Interleukin-6 and tumor necrosis factor alpha in relation to myocardial infarct size and collagen formation

Background: Interleukin-6 (IL-6) and tumor necrosis factor alpha (TNF-α) levels increase after acute myocardial infarction (AMI) in humans. Experimental data suggest that these cytokines regulate the initiation of scar formation after AMI. We investigated the interrelationships of IL-6 and TNF-α, ti...

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Published inJournal of cardiac failure Vol. 9; no. 4; pp. 325 - 332
Main Authors Puhakka, Mikko, Magga, Jarkko, Hietakorpi, Seppo, Penttilä, Ilkka, Uusimaa, Paavo, Risteli, Juha, Peuhkurinen, Keijo
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.08.2003
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Summary:Background: Interleukin-6 (IL-6) and tumor necrosis factor alpha (TNF-α) levels increase after acute myocardial infarction (AMI) in humans. Experimental data suggest that these cytokines regulate the initiation of scar formation after AMI. We investigated the interrelationships of IL-6 and TNF-α, tissue injury, infarct size, cardiac function, and collagen formation in humans. Methods: Serum and plasma samples were taken on 93 patients receiving thrombolytic treatment for their first AMI. Collagen formation was evaluated by measuring concentrations of serum aminoterminal propeptide of type III procollagen (PIIINP). Results: IL-6 levels increased by 44% (P <.001) and peaked at 24 hours. Peak IL-6 levels correlated positively with area under the curve of creatine kinase MB mass (r =.31, P <.01), peak troponin T level (r =.34, P <.005), and PIIINP measured at discharge (r =.46, P <.001). There were no changes in TNF-α levels, and patients with left ventricular dysfunction (EF < 40 %) had similar TNF-α levels as those with preserved left ventricular function. Conclusions: IL-6 may regulate collagen formation and thus remodeling of the left ventricle after AMI. In addition, TNF-α measurement is useless in the assessment of infarct size or left ventricular function during the immediate post-infarction period.
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ISSN:1071-9164
1532-8414
DOI:10.1054/jcaf.2003.38