BDNF function as a potential mediator of bipolar disorder and post-traumatic stress disorder comorbidity

被引:81
作者
Rakofsky, J. J. [1 ]
Ressler, K. J. [2 ]
Dunlop, B. W. [1 ]
机构
[1] Emory Univ, Dept Psychiat & Behav Sci, Mood & Anxiety Disorders Program, Bipolar Disorders Clin, Atlanta, GA 30306 USA
[2] Emory Univ, Dept Psychiat & Behav Sci, Ctr Behav Neurosci, Yerkes Res Ctr, Atlanta, GA 30306 USA
关键词
bipolar disorder; post-traumatic stress disorder; brain-derived neurotrophic factor; NEUROTROPHIC-FACTOR BDNF; FACTOR VAL66MET POLYMORPHISM; NERVE GROWTH-FACTOR; AGE-OF-ONSET; VENTROMEDIAL PREFRONTAL CORTEX; ACTIVITY-DEPENDENT SECRETION; GENE CONFERS SUSCEPTIBILITY; CHILDHOOD SEXUAL-ABUSE; ANXIETY-RELATED TRAITS; FACTOR MESSENGER-RNA;
D O I
10.1038/mp.2011.121
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Bipolar disorder (BD) and post-traumatic stress disorder (PTSD) frequently co-occur among psychiatric patients, leading to increased morbidity and mortality. Brain-derived neurotrophic factor (BDNF) function is associated with core characteristics of both BD and PTSD. We propose a neurobiological model that underscores the role of reduced BDNF function resulting from several contributing sources, including the met variant of the BDNF val66met (rs6265) single-nucleotide polymorphism, trauma-induced epigenetic regulation and current stress, as a contributor to the onset of both illnesses within the same person. Further studies are needed to evaluate the genetic association between the val66met allele and the BD-PTSD population, along with central/peripheral BDNF levels and epigenetic patterns of BDNF gene regulation within these patients. Molecular Psychiatry (2012) 17, 22-35; doi:10.1038/mp.2011.121; published online 20 September 2011
引用
收藏
页码:22 / 35
页数:14
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