The impact of left ventricle assist device on circulating endothelial microparticles - pilot study
Language English Country Sweden Media print
Document type Clinical Trial, Journal Article, Research Support, Non-U.S. Gov't
PubMed
23183513
PII: NEL330812A13
Knihovny.cz E-resources
- MeSH
- Biomarkers blood MeSH
- Endothelium, Vascular metabolism pathology MeSH
- Cardiomyopathy, Dilated blood surgery MeSH
- Adult MeSH
- Hemodynamics physiology MeSH
- Myocardial Ischemia blood surgery MeSH
- Middle Aged MeSH
- Humans MeSH
- Cell-Derived Microparticles metabolism pathology MeSH
- Pilot Projects MeSH
- Heart-Assist Devices adverse effects MeSH
- Prospective Studies MeSH
- Aged MeSH
- Heart Failure blood surgery MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Publication type
- Journal Article MeSH
- Clinical Trial MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Biomarkers MeSH
OBJECTIVES: Recent technological breakthroughs in the design of reliable systems for long term non-pulsatile mechanical heart support offer the possibility to study the effect of continuous blood flow in the vascular system. Generally, it is assumed that the absence of physiological pulsatile flow leads to prothrombogenic and proatherogenic changes. We investigated the change in the circulating endothelial microparticle concentration as a marker of endothelial damage in patients implanted with a continuous-flow left ventricle assist device (LVAD). METHODS: Endothelial microparticles were measured in 8 males (mean age 54.1±11.5 years) with terminal heart failure before and 3 months after implantation of an LVAD. The group consisted of 3 patients with dilated cardiomyopathy, 3 patients with ischemic cardiomyopathy, 1 patient with both conditions and 1 patient with congenital valvular disease. The concentration of endothelial microparticles was determined by ELISA Zymutest MP activity test. RESULTS: We did not observe a significant change in the concentration of circulating endothelial microparticles measured before and 3 months after implantation (p=0.669). High inter-individual variability in response to implantation was found. However, no association between a change in endothelial microparticle concentration and heart failure aetiology or a significant clinical complication attributed to LVAD implantation was observed. CONCLUSION: Results from this preliminary pilot study do not indicate that LVADs contribute to short-term vascular damage as defined by an increase in circulating endothelial microparticles.