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Influence of Belatacept- vs. CNI-Based Immunosuppression on Vascular Stiffness and Body Composition
Background: Arterial stiffness and phase angle (PhA) have gained importance as a diagnostic and prognostic parameter in the management of cardiovascular disease. There are few studies regarding the differences in arterial stiffness and body composition between renal transplant recipients (RTRs) rece...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8911184/ https://www.ncbi.nlm.nih.gov/pubmed/35268310 http://dx.doi.org/10.3390/jcm11051219 |
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author | Heleniak, Zbigniew Illersperger, Sarah Naik, Marcel G. Osmanodja, Bilgin Ronicke, Simon Eleftheriadis, Georgios Halleck, Fabian Budde, Klemens |
author_facet | Heleniak, Zbigniew Illersperger, Sarah Naik, Marcel G. Osmanodja, Bilgin Ronicke, Simon Eleftheriadis, Georgios Halleck, Fabian Budde, Klemens |
author_sort | Heleniak, Zbigniew |
collection | PubMed |
description | Background: Arterial stiffness and phase angle (PhA) have gained importance as a diagnostic and prognostic parameter in the management of cardiovascular disease. There are few studies regarding the differences in arterial stiffness and body composition between renal transplant recipients (RTRs) receiving belatacept (BELA) vs. calcineurin inhibitors (CNI). Therefore, we investigated the differences in arterial stiffness and body composition between RTRs treated with different immunosuppressants, including BELA. Methods: In total, 325 RTRs were enrolled in the study (mean age 52.2 years, M −62.7%). Arterial stiffness was determined with an automated oscillometric device. All body composition parameters were assessed, based on bioelectrical impedance analysis (BIA), and laboratory parameters were obtained from the medical files of the patients. Results: We did not detect any significant difference in terms of arterial stiffness and PhA in RTRs undergoing different immunosuppressive regimens, based on CsA, Tac, or BELA. Age was an essential risk factor for greater arterial stiffness. The PhA was associated with age, BMI, time of dialysis before transplantation, and kidney graft function. Conclusion: No significant differences in arterial stiffness and PhA were observed in RTRs under different immunosuppressive regimens. While our data provide additional evidence for arterial stiffness and PhA in RTRs, more research is needed to fully explore these cardiovascular risk factors and the impact of different immunosuppressive regimens. |
format | Online Article Text |
id | pubmed-8911184 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-89111842022-03-11 Influence of Belatacept- vs. CNI-Based Immunosuppression on Vascular Stiffness and Body Composition Heleniak, Zbigniew Illersperger, Sarah Naik, Marcel G. Osmanodja, Bilgin Ronicke, Simon Eleftheriadis, Georgios Halleck, Fabian Budde, Klemens J Clin Med Article Background: Arterial stiffness and phase angle (PhA) have gained importance as a diagnostic and prognostic parameter in the management of cardiovascular disease. There are few studies regarding the differences in arterial stiffness and body composition between renal transplant recipients (RTRs) receiving belatacept (BELA) vs. calcineurin inhibitors (CNI). Therefore, we investigated the differences in arterial stiffness and body composition between RTRs treated with different immunosuppressants, including BELA. Methods: In total, 325 RTRs were enrolled in the study (mean age 52.2 years, M −62.7%). Arterial stiffness was determined with an automated oscillometric device. All body composition parameters were assessed, based on bioelectrical impedance analysis (BIA), and laboratory parameters were obtained from the medical files of the patients. Results: We did not detect any significant difference in terms of arterial stiffness and PhA in RTRs undergoing different immunosuppressive regimens, based on CsA, Tac, or BELA. Age was an essential risk factor for greater arterial stiffness. The PhA was associated with age, BMI, time of dialysis before transplantation, and kidney graft function. Conclusion: No significant differences in arterial stiffness and PhA were observed in RTRs under different immunosuppressive regimens. While our data provide additional evidence for arterial stiffness and PhA in RTRs, more research is needed to fully explore these cardiovascular risk factors and the impact of different immunosuppressive regimens. MDPI 2022-02-24 /pmc/articles/PMC8911184/ /pubmed/35268310 http://dx.doi.org/10.3390/jcm11051219 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Heleniak, Zbigniew Illersperger, Sarah Naik, Marcel G. Osmanodja, Bilgin Ronicke, Simon Eleftheriadis, Georgios Halleck, Fabian Budde, Klemens Influence of Belatacept- vs. CNI-Based Immunosuppression on Vascular Stiffness and Body Composition |
title | Influence of Belatacept- vs. CNI-Based Immunosuppression on Vascular Stiffness and Body Composition |
title_full | Influence of Belatacept- vs. CNI-Based Immunosuppression on Vascular Stiffness and Body Composition |
title_fullStr | Influence of Belatacept- vs. CNI-Based Immunosuppression on Vascular Stiffness and Body Composition |
title_full_unstemmed | Influence of Belatacept- vs. CNI-Based Immunosuppression on Vascular Stiffness and Body Composition |
title_short | Influence of Belatacept- vs. CNI-Based Immunosuppression on Vascular Stiffness and Body Composition |
title_sort | influence of belatacept- vs. cni-based immunosuppression on vascular stiffness and body composition |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8911184/ https://www.ncbi.nlm.nih.gov/pubmed/35268310 http://dx.doi.org/10.3390/jcm11051219 |
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