Simulating pharmaceutical treatment effects on osteoporosis via a bone remodeling algorithm targeting hypermineralized sites. (February 2020)
- Record Type:
- Journal Article
- Title:
- Simulating pharmaceutical treatment effects on osteoporosis via a bone remodeling algorithm targeting hypermineralized sites. (February 2020)
- Main Title:
- Simulating pharmaceutical treatment effects on osteoporosis via a bone remodeling algorithm targeting hypermineralized sites
- Authors:
- Jean-Louis, Milan
Claudia, Chan Yone
Jean-Marie, Rossi
Patrick, Chabrand - Abstract:
- Highlights: An in silico model of bone remodeling is proposed. The algorithm considers hypermineralized sites as prime targets for the bone remodeling process. Imbalance between osteoclastic and osteoblastic activities is considered. Representation of pathologies such as osteoporosis and pharmaceutical treatment is achieved. The model predicts evolution of bone with time and effect of treatment. Abstract: Pharmaceutical treatments can slow bone degradation, thus reducing the fracture risk inherent in osteoporosis. Antiresorptive treatments block the over-activation of osteoclasts vs osteoblasts, but the resulting decrease in bone remodeling frequency may weaken bone structure over time, with no gain in bone volume. Anabolic treatments, however, induce gain in bone volume. The quantitative results from existing studies on the effects of treatments over time are general and non-patient-specific, while numerical models simulating evolution of patient-specific bone microarchitecture consider a spatially random distribution of the remodeling process. Here, we propose a new approach to simulate the remodeling over decades of an individual patient's bone microarchitecture, based on the hypothesis that the oldest sites, which are hypermineralized and more brittle, are remodeled first. Taking these older sites as prime targets of remodeling, simulations show that severe osteoporosis profoundly degrades the mechanical properties of the bone structure, which can be restored and evenHighlights: An in silico model of bone remodeling is proposed. The algorithm considers hypermineralized sites as prime targets for the bone remodeling process. Imbalance between osteoclastic and osteoblastic activities is considered. Representation of pathologies such as osteoporosis and pharmaceutical treatment is achieved. The model predicts evolution of bone with time and effect of treatment. Abstract: Pharmaceutical treatments can slow bone degradation, thus reducing the fracture risk inherent in osteoporosis. Antiresorptive treatments block the over-activation of osteoclasts vs osteoblasts, but the resulting decrease in bone remodeling frequency may weaken bone structure over time, with no gain in bone volume. Anabolic treatments, however, induce gain in bone volume. The quantitative results from existing studies on the effects of treatments over time are general and non-patient-specific, while numerical models simulating evolution of patient-specific bone microarchitecture consider a spatially random distribution of the remodeling process. Here, we propose a new approach to simulate the remodeling over decades of an individual patient's bone microarchitecture, based on the hypothesis that the oldest sites, which are hypermineralized and more brittle, are remodeled first. Taking these older sites as prime targets of remodeling, simulations show that severe osteoporosis profoundly degrades the mechanical properties of the bone structure, which can be restored and even improved by anabolic, more than by antiresorptive, therapies. … (more)
- Is Part Of:
- Medical engineering & physics. Volume 76(2020)
- Journal:
- Medical engineering & physics
- Issue:
- Volume 76(2020)
- Issue Display:
- Volume 76, Issue 2020 (2020)
- Year:
- 2020
- Volume:
- 76
- Issue:
- 2020
- Issue Sort Value:
- 2020-0076-2020-0000
- Page Start:
- 56
- Page End:
- 68
- Publication Date:
- 2020-02
- Subjects:
- Bone remodeling -- Osteoporosis -- Antiresorptive -- Anabolic -- Bone biomechanics -- Hypermineralization -- Finite element analysis
Biomedical engineering -- Periodicals
Biomedical Engineering -- Periodicals
Physics -- Periodicals
Génie biomédical -- Périodiques
Biomedical engineering
Electronic journals
Periodicals
610.28 - Journal URLs:
- http://www.medengphys.com ↗
http://www.sciencedirect.com/science/journal/13504533 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/13504533 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/13504533 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.medengphy.2019.10.011 ↗
- Languages:
- English
- ISSNs:
- 1350-4533
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5527.323000
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- 12813.xml