A multiscale model to predict current absolute risk of femoral fracture in a postmenopausal population.


Journal

Biomechanics and modeling in mechanobiology
ISSN: 1617-7940
Titre abrégé: Biomech Model Mechanobiol
Pays: Germany
ID NLM: 101135325

Informations de publication

Date de publication:
Apr 2019
Historique:
received: 24 02 2018
accepted: 24 09 2018
pubmed: 3 10 2018
medline: 12 7 2019
entrez: 3 10 2018
Statut: ppublish

Résumé

Osteoporotic hip fractures are a major healthcare problem. Fall severity and bone strength are important risk factors of hip fracture. This study aims to obtain a mechanistic explanation for fracture risk in dependence of these risk factors. A novel modelling approach is developed that combines models at different scales to overcome the challenge of a large space-time domain of interest and considers the variability of impact forces between potential falls in a subject. The multiscale model and its component models are verified with respect to numerical approximations made therein, the propagation of measurement uncertainties of model inputs is quantified, and model predictions are validated against experimental and clinical data. The main results are model predicted absolute risk of current fracture (ARF0) that ranged from 1.93 to 81.6% (median 36.1%) for subjects in a retrospective cohort of 98 postmenopausal British women (49 fracture cases and 49 controls); ARF0 was computed up to a precision of 1.92 percentage points (pp) due to numerical approximations made in the model; ARF0 possessed an uncertainty of 4.00 pp due to uncertainties in measuring model inputs; ARF0 classified observed fracture status in the above cohort with AUC = 0.852 (95% CI 0.753-0.918), 77.6% specificity (95% CI 63.4-86.5%) and 81.6% sensitivity (95% CI 68.3-91.1%). These results demonstrate that ARF0 can be computed using the model with sufficient precision to distinguish between subjects and that the novel mechanism of fracture risk determination based on fall dynamics, hip impact and bone strength can be considered validated.

Identifiants

pubmed: 30276488
doi: 10.1007/s10237-018-1081-0
pii: 10.1007/s10237-018-1081-0
pmc: PMC6418062
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

301-318

Subventions

Organisme : Engineering and Physical Sciences Research Council
ID : EP/K03877X/1
Organisme : Horizon 2020 Framework Programme
ID : H2020-EINFRA-2015-1-675451
Organisme : National Institute for Health Research
ID : Sheffield Biomedical Research Centre (Translational Neuroscience)

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Auteurs

Pinaki Bhattacharya (P)

Department of Mechanical Engineering, University of Sheffield, The Sir Frederick Mappin Building, Mappin Street, Sheffield, S1 3JD, UK. p.bhattacharya@sheffield.ac.uk.
INSIGNEO Institute for in Silico Medicine, University of Sheffield, The Pam Liversidge Building, Mappin Street, Sheffield, S1 3JD, UK. p.bhattacharya@sheffield.ac.uk.

Zainab Altai (Z)

Department of Mechanical Engineering, University of Sheffield, The Sir Frederick Mappin Building, Mappin Street, Sheffield, S1 3JD, UK.
INSIGNEO Institute for in Silico Medicine, University of Sheffield, The Pam Liversidge Building, Mappin Street, Sheffield, S1 3JD, UK.

Muhammad Qasim (M)

Department of Mechanical Engineering, University of Sheffield, The Sir Frederick Mappin Building, Mappin Street, Sheffield, S1 3JD, UK.
INSIGNEO Institute for in Silico Medicine, University of Sheffield, The Pam Liversidge Building, Mappin Street, Sheffield, S1 3JD, UK.

Marco Viceconti (M)

Department of Mechanical Engineering, University of Sheffield, The Sir Frederick Mappin Building, Mappin Street, Sheffield, S1 3JD, UK.
INSIGNEO Institute for in Silico Medicine, University of Sheffield, The Pam Liversidge Building, Mappin Street, Sheffield, S1 3JD, UK.

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