{"title":"Sclerostin in ankylosing spondylitis: A meta-analysis","authors":"Li-Wei Jiang , Mei-Ling Yuan , Li-Na Jiang , Ai-Xin Xia , Jia-Qing Chen , Yan-Ping Li , Cheng-Gui Miao , Yan-Mei Mao","doi":"10.1016/j.cca.2025.120375","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><div>This study aims to assess circulating sclerostin levels in patients with ankylosing spondylitis (AS).</div></div><div><h3>Methods</h3><div>The databases of PubMed, Embase, Medline, Web of Science, The Cochrane Library, China National Knowledge Infrastructure Database (CNKI), China Biomedical Literature Database (CBM), Wanfang Med Online Database (Wanfang), China Science and Technology Journal Database (VIP) were used to collect all relevant published articles (up to 26 August 2024). The pooled standardized mean difference (<em>SMD</em>) with 95% confidence interval (CI) was calculated by the random-effect model.</div></div><div><h3>Results</h3><div>A total of 22 studies were included, including 1354 AS patients and 871 normal controls. There was no significant difference in the circulating sclerostin levels between AS patients and normal controls (<em>SMD</em> = −0.03, 95%CI = −0.51 to 0.46, <em>P</em> = 0.92). Subgroup analysis showed that the South America group, the Africa group, cohort study group, bath ankylosing spondylitis disease activity index (BASDAI) score < 4 group, bath ankylosing spondylitis functional index (BASFI) score < 4 group, C-reactive protein (CRP) ≤ 10 mg/L group, modified stoke ankylosing spondylitis spinal score (mSASSS) ≥ 30 group, TECO medical group and other enzyme-linked immunosorbent assay (ELISA) kits group had lower levels of the circulating sclerostin. Egger’s linear regression test indicated that there was no significant publication bias. Sensitivity analysis showed that the results were stable.</div></div><div><h3>Conclusion</h3><div>There was no significant difference in circulating sclerostin levels between AS patients and normal controls. However, the circulating sclerostin levels in AS patients were influenced by region, type of study, BASDAI score, BASFI score, CRP, mSASSS, and ELISA kits. Therefore, it may serve as an indicator to evaluate disease activity, functional status, inflammation and imaging progression in AS patients.</div></div>","PeriodicalId":10205,"journal":{"name":"Clinica Chimica Acta","volume":"575 ","pages":"Article 120375"},"PeriodicalIF":3.2000,"publicationDate":"2025-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinica Chimica Acta","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0009898125002542","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MEDICAL LABORATORY TECHNOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Objective
This study aims to assess circulating sclerostin levels in patients with ankylosing spondylitis (AS).
Methods
The databases of PubMed, Embase, Medline, Web of Science, The Cochrane Library, China National Knowledge Infrastructure Database (CNKI), China Biomedical Literature Database (CBM), Wanfang Med Online Database (Wanfang), China Science and Technology Journal Database (VIP) were used to collect all relevant published articles (up to 26 August 2024). The pooled standardized mean difference (SMD) with 95% confidence interval (CI) was calculated by the random-effect model.
Results
A total of 22 studies were included, including 1354 AS patients and 871 normal controls. There was no significant difference in the circulating sclerostin levels between AS patients and normal controls (SMD = −0.03, 95%CI = −0.51 to 0.46, P = 0.92). Subgroup analysis showed that the South America group, the Africa group, cohort study group, bath ankylosing spondylitis disease activity index (BASDAI) score < 4 group, bath ankylosing spondylitis functional index (BASFI) score < 4 group, C-reactive protein (CRP) ≤ 10 mg/L group, modified stoke ankylosing spondylitis spinal score (mSASSS) ≥ 30 group, TECO medical group and other enzyme-linked immunosorbent assay (ELISA) kits group had lower levels of the circulating sclerostin. Egger’s linear regression test indicated that there was no significant publication bias. Sensitivity analysis showed that the results were stable.
Conclusion
There was no significant difference in circulating sclerostin levels between AS patients and normal controls. However, the circulating sclerostin levels in AS patients were influenced by region, type of study, BASDAI score, BASFI score, CRP, mSASSS, and ELISA kits. Therefore, it may serve as an indicator to evaluate disease activity, functional status, inflammation and imaging progression in AS patients.
期刊介绍:
The Official Journal of the International Federation of Clinical Chemistry and Laboratory Medicine (IFCC)
Clinica Chimica Acta is a high-quality journal which publishes original Research Communications in the field of clinical chemistry and laboratory medicine, defined as the diagnostic application of chemistry, biochemistry, immunochemistry, biochemical aspects of hematology, toxicology, and molecular biology to the study of human disease in body fluids and cells.
The objective of the journal is to publish novel information leading to a better understanding of biological mechanisms of human diseases, their prevention, diagnosis, and patient management. Reports of an applied clinical character are also welcome. Papers concerned with normal metabolic processes or with constituents of normal cells or body fluids, such as reports of experimental or clinical studies in animals, are only considered when they are clearly and directly relevant to human disease. Evaluation of commercial products have a low priority for publication, unless they are novel or represent a technological breakthrough. Studies dealing with effects of drugs and natural products and studies dealing with the redox status in various diseases are not within the journal''s scope. Development and evaluation of novel analytical methodologies where applicable to diagnostic clinical chemistry and laboratory medicine, including point-of-care testing, and topics on laboratory management and informatics will also be considered. Studies focused on emerging diagnostic technologies and (big) data analysis procedures including digitalization, mobile Health, and artificial Intelligence applied to Laboratory Medicine are also of interest.