Glutathione alterations in depression: a meta-analysis and systematic review of proton magnetic resonance spectroscopy studies.

IF 3.5 3区 医学 Q2 NEUROSCIENCES
Charles J M Bell, Mitul Mehta, Luwaiza Mirza, Allan H Young, Katherine Beck
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Abstract

Background: Major depressive disorder (MDD) is a common and serious psychiatric disorder associated with significant morbidity. There is mounting evidence for the role of oxidative stress in the pathophysiology of depression.

Objective: To investigate alterations in the brain antioxidant glutathione in depression by undertaking a meta-analysis of proton magnetic resonance spectroscopy (1H-MRS).

Methods: MEDLINE, EMBASE and Psych Info databases were searched for case-control studies that reported brain glutathione levels in patients with depression and healthy controls. Means and variances (SDS) were extracted for each measure to calculate effect sizes. Hedges g was used to quantify mean differences. The Meta-analysis of Observational Studies in Epidemiology (MOOSE) and Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) guidelines were followed.

Results: 8 studies that reported measurements for 230 patients with depression and 216 controls were included. Three studies included data for the occipital cortex and five studies for the medial frontal cortex. In the occipital cortex, GSH was lower in the patient group as compared to controls (g = -0.98, 95% [CI, -1.45--0.50], P = < 0.001). In both the medial frontal cortex and in the combined all areas analysis there was no significant difference in GSH levels between cases and controls.

Conclusions: This study found reduced levels of GSH specifically in the occipital region of patients with MDD. This provides some support for the role of oxidative stress in depression and suggests that targeting this system may provide future therapeutic opportunities. However, the meta-analysis was limited by the small number and quality of the included studies. More studies using high quality MRS methods in a variety of brain regions are needed in the future to test this putative hypothesis.

抑郁症的谷胱甘肽改变:质子磁共振波谱研究的荟萃分析和系统回顾。
背景:重度抑郁障碍(MDD)是一种常见的严重精神障碍,发病率高。越来越多的证据表明,氧化应激在抑郁症的病理生理中起着重要作用。目的:通过质子磁共振波谱(1H-MRS) meta分析,探讨抑郁症患者脑内抗氧化剂谷胱甘肽的变化。方法:检索MEDLINE、EMBASE和Psych Info数据库中报道抑郁症患者和健康对照者脑谷胱甘肽水平的病例对照研究。提取每个测量的均值和方差(SDS)来计算效应大小。套期保值被用来量化平均差异。遵循流行病学观察性研究的荟萃分析(MOOSE)和系统评价和荟萃分析的首选报告项目(PRISMA)指南。结果:8项研究报告了230名抑郁症患者和216名对照组的测量结果。三项研究包括枕叶皮层的数据,五项研究包括内侧额叶皮层的数据。在枕叶皮层,与对照组相比,患者组的GSH水平较低(g = -0.98, 95% [CI, -1.45- 0.50], P =结论:该研究发现,重度抑郁症患者枕叶区特异性GSH水平降低。这为氧化应激在抑郁症中的作用提供了一些支持,并表明靶向该系统可能为未来的治疗提供机会。然而,meta分析受到纳入研究的数量和质量的限制。未来需要更多的研究使用高质量的磁共振成像方法在不同的大脑区域来验证这一假设。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Psychopharmacology
Psychopharmacology 医学-精神病学
CiteScore
7.10
自引率
5.90%
发文量
257
审稿时长
2-4 weeks
期刊介绍: Official Journal of the European Behavioural Pharmacology Society (EBPS) Psychopharmacology is an international journal that covers the broad topic of elucidating mechanisms by which drugs affect behavior. The scope of the journal encompasses the following fields: Human Psychopharmacology: Experimental This section includes manuscripts describing the effects of drugs on mood, behavior, cognition and physiology in humans. The journal encourages submissions that involve brain imaging, genetics, neuroendocrinology, and developmental topics. Usually manuscripts in this section describe studies conducted under controlled conditions, but occasionally descriptive or observational studies are also considered. Human Psychopharmacology: Clinical and Translational This section comprises studies addressing the broad intersection of drugs and psychiatric illness. This includes not only clinical trials and studies of drug usage and metabolism, drug surveillance, and pharmacoepidemiology, but also work utilizing the entire range of clinically relevant methodologies, including neuroimaging, pharmacogenetics, cognitive science, biomarkers, and others. Work directed toward the translation of preclinical to clinical knowledge is especially encouraged. The key feature of submissions to this section is that they involve a focus on clinical aspects. Preclinical psychopharmacology: Behavioral and Neural This section considers reports on the effects of compounds with defined chemical structures on any aspect of behavior, in particular when correlated with neurochemical effects, in species other than humans. Manuscripts containing neuroscientific techniques in combination with behavior are welcome. We encourage reports of studies that provide insight into the mechanisms of drug action, at the behavioral and molecular levels. Preclinical Psychopharmacology: Translational This section considers manuscripts that enhance the confidence in a central mechanism that could be of therapeutic value for psychiatric or neurological patients, using disease-relevant preclinical models and tests, or that report on preclinical manipulations and challenges that have the potential to be translated to the clinic. Studies aiming at the refinement of preclinical models based upon clinical findings (back-translation) will also be considered. The journal particularly encourages submissions that integrate measures of target tissue exposure, activity on the molecular target and/or modulation of the targeted biochemical pathways. Preclinical Psychopharmacology: Molecular, Genetic and Epigenetic This section focuses on the molecular and cellular actions of neuropharmacological agents / drugs, and the identification / validation of drug targets affecting the CNS in health and disease. We particularly encourage studies that provide insight into the mechanisms of drug action at the molecular level. Manuscripts containing evidence for genetic or epigenetic effects on neurochemistry or behavior are welcome.
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