Yu Younger W-Y, Chen Tai-Jui, Hong Chen-Jee, Chen Hung-Mei, Tsai Shih-Jen
Yu's Psychiatric Clinic, Kaohsiung, Taiwan, ROC.
Neuropsychopharmacology. 2003 Jun;28(6):1182-5. doi: 10.1038/sj.npp.1300172. Epub 2003 Apr 2.
Proinflammatory cytokines, including interleukin (IL)-1beta, are suggested to have a role in the pathogenesis of major depressive disorder (MDD) and be related to the therapeutic effects of antidepressants. To elucidate a genetic predisposition of MDD, we studied biallelic polymorphism in the promoter region (position -511) of the IL-1beta gene in 157 patients with MDD and in 112 controls. We also examined the association of this polymorphism and fluoxetine therapeutic response in 119 MDD patients who received a 4-week fluoxetine treatment. No significant difference was found in the genetic polymorphism between MDD patients and controls. However, MDD patients who were homozygous for the -511T allele of the IL-1beta gene had a trend of less severity of depressive symptoms and more favorable fluoxetine therapeutic response than -511C carriers. Further study with a larger sample is needed to clarify the role of the IL-1beta genetic polymorphisms in the symptoms and treatment effects in MDD.
包括白细胞介素(IL)-1β在内的促炎细胞因子被认为在重度抑郁症(MDD)的发病机制中起作用,并且与抗抑郁药的治疗效果相关。为了阐明MDD的遗传易感性,我们研究了157例MDD患者和112例对照者中IL-1β基因启动子区域(-511位点)的双等位基因多态性。我们还检查了119例接受4周氟西汀治疗的MDD患者中这种多态性与氟西汀治疗反应的关联。MDD患者和对照者之间的基因多态性没有显著差异。然而,IL-1β基因-511T等位基因纯合的MDD患者与-511C携带者相比,有抑郁症状严重程度较低和氟西汀治疗反应较好的趋势。需要更大样本的进一步研究来阐明IL-1β基因多态性在MDD症状和治疗效果中的作用。