Evidence map›Paper›PMID 40092571›Full record

ArticleVascular health and risk management2025

Circulating Inflammatory Factors and Bidirectional Mendelian Randomization Analysis in Patients with Kawasaki Disease.

Muqing Niu, Jinyong Pan, Kui Wang, Li Zhang, Zhaotang Lin, Fengling Zhang

Abstract read
In one paragraph

Article in Vascular health and risk management, 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Muqing NiuThe First Affiliated Hospital of Shihezi University, Shihezi, Xinjiang, People's Republic of China.ORCID 0009-0008-9888-2705
Jinyong PanDepartment of Pediatrics, The First Affiliated Hospital of Shihezi University, Shihezi, Xinjiang, People's Republic of China.
Kui WangShihezi University School of Medicine, Shihezi, Xinjiang, People's Republic of China.
Li ZhangDepartment of Pediatrics, The First Affiliated Hospital of Shihezi University, Shihezi, Xinjiang, People's Republic of China.
Zhaotang LinDepartment of Pediatrics, The First Affiliated Hospital of Shihezi University, Shihezi, Xinjiang, People's Republic of China.
Fengling ZhangThe First Affiliated Hospital of Shihezi University, Shihezi, Xinjiang, People's Republic of China.ORCID 0009-0008-0661-5942

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Kawasaki disease (KD), also known as mucocutaneous lymph node syndrome, is a systemic immune vasculitis with an unclear etiology. It is often complicated by coronary artery disease. This study uses bidirectional Mendelian randomization (MR) to investigate the interaction between KD and circulating inflammatory factors, providing insights into their causal relationships. Methods: We conducted a two-way pooled MR analysis to examine the causal links between 41 circulating inflammatory regulators and the risk of KD. Genetic data related to inflammation were sourced from three genome-wide association studies (GWASs) involving CRP, PCT, and cytokines, while KD data were derived from other studies. Inverse-variance weighting (IVW) was the primary MR method, with sensitivity analyses performed using MR‒Egger, weighted median, weighted mode, and MR-PRESSO to ensure robustness. Results: Forward MR analyses showed no significant relationship between inflammatory factors and KD outcomes. In contrast, reverse MR, with KD as the exposure factor, revealed that interleukin-2 (IL-2) and interleukin-8 (IL-8) were significantly associated with KD (IL-2: OR=1.0085, P=0.037; IL-8: OR=1.0099, P=0.014). Borderline significant associations were observed for factors such as B_NGF, EOTAXIN, HGF, and IL_12_P70 in MR‒Egger and weighted median analyses. Conclusion: This bidirectional MR study highlights the role of circulating inflammatory modulators in KD risk, offering insights into KD pathogenesis and potential therapeutic targets.

Indexed as

CytokinesInflammation MediatorsMucocutaneous Lymph Node SyndromeBiomarkersChildChild, PreschoolFemaleGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansMaleMendelian Randomization AnalysisPhenotypePolymorphism, Single NucleotideRisk AssessmentRisk FactorsBiomarkersCytokinesInflammation Mediatorsbidirectional Mendelian randomizationcirculating inflammatory regulatorsGWAS catalogKawasaki diseaseMendelian randomization

Identifiers

PMID40092571
PMCPMC11910938

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