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Vitamin D and Calcium Supplementation Accelerate Vascular Calcification in a Model of Pseudoxanthoma Elasticum

Arterial calcification is a common feature of pseudoxanthoma elasticum (PXE), a disease characterized by ABCC6 mutations, inducing a deficiency in pyrophosphate, a key inhibitor of calcium phosphate crystallization in arteries. Methods: we analyzed whether long-term exposure of Abcc6(−/−) mice (a mu...

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Autores principales: Bouderlique, Elise, Tang, Ellie, Zaworski, Jeremy, Coudert, Amélie, Bazin, Dominique, Borondics, Ferenc, Haymann, Jean-Philippe, Leftheriotis, Georges, Martin, Ludovic, Daudon, Michel, Letavernier, Emmanuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8878394/
https://www.ncbi.nlm.nih.gov/pubmed/35216422
http://dx.doi.org/10.3390/ijms23042302
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author Bouderlique, Elise
Tang, Ellie
Zaworski, Jeremy
Coudert, Amélie
Bazin, Dominique
Borondics, Ferenc
Haymann, Jean-Philippe
Leftheriotis, Georges
Martin, Ludovic
Daudon, Michel
Letavernier, Emmanuel
author_facet Bouderlique, Elise
Tang, Ellie
Zaworski, Jeremy
Coudert, Amélie
Bazin, Dominique
Borondics, Ferenc
Haymann, Jean-Philippe
Leftheriotis, Georges
Martin, Ludovic
Daudon, Michel
Letavernier, Emmanuel
author_sort Bouderlique, Elise
collection PubMed
description Arterial calcification is a common feature of pseudoxanthoma elasticum (PXE), a disease characterized by ABCC6 mutations, inducing a deficiency in pyrophosphate, a key inhibitor of calcium phosphate crystallization in arteries. Methods: we analyzed whether long-term exposure of Abcc6(−/−) mice (a murine model of PXE) to a mild vitamin D supplementation, with or without calcium, would impact the development of vascular calcification. Eight groups of mice (including Abcc6(−/−) and wild-type) received vitamin D supplementation every 2 weeks, a calcium-enriched diet alone (calcium in drinking water), both vitamin D supplementation and calcium-enriched diet, or a standard diet (controls) for 6 months. Aorta and kidney artery calcification was assessed by 3D-micro-computed tomography, Optical PhotoThermal IR (OPTIR) spectroscopy, scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy (SEM-EDS) and Yasue staining. Results: at 6 months, although vitamin D and/or calcium did not significantly increase serum calcium levels, vitamin D and calcium supplementation significantly worsened aorta and renal artery calcification in Abcc6(−/−) mice. Conclusions: vitamin D and/or calcium supplementation accelerate vascular calcification in a murine model of PXE. These results sound a warning regarding the use of these supplementations in PXE patients and, to a larger extent, patients with low systemic pyrophosphate levels.
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spelling pubmed-88783942022-02-26 Vitamin D and Calcium Supplementation Accelerate Vascular Calcification in a Model of Pseudoxanthoma Elasticum Bouderlique, Elise Tang, Ellie Zaworski, Jeremy Coudert, Amélie Bazin, Dominique Borondics, Ferenc Haymann, Jean-Philippe Leftheriotis, Georges Martin, Ludovic Daudon, Michel Letavernier, Emmanuel Int J Mol Sci Article Arterial calcification is a common feature of pseudoxanthoma elasticum (PXE), a disease characterized by ABCC6 mutations, inducing a deficiency in pyrophosphate, a key inhibitor of calcium phosphate crystallization in arteries. Methods: we analyzed whether long-term exposure of Abcc6(−/−) mice (a murine model of PXE) to a mild vitamin D supplementation, with or without calcium, would impact the development of vascular calcification. Eight groups of mice (including Abcc6(−/−) and wild-type) received vitamin D supplementation every 2 weeks, a calcium-enriched diet alone (calcium in drinking water), both vitamin D supplementation and calcium-enriched diet, or a standard diet (controls) for 6 months. Aorta and kidney artery calcification was assessed by 3D-micro-computed tomography, Optical PhotoThermal IR (OPTIR) spectroscopy, scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy (SEM-EDS) and Yasue staining. Results: at 6 months, although vitamin D and/or calcium did not significantly increase serum calcium levels, vitamin D and calcium supplementation significantly worsened aorta and renal artery calcification in Abcc6(−/−) mice. Conclusions: vitamin D and/or calcium supplementation accelerate vascular calcification in a murine model of PXE. These results sound a warning regarding the use of these supplementations in PXE patients and, to a larger extent, patients with low systemic pyrophosphate levels. MDPI 2022-02-19 /pmc/articles/PMC8878394/ /pubmed/35216422 http://dx.doi.org/10.3390/ijms23042302 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
Bouderlique, Elise
Tang, Ellie
Zaworski, Jeremy
Coudert, Amélie
Bazin, Dominique
Borondics, Ferenc
Haymann, Jean-Philippe
Leftheriotis, Georges
Martin, Ludovic
Daudon, Michel
Letavernier, Emmanuel
Vitamin D and Calcium Supplementation Accelerate Vascular Calcification in a Model of Pseudoxanthoma Elasticum
title Vitamin D and Calcium Supplementation Accelerate Vascular Calcification in a Model of Pseudoxanthoma Elasticum
title_full Vitamin D and Calcium Supplementation Accelerate Vascular Calcification in a Model of Pseudoxanthoma Elasticum
title_fullStr Vitamin D and Calcium Supplementation Accelerate Vascular Calcification in a Model of Pseudoxanthoma Elasticum
title_full_unstemmed Vitamin D and Calcium Supplementation Accelerate Vascular Calcification in a Model of Pseudoxanthoma Elasticum
title_short Vitamin D and Calcium Supplementation Accelerate Vascular Calcification in a Model of Pseudoxanthoma Elasticum
title_sort vitamin d and calcium supplementation accelerate vascular calcification in a model of pseudoxanthoma elasticum
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8878394/
https://www.ncbi.nlm.nih.gov/pubmed/35216422
http://dx.doi.org/10.3390/ijms23042302
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