Literature DB >> 16435069

Levosimendan use reduces matrix metalloproteinase-2 in patients with decompensated heart failure.

Dimitrios N Tziakas1, Georgios K Chalikias, Helen I Hatzinikolaou, Dimitrios A Stakos, Nikolaos Papanas, Ioannis K Tentes, Alexandros X Kortsaris, Efstratios Maltezos, Dimitrios I Hatseras, Juan Carlos Kaski.   

Abstract

BACKGROUND: Extracellular matrix metabolism (ECM) has an important role in left ventricular (LV) remodeling in chronic heart failure (CHF). Matrix metalloproteinases (MMPs) are involved in the regulation of extracellular matrix (ECM) metabolism. We investigated the effect of levosimendan, a novel calcium sensitizer, on serum levels of MMP-2.
METHODS: Our study population consisted of 60 consecutive patients with advanced heart failure who were admitted to hospital with an acute decompensation of their CHF. Patients were randomized to levosimendan (n = 30; 18 men, aged 65 +/- 3 years) or placebo (n = 30; 15 men, aged 67 +/- 4 years). Serum MMP-2 levels were assessed before and after treatment with levosimendan or placebo, using a commercially available ELISA.
RESULTS: Serum levels of MMP-2 were reduced from 427 ng/ml 95%CI 372-484 to 371 ng/ml 95%CI 329-413 in the levosimendan treated group and from 433 ng/ml 95%CI 422-444 to 425 ng/ml 95%CI 414-436 in the placebo group. Repeated measurements ANOVA showed that treatment with levosimendan significantly affected levels of MMP-2 (p = 0.019).
CONCLUSIONS: The present study showed that levosimendan may beneficially affect ECM remodeling in patients with acutely decompensated CHF. Whether these effects translate into added clinical benefits, as suggested by an improved ejection fraction in the levosimendan group, deserves further investigation.

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Year:  2005        PMID: 16435069     DOI: 10.1007/s10557-005-5417-5

Source DB:  PubMed          Journal:  Cardiovasc Drugs Ther        ISSN: 0920-3206            Impact factor:   3.727


  6 in total

Review 1.  Extracellular matrix molecules: potential targets in pharmacotherapy.

Authors:  Hannu Järveläinen; Annele Sainio; Markku Koulu; Thomas N Wight; Risto Penttinen
Journal:  Pharmacol Rev       Date:  2009-06       Impact factor: 25.468

2.  Changes in extracellular matrix cause RPE cells to make basal deposits and activate the alternative complement pathway.

Authors:  Rosario Fernandez-Godino; Kinga M Bujakowska; Eric A Pierce
Journal:  Hum Mol Genet       Date:  2018-01-01       Impact factor: 6.150

Review 3.  Clinical pharmacology of levosimendan.

Authors:  Saila Antila; Stig Sundberg; Lasse A Lehtonen
Journal:  Clin Pharmacokinet       Date:  2007       Impact factor: 6.447

Review 4.  Acute heart failure: patient characteristics and pathophysiology.

Authors:  Catherine N Marti; Vasiliki V Georgiopoulou; Andreas P Kalogeropoulos
Journal:  Curr Heart Fail Rep       Date:  2013-12

Review 5.  A review of levosimendan in the treatment of heart failure.

Authors:  Hulya Akhan Kasikcioglu; Nese Cam
Journal:  Vasc Health Risk Manag       Date:  2006

6.  Influence of spironolactone on matrix metalloproteinase-2 in acute decompensated heart failure.

Authors:  João Pedro Ferreira; Mário Santos; José Carlos Oliveira; Irene Marques; Paulo Bettencourt; Henrique Carvalho
Journal:  Arq Bras Cardiol       Date:  2015-01-23       Impact factor: 2.000

  6 in total

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