{"title":"可溶性 TREM2 与阿尔茨海默病和轻度认知障碍的关系:系统回顾和荟萃分析","authors":"Ruiqi Wang, Yi-jun Zhan, Wen-Qing Zhu, Qianwen Yang, Jian Pei","doi":"10.3389/fnagi.2024.1407980","DOIUrl":null,"url":null,"abstract":"Soluble triggering receptor expressed on myeloid cells 2 (sTREM2) is a potential neuroinflammatory biomarker linked to the pathogenesis of Alzheimer’s disease (AD) and mild cognitive impairment (MCI). Previous studies have produced inconsistent results regarding sTREM2 levels in various clinical stages of AD. This study aims to establish the correlation between sTREM2 levels and AD progression through a meta-analysis of sTREM2 levels in cerebrospinal fluid (CSF) and blood.Comprehensive searches were conducted in PubMed, Embase, Web of Science, and the Cochrane Library to identify observational studies reporting CSF and blood sTREM2 levels in AD patients, MCI patients, and healthy controls. A random effects meta-analysis was used to calculate the standardized mean difference (SMD) and 95% confidence intervals (CIs).Thirty-six observational studies involving 3,016 AD patients, 3,533 MCI patients, and 4,510 healthy controls were included. CSF sTREM2 levels were significantly higher in both the AD [SMD = 0.28, 95% CI (0.15, 0.41)] and MCI groups [SMD = 0.30, 95% CI (0.13, 0.47)] compared to the healthy control group. However, no significant differences in expression were detected between the AD and MCI groups [SMD = 0.09, 95% CI (−0.09, 0.26)]. Furthermore, increased plasma sTREM2 levels were associated with a higher risk of AD [SMD = 0.42, 95% CI (0.01, 0.83)].CSF sTREM2 levels are positively associated with an increased risk of AD and MCI. Plasma sTREM2 levels were notably higher in the AD group than in the control group and may serve as a promising biomarker for diagnosing AD. However, sTREM2 levels are not effective for distinguishing between different disease stages of AD. Further investigations are needed to explore the longitudinal changes in sTREM2 levels, particularly plasma sTREM2 levels, during AD progression.https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42024514593","PeriodicalId":503985,"journal":{"name":"Frontiers in Aging Neuroscience","volume":"62 40","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-05-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Association of soluble TREM2 with Alzheimer’s disease and mild cognitive impairment: a systematic review and meta-analysis\",\"authors\":\"Ruiqi Wang, Yi-jun Zhan, Wen-Qing Zhu, Qianwen Yang, Jian Pei\",\"doi\":\"10.3389/fnagi.2024.1407980\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Soluble triggering receptor expressed on myeloid cells 2 (sTREM2) is a potential neuroinflammatory biomarker linked to the pathogenesis of Alzheimer’s disease (AD) and mild cognitive impairment (MCI). 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However, no significant differences in expression were detected between the AD and MCI groups [SMD = 0.09, 95% CI (−0.09, 0.26)]. Furthermore, increased plasma sTREM2 levels were associated with a higher risk of AD [SMD = 0.42, 95% CI (0.01, 0.83)].CSF sTREM2 levels are positively associated with an increased risk of AD and MCI. Plasma sTREM2 levels were notably higher in the AD group than in the control group and may serve as a promising biomarker for diagnosing AD. However, sTREM2 levels are not effective for distinguishing between different disease stages of AD. 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引用次数: 0
摘要
髓系细胞上表达的可溶性触发受体 2(sTREM2)是一种潜在的神经炎症生物标志物,与阿尔茨海默病(AD)和轻度认知障碍(MCI)的发病机制有关。以往的研究对不同临床阶段阿尔茨海默病的 sTREM2 水平得出了不一致的结果。本研究旨在通过对脑脊液(CSF)和血液中的sTREM2水平进行荟萃分析,确定sTREM2水平与AD进展之间的相关性。我们在PubMed、Embase、Web of Science和Cochrane图书馆进行了全面检索,以确定报告AD患者、MCI患者和健康对照者CSF和血液中sTREM2水平的观察性研究。该研究纳入了36项观察性研究,涉及3016名AD患者、3533名MCI患者和4510名健康对照者。与健康对照组相比,AD 组[SMD = 0.28,95% CI (0.15,0.41)]和 MCI 组[SMD = 0.30,95% CI (0.13,0.47)]的 CSF sTREM2 水平均显著升高。然而,在AD组和MCI组之间没有发现明显的表达差异[SMD = 0.09, 95% CI (-0.09, 0.26)]。此外,血浆sTREM2水平升高与AD风险升高有关[SMD = 0.42,95% CI (0.01,0.83)]。AD组血浆sTREM2水平明显高于对照组,可作为诊断AD的一种有前途的生物标志物。然而,sTREM2水平并不能有效区分AD的不同疾病阶段。在AD进展过程中,sTREM2水平,尤其是血浆sTREM2水平的纵向变化还需要进一步研究。https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42024514593
Association of soluble TREM2 with Alzheimer’s disease and mild cognitive impairment: a systematic review and meta-analysis
Soluble triggering receptor expressed on myeloid cells 2 (sTREM2) is a potential neuroinflammatory biomarker linked to the pathogenesis of Alzheimer’s disease (AD) and mild cognitive impairment (MCI). Previous studies have produced inconsistent results regarding sTREM2 levels in various clinical stages of AD. This study aims to establish the correlation between sTREM2 levels and AD progression through a meta-analysis of sTREM2 levels in cerebrospinal fluid (CSF) and blood.Comprehensive searches were conducted in PubMed, Embase, Web of Science, and the Cochrane Library to identify observational studies reporting CSF and blood sTREM2 levels in AD patients, MCI patients, and healthy controls. A random effects meta-analysis was used to calculate the standardized mean difference (SMD) and 95% confidence intervals (CIs).Thirty-six observational studies involving 3,016 AD patients, 3,533 MCI patients, and 4,510 healthy controls were included. CSF sTREM2 levels were significantly higher in both the AD [SMD = 0.28, 95% CI (0.15, 0.41)] and MCI groups [SMD = 0.30, 95% CI (0.13, 0.47)] compared to the healthy control group. However, no significant differences in expression were detected between the AD and MCI groups [SMD = 0.09, 95% CI (−0.09, 0.26)]. Furthermore, increased plasma sTREM2 levels were associated with a higher risk of AD [SMD = 0.42, 95% CI (0.01, 0.83)].CSF sTREM2 levels are positively associated with an increased risk of AD and MCI. Plasma sTREM2 levels were notably higher in the AD group than in the control group and may serve as a promising biomarker for diagnosing AD. However, sTREM2 levels are not effective for distinguishing between different disease stages of AD. Further investigations are needed to explore the longitudinal changes in sTREM2 levels, particularly plasma sTREM2 levels, during AD progression.https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42024514593