{"title":"Galectin-3 in systemic lupus erythematosus: a meta-analysis.","authors":"Yang Wu, Li-Na Jiang, Jing-Ru Wu, Yi-Ran Lu, Ting-Ting Lu, Ji-Min Zhu, Jing Li, Shanshan Xu, Bai-Kun Li, Cheng-Gui Miao, Yan-Mei Mao","doi":"10.1007/s12026-026-09793-z","DOIUrl":null,"url":null,"abstract":"<p><p>This study aims to assess the circulating galectin-3 (Gal-3) levels in patients with systemic lupus erythematosus (SLE) and explore the major related influencing factors. Systematic searches of all relevant English articles were conducted in PubMed, Embase, Web of Science, and the Cochrane Library from inception to September 22nd, 2025. Continuous variable data from multiple studies were subjected to a random-effects meta-analysis using Stata 12.0 software to estimate the pooled effect size. Data on circulating Gal-3 levels were analyzed using the standard mean difference (SMD) with 95% confidence intervals (CI) and 95% prediction intervals (PI) in the presence of significant heterogeneity. A total of 8 studies were finally included in this meta-analysis, involving 397 patients with SLE and 433 normal controls. The combined effect showed that SLE patients had significantly higher circulating Gal-3 levels than normal controls (SMD = 1.290, 95% CI: 0.713-1.868, 95% PI: -0.25-2.80, P < 0.001). Subgroup analyses stratified by age, region, assay method, sample size and Newcastle-Ottawa Quality Assessment Scale score also demonstrated consistent results. Egger's linear regression test indicated no significant publication bias (P>0.05). Sensitivity analysis showed that the results were stable. SLE patients have higher circulating levels of Gal-3 than normal controls. Given the crucial role of Gal-3 in SLE, it is worthwhile to investigate its potential as a therapeutic target and biomarker.</p>","PeriodicalId":13389,"journal":{"name":"Immunologic Research","volume":"74 1","pages":""},"PeriodicalIF":2.7000,"publicationDate":"2026-08-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Immunologic Research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s12026-026-09793-z","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
This study aims to assess the circulating galectin-3 (Gal-3) levels in patients with systemic lupus erythematosus (SLE) and explore the major related influencing factors. Systematic searches of all relevant English articles were conducted in PubMed, Embase, Web of Science, and the Cochrane Library from inception to September 22nd, 2025. Continuous variable data from multiple studies were subjected to a random-effects meta-analysis using Stata 12.0 software to estimate the pooled effect size. Data on circulating Gal-3 levels were analyzed using the standard mean difference (SMD) with 95% confidence intervals (CI) and 95% prediction intervals (PI) in the presence of significant heterogeneity. A total of 8 studies were finally included in this meta-analysis, involving 397 patients with SLE and 433 normal controls. The combined effect showed that SLE patients had significantly higher circulating Gal-3 levels than normal controls (SMD = 1.290, 95% CI: 0.713-1.868, 95% PI: -0.25-2.80, P < 0.001). Subgroup analyses stratified by age, region, assay method, sample size and Newcastle-Ottawa Quality Assessment Scale score also demonstrated consistent results. Egger's linear regression test indicated no significant publication bias (P>0.05). Sensitivity analysis showed that the results were stable. SLE patients have higher circulating levels of Gal-3 than normal controls. Given the crucial role of Gal-3 in SLE, it is worthwhile to investigate its potential as a therapeutic target and biomarker.
期刊介绍:
IMMUNOLOGIC RESEARCH represents a unique medium for the presentation, interpretation, and clarification of complex scientific data. Information is presented in the form of interpretive synthesis reviews, original research articles, symposia, editorials, and theoretical essays. The scope of coverage extends to cellular immunology, immunogenetics, molecular and structural immunology, immunoregulation and autoimmunity, immunopathology, tumor immunology, host defense and microbial immunity, including viral immunology, immunohematology, mucosal immunity, complement, transplantation immunology, clinical immunology, neuroimmunology, immunoendocrinology, immunotoxicology, translational immunology, and history of immunology.