Evidence map›Paper›PMID 40688201›Full record

ArticleTranslational pediatrics2025

Up-regulated vitronectin in Kawasaki disease shock syndrome serves as a potential biomarker.

Zhimiao Wei, Baoling Bai, Yang Zheng, Hongmao Wang, Mingming Zhang, Qin Zhang, Xiaohui Li

Abstract read
In one paragraph

Article in Translational pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Zhimiao WeiDepartment of Cardiovascular Medicine, Children's Hospital Capital Institute of Pediatrics, Beijing, China.
Baoling BaiBeijing Municipal Key Laboratory of Child Development and Nutriomics, Capital Institute of Pediatrics, Beijing, China.
Yang ZhengDepartment of Cardiovascular Medicine, Children's Hospital Capital Institute of Pediatrics, Peking Union Medical College Graduate School, Beijing, China.
Hongmao WangDepartment of Cardiovascular Medicine, Children's Hospital Capital Institute of Pediatrics, Beijing, China.
Mingming ZhangDepartment of Cardiovascular Medicine, Children's Hospital Capital Institute of Pediatrics, Beijing, China.
Qin ZhangBeijing Municipal Key Laboratory of Child Development and Nutriomics, Capital Institute of Pediatrics, Beijing, China.
Xiaohui LiDepartment of Cardiovascular Medicine, Children's Hospital Capital Institute of Pediatrics, Beijing, China.ORCID https://orcid.org/0000-0003-1882-5898

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Kawasaki disease shock syndrome (KDSS) pathogenesis involves an immune inflammatory response related to Kawasaki disease (KD) that damages microvessel endothelial cells, leading to microcirculatory disorders. Its clinical manifestations are characterized by hypotension, poor peripheral perfusion, and a high risk of coronary artery lesions (CALs). Currently, there are few reports on biomarkers based on endothelial cell dysfunction in KDSS. This study aims to identify potential biomarkers of endothelial dysfunction in KDSS at the protein level. Methods: In this study, we recruited age- and sex-matched participants, consisting of KDSS patients, KD patients, and healthy control (HC) children. The inflammatory indicators and cytokines were compared between the KD and KDSS groups. The endothelial barrier function was assessed by dynamically measuring the cell impedance in human coronary artery endothelial cells (HCAECs). Tandem mass tag (TMT)-based proteomics was used to profile the differentially expressed proteins (DEPs) in KDSS plasma. Function and pathway enrichment analyses were performed for related pathways involved in KDSS pathology. Key proteins were validated through Western blotting. Results: Inflammatory cytokines were significantly higher in the KDSS group than in the KD group, and included interleukin-6 (IL-6) (259.37±385.20 Conclusions: This study provides a potential plasma proteomic profile for KDSS. Vitronectin may serve as a pathogenesis-based diagnostic biomarker for KDSS.

Indexed as

coronary arteryKawasaki disease shock syndrome (KDSS)proteomics analysisvitronectin

Identifiers

PMID40688201
PMCPMC12268671

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.