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Interleukin-21 – A biomarker of importance in predicting myocardial function following acute infarction?

Authors :
Weir, Robin A.P.
Miller, Ashley M.
Petrie, Colin J.
Clements, Suzanne
Steedman, Tracey
Dargie, Henry J.
Squire, Iain B.
Ng, Leong L.
McInnes, Iain B.
McMurray, John J.V.
Source :
Cytokine. Oct2012, Vol. 60 Issue 1, p220-225. 6p.
Publication Year :
2012

Abstract

Abstract: Introduction: Following acute myocardial infarction (AMI), the acute inflammatory response contributes to wound healing but also to progressive myocardial injury. Interleukin-21 (IL-21) plays a key role in immunoregulation; whether IL-21 is associated with left ventricular (LV) remodelling after AMI is unknown. Methods: Plasma IL-21 concentrations were measured in 100 patients (age 58.9±12.0years, 77% male) admitted with AMI and LV dysfunction, at baseline (mean 46h) and again at 24weeks; cardiac magnetic resonance and measurement of B-type natriuretic peptide, monocyte chemoattractant protein-1, matrix metalloproteinase (MMP)-2, -3, -9, and tissue inhibitor of metalloproteinase (TIMP)-1, -2, -4 occurred at both time-points. Remodelling was defined as change in LV end-systolic volume index (ΔLVESVI). Results: Plasma IL-21 concentration was unchanged over time (48.1 [SD 35.4]pg/mL at baseline vs. 48.8 [61.3]pg/mL at 24weeks, p =0.92). Baseline IL-21 correlated significantly with ΔLVESVI (r =0.30, p =0.005) and change in LV end-diastolic volume index (r =0.33, p =0.003). On multivariate analysis, plasma IL-21 was an independent predictor of remodelling. IL-21 was also significantly associated with higher TIMP-4 concentrations and lower MMP-9 concentrations at baseline. Conclusions: IL-21 predicts adverse remodelling following AMI in patients with LV dysfunction. Whether it plays a direct pathophysiological role in remodelling merits further study. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
10434666
Volume :
60
Issue :
1
Database :
Academic Search Index
Journal :
Cytokine
Publication Type :
Academic Journal
Accession number :
79341858
Full Text :
https://doi.org/10.1016/j.cyto.2012.06.002