4.5 Article

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

Journal

BIOMECHANICS AND MODELING IN MECHANOBIOLOGY
Volume 18, Issue 2, Pages 301-318

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s10237-018-1081-0

Keywords

Osteoporotic hip fracture; Multiscale model; Verification; Uncertainty quantification; Validation

Funding

  1. UK Engineering and Physical Sciences Research Council through the MultiSim Project [EP/K03877X/1]
  2. European Commission H2020 programme through the CompBioMed Centre of Excellence [H2020-EINFRA-2015-1-675451]
  3. UK National Institute for Health Research (NIHR) through the Sheffield Biomedical Research Centre (Translational Neuroscience)
  4. EPSRC [EP/K03877X/1] Funding Source: UKRI

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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 4.00pp 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.

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