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Influence of lipid profile and statin administration on arterial stiffness in renal transplant recipients

BACKGROUND: Hyperlipidemia is one of the major risk factors for developing a cardiovascular disease (CVD) and it is a frequent post-transplant complication, occurring in up to 60% of the renal transplant recipients (RTRs). Lipid lowering therapy with HMG-CoA reductase inhibitors (statins) is general...

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Autores principales: Heleniak, Zbigniew T., Illersperger, Sarah, Brakemeier, Susanne, Dębska-Ślizień, Alicja, Bach, Paul, Budde, Klemens, Halleck, Fabian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Via Medica 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9007483/
https://www.ncbi.nlm.nih.gov/pubmed/32329037
http://dx.doi.org/10.5603/CJ.a2020.0063
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author Heleniak, Zbigniew T.
Illersperger, Sarah
Brakemeier, Susanne
Dębska-Ślizień, Alicja
Bach, Paul
Budde, Klemens
Halleck, Fabian
author_facet Heleniak, Zbigniew T.
Illersperger, Sarah
Brakemeier, Susanne
Dębska-Ślizień, Alicja
Bach, Paul
Budde, Klemens
Halleck, Fabian
author_sort Heleniak, Zbigniew T.
collection PubMed
description BACKGROUND: Hyperlipidemia is one of the major risk factors for developing a cardiovascular disease (CVD) and it is a frequent post-transplant complication, occurring in up to 60% of the renal transplant recipients (RTRs). Lipid lowering therapy with HMG-CoA reductase inhibitors (statins) is generally recommended and may reduce the overall cardiovascular risk. The aim of this study was to evaluate the lipid profile, statin administration and their relationship with arterial stiffness parameters in RTRs. METHODS: Three hundred and forty-four stable RTRs (62.5% male) transplanted between 1994 and 2018 were randomly enrolled to the study. The following parameters of arterial stiffness was measured in each patient: ankle brachial index, carotid femoral pulse wave velocity (baPWV left and right, cfPWV) and pulse pressure (PP right and left). The study group was divided based on the use statins: 143 (41.6%) and 201 (58.4%). RTRs were qualified to the statin (+) and the statin (−) group, respectively. RESULTS: In the statin (+) as compared to statin (−) group there were more patients with a CVD (32.9% vs. 14.9%) and diabetes (25.2% vs. 14.4%). In the whole study group, CVD was associated with a significant increase of both baPWV and cfPWV as well as PP (8.5 mmHg). There were significant differences in arterial stiffness parameters (baPWV, cfPWV, PP) between the statin (+) and the statin (−) group. CONCLUSIONS: Arterial stiffness was increased in RTRs with CVD and hyperlipidemia. The control of hyperlipidemia was poor in RTRs.
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spelling pubmed-90074832022-04-14 Influence of lipid profile and statin administration on arterial stiffness in renal transplant recipients Heleniak, Zbigniew T. Illersperger, Sarah Brakemeier, Susanne Dębska-Ślizień, Alicja Bach, Paul Budde, Klemens Halleck, Fabian Cardiol J Clinical Cardiology BACKGROUND: Hyperlipidemia is one of the major risk factors for developing a cardiovascular disease (CVD) and it is a frequent post-transplant complication, occurring in up to 60% of the renal transplant recipients (RTRs). Lipid lowering therapy with HMG-CoA reductase inhibitors (statins) is generally recommended and may reduce the overall cardiovascular risk. The aim of this study was to evaluate the lipid profile, statin administration and their relationship with arterial stiffness parameters in RTRs. METHODS: Three hundred and forty-four stable RTRs (62.5% male) transplanted between 1994 and 2018 were randomly enrolled to the study. The following parameters of arterial stiffness was measured in each patient: ankle brachial index, carotid femoral pulse wave velocity (baPWV left and right, cfPWV) and pulse pressure (PP right and left). The study group was divided based on the use statins: 143 (41.6%) and 201 (58.4%). RTRs were qualified to the statin (+) and the statin (−) group, respectively. RESULTS: In the statin (+) as compared to statin (−) group there were more patients with a CVD (32.9% vs. 14.9%) and diabetes (25.2% vs. 14.4%). In the whole study group, CVD was associated with a significant increase of both baPWV and cfPWV as well as PP (8.5 mmHg). There were significant differences in arterial stiffness parameters (baPWV, cfPWV, PP) between the statin (+) and the statin (−) group. CONCLUSIONS: Arterial stiffness was increased in RTRs with CVD and hyperlipidemia. The control of hyperlipidemia was poor in RTRs. Via Medica 2022-04-07 /pmc/articles/PMC9007483/ /pubmed/32329037 http://dx.doi.org/10.5603/CJ.a2020.0063 Text en Copyright © 2022 Via Medica https://creativecommons.org/licenses/by-nc-nd/4.0/This article is available in open access under Creative Common Attribution-Non-Commercial-No Derivatives 4.0 International (CC BY-NC-ND 4.0) license, allowing to download articles and share them with others as long as they credit the authors and the publisher, but without permission to change them in any way or use them commercially
spellingShingle Clinical Cardiology
Heleniak, Zbigniew T.
Illersperger, Sarah
Brakemeier, Susanne
Dębska-Ślizień, Alicja
Bach, Paul
Budde, Klemens
Halleck, Fabian
Influence of lipid profile and statin administration on arterial stiffness in renal transplant recipients
title Influence of lipid profile and statin administration on arterial stiffness in renal transplant recipients
title_full Influence of lipid profile and statin administration on arterial stiffness in renal transplant recipients
title_fullStr Influence of lipid profile and statin administration on arterial stiffness in renal transplant recipients
title_full_unstemmed Influence of lipid profile and statin administration on arterial stiffness in renal transplant recipients
title_short Influence of lipid profile and statin administration on arterial stiffness in renal transplant recipients
title_sort influence of lipid profile and statin administration on arterial stiffness in renal transplant recipients
topic Clinical Cardiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9007483/
https://www.ncbi.nlm.nih.gov/pubmed/32329037
http://dx.doi.org/10.5603/CJ.a2020.0063
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