Michal Kuchař, Alexander Morávek, Niels Hammer, Petr Henyš
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引用次数: 0
Abstract
Walking, posture and childbirth all depend on the pelvic ring, yet human pelvic dimorphism is usually interpreted from static birth-canal dimensions. We asked whether sex differences in pelvic function are explained by overall size and static pelvimetry or by available mechanical deformation pathways. We analysed 278 anatomically standardized lumbopelvic finite-element models built from clinical computed tomography scans. In each model, modal decomposition separated pelvic deformation into a shared, ranked set of pathways, allowing us to compare pathway stiffness, load recruitment and sensitivity to ligamentous and cartilaginous constraints. Overall pelvic size accounted for much of the baseline stiffness spectrum, confirming a strong size-dependent component. However, size- and age-adjusted sex differences remained: male pelves showed approximately 20% higher eigenvalues than female pelves in modes 2 and 9. Loading probes showed a common backbone in both sexes during habitual support, whereas inlet opening revealed a different response organization, with female pelves distributing deformation across a broader, coordinated set and a higher effective number of participating modes. The principal inlet-opening pathway was most sensitive to the pubic symphysis and anterior sacroiliac ligamentous constraints. Pelvic dimorphism, therefore, lies not only in canal shape, but in the organization of mechanical pathways that balance support with deformation.
期刊介绍:
J. R. Soc. Interface welcomes articles of high quality research at the interface of the physical and life sciences. It provides a high-quality forum to publish rapidly and interact across this boundary in two main ways: J. R. Soc. Interface publishes research applying chemistry, engineering, materials science, mathematics and physics to the biological and medical sciences; it also highlights discoveries in the life sciences of relevance to the physical sciences. Both sides of the interface are considered equally and it is one of the only journals to cover this exciting new territory. J. R. Soc. Interface welcomes contributions on a diverse range of topics, including but not limited to; biocomplexity, bioengineering, bioinformatics, biomaterials, biomechanics, bionanoscience, biophysics, chemical biology, computer science (as applied to the life sciences), medical physics, synthetic biology, systems biology, theoretical biology and tissue engineering.