A predictive mechanical model for evaluating vertebral fracture probability in lumbar spine under different osteoporotic drug therapies. Issue 131 (July 2016)

• Record Type: Journal Article
• Authors: López, E.; Ibarz, E.; Herrera, A.; Puértolas, S.; Gabarre, S.; Más, Y.; Mateo, J.; Gil-Albarova, J.; Gracia, L.
• Is Part Of: Computer methods and programs in biomedicine. Issue 131(2016)
• Page Start: 37
• Page End: 50
• Publication Date: 2016-07
• Subjects: Osteoporotic vertebral fracture -- Predictive model -- Finite elements -- Fracture risk -- Fracture probability -- Osteoporosis treatments; BMD Bone Mineral Density -- CT Computed Tomography -- DXA Dual-energy X-ray Absorptiometry -- FE Finite Elements -- FRAX Fracture Risk Assessment Tool -- L1 to L5 Lumbar vertebrae -- PTH Parathyroid Hormone -- QCT Quantitative Computed Tomography -- S1 Sacrum -- T12 Last thoracic vertebrae -- WHO World Health Organization; Medicine -- Computer programs -- Periodicals; Biology -- Computer programs -- Periodicals; Computers -- Periodicals; Medicine -- Periodicals; Médecine -- Logiciels -- Périodiques; Biologie -- Logiciels -- Périodiques; Biology -- Computer programs; Medicine -- Computer programs; Periodicals; Electronic journals; 610.28
• DOI: 10.1016/j.cmpb.2016.04.006
• Languages: English
• ISSNs: 0169-2607

Abstract

Highlights: Method for estimating the fracture risk in osteoporotic patients based on Damage and Fracture Mechanics and DXA measurements. The method evaluates the evolution over time of the mechanical strength of bone from BMD, for different treatments. Evolutionary algorithm and a finite element model of the lumbar spine allow the prediction of fracture probability. The incorporation of clinical measurements and simulation results will be useful for an individualized treatment in patients. The model predicts the evolution of vertebral fracture probability and the expected evolution under different therapies. Abstract: Osteoporotic vertebral fractures represent a major cause of disability, loss of quality of life and even mortality among the elderly population. Decisions on drug therapy are based on the assessment of risk factors for fracture from bone mineral density (BMD) measurements. A previously developed model, based on the Damage and Fracture Mechanics, was applied for the evaluation of the mechanical magnitudes involved in the fracture process from clinical BMD measurements. BMD evolution in untreated patients and in patients with seven different treatments was analyzed from clinical studies in order to compare the variation in the risk of fracture. The predictive model was applied in a finite element simulation of the whole lumbar spine, obtaining detailed maps of damage and fracture probability, identifying high-risk local zones at vertebral body. For every vertebra, strontium ranelate exhibits the highest decrease, whereas minimum decrease is achieved with oral ibandronate. All the treatments manifest similar trends for every vertebra. Conversely, for the natural BMD evolution, as bone stiffness decreases, the mechanical damage and fracture probability show a significant increase (as it occurs in the natural history of BMD). Vertebral walls and external areas of vertebral end plates are the zones at greatest risk, in coincidence with the typical locations of osteoporotic fractures, characterized by a vertebral crushing due to the collapse of vertebral walls. This methodology could be applied for an individual patient, in order to obtain the trends corresponding to different treatments, in identifying at-risk individuals in early stages of osteoporosis and might be helpful for treatment decisions.