Sex differences in the inflammation-depression link: A systematic review and meta-analysis

IF 8.8 2区 医学 Q1 IMMUNOLOGY Brain, Behavior, and Immunity Pub Date : 2024-07-30 DOI:10.1016/j.bbi.2024.07.037
{"title":"Sex differences in the inflammation-depression link: A systematic review and meta-analysis","authors":"","doi":"10.1016/j.bbi.2024.07.037","DOIUrl":null,"url":null,"abstract":"<div><p>Major Depressive Disorder (MDD) is a heterogeneous disorder that affects twice as many women than men. Precluding advances in more tailored and efficacious treatments for depression is the lack of reliable biomarkers. While depression is linked to elevations in inflammatory immune system functioning, this relationship is not evident among all individuals with depression and may vary based on symptom subtypes and/or sex. This systematic review and meta-analysis examined whether inflammatory immune peripheral markers of depression are sex-specific. PRISMA guidelines were followed for the systematic review, and a comprehensive search strategy that identified studies from PubMed and PsycInfo was applied. Studies were included if they reported C-reactive protein (CRP), interleukin (IL)-6, tumor necrosis factor (TNF)-α and/or IL-1β for males and/or females among depressed and healthy adults. We identified 23 studies that satisfied these inclusion criteria. Random-effects meta-analysis models were fit, and measures of association were summarized between levels of circulating markers of inflammation in depressed and healthy males and females. Sex-based analyses revealed elevated levels of CRP among females with depression (Cohen’s d = 0.19) relative to their healthy counterparts (p = 0.02), an effect not apparent among males (Cohen’s d = -0.01). Similarly, levels of IL-6 were increased among females with depression compared to healthy controls (Cohen’s d = 0.51; p = 0.04), but once again this was not found among males (Cohen’s d = 0.16). While TNF-α levels were elevated among individuals with depression compared to controls (p = 0.01), no statistically significant sex differences were found. The meta-analysis for IL-1β resulted in only three articles, and thus, results are presented in the supplemental section. This meta-analysis advances our understanding of the unique involvement of inflammatory biomarkers in depression among men and women, which may help inform more tailored sex-specific treatment approaches in the future.</p></div>","PeriodicalId":9199,"journal":{"name":"Brain, Behavior, and Immunity","volume":null,"pages":null},"PeriodicalIF":8.8000,"publicationDate":"2024-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S0889159124005129/pdfft?md5=7c40a6d19db33bcffcbe502742bc88a6&pid=1-s2.0-S0889159124005129-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Brain, Behavior, and Immunity","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0889159124005129","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Major Depressive Disorder (MDD) is a heterogeneous disorder that affects twice as many women than men. Precluding advances in more tailored and efficacious treatments for depression is the lack of reliable biomarkers. While depression is linked to elevations in inflammatory immune system functioning, this relationship is not evident among all individuals with depression and may vary based on symptom subtypes and/or sex. This systematic review and meta-analysis examined whether inflammatory immune peripheral markers of depression are sex-specific. PRISMA guidelines were followed for the systematic review, and a comprehensive search strategy that identified studies from PubMed and PsycInfo was applied. Studies were included if they reported C-reactive protein (CRP), interleukin (IL)-6, tumor necrosis factor (TNF)-α and/or IL-1β for males and/or females among depressed and healthy adults. We identified 23 studies that satisfied these inclusion criteria. Random-effects meta-analysis models were fit, and measures of association were summarized between levels of circulating markers of inflammation in depressed and healthy males and females. Sex-based analyses revealed elevated levels of CRP among females with depression (Cohen’s d = 0.19) relative to their healthy counterparts (p = 0.02), an effect not apparent among males (Cohen’s d = -0.01). Similarly, levels of IL-6 were increased among females with depression compared to healthy controls (Cohen’s d = 0.51; p = 0.04), but once again this was not found among males (Cohen’s d = 0.16). While TNF-α levels were elevated among individuals with depression compared to controls (p = 0.01), no statistically significant sex differences were found. The meta-analysis for IL-1β resulted in only three articles, and thus, results are presented in the supplemental section. This meta-analysis advances our understanding of the unique involvement of inflammatory biomarkers in depression among men and women, which may help inform more tailored sex-specific treatment approaches in the future.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
炎症与抑郁之间的性别差异:系统回顾与荟萃分析
重度抑郁症(MDD)是一种异质性疾病,女性患者人数是男性的两倍。由于缺乏可靠的生物标志物,无法对抑郁症进行更有针对性、更有效的治疗。虽然抑郁症与炎症性免疫系统功能的升高有关,但这种关系在所有抑郁症患者中并不明显,而且可能因症状亚型和/或性别而异。本系统综述和荟萃分析研究了抑郁症的炎症免疫外周标志物是否具有性别特异性。该系统性综述遵循了 PRISMA 指南,并采用了从 PubMed 和 PsycInfo 中确定研究的综合搜索策略。如果研究报告了男性和/或女性抑郁症患者和/或健康成年人的 C 反应蛋白 (CRP)、白细胞介素 (IL)-6、肿瘤坏死因子 (TNF)-α 和/或 IL-1β 的情况,则纳入该研究。我们确定了 23 项符合上述纳入标准的研究。我们拟合了随机效应荟萃分析模型,并总结了抑郁症患者与健康男性和女性的循环炎症标志物水平之间的关联性。基于性别的分析表明,女性抑郁症患者的 CRP 水平(Cohen's d = 0.19)高于健康女性(p = 0.02),而这一效应在男性中并不明显(Cohen's d = -0.01)。同样,与健康对照组相比,女性抑郁症患者的 IL-6 水平也有所升高(Cohen's d = 0.51; p = 0.04),但男性抑郁症患者的 IL-6 水平同样没有升高(Cohen's d = 0.16)。虽然与对照组相比,抑郁症患者的 TNF-α 水平升高(p = 0.01),但在统计学上没有发现显著的性别差异。关于IL-1β的荟萃分析仅有三篇文章,因此结果将在补充部分介绍。这项荟萃分析加深了我们对炎症生物标志物在男性和女性抑郁症中的独特作用的了解,这可能有助于为将来更有针对性的性别治疗方法提供依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
29.60
自引率
2.00%
发文量
290
审稿时长
28 days
期刊介绍: Established in 1987, Brain, Behavior, and Immunity proudly serves as the official journal of the Psychoneuroimmunology Research Society (PNIRS). This pioneering journal is dedicated to publishing peer-reviewed basic, experimental, and clinical studies that explore the intricate interactions among behavioral, neural, endocrine, and immune systems in both humans and animals. As an international and interdisciplinary platform, Brain, Behavior, and Immunity focuses on original research spanning neuroscience, immunology, integrative physiology, behavioral biology, psychiatry, psychology, and clinical medicine. The journal is inclusive of research conducted at various levels, including molecular, cellular, social, and whole organism perspectives. With a commitment to efficiency, the journal facilitates online submission and review, ensuring timely publication of experimental results. Manuscripts typically undergo peer review and are returned to authors within 30 days of submission. It's worth noting that Brain, Behavior, and Immunity, published eight times a year, does not impose submission fees or page charges, fostering an open and accessible platform for scientific discourse.
期刊最新文献
Differential effects of social versus monetary incentives on inhibitory control under acute inflammation. Depletion of the paternal gut microbiome alters sperm small RNAs and impacts offspring physiology and behavior in mice. Biobehavioral mechanisms underlying symptoms in cancer patients with chronic graft-versus-host disease Astrocyte-neuron communication through the complement C3-C3aR pathway in Parkinson's disease. Depression-like behavior is associated with deficits in cognition and hippocampal neurogenesis in a subset of spinally contused male, but not female, rats.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1