期刊文献+

抑郁易感性因素的神经机制 被引量:6

Neural mechanisms underlying susceptibility factors in depression
原文传递
导出
摘要 抑郁症是一种常见的精神类疾病,导致其发病的影响因素众多,但其神经机制尚不清楚.本文首先回顾了与抑郁易感性有关的认知理论,包括Beck提出的认知模型理论以及Abramson提出的抑郁无望理论模型.其次,从遗传因素、外部环境因素以及个体心理因素3个方面阐述了易感性因素对抑郁影响及其作用的神经机制.最后,基于认知神经科学的现状和局限性并结合抑郁研究现状,提出了抑郁研究可能面临的挑战和对未来研究展望.具体而言,未来研究应从统计建模的角度出发,整合基因-脑影像-行为大数据,先从横向研究角度比较探讨和分析抑郁形成的各种影响因素,建立有效的因素模型;再从纵向跟踪的角度探明各种易感因素在抑郁发生中的作用机制,建立抑郁的预测模型;最终实现基于基因-脑影像-行为大数据的融合,从而对抑郁的发生和发展进行有效的预测和早期干预,降低抑郁症的发病率. Major depressive disorder(MDD) is one of the most common mental disorders. The World Health Organization currently estimates that there are approximately 350 million depressive patients worldwide. MDD not only affects the life quality of individuals and their families, but also brings about a heavy financial burden to the society. The factors that contribute to the onset of MDD are complex and its underlying neural mechanisms have remained unclear. The modern medical science proposes "early detection, early treatment" of diseases. Therefore, early prediction and diagnosis of the MDD onsets are becoming a trend in depressive studies. This review firstly sketched the related cognitive theories of susceptibility in depression, including Beck's Cognitive Model of Depression and Abramson's Theory of Helplessness and Depression. Secondly, we elaborated the way in which susceptibility factors exerted their influences on depression and its underlying neural mechanisms from the perspectives of gene, external environment and individual psychological factors, respectively. Among the depressionrelated candidate genes, 5-HTTLPR(serotonin-transporter-linked polymorphic region) plays a critical role in modulating the cognitive-affective system which is associated with depression. The factors of the external environment which might lead to depression mainly involve the perceived stress and the social support when individuals experience negative life events. Those factors exert lasting and overwhelming influences on the structure and function of brain regions which are related to abnormalities of the cognitive-affective modulating system. Stress may affect the hippocampus and the prefrontal cortex which are closely related to depression, while social support involves the prefrontal cortex, the anterior cingulate cortex and the corpus striatum which are associated with cognition-affection modulating system. The individual psychological factors that might contribute to depression include rumination, attribution, neuroticism and extraversion and are believed to be associated with the prefrontal cortex, the cingulate cortex, the subcortical nuclei such as hippocampus and amygdala. Finally, we analyzed the limitations of cognitive neuroscience, such as low statistical testing power, verifiability and reproducibility, and the fact that multimodal brain imaging is currently not sufficient to uncover the neural mechanisms of the brains. Based on the status quo of research into cognitive neuroscience and depression, we put forward the prospective challenges and outlooks for future research into depression. Specifically, the future research is expected to start from the perspective of statistical modeling and to aim at gene-brain-behavior integration. Then, cross-sectional studies are expected to explore and analyze the various factors affecting the depression and to establish an effective factorial model. Structural equation model(SEM) and machine learning model are effective approaches to build, estimate and verify causal models. On the other hand, the longitudinal studies are expected to ascertain the roles of various risk factors in depressive progression and to establish the predictive model of depression. The clinical practice of the built model is yet to be verified from the perspective of intervention and treatment. For instance, transcranial magnetic stimulation(TMS), transcranial electrical stimulation(TES) and other approaches could be used to verify the effects of treatment. Eventually, based on the gene-brain-behavior interplay, it could provide a valuable model for predicting the occurrence and development of depression, conducting early intervention and thus reducing the incidence of depression.
出处 《科学通报》 EI CAS CSCD 北大核心 2016年第6期654-667,共14页 Chinese Science Bulletin
基金 国家自然科学基金(31571137 31271087) 重庆市自然科学基金(cstc2015jcyj A10106) 中央高校基本业务费创新团队项目(SWU1509383)资助
关键词 抑郁 易感性因素 神经机制 预测模型 depression susceptibility factors neural mechanisms predictive model
  • 相关文献

参考文献123

  • 1Mrazek D A, Hornberger J C, Altar C A, et al. A review of the clinical, economic, and societal burden of treatment-resistant depression:1996-2013. Psychiat Serv, 2014, 65:977-987.
  • 2Lépine J P, Briley M. The increasing burden of depression. Neuropsych Dis Treat, 2011, 7:3-7.
  • 3乔婧,邱江,李迪康,熊清.重度抑郁症多脑区基因表达谱分析[J].科学通报,2015,60(11):1010-1021. 被引量:4
  • 4Sullivan P F, Neale M C, Kendler K S. Genetic epidemiology of major depression:Review and meta-analysis. Am J Geriat Psychiat, 2014, 157:1552-1562.
  • 5Dunn E C, Brown R C, Dai Y, et al. Genetic determinants of depression:Recent findings and future directions. Harvard Rev Psychiat, 2015, 23:1-18.
  • 6抑郁症的蛋白质组学和多肽组学研究[J].中国科技成果,2013(22):71-72. 被引量:2
  • 7Beck A T. Cognitive models of depression. Clin Adv Cognitive Psychother:Theory Appl, 2002, 14:29-61.
  • 8Disner S G, Beevers C G, Haigh E A P, et al. Neural mechanisms of the cognitive model of depression. Nat Rev Neurosci, 2011, 12:467-477.
  • 9Cole M G, Dendukuri N. Risk factors for depression among elderly community subjects:A systematic review and meta-analysis. Am J Geriat Psychiat, 2014, 160:1147-1156.
  • 10Letourneau N L, Tramonte L, Willms J D. Maternal depression, family functioning and children's longitudinal development. J Pediatr Nurs, 2013, 28:223-234.

二级参考文献223

  • 1刘玉新,张建卫,金盛华.社会支持与人格对大学生压力的影响[J].心理学报,2005,37(1):92-99. 被引量:77
  • 2叶俊杰.大学生领悟社会支持的影响因素研究[J].心理科学,2005,28(6):1468-1471. 被引量:155
  • 3汪向东 王希林 马弘.心理卫生评定量表手册.中国心理卫生杂志,1999,12:217-217.
  • 4Ametz B B, Brenner S O, Levi L. Neuroendocrine and immunologic effects of unemployment and job insecurity. Psychotherapy and Psychosomatics., 1991 (55) :76.
  • 5Aradal-Erikson E, Erikson T E, Holm A C, et aL Salivary cortisol and serum prolactin in relation to stress rating scales in a group of rescue workers. Biol. Psychiatry. 1999(46) :850.
  • 6Kirschbaum C, Wolf O T. May M, et al. Stress and treatment induced elevations of cortisol levels associated with impaired declarative memory in healthy adults. Life Science, 1996 (58): 1475.
  • 7Whelan T B, Schteingart D E, Starkkman M N, et al. Neuropsychological deficits in Cushing's syndrome. J Nerv. Ment. Dis. 1980,168:753.
  • 8Starkman MN, Gebarski SS, Berent S. Hippocampal formation volume, memory dysfunction, and eortisol levels in patients with Cushing's syndrome. Biological Psychiatry. 1992,1 32(9) : 756.
  • 9Starkman M, Giordani B, Gebarski S, et al. Decrease in cortisol reverses human hippocampal atrophy following treatment of Cushing's disease. Biol Psychiatry, in press.
  • 10O'Brien JT, Schweitzer I, Ames D. The function of the hypothalamic-pituitary-adrenal axis in Alzheimer's disease. Response to insulin hypoglycaemia. British Journal of Psychiatry. 1994, 165(5):650.

共引文献133

同被引文献102

引证文献6

二级引证文献23

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部