{"title":"Serum endocan as a dual-function biomarker in Kawasaki disease: early diagnostic potential and prediction of coronary arterial aneurysms","authors":"Chang Liu, Yi Wei, Fengchuan Jing , Qijian Yi","doi":"10.1016/j.cyto.2025.157052","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>Kawasaki disease (KD), an acute vasculitis of unclear etiology, is an important contributor to childhood-acquired heart disease due to coronary arterial aneurysms (CAAs). Current diagnosis lacks specific biomarkers, risking delayed treatment. Endocan, a proteoglycan implicated in vascular inflammation, may address this gap. This study evaluates serum endocan in acute KD for its utility in early KD diagnosis and CAA risk prediction.</div></div><div><h3>Method</h3><div>This prospective cohort study enrolled 79 KD patients and 48 healthy controls. The KD group was further divided into KD with CAA (KD-CAA) and KD non-CAA (KD-NCAA) subgroups. Serum endocan levels were quantified via enzyme-linked immunosorbent assay. Clinical parameters including inflammatory markers were systematically analyzed using SPSS and GraphPad Prism.</div></div><div><h3>Results</h3><div>Serum endocan levels were significantly elevated in KD patients compared to HCs (median [25th–75th percentile], 1803.69 pg/ml [1478.97–2038.87] vs. 931.73 [815.57–1138.72] pg/ml, <em>P</em> < 0.001), with higher concentrations in KD-CAA versus KD-NCAA (mean ± SD, 1962.43 ± 321.48 vs. 1702.46 ± 458.54 pg/ml, <em>P</em> = 0.024).</div><div>Endocan demonstrated excellent performance in distinguishing KD patients from HCs (AUC = 0.915, 95 % CI: 0.863–0.968; sensitivity 88.6 %, specificity 85.4 %). It also showed a modest but statistically significant predictive value for CAAs within the KD cohort (AUC = 0.675, 95 % CI: 0.548–0.801; sensitivity 73.7 %, specificity 58.3 %).</div></div><div><h3>Conclusion</h3><div>Serum endocan is a high-performance biomarker for differentiating KD from HCs. Despite modest performance in predicting CAAs and undetermined specificity, it may serve as a valuable supportive tool for risk stratification in KD patients.</div></div>","PeriodicalId":297,"journal":{"name":"Cytokine","volume":"196 ","pages":"Article 157052"},"PeriodicalIF":3.6000,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cytokine","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1043466625001991","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/10/22 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Background
Kawasaki disease (KD), an acute vasculitis of unclear etiology, is an important contributor to childhood-acquired heart disease due to coronary arterial aneurysms (CAAs). Current diagnosis lacks specific biomarkers, risking delayed treatment. Endocan, a proteoglycan implicated in vascular inflammation, may address this gap. This study evaluates serum endocan in acute KD for its utility in early KD diagnosis and CAA risk prediction.
Method
This prospective cohort study enrolled 79 KD patients and 48 healthy controls. The KD group was further divided into KD with CAA (KD-CAA) and KD non-CAA (KD-NCAA) subgroups. Serum endocan levels were quantified via enzyme-linked immunosorbent assay. Clinical parameters including inflammatory markers were systematically analyzed using SPSS and GraphPad Prism.
Results
Serum endocan levels were significantly elevated in KD patients compared to HCs (median [25th–75th percentile], 1803.69 pg/ml [1478.97–2038.87] vs. 931.73 [815.57–1138.72] pg/ml, P < 0.001), with higher concentrations in KD-CAA versus KD-NCAA (mean ± SD, 1962.43 ± 321.48 vs. 1702.46 ± 458.54 pg/ml, P = 0.024).
Endocan demonstrated excellent performance in distinguishing KD patients from HCs (AUC = 0.915, 95 % CI: 0.863–0.968; sensitivity 88.6 %, specificity 85.4 %). It also showed a modest but statistically significant predictive value for CAAs within the KD cohort (AUC = 0.675, 95 % CI: 0.548–0.801; sensitivity 73.7 %, specificity 58.3 %).
Conclusion
Serum endocan is a high-performance biomarker for differentiating KD from HCs. Despite modest performance in predicting CAAs and undetermined specificity, it may serve as a valuable supportive tool for risk stratification in KD patients.
期刊介绍:
The journal Cytokine has an open access mirror journal Cytokine: X, sharing the same aims and scope, editorial team, submission system and rigorous peer review.
* Devoted exclusively to the study of the molecular biology, genetics, biochemistry, immunology, genome-wide association studies, pathobiology, diagnostic and clinical applications of all known interleukins, hematopoietic factors, growth factors, cytotoxins, interferons, new cytokines, and chemokines, Cytokine provides comprehensive coverage of cytokines and their mechanisms of actions, 12 times a year by publishing original high quality refereed scientific papers from prominent investigators in both the academic and industrial sectors.
We will publish 3 major types of manuscripts:
1) Original manuscripts describing research results.
2) Basic and clinical reviews describing cytokine actions and regulation.
3) Short commentaries/perspectives on recently published aspects of cytokines, pathogenesis and clinical results.