4.6 Article

IMPACT OF THE HTR3A GENE WITH EARLY LIFE TRAUMA ON EMOTIONAL BRAIN NETWORKS AND DEPRESSED MOOD

期刊

DEPRESSION AND ANXIETY
卷 27, 期 8, 页码 752-759

出版社

WILEY
DOI: 10.1002/da.20726

关键词

depression; HTR3A; stress; emotional brain imaging; Brain Resource International Database; Brain Research and Integrative Neuroscience Network (BRAINnet)

资金

  1. ARC-linkage [LP0455104]
  2. NIMH [MH-52899, MH-39415]
  3. Pfizer foundation Senior Research Fellowship
  4. UNSW Vice-Chancellors Post-doctoral fellowshi
  5. European Molecular Biology Organisation [ALTF 166-2004]
  6. Australian Research Council [LP0455104] Funding Source: Australian Research Council

向作者/读者索取更多资源

Background: The risk for mental illnesses such as depression is increasingly conceptualized as the product of gene environment interactions and their impact on brain structure and function. The role of serotonin 3A receptor gene (HTR3A -42C>T polymorphism) and its interaction with early life stress (ELS) was investigated in view of the receptor's localization to brain regions central to emotion processing. Methods: Fronto-limbic grey matter (GM) loss was measured using magnetic resonance imaging and assessed using voxel-based morphometry analysis in 397 nonclinical individuals front the Brain Resource International Database. Negative mood symptoms were also assessed. Results: The HTR3A CC genotype group, compared to the T carriers, demonstrated comparative loss to GM in hippocampal structures, which extended to the frontal cortices for those CC genotype individuals also exposed to ELS. Elevations in depressed mood were also evident. Conclusions: These findings suggest that the HTR3A CC genotype may be associated with alterations in brain structures central to emotion processing, particularly when exposed to stress, and further highlight the potential role of the serotonin system in the pathophysiology of affective disorders. In contrast, those individuals with the T allele, in particular the TT genotype, may be more protected from such alterations combined with minimal exposure to ELS events. Depression and Anxiety 27:752-759, 2010. (C) 2010 Wiley-Liss, Inc.

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