Cargando…

Pathophysiology of Vascular Calcification and Bone Loss: Linked Disorders of Ageing?

Vascular Calcification (VC), low bone mass and fragility fractures are frequently observed in ageing subjects. Although this clinical observation could be the mere coincidence of frequent age-dependent disorders, clinical and experimental data suggest that VC and bone loss could share pathophysiolog...

Descripción completa

Detalles Bibliográficos
Autores principales: Cannata-Andía, Jorge B., Carrillo-López, Natalia, Messina, Osvaldo D., Hamdy, Neveen A. T., Panizo, Sara, Ferrari, Serge L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8623966/
https://www.ncbi.nlm.nih.gov/pubmed/34836090
http://dx.doi.org/10.3390/nu13113835
_version_ 1784606058689331200
author Cannata-Andía, Jorge B.
Carrillo-López, Natalia
Messina, Osvaldo D.
Hamdy, Neveen A. T.
Panizo, Sara
Ferrari, Serge L.
author_facet Cannata-Andía, Jorge B.
Carrillo-López, Natalia
Messina, Osvaldo D.
Hamdy, Neveen A. T.
Panizo, Sara
Ferrari, Serge L.
author_sort Cannata-Andía, Jorge B.
collection PubMed
description Vascular Calcification (VC), low bone mass and fragility fractures are frequently observed in ageing subjects. Although this clinical observation could be the mere coincidence of frequent age-dependent disorders, clinical and experimental data suggest that VC and bone loss could share pathophysiological mechanisms. Indeed, VC is an active process of calcium and phosphate precipitation that involves the transition of the vascular smooth muscle cells (VSMCs) into osteoblast-like cells. Among the molecules involved in this process, parathyroid hormone (PTH) plays a key role acting through several mechanisms which includes the regulation of the RANK/RANKL/OPG system and the Wnt/ß-catenin pathway, the main pathways for bone resorption and bone formation, respectively. Furthermore, some microRNAs have been implicated as common regulators of bone metabolism, VC, left ventricle hypertrophy and myocardial fibrosis. Elucidating the common mechanisms between ageing; VC and bone loss could help to better understand the potential effects of osteoporosis drugs on the CV system.
format Online
Article
Text
id pubmed-8623966
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-86239662021-11-27 Pathophysiology of Vascular Calcification and Bone Loss: Linked Disorders of Ageing? Cannata-Andía, Jorge B. Carrillo-López, Natalia Messina, Osvaldo D. Hamdy, Neveen A. T. Panizo, Sara Ferrari, Serge L. Nutrients Review Vascular Calcification (VC), low bone mass and fragility fractures are frequently observed in ageing subjects. Although this clinical observation could be the mere coincidence of frequent age-dependent disorders, clinical and experimental data suggest that VC and bone loss could share pathophysiological mechanisms. Indeed, VC is an active process of calcium and phosphate precipitation that involves the transition of the vascular smooth muscle cells (VSMCs) into osteoblast-like cells. Among the molecules involved in this process, parathyroid hormone (PTH) plays a key role acting through several mechanisms which includes the regulation of the RANK/RANKL/OPG system and the Wnt/ß-catenin pathway, the main pathways for bone resorption and bone formation, respectively. Furthermore, some microRNAs have been implicated as common regulators of bone metabolism, VC, left ventricle hypertrophy and myocardial fibrosis. Elucidating the common mechanisms between ageing; VC and bone loss could help to better understand the potential effects of osteoporosis drugs on the CV system. MDPI 2021-10-27 /pmc/articles/PMC8623966/ /pubmed/34836090 http://dx.doi.org/10.3390/nu13113835 Text en © 2021 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 Review
Cannata-Andía, Jorge B.
Carrillo-López, Natalia
Messina, Osvaldo D.
Hamdy, Neveen A. T.
Panizo, Sara
Ferrari, Serge L.
Pathophysiology of Vascular Calcification and Bone Loss: Linked Disorders of Ageing?
title Pathophysiology of Vascular Calcification and Bone Loss: Linked Disorders of Ageing?
title_full Pathophysiology of Vascular Calcification and Bone Loss: Linked Disorders of Ageing?
title_fullStr Pathophysiology of Vascular Calcification and Bone Loss: Linked Disorders of Ageing?
title_full_unstemmed Pathophysiology of Vascular Calcification and Bone Loss: Linked Disorders of Ageing?
title_short Pathophysiology of Vascular Calcification and Bone Loss: Linked Disorders of Ageing?
title_sort pathophysiology of vascular calcification and bone loss: linked disorders of ageing?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8623966/
https://www.ncbi.nlm.nih.gov/pubmed/34836090
http://dx.doi.org/10.3390/nu13113835
work_keys_str_mv AT cannataandiajorgeb pathophysiologyofvascularcalcificationandbonelosslinkeddisordersofageing
AT carrillolopeznatalia pathophysiologyofvascularcalcificationandbonelosslinkeddisordersofageing
AT messinaosvaldod pathophysiologyofvascularcalcificationandbonelosslinkeddisordersofageing
AT hamdyneveenat pathophysiologyofvascularcalcificationandbonelosslinkeddisordersofageing
AT panizosara pathophysiologyofvascularcalcificationandbonelosslinkeddisordersofageing
AT ferrarisergel pathophysiologyofvascularcalcificationandbonelosslinkeddisordersofageing
AT pathophysiologyofvascularcalcificationandbonelosslinkeddisordersofageing