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Vascular Calcification Slows But Does Not Regress After Kidney Transplantation

INTRODUCTION: Medial arterial calcification is a common and progressive lesion in end-stage renal disease that is associated with poor cardiovascular outcomes. Whether this lesion can be arrested or reversed is unknown, and was examined retrospectively by measuring progression of breast arterial cal...

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Autores principales: Alappan, Harish R., Vasanth, Payaswini, Manzoor, Shumila, O’Neill, W. Charles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7710884/
https://www.ncbi.nlm.nih.gov/pubmed/33305114
http://dx.doi.org/10.1016/j.ekir.2020.09.039
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author Alappan, Harish R.
Vasanth, Payaswini
Manzoor, Shumila
O’Neill, W. Charles
author_facet Alappan, Harish R.
Vasanth, Payaswini
Manzoor, Shumila
O’Neill, W. Charles
author_sort Alappan, Harish R.
collection PubMed
description INTRODUCTION: Medial arterial calcification is a common and progressive lesion in end-stage renal disease that is associated with poor cardiovascular outcomes. Whether this lesion can be arrested or reversed is unknown, and was examined retrospectively by measuring progression of breast arterial calcification before and after kidney transplantation. METHODS: Arterial calcification was measured on serial mammograms from patients with previous kidney transplantation and compared to measurements performed before transplantation or in patients on the active waitlist. Serum creatinine >2.0 mg/dl after transplantation or warfarin use were exclusions. RESULTS: Median (interquartile range) progression of arterial calcification was 12.9 mm/breast per year (5.9 to 32.6) in 34 patients before or awaiting transplantation compared to just 1.2 mm/breast per year (−0.54 to 5.1) in 34 patients after transplantation (P < 0.001). Slowing of progression was also seen in longitudinal analyses of patients with mammograms performed both before and after transplantation. Duration of end-stage renal disease before transplantation but not age, diabetes, baseline calcification, or serum chemistries correlated with progression after transplantation. Significant regression was not observed in any patient. CONCLUSION: In this first quantitative study of the effect of kidney transplantation, medial arterial calcification appeared to slow to rates seen in patients with normal renal function, indicating that the effect of renal failure may be completely abrogated. Overall, however, there was no significant regression, suggesting that calcification is irreversible and emphasizing the importance of prevention. Duration of pretransplant end-stage renal disease but not baseline calcification was a determinant of progression, consistent with cumulative, permanent changes to arteries that promote calcification.
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spelling pubmed-77108842020-12-09 Vascular Calcification Slows But Does Not Regress After Kidney Transplantation Alappan, Harish R. Vasanth, Payaswini Manzoor, Shumila O’Neill, W. Charles Kidney Int Rep Clinical Research INTRODUCTION: Medial arterial calcification is a common and progressive lesion in end-stage renal disease that is associated with poor cardiovascular outcomes. Whether this lesion can be arrested or reversed is unknown, and was examined retrospectively by measuring progression of breast arterial calcification before and after kidney transplantation. METHODS: Arterial calcification was measured on serial mammograms from patients with previous kidney transplantation and compared to measurements performed before transplantation or in patients on the active waitlist. Serum creatinine >2.0 mg/dl after transplantation or warfarin use were exclusions. RESULTS: Median (interquartile range) progression of arterial calcification was 12.9 mm/breast per year (5.9 to 32.6) in 34 patients before or awaiting transplantation compared to just 1.2 mm/breast per year (−0.54 to 5.1) in 34 patients after transplantation (P < 0.001). Slowing of progression was also seen in longitudinal analyses of patients with mammograms performed both before and after transplantation. Duration of end-stage renal disease before transplantation but not age, diabetes, baseline calcification, or serum chemistries correlated with progression after transplantation. Significant regression was not observed in any patient. CONCLUSION: In this first quantitative study of the effect of kidney transplantation, medial arterial calcification appeared to slow to rates seen in patients with normal renal function, indicating that the effect of renal failure may be completely abrogated. Overall, however, there was no significant regression, suggesting that calcification is irreversible and emphasizing the importance of prevention. Duration of pretransplant end-stage renal disease but not baseline calcification was a determinant of progression, consistent with cumulative, permanent changes to arteries that promote calcification. Elsevier 2020-10-08 /pmc/articles/PMC7710884/ /pubmed/33305114 http://dx.doi.org/10.1016/j.ekir.2020.09.039 Text en © 2020 International Society of Nephrology. Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Clinical Research
Alappan, Harish R.
Vasanth, Payaswini
Manzoor, Shumila
O’Neill, W. Charles
Vascular Calcification Slows But Does Not Regress After Kidney Transplantation
title Vascular Calcification Slows But Does Not Regress After Kidney Transplantation
title_full Vascular Calcification Slows But Does Not Regress After Kidney Transplantation
title_fullStr Vascular Calcification Slows But Does Not Regress After Kidney Transplantation
title_full_unstemmed Vascular Calcification Slows But Does Not Regress After Kidney Transplantation
title_short Vascular Calcification Slows But Does Not Regress After Kidney Transplantation
title_sort vascular calcification slows but does not regress after kidney transplantation
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7710884/
https://www.ncbi.nlm.nih.gov/pubmed/33305114
http://dx.doi.org/10.1016/j.ekir.2020.09.039
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