4.8 Article

Sequence variations in CREB1 cosegregate with depressive disorders in women

期刊

MOLECULAR PSYCHIATRY
卷 8, 期 6, 页码 611-618

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/sj.mp.4001354

关键词

genetics; CREB1; depression; sex-specific; women

资金

  1. NCRR NIH HHS [1-P41-RR03655] Funding Source: Medline
  2. NIMH NIH HHS [MH00540, MH60866, MH48969] Funding Source: Medline
  3. NATIONAL CENTER FOR RESEARCH RESOURCES [P41RR003655] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE OF MENTAL HEALTH [R01MH060866, R01MH048969] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Major depressive disorder (MDD) constitutes a major public health problem worldwide and affects women twice as frequently as men. Previous linkage studies have identified a 451 kb region of 2q33-35 that exhibited significant evidence of linkage to Mood Disorders among women ( but not men) from families with recurrent, early-onset MDD (RE-MDD), a severe and strongly familial subtype of MDD. This 451 kb region includes CREB1, an attractive susceptibility gene for MDD and related disorders. Sequence variations in the CREB1 promoter and intron 8 have been detected that cosegregate with Mood Disorders, or their absence, in women from these families, identifying CREB1 as a sex-limited susceptibility gene for unipolar Mood Disorders. These findings implicate the cAMP signaling pathway in the pathophysiology of Mood Disorders and related conditions.

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