Molecular Signatures of Major Depression

نویسندگان

  • Na Cai
  • Simon Chang
  • Yihan Li
  • Qibin Li
  • Jingchu Hu
  • Jieqin Liang
  • Li Song
  • Warren Kretzschmar
  • Xiangchao Gan
  • Jerome Nicod
  • Margarita Rivera
  • Hong Deng
  • Bo Du
  • Keqing Li
  • Wenhu Sang
  • Jingfang Gao
  • Shugui Gao
  • Baowei Ha
  • Hung-Yao Ho
  • Chunmei Hu
  • Jian Hu
  • Zhenfei Hu
  • Guoping Huang
  • Guoqing Jiang
  • Tao Jiang
  • Wei Jin
  • Gongying Li
  • Kan Li
  • Yi Li
  • Yingrui Li
  • Youhui Li
  • Yu-Ting Lin
  • Lanfen Liu
  • Tiebang Liu
  • Ying Liu
  • Yuan Liu
  • Yao Lu
  • Luxian Lv
  • Huaqing Meng
  • Puyi Qian
  • Hong Sang
  • Jianhua Shen
  • Jianguo Shi
  • Jing Sun
  • Ming Tao
  • Gang Wang
  • Guangbiao Wang
  • Jian Wang
  • Linmao Wang
  • Xueyi Wang
  • Xumei Wang
  • Huanming Yang
  • Lijun Yang
  • Ye Yin
  • Jinbei Zhang
  • Kerang Zhang
  • Ning Sun
  • Wei Zhang
  • Xiuqing Zhang
  • Zhen Zhang
  • Hui Zhong
  • Gerome Breen
  • Jun Wang
  • Jonathan Marchini
  • Yiping Chen
  • Qi Xu
  • Xun Xu
  • Richard Mott
  • Guo-Jen Huang
  • Kenneth Kendler
  • Jonathan Flint
چکیده

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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عنوان ژورنال:

دوره 25  شماره 

صفحات  -

تاریخ انتشار 2015