Tissue inhibitor of metalloproteinases levels in patients with chronic heart failure: An independent predictor of mortality

Background: Matrix metalloproteinases (MMP) and their tissue inhibitors (TIMP) are involved in cardiac remodelling. The prognostic utility of TIMP is unknown in chronic heart failure (CHF). Aims: We investigated the association of plasma levels of soluble MMP-9 and TIMP-1 with clinical, laboratory a...

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Veröffentlicht in:European journal of heart failure 2008-04, Vol.10 (4), p.388-395
Hauptverfasser: Frantz, S., Störk, S., Michels, K., Eigenthaler, M., Ertl, G., Bauersachs, J., Angermann, C.E.
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Sprache:eng
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Zusammenfassung:Background: Matrix metalloproteinases (MMP) and their tissue inhibitors (TIMP) are involved in cardiac remodelling. The prognostic utility of TIMP is unknown in chronic heart failure (CHF). Aims: We investigated the association of plasma levels of soluble MMP-9 and TIMP-1 with clinical, laboratory and echocardiographic parameters and estimated their prognostic value in the prediction of all-cause death. Methods: MMP-9, TIMP-1, tumour necrosis factor-α, and amino-terminal pro-brain natriuretic peptide were measured in 249 consecutively enrolled CHF patients and 74 healthy individuals. Results: After adjustment for age, sex and creatinine, levels of TIMP-1 (1640 vs. 735 ng/ml, P < 0.001) but not MMP-9 were elevated in CHF patients compared to controls. During a median follow-up period of 2.5 years, 66 patients (27%) died. In multivariable Cox regression models TIMP-1 but not MMP-9 emerged as an independent predictor of all-cause death (hazard ratio per tertile, 3.5; 95% confidence interval [CI], 2.2-5.1). In addition to the full set of univariately predictive clinical and serological markers, information on TIMP-1 significantly increased the area under the receiver operating characteristic curve from 0.77 (95% CI, 0.71-0.84) to 0.87 (95% CI, 0.82-0.92). Conclusion: In stable CHF patients, TIMP-1 but not MMP-9 is of independent and incremental value regarding the prediction of all-cause death.
ISSN:1388-9842
1879-0844
DOI:10.1016/j.ejheart.2008.02.015