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Cai, N. ; Chang, S.* ; Li, Y.* ; Li, Q.* ; Hu, J.* ; Liang, J.* ; Song, L.* ; Kretzschmar, W.* ; Gan, X.* ; Nicod, J.* ; Rivera, M.* ; Deng, H.* ; Du, B.* ; Li, K.* ; Sang, W.* ; Gao, J.* ; Gao, S.* ; Ha, B.* ; Ho, H.Y.* ; Hu, C.* ; Hu, Z.* ; Huang, G.* ; Jiang, G.* ; Jiang, T.* ; Jin, W.* ; Li, G.* ; Lin, Y.T.* ; Liu, L.* ; Liu, T.* ; Liu, Y.* ; Lu, Y.* ; Lv, L.* ; Meng, H.* ; Qian, P.* ; Sang, H.* ; Shen, J.* ; Shi, J.* ; Sun, J.* ; Tao, M.* ; Wang, G.* ; Wang, J.* ; Wang, L.* ; Wang, X.* ; Yang, H.* ; Yang, L.* ; Yin, Y.* ; Zhang, J.* ; Zhang, K.* ; Sun, N.* ; Zhang, W.* ; Zhang, X.* ; Zhang, Z.* ; Zhong, H.* ; Breen, G.* ; Marchini, J.* ; Chen, Y.* ; Xu, Q.* ; Xu, X.* ; Mott, R.* ; Huang, G.J.* ; Kendler, K.* ; Flint, J.*

Molecular signatures of major depression.

Curr. Biol. 25, 1146-1156 (2015)
Verlagsversion DOI PMC
Closed
Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
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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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Sprache englisch
Veröffentlichungsjahr 2015
HGF-Berichtsjahr 2015
ISSN (print) / ISBN 0960-9822
e-ISSN 1879-0445
Zeitschrift Current Biology
Quellenangaben Band: 25, Heft: 9, Seiten: 1146-1156 Artikelnummer: , Supplement: ,
Verlag Elsevier
Begutachtungsstatus Peer reviewed
Institut(e) Helmholtz Pioneer Campus (HPC)
DOI 10.1016/j.cub.2015.03.008
PubMed ID 25913401
Erfassungsdatum 2019-12-09
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