Molecular Signatures of Major Depression

Na Cai(Centre for Human Genetics), Simon Chang(Chang Gung University), Yihan Li(BGI Group (China)), Qibin Li(BGI Group (China)), Jingchu Hu(BGI Group (China)), Jieqin Liang(BGI Group (China)), Li Song(BGI Group (China)), Warren W. Kretzschmar(Centre for Human Genetics), Xiangchao Gan(Max Planck Institute for Plant Breeding Research), Jérôme Nicod(Centre for Human Genetics), Margarita Rivera(Universidad de Granada), Hong Deng(Sichuan University), Bo Du(Hebei Mental Health Center), Keqing Li(Jiangxi Mental Health Center), Wenhu Sang(Hebei Mental Health Center), Jingfang Gao, Shugui Gao(Ningbo Kangning Hospital), Baowei Ha(Liaocheng People's Hospital), Hung‐Yao Ho(Chang Gung University), Chunmei Hu(Heilongjiang Provincial Hospital), Jian Hu(BGI Group (China)), Zhenfei Hu(BGI Group (China)), Guoping Huang(Chang Gung University), Guoqing Jiang(Chongqing City Mental Health Center), Tao Jiang(BGI Group (China)), Wei Jin(BGI Group (China)), Gongying Li(Jining Medical University), Kan Li(Jiangxi Mental Health Center), Yi Li(BGI Group (China)), Yingrui Li(BGI Group (China)), Youhui Li(BGI Group (China)), Yu-Ting Lin(Chang Gung University), Lanfen Liu(Shandong Mental Health Center), Tiebang Liu(Shenzhen KangNing Hospital), Ying Liu(BGI Group (China)), Yuan Liu(BGI Group (China)), Yao Lu(BGI Group (China)), Luxian Lv(Henan Psychiatric Hospital), Huaqing Meng(Chongqing Medical University), Puyi Qian(BGI Group (China)), Hong Sang(Sixth Hospital of Changchun City), Jianhua Shen(Tianjin Anding Hospital), Jianguo Shi(Xian Mental Health Center), Jing Sun(Nanjing Brain Hospital), Ming Tao(Zhejiang Chinese Medical University), Gang Wang(BGI Group (China)), Guangbiao Wang(BGI Group (China)), Jian Wang(BGI Group (China)), Linmao Wang(BGI Group (China)), Xueyi Wang(Hebei Medical University), Xumei Wang(Hebei Medical University), Huanming Yang(BGI Group (China)), Lijun Yang(Brain Hospital of Jilin), Ye Yin(BGI Group (China)), Jinbei Zhang(Sun Yat-sen University), Kerang Zhang(Shanxi Medical University), Ning Sun(Shanxi Medical University), Wei Zhang(Harbin Medical University), Xiuqing Zhang(BGI Group (China)), Zhen Zhang(Jiangsu University), Hui Zhong(Anhui Mental Health Center), Gerome Breen(King's College London), Jun Wang(BGI Group (China)), Jonathan Marchini(Centre for Human Genetics), Yiping Chen(University of Oxford), Qi Xu(Chinese Academy of Medical Sciences & Peking Union Medical College), Xun Xu(BGI Group (China)), Richard Mott(Centre for Human Genetics), Guo‐Jen Huang(Chang Gung University), Kenneth S. Kendler(Virginia Commonwealth University), Jonathan Flint(Centre for Human Genetics)
Current Biology
April 25, 2015
Cited by 288Open Access
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Abstract

Adversity, particularly in early life, can cause illness. Clues to the responsible mechanisms may lie with the discovery of molecular signatures of stress, some of which include alterations to an individual's somatic genome. Here, using genome sequences from 11,670 women, we observed a highly significant association between a stress-related disease, major depression, and the amount of mtDNA (p = 9.00 × 10(-42), odds ratio 1.33 [95% confidence interval [CI] = 1.29-1.37]) and telomere length (p = 2.84 × 10(-14), odds ratio 0.85 [95% CI = 0.81-0.89]). While both telomere length and mtDNA amount were associated with adverse life events, conditional regression analyses showed the molecular changes were contingent on the depressed state. We tested this hypothesis with experiments in mice, demonstrating that stress causes both molecular changes, which are partly reversible and can be elicited by the administration of corticosterone. Together, these results demonstrate that changes in the amount of mtDNA and telomere length are consequences of stress and entering a depressed state. These findings identify increased amounts of mtDNA as a molecular marker of MD and have important implications for understanding how stress causes the disease.


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