Bone fragility in diabetes: novel concepts and clinical implications
Research output: Contribution to journal › Review article › Contributed › peer-review
Contributors
Abstract
Increased fracture risk represents an emerging and severe complication of diabetes. The resulting prolonged immobility and hospitalisations can lead to substantial morbidity and mortality. In type 1 diabetes, bone mass and bone strength are reduced, resulting in up to a five-times greater risk of fractures throughout life. In type 2 diabetes, fracture risk is increased despite a normal bone mass. Conventional dual-energy x-ray absorptiometry might underestimate fracture risk, but can be improved by applying specific adjustments. Bone fragility in diabetes can result from cellular abnormalities, matrix interactions, immune and vascular changes, and musculoskeletal maladaptation to chronic hyperglycaemia. This Review summarises how the bone microenvironment responds to type 1 and type 2 diabetes, and the mechanisms underlying fragility fractures. We describe the value of novel imaging technologies and the clinical utility of biomarkers, and discuss current and future therapeutic approaches that protect bone health in people with diabetes.
Details
Original language | English |
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Pages (from-to) | 207-220 |
Number of pages | 14 |
Journal | The Lancet. Diabetes & endocrinology |
Volume | 10 |
Issue number | 3 |
Publication status | Published - Mar 2022 |
Peer-reviewed | Yes |
External IDs
Scopus | 85124890010 |
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unpaywall | 10.1016/s2213-8587(21)00347-8 |
WOS | 000761942900014 |
ORCID | /0000-0002-8691-8423/work/142236012 |
Keywords
Research priority areas of TU Dresden
DFG Classification of Subject Areas according to Review Boards
Subject groups, research areas, subject areas according to Destatis
Sustainable Development Goals
ASJC Scopus subject areas
Keywords
- Absorptiometry, Photon, Bone Density, Bone and Bones/diagnostic imaging, Diabetes Mellitus, Type 2/complications, Fractures, Bone/complications, Humans, Musculoskeletal health, Mineral density, Postmenopausal women, Older-adults, Serum sclerostin, Defect regeneration, Glycation end-products, Hip fracture, Vertebral fracture risk, Marrow adiposity