Department of Neuropsychiatry, Eulji University School of Medicine, Daejeon, Republic of Korea. ; Department of Psychiatry, Eulji General Hospital, Seoul, Republic of Korea.
Department of Neuropsychiatry, Eulji University School of Medicine, Daejeon, Republic of Korea. ; Department of Psychiatry, Eulji University Hospital, Daejeon, Republic of Korea.
Psychiatry Investig. 2014 Apr;11(2):192-9. doi: 10.4306/pi.2014.11.2.192. Epub 2014 Apr 11.
We investigated possible association between depressive disorders and BDNF Val66Met and 5-HTTLPR. Brain derived neurotrophic factor (BDNF) gene and serotonin transporter (SLC6A4) gene are promising candidate genes for depressive disorders. It has been suggested that BDNF promotes the survival and differentiation of serotonergic neurons and that serotonergic transmission exerts powerful control over BDNF gene expression.
Final analyses were performed on 186 patients with depressive disorders and 1032 controls. Val66Met polymorphism of BDNF gene and 5-HTTLPR polymorphism of serotonin transporter gene were genotyped and allele and genotypic associations on the diagnosis of depression and age at onset of depression were analyzed.
The 5-HTTLPR was positively associated with depressive affected status in the total sample and in females (p=0.038 for allelewise, p=0.015 for genotype-wise associations), but, not in males. The BDNF Val66Met showed no association with depression. BDNF Val66Met and 5-HTTLPR alone were not associated with age at onset of depression. Additional analysis on the interaction between BDNF Val66Met and 5-HTTLPR found a significant association with age at onset of depression in the entire patient group. This association was also found in the female but not in the male patient group. None of the positive results survived Bonferroni correction for multiple testing.
This result suggested that BDNF Val66Met and 5-HTTLPR may contribute to depressive disorders in a complex way and that the genetic effect could differ by gender. Further studies with large number of patients will be necessary.
我们研究了抑郁障碍与脑源性神经营养因子(BDNF) Val66Met 和 5-羟色胺转运体(SLC6A4)基因多态性的可能相关性。脑源性神经营养因子(BDNF)基因和 5-羟色胺转运体(SLC6A4)基因是抑郁障碍的有希望的候选基因。有研究表明,BDNF 促进 5-羟色胺能神经元的存活和分化,5-羟色胺能传递对 BDNF 基因表达有强大的控制作用。
对 186 例抑郁障碍患者和 1032 例对照进行了最终分析。对 BDNF 基因 Val66Met 多态性和 5-羟色胺转运体基因 5-HTTLPR 多态性进行了基因分型,并分析了等位基因和基因型与抑郁障碍诊断和抑郁障碍发病年龄的相关性。
5-HTTLPR 与总样本和女性的抑郁状态呈正相关(等位基因分析:p=0.038,基因型分析:p=0.015),但与男性无关。BDNF Val66Met 与抑郁无关。BDNF Val66Met 和 5-HTTLPR 单独与抑郁障碍的发病年龄无关。对 BDNF Val66Met 和 5-HTTLPR 之间相互作用的进一步分析发现,在整个患者组中与发病年龄有显著相关性。这一关联在女性患者中也存在,但在男性患者中不存在。这些阳性结果在多重检验的 Bonferroni 校正后均未得到验证。
这一结果表明,BDNF Val66Met 和 5-HTTLPR 可能以复杂的方式导致抑郁障碍,遗传效应可能因性别而异。需要对更多患者进行进一步的研究。