Evidence map›Paper›PMID 41543139›Full record

ArticleJournal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research2026

QCT-based geometric, densitometric, and biomechanical properties of the aging human thoracolumbar spine.

Jianzhong Xu, Hossein Hemmatazad, Michael Indermaur, Alice Dudle, Alicia Feist, Rainer J Egli, Jasmin Wandel, Philippe Zysset

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Article in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Jianzhong XuARTORG Center for Biomedical Engineering Research, University of Bern, 3010 Bern, Switzerland.
Hossein HemmatazadDepartment of Radiation Oncology, Inselspital, Bern University Hospital and University of Bern, 3010 Bern, Switzerland.
Michael IndermaurARTORG Center for Biomedical Engineering Research, University of Bern, 3010 Bern, Switzerland.
Alice DudleARTORG Center for Biomedical Engineering Research, University of Bern, 3010 Bern, Switzerland.
Alicia FeistARTORG Center for Biomedical Engineering Research, University of Bern, 3010 Bern, Switzerland.
Rainer J EgliDepartment of Diagnostic, Interventional, and Pediatric Radiology, Inselspital, Bern University Hospital and University of Bern, 3010 Bern, Switzerland.
Jasmin WandelInstitute for Optimization and Data Analysis, Bern University of Applied Sciences, 2501 Biel, Switzerland.
Philippe ZyssetARTORG Center for Biomedical Engineering Research, University of Bern, 3010 Bern, Switzerland.ORCID 0000-0002-4712-7047

Funding

Swiss National Science Foundation 200365
6 · The paper itself

Abstract

Vertebral fractures represent a growing health issue in our aging societies. We performed a large-scale quantitative assessment of the geometric, densitometric, and biomechanical characteristics of the aging thoracolumbar spine using QCT and homogenized finite element (hFE) analysis. A total of 9298 intact vertebral bodies from T1 to L5 were evaluated across 629 radiologically healthy post-mortem spines (194 female, 435 male). We quantified vertebral height, cross-sectional area (CSA), BMC, BMD, synthetic areal BMD, and hFE-derived yield strength and applied a mixed linear regression model to investigate their dependence on age, sex, BMI, and spinal level. We found that vertebral height was greatest in the lumbar region, while CSA increased caudally and showed positive associations with both age and BMI. Both BMD and yield strength declined with advancing age, with significantly steeper reductions observed in females and in individuals with lower BMI. Interestingly, not yield force, but yield strength was found to be minimal at the thoracolumbar junction (T12-L1), which coincides with the highest occurrence of vertebral fractures. Despite inter-individual variability, BMD demonstrated strong segmental correlations, particularly between adjacent vertebrae, with correlation strength increasing with anatomical proximity. We established a robust power-law relationship (R2 = 0.91) between BMD and yield strength, which generalized across all vertebral levels. Collectively, these findings delineate spatial and demographic patterns in vertebral strength degeneration and provide normative QCT-based reference data for biomechanical modeling. The derived regression framework enables non-invasive estimation of vertebral yield strength, supporting future applications in fracture risk prediction and spine biomechanics research.

Indexed as

AgingBone DensityDensitometryLumbar VertebraeThoracic VertebraeTomography, X-Ray ComputedAdultAgedAged, 80 and overBiomechanical PhenomenaFemaleFinite Element AnalysisHumansMaleMiddle Ageddensitometryfinite element analysisspine anatomythoracolumbar spinevertebral strength

Identifiers

PMID41543139
PMCPMC13525206

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.