{"title":"Association between transthyretin levels and Alzheimer's disease: A meta-analysis.","authors":"Bing-Qiu Li, Fang-Yu Li, Ling-Zhi Xu, Ying Li, Jian-Ping Jia","doi":"10.1177/25424823261478024","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Transthyretin (TTR) has been implicated in amyloid-β (Aβ) binding, cerebrospinal fluid homeostasis, and neurodegenerative processes in Alzheimer's disease (AD), but clinical evidence regarding its levels in AD and mild cognitive impairment (MCI) remains inconsistent.</p><p><strong>Objective: </strong>This meta-analysis aimed to clarify the association between blood/cerebrospinal fluid (CSF) TTR levels and AD/MCI.</p><p><strong>Methods: </strong>Following the PRISMA guidelines, this meta-analysis systematically identified and included 18 eligible studies from databases including PubMed, Web of Science, Embase, and Cochrane Library.</p><p><strong>Results: </strong>Random-effects meta-analysis showed lower TTR levels in AD versus healthy controls (HC) (Hedges' g = -0.77, 95% CI: -1.50, -0.04; p = 0.04), with no significant differences in MCI versus HC. Subgroup analyses confirmed a significant reduction in TTR levels across multiple dimensions: 1) sample types (serum); 2) population characteristics (age difference < 5 years and sex difference ≥ 10%); and 3) detection methods (immunoassay). Multivariate meta-regression with region, sample source, detection technology, and female ratio difference as covariates, accounted for 36.81% of the between-study heterogeneity. Sensitivity analysis verified result robustness, and publication bias was resolved after excluding an outlier study.</p><p><strong>Conclusions: </strong>Lower TTR levels are significantly associated with AD. This finding suggests that TTR warrants further investigation as a candidate biomarker for AD, although prospective studies are needed to validate its clinical utility.</p>","PeriodicalId":73594,"journal":{"name":"Journal of Alzheimer's disease reports","volume":"10 ","pages":"25424823261478024"},"PeriodicalIF":2.8000,"publicationDate":"2026-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13662339/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Alzheimer's disease reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/25424823261478024","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Transthyretin (TTR) has been implicated in amyloid-β (Aβ) binding, cerebrospinal fluid homeostasis, and neurodegenerative processes in Alzheimer's disease (AD), but clinical evidence regarding its levels in AD and mild cognitive impairment (MCI) remains inconsistent.
Objective: This meta-analysis aimed to clarify the association between blood/cerebrospinal fluid (CSF) TTR levels and AD/MCI.
Methods: Following the PRISMA guidelines, this meta-analysis systematically identified and included 18 eligible studies from databases including PubMed, Web of Science, Embase, and Cochrane Library.
Results: Random-effects meta-analysis showed lower TTR levels in AD versus healthy controls (HC) (Hedges' g = -0.77, 95% CI: -1.50, -0.04; p = 0.04), with no significant differences in MCI versus HC. Subgroup analyses confirmed a significant reduction in TTR levels across multiple dimensions: 1) sample types (serum); 2) population characteristics (age difference < 5 years and sex difference ≥ 10%); and 3) detection methods (immunoassay). Multivariate meta-regression with region, sample source, detection technology, and female ratio difference as covariates, accounted for 36.81% of the between-study heterogeneity. Sensitivity analysis verified result robustness, and publication bias was resolved after excluding an outlier study.
Conclusions: Lower TTR levels are significantly associated with AD. This finding suggests that TTR warrants further investigation as a candidate biomarker for AD, although prospective studies are needed to validate its clinical utility.