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抑郁发病机制与治疗:从血液 mRNA 表达中我们能学到什么?

Depression pathogenesis and treatment: what can we learn from blood mRNA expression?

机构信息

Section of Perinatal Psychiatry & Stress, Department of Psychological Medicine, Institute of Psychiatry, King's College London, 125 Coldharbour Lane, London, SE5 9NU, UK.

出版信息

BMC Med. 2013 Feb 5;11:28. doi: 10.1186/1741-7015-11-28.

DOI:10.1186/1741-7015-11-28
PMID:23384232
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3606439/
Abstract

Alterations in several biological systems, including the neuroendocrine and immune systems, have been consistently demonstrated in patients with major depressive disorder. These alterations have been predominantly studied using easily accessible systems such as blood and saliva. In recent years there has been an increasing body of evidence supporting the use of peripheral blood gene expression to investigate the pathogenesis of depression, and to identify relevant biomarkers. In this paper we review the current literature on gene expression alterations in depression, focusing in particular on three important and interlinked biological domains: inflammation, glucocorticoid receptor functionality and neuroplasticity. We also briefly review the few existing transcriptomics studies. Our review summarizes data showing that patients with major depressive disorder exhibit an altered pattern of expression in several genes belonging to these three biological domains when compared with healthy controls. In particular, we show evidence for a pattern of 'state-related' gene expression changes that are normalized either by remission or by antidepressant treatment. Taken together, these findings highlight the use of peripheral blood gene expression as a clinically relevant biomarker approach.

摘要

在患有重度抑郁症的患者中,已经一致证明了几种生物系统(包括神经内分泌和免疫系统)的改变。这些改变主要使用易于获取的系统(如血液和唾液)进行研究。近年来,越来越多的证据支持使用外周血基因表达来研究抑郁症的发病机制,并确定相关的生物标志物。在本文中,我们综述了有关抑郁症基因表达改变的现有文献,特别关注三个重要且相互关联的生物学领域:炎症、糖皮质激素受体功能和神经可塑性。我们还简要回顾了少数现有的转录组学研究。我们的综述总结了数据,表明与健康对照组相比,患有重度抑郁症的患者在这三个生物学领域的几个基因中表现出改变的表达模式。特别是,我们证明了存在一种“与状态相关”的基因表达变化模式,这种模式可以通过缓解或抗抑郁治疗来正常化。综上所述,这些发现强调了使用外周血基因表达作为一种有临床意义的生物标志物方法。

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本文引用的文献

1
Glucocorticoid-related molecular signaling pathways regulating hippocampal neurogenesis.调控海马神经发生的糖皮质激素相关分子信号通路。
Neuropsychopharmacology. 2013 Apr;38(5):872-83. doi: 10.1038/npp.2012.253. Epub 2012 Dec 6.
2
Candidate genes expression profile associated with antidepressants response in the GENDEP study: differentiating between baseline 'predictors' and longitudinal 'targets'.候选基因表达谱与 GENDEP 研究中抗抑郁药反应相关:区分基线“预测因子”和纵向“靶标”。
Neuropsychopharmacology. 2013 Feb;38(3):377-85. doi: 10.1038/npp.2012.191. Epub 2012 Sep 19.
3
Inflammation and depression.炎症与抑郁症。
Curr Top Behav Neurosci. 2013;14:135-51. doi: 10.1007/7854_2012_211.
4
The neuroprogressive nature of major depressive disorder: pathways to disease evolution and resistance, and therapeutic implications.重性抑郁障碍的神经进展性:疾病演变和抵抗的途径,以及治疗意义。
Mol Psychiatry. 2013 May;18(5):595-606. doi: 10.1038/mp.2012.33. Epub 2012 Apr 24.
5
Blood-based gene expression profiles models for classification of subsyndromal symptomatic depression and major depressive disorder.基于血液的基因表达谱模型用于亚综合征症状性抑郁和重性抑郁障碍的分类。
PLoS One. 2012;7(2):e31283. doi: 10.1371/journal.pone.0031283. Epub 2012 Feb 13.
6
The expression of genes encoding for COX-2, MPO, iNOS, and sPLA2-IIA in patients with recurrent depressive disorder.在复发性抑郁症患者中,COX-2、MPO、iNOS 和 sPLA2-IIA 基因的表达。
J Affect Disord. 2012 May;138(3):360-6. doi: 10.1016/j.jad.2012.01.016. Epub 2012 Feb 12.
7
The roles of neurotrophic factor and Wnt signaling in depression.神经营养因子和 Wnt 信号通路在抑郁症中的作用。
Clin Pharmacol Ther. 2012 Feb;91(2):333-8. doi: 10.1038/clpt.2011.296. Epub 2011 Dec 28.
8
Mechanistic explanations how cell-mediated immune activation, inflammation and oxidative and nitrosative stress pathways and their sequels and concomitants play a role in the pathophysiology of unipolar depression.细胞介导的免疫激活、炎症以及氧化和硝化应激途径及其后果和伴随事件如何在单相抑郁症的病理生理学中发挥作用的机制解释。
Neurosci Biobehav Rev. 2012 Feb;36(2):764-85. doi: 10.1016/j.neubiorev.2011.12.005. Epub 2011 Dec 19.
9
Regulation of mRNA expression encoding chaperone and co-chaperone proteins of the glucocorticoid receptor in peripheral blood: association with depressive symptoms during pregnancy.调控糖皮质激素受体伴侣蛋白和共伴侣蛋白编码 mRNA 的表达:与孕期抑郁症状的相关性。
Psychol Med. 2012 May;42(5):943-56. doi: 10.1017/S0033291711002121.
10
Can adult neurogenesis buffer stress responses and depressive behaviour?成年神经发生能否缓冲应激反应和抑郁行为?
Mol Psychiatry. 2012 Jan;17(1):9-10. doi: 10.1038/mp.2011.133. Epub 2011 Oct 11.