The neuroprogressive nature of major depressive disorder: pathways to disease evolution and resistance, and therapeutic implications

被引:419
作者
Moylan, S. [1 ]
Maes, M. [2 ]
Wray, N. R. [3 ]
Berk, M. [1 ,4 ,5 ,6 ]
机构
[1] Deakin Univ, Sch Med, Geelong, Vic 3220, Australia
[2] Piyavate Hosp, Bangkok, Thailand
[3] Univ Queensland, Queensland Brain Inst, Brisbane, Qld, Australia
[4] Ctr Youth Mental Hlth, Orygen Youth Hlth Res Ctr, Parkville, Vic, Australia
[5] Mental Hlth Res Inst Victoria, Parkville, Vic, Australia
[6] Univ Melbourne, Dept Psychiat, Parkville, Vic 3052, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
cytokines; depression; inflammation; neuroprogression; nitrosative stress; oxidative stress; NITRIC-OXIDE SYNTHASE; NEUROTROPHIC FACTOR EXPRESSION; SUBGENUAL PREFRONTAL CORTEX; MEDIATED IMMUNE ACTIVATION; LIPID-PEROXIDATION PRODUCT; STRESS-INDUCED DEPRESSION; METHYL-D-ASPARTATE; HIPPOCAMPAL VOLUME; OXIDATIVE STRESS; DOUBLE-BLIND;
D O I
10.1038/mp.2012.33
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
In some patients with major depressive disorder (MDD), individual illness characteristics appear consistent with those of a neuroprogressive illness. Features of neuroprogression include poorer symptomatic, treatment and functional outcomes in patients with earlier disease onset and increased number and length of depressive episodes. In such patients, longer and more frequent depressive episodes appear to increase vulnerability for further episodes, precipitating an accelerating and progressive illness course leading to functional decline. Evidence from clinical, biochemical and neuroimaging studies appear to support this model and are informing novel therapeutic approaches. This paper reviews current knowledge of the neuroprogressive processes that may occur in MDD, including structural brain consequences and potential molecular mechanisms including the role of neurotransmitter systems, inflammatory, oxidative and nitrosative stress pathways, neurotrophins and regulation of neurogenesis, cortisol and the hypothalamic-pituitary-adrenal axis modulation, mitochondrial dysfunction and epigenetic and dietary influences. Evidence-based novel treatments informed by this knowledge are discussed. Molecular Psychiatry (2013) 18, 595-606; doi:10.1038/mp.2012.33; published online 24 April 2012
引用
收藏
页码:595 / 606
页数:12
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