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A multi-stage association study of plasma cytokines identifies osteopontin as a biomarker for acute coronary syndrome risk and severity

Authors :
Xinwen Min
Binyao Yang
Kuai Yu
Tangchun Wu
Xuezhen Liu
Ce Zhang
Lue Zhou
Kai Yan
Xiulou Li
Liyun Zhang
Haijing Jiang
Xiaoting Luo
Xiang Cheng
Xiaomin Zhang
Jun Li
An Pan
Shunchang Sun
Frank B. Hu
Meian He
Wenhua Mei
Handong Yang
Source :
Scientific Reports, Vol 9, Iss 1, Pp 1-9 (2019), Scientific Reports
Publication Year :
2019
Publisher :
Nature Portfolio, 2019.

Abstract

Cytokines play a critical role in the pathogenesis and development of cardiovascular diseases. However, data linking cytokines to risk and severity of acute coronary syndrome (ACS) are still limited. We measured plasma profile of 280 cytokines using a quantitative protein microarray in 12 ACS patients and 16 healthy controls, and identified 15 differentially expressed cytokines for ACS. Osteopontin, chemokine ligand 23, brain derived neurotrophic factor and C-reactive protein (CRP) were further validated using immunoassay in two independent case-control studies with a total of 210 ACS patients and 210 controls. We further examined their relations with incident ACS among 318 case-control pairs nested within the Dongfeng-Tongji cohort, and found plasma osteopontin and CRP concentrations were associated with incident ACS, and the multivariable-adjusted odds ratio (95% confidence interval) was 1.29 (1.06–1.57) per 1-SD increase for osteopontin and 1.30 (1.02–1.66) for CRP, respectively. Higher levels of circulating osteopontin were also correlated with higher severity of ACS, and earlier ACS onset time. Adding osteopontin alone or in combination with CRP modestly improved the predictive ability of ACS beyond the Framingham risk scores. Our findings suggested that osteopontin might be a biomarker for incident ACS, using osteopontin adds moderately to traditional cardiovascular risk factors.

Details

Language :
English
ISSN :
20452322
Volume :
9
Issue :
1
Database :
OpenAIRE
Journal :
Scientific Reports
Accession number :
edsair.doi.dedup.....8e0c4d92646c5d89a1844a143074bdd0