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Diabetes Mellitus-induced Bone Fragility

Accumulating evidence has shown that the risk of osteoporotic fractures is increased in patients with diabetes mellitus (DM). Thus, DM-induced bone fragility has been recently recognized as a diabetic complication. Because the fracture risk is independent of the reduction in bone mineral density, de...

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Detalles Bibliográficos
Autores principales: Kanazawa, Ippei, Sugimoto, Toshitsugu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Internal Medicine 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6207820/
https://www.ncbi.nlm.nih.gov/pubmed/29780142
http://dx.doi.org/10.2169/internalmedicine.0905-18
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author Kanazawa, Ippei
Sugimoto, Toshitsugu
author_facet Kanazawa, Ippei
Sugimoto, Toshitsugu
author_sort Kanazawa, Ippei
collection PubMed
description Accumulating evidence has shown that the risk of osteoporotic fractures is increased in patients with diabetes mellitus (DM). Thus, DM-induced bone fragility has been recently recognized as a diabetic complication. Because the fracture risk is independent of the reduction in bone mineral density, deterioration of the bone quality may be the main cause of bone fragility. Although its mechanism remains poorly understood, accumulated collagen cross-links of advanced glycation end-products (AGEs) and dysfunctions of osteoblast and osteocyte may be involved. Previous studies have suggested that various diabetes-related factors, such as chronic hyperglycemia, insulin, insulin-like growth factor-I, AGEs, and homocysteine, are associated with the risk of bone fragility caused by impaired bone formation and bone remodeling. Furthermore, several anti-diabetic drugs are known to affect bone metabolism and fracture risk. We herein review the association between DM and fracture risk as well as the mechanism of DM-induced bone fragility based on recent evidence.
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spelling pubmed-62078202018-10-31 Diabetes Mellitus-induced Bone Fragility Kanazawa, Ippei Sugimoto, Toshitsugu Intern Med Review Article Accumulating evidence has shown that the risk of osteoporotic fractures is increased in patients with diabetes mellitus (DM). Thus, DM-induced bone fragility has been recently recognized as a diabetic complication. Because the fracture risk is independent of the reduction in bone mineral density, deterioration of the bone quality may be the main cause of bone fragility. Although its mechanism remains poorly understood, accumulated collagen cross-links of advanced glycation end-products (AGEs) and dysfunctions of osteoblast and osteocyte may be involved. Previous studies have suggested that various diabetes-related factors, such as chronic hyperglycemia, insulin, insulin-like growth factor-I, AGEs, and homocysteine, are associated with the risk of bone fragility caused by impaired bone formation and bone remodeling. Furthermore, several anti-diabetic drugs are known to affect bone metabolism and fracture risk. We herein review the association between DM and fracture risk as well as the mechanism of DM-induced bone fragility based on recent evidence. The Japanese Society of Internal Medicine 2018-05-18 2018-10-01 /pmc/articles/PMC6207820/ /pubmed/29780142 http://dx.doi.org/10.2169/internalmedicine.0905-18 Text en Copyright © 2018 by The Japanese Society of Internal Medicine https://creativecommons.org/licenses/by-nc-nd/4.0/ The Internal Medicine is an Open Access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review Article
Kanazawa, Ippei
Sugimoto, Toshitsugu
Diabetes Mellitus-induced Bone Fragility
title Diabetes Mellitus-induced Bone Fragility
title_full Diabetes Mellitus-induced Bone Fragility
title_fullStr Diabetes Mellitus-induced Bone Fragility
title_full_unstemmed Diabetes Mellitus-induced Bone Fragility
title_short Diabetes Mellitus-induced Bone Fragility
title_sort diabetes mellitus-induced bone fragility
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6207820/
https://www.ncbi.nlm.nih.gov/pubmed/29780142
http://dx.doi.org/10.2169/internalmedicine.0905-18
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