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Alterations of multiple peripheral inflammatory cytokine levels after repeated ketamine infusions in major depressive disorder.在重度抑郁症患者中,反复给予氯胺酮后,多种外周炎症细胞因子水平的改变。
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单相抑郁症患者与健康对照个体的脑脊液生物标志物比较:系统评价和荟萃分析。

Cerebrospinal Fluid Biomarkers in Patients With Unipolar Depression Compared With Healthy Control Individuals: A Systematic Review and Meta-analysis.

机构信息

Biological and Precision Psychiatry, Copenhagen Research Centre for Mental Health, Mental Health Centre Copenhagen, Copenhagen University Hospital, Copenhagen, Denmark.

Department of Immunology and Microbiology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.

出版信息

JAMA Psychiatry. 2022 Jun 1;79(6):571-581. doi: 10.1001/jamapsychiatry.2022.0645.

DOI:10.1001/jamapsychiatry.2022.0645
PMID:35442429
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9021989/
Abstract

IMPORTANCE

Depression has been associated with alterations in neurotransmitters, hormones, and inflammatory and neurodegenerative biomarkers, and biomarkers quantified in the cerebrospinal fluid (CSF) are more likely to reflect ongoing biochemical changes within the brain. However, a comprehensive overview of CSF biomarkers is lacking and could contribute to the pathophysiological understanding of depression.

OBJECTIVE

To investigate differences in quantified CSF biomarkers in patients with unipolar depression compared with healthy control individuals.

DATA SOURCES

PubMed, EMBASE, PsycINFO, Cochrane Library, Web of Science, and ClinicalTrials.gov were searched for eligible trials from database inception to August 25, 2021.

STUDY SELECTION

All studies investigating CSF biomarkers in individuals 18 years and older with unipolar depression and healthy control individuals were included. One author screened titles and abstracts, and 2 independent reviewers examined full-text reports. Studies that did not include healthy control individuals or included control individuals with recent hospital contacts or admissions that might affect CSF biomarker concentrations were excluded.

DATA EXTRACTION AND SYNTHESIS

Data extraction and quality assessment were performed by 2 reviewers following the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) and Meta-analysis of Observational Studies in Epidemiology (MOOSE) reporting guidelines. Meta-analyses were performed using standardized mean differences (SMDs) calculated with random-effects models. A third investigator was consulted if the 2 reviewers reached different decisions or when in doubt.

MAIN OUTCOMES AND MEASURES

Quantifiable CSF biomarkers.

RESULTS

A total of 167 studies met eligibility criteria, and 97 had available data and were included in the meta-analysis. These 97 studies comprised 165 biomarkers, 42 of which were quantified in 2 or more studies. CSF levels of interleukin 6 (7 studies; SMD, 0.35; 95% CI, 0.12 to 0.59; I2 = 16%), total protein (5 studies; SMD, 0.53; 95% CI, 0.35 to 0.72; I2 = 0%), and cortisol (2 studies; SMD, 1.23; 95% CI, 0.89 to 1.57; I2 = 0%) were higher in patients with unipolar depression compared with healthy control individuals, whereas homovanillic acid (17 studies; SMD, -0.26; 95% CI, -0.39 to -0.14; I2 = 11%), γ-aminobutyric acid (4 studies; SMD, -0.50; 95% CI, -0.92 to -0.08; I2 = 55%), somatostatin (5 studies; SMD, -1.49; 95% CI, -2.53 to -0.45; I2 = 91%), brain-derived neurotrophic factor (3 studies; SMD, -0.58; 95% CI, -0.97 to -0.19; I2 = 0%), amyloid-β 40 (3 studies; SMD, -0.80; 95% CI, -1.14 to -0.46; I2 = 0%), and transthyretin (2 studies; SMD, -0.82; 95% CI, -1.37 to -0.27; I2 = 0%) were lower. The remaining 33 biomarkers had nonsignificant results.

CONCLUSIONS AND RELEVANCE

The findings of this systematic review and meta-analysis point toward a dysregulated dopaminergic system, a compromised inhibitory system, hypothalamic-pituitary-adrenal axis hyperactivity, increased neuroinflammation and blood-brain barrier permeability, and impaired neuroplasticity as important factors in depression pathophysiology.

摘要

重要性

抑郁症与神经递质、激素、炎症和神经退行性生物标志物的改变有关,而脑脊液(CSF)中定量的生物标志物更有可能反映大脑内持续的生化变化。然而,目前缺乏对 CSF 生物标志物的全面概述,这可能有助于对抑郁症的病理生理学的理解。

目的

研究与健康对照组相比,单相抑郁症患者 CSF 生物标志物的差异。

数据来源

从数据库成立到 2021 年 8 月 25 日,通过 PubMed、EMBASE、PsycINFO、Cochrane 图书馆、Web of Science 和 ClinicalTrials.gov 搜索了合格的试验。

研究选择

所有研究了 18 岁及以上单相抑郁症患者和健康对照组个体 CSF 生物标志物的研究均被纳入。一名作者筛选标题和摘要,两名独立的审稿人检查全文报告。未包括健康对照组或包括最近住院或入院可能影响 CSF 生物标志物浓度的对照组的研究被排除。

数据提取和综合

两名审稿人按照系统评价和荟萃分析的 Preferred Reporting Items(PRISMA)和观察性研究荟萃分析的 MOOSE 报告指南进行数据提取和质量评估。使用随机效应模型计算标准化均数差(SMD)进行荟萃分析。如果两名审稿人做出不同的决定或有疑问,将咨询第三名研究人员。

主要结果和措施

可量化的 CSF 生物标志物。

结果

共有 167 项研究符合入选标准,其中 97 项有可用数据并纳入荟萃分析。这 97 项研究包括 165 项生物标志物,其中 42 项在 2 项或更多研究中进行了定量。与健康对照组相比,抑郁症患者的 CSF 白细胞介素 6(7 项研究;SMD,0.35;95%CI,0.12 至 0.59;I2=16%)、总蛋白(5 项研究;SMD,0.53;95%CI,0.35 至 0.72;I2=0%)和皮质醇(2 项研究;SMD,1.23;95%CI,0.89 至 1.57;I2=0%)水平更高,而单胺氧化酶(17 项研究;SMD,-0.26;95%CI,-0.39 至 -0.14;I2=11%)、γ-氨基丁酸(4 项研究;SMD,-0.50;95%CI,-0.92 至 -0.08;I2=55%)、生长抑素(5 项研究;SMD,-1.49;95%CI,-2.53 至 -0.45;I2=91%)、脑源性神经营养因子(3 项研究;SMD,-0.58;95%CI,-0.97 至 -0.19;I2=0%)、β-淀粉样蛋白 40(3 项研究;SMD,-0.80;95%CI,-1.14 至 -0.46;I2=0%)和转甲状腺素(2 项研究;SMD,-0.82;95%CI,-1.37 至 -0.27;I2=0%)水平较低。其余 33 项生物标志物的结果无统计学意义。

结论和相关性

这项系统评价和荟萃分析的结果表明,多巴胺能系统失调、抑制系统受损、下丘脑-垂体-肾上腺轴活性亢进、神经炎症和血脑屏障通透性增加以及神经可塑性受损可能是抑郁症病理生理学的重要因素。