Li Xinrong, Sun Ning, Xu Yong, Wang Yanfang, Li Suping, Du Qiaorong, Peng Juyi, Luo Jinxiu, Zhang Kerang
Department of Psychiatry, First Hospital of Shanxi Medical University, Taiyuan 030001, Shanxi Province, China.
Department of Psychiatry, First Hospital of Shanxi Medical University, Taiyuan 030001, Shanxi Province, China ; Nursing College of Shanxi Medical University, Taiyuan 030001, Shanxi Province, China.
Neural Regen Res. 2012 Sep 5;7(25):1985-91. doi: 10.3969/j.issn.1673-5374.2012.25.010.
The norepinephrine transporter plays an important role in the pathophysiology and pharmacological treatment of major depressive disorder. Consequently, the norepinephrine transporter gene is an attractive candidate in major depressive disorder research. In the present study, we evaluated the depression symptoms of subjects with major depressive disorder, who were all from the North of China and of Han Chinese origin, using the Hamilton Depression Scale. We examined the relationship between two single nucleotide polymorphisms in the norepinephrine transporter, rs2242446 and rs5569, and the retardation symptoms of major depressive disorder using quantitative trait testing with the UNPHASED program. rs5569 was associated with depressed mood, and the GG genotype may be a risk factor for this; rs2242446 was associated with work and interest, and the TT genotype may be a risk factor for loss of interest. Our findings suggest that rs2242446 and rs5569 in the norepinephrine transporter gene are associated with the retardation symptoms of depression in the Han Chinese population.
去甲肾上腺素转运体在重度抑郁症的病理生理学和药物治疗中发挥着重要作用。因此,去甲肾上腺素转运体基因是重度抑郁症研究中一个有吸引力的候选基因。在本研究中,我们使用汉密尔顿抑郁量表评估了所有来自中国北方且为汉族的重度抑郁症患者的抑郁症状。我们使用UNPHASED程序进行数量性状测试,研究了去甲肾上腺素转运体中的两个单核苷酸多态性rs2242446和rs5569与重度抑郁症迟缓症状之间的关系。rs5569与情绪低落有关,GG基因型可能是其危险因素;rs2242446与工作和兴趣有关,TT基因型可能是兴趣丧失的危险因素。我们的研究结果表明,去甲肾上腺素转运体基因中的rs2242446和rs5569与汉族人群抑郁症的迟缓症状有关。