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Dinamica de durată a markerilor stresului oxidativ la pacienţii cu restenoză intra-stent după revascularizarea repetată ţintă

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dc.contributor.author Ciobanu, L.
dc.date.accessioned 2020-01-18T10:50:41Z
dc.date.available 2020-01-18T10:50:41Z
dc.date.issued 2014
dc.identifier.citation CIOBANU, L. Dinamica de durată a markerilor stresului oxidativ la pacienţii cu restenoză intra-stent după revascularizarea repetată ţintă. In: Curierul Medical. 2014, nr. 1(57), pp. 30-35. ISSN 1875-0666. en_US
dc.identifier.issn 1875-0666
dc.identifier.uri http://repository.usmf.md/handle/20.500.12710/7296
dc.identifier.uri http://moldmedjournal.md/wp-content/uploads/2016/09/Cm-1-57-1.pdf
dc.description Department of Interventional Cardiology, Institute of Cardiology, Chisinau, the Republic of Moldova en_US
dc.description.abstract Background: The oxidative stress as a key mechanism of vascular injury and remodeling represents an important subject of in-stent restenosis (ISR) pathogenesis study. Material and methods: This article is aimed at the evaluation of the circulating levels of oxidative stress markers in 68 patients with ISR, which are the following: malonic dialdehyde (MDA) advanced oxidized protein products (AOPP), glutathione peroxidase, glutathione reductase, catalase, superoxide dismutase, total antioxidant activity (TAA), advanced glycation end products (AGEPs) and arginase. These markers were assayed before the repetitive target revascularization and after 1, 3, 6 and 12 months (40 healthy persons served as a control group). Results: The obtained outcomes indicate that the oxidative stress activity has been markedly increased in the patients with ISR and has remained raised after the revascularization what has been demonstrated by significantly increased MDA and AOPP levels compared to the control markers during all study period. Antioxidant enzymes have been decreased in restenosis, and the most conspicuous reduction has been found for TAA – by 56%. After the revascularization this marker practically has not been changed. The levels of AGEPs and arginase have had a similar dynamics whose main trait has been their rise by 20-28% after 3 months compared to pre-conditioning indices. The pathophysiological significance of the period concerning implication of both factors in free oxygen radicals release and endothelium dysfunction cannot be overestimated. Conclusions: The results confirm the pathogenetic role of oxidative stress in the in-stent restenosis evolution, whose activity assay in practice may be supported by MDA, AOPP, TAA, AGEPs and arginase circulating levels estimation. en_US
dc.language.iso ro en_US
dc.publisher The Scientific Medical Association of the Republic of Moldova en_US
dc.relation.ispartof Curierul Medical
dc.subject in-stent restenosis en_US
dc.subject oxidative stress en_US
dc.subject markers en_US
dc.subject.mesh Oxidative Stress en_US
dc.subject.mesh Coronary Restenosis en_US
dc.subject.mesh Malondialdehyde en_US
dc.subject.mesh Myocardial Revascularization en_US
dc.subject.mesh Biomarkers en_US
dc.title Dinamica de durată a markerilor stresului oxidativ la pacienţii cu restenoză intra-stent după revascularizarea repetată ţintă en_US
dc.title.alternative Long duration dynamics of oxidative stress markers in patients with in-stent restenosis after target repetitive revascularization en_US
dc.type Article en_US


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