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...

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Autores principales: Jorge B. Cannata-Andía, Natalia Carrillo-López, Osvaldo D. Messina, Neveen A. T. Hamdy, Sara Panizo, Serge L. Ferrari, on behalf of the International Osteoporosis Foundation (IOF) Working Group on Bone and Cardiovascular Diseases
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Publicado: MDPI AG 2021
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Acceso en línea:https://doaj.org/article/9bdec82e057a4d86a952598e80781662
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spelling oai:doaj.org-article:9bdec82e057a4d86a952598e807816622021-11-25T18:34:31ZPathophysiology of Vascular Calcification and Bone Loss: Linked Disorders of Ageing?10.3390/nu131138352072-6643https://doaj.org/article/9bdec82e057a4d86a952598e807816622021-10-01T00:00:00Zhttps://www.mdpi.com/2072-6643/13/11/3835https://doaj.org/toc/2072-6643Vascular 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.Jorge B. Cannata-AndíaNatalia Carrillo-LópezOsvaldo D. MessinaNeveen A. T. HamdySara PanizoSerge L. Ferrarion behalf of the International Osteoporosis Foundation (IOF) Working Group on Bone and Cardiovascular DiseasesMDPI AGarticleosteoporosisvascular calcificationmineral bone disordersbone lossbone fracturesfracture riskNutrition. Foods and food supplyTX341-641ENNutrients, Vol 13, Iss 3835, p 3835 (2021)
institution DOAJ
collection DOAJ
language EN
topic osteoporosis
vascular calcification
mineral bone disorders
bone loss
bone fractures
fracture risk
Nutrition. Foods and food supply
TX341-641
spellingShingle osteoporosis
vascular calcification
mineral bone disorders
bone loss
bone fractures
fracture risk
Nutrition. Foods and food supply
TX341-641
Jorge B. Cannata-Andía
Natalia Carrillo-López
Osvaldo D. Messina
Neveen A. T. Hamdy
Sara Panizo
Serge L. Ferrari
on behalf of the International Osteoporosis Foundation (IOF) Working Group on Bone and Cardiovascular Diseases
Pathophysiology of Vascular Calcification and Bone Loss: Linked Disorders of Ageing?
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 article
author Jorge B. Cannata-Andía
Natalia Carrillo-López
Osvaldo D. Messina
Neveen A. T. Hamdy
Sara Panizo
Serge L. Ferrari
on behalf of the International Osteoporosis Foundation (IOF) Working Group on Bone and Cardiovascular Diseases
author_facet Jorge B. Cannata-Andía
Natalia Carrillo-López
Osvaldo D. Messina
Neveen A. T. Hamdy
Sara Panizo
Serge L. Ferrari
on behalf of the International Osteoporosis Foundation (IOF) Working Group on Bone and Cardiovascular Diseases
author_sort Jorge B. Cannata-Andía
title 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_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_sort pathophysiology of vascular calcification and bone loss: linked disorders of ageing?
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/9bdec82e057a4d86a952598e80781662
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