(一种SSRI)的治疗反应相关。氟伏沙明(50至200毫克)每日给药两次,持续6周。54名患者完成了本研究。应答者和无应答者之间的基因型分布和等位基因频率无显著差异。蒙哥马利-阿斯伯格抑郁评定量表评分的时间进程在-1438G/G、-1438G/A和-1438A/A基因型组之间无显著差异。结果表明,5-HT(2A)受体基因中的-1438G/A启动子多态性在日本重度抑郁症患者对氟伏沙明的治疗反应中不太可能起主要作用。