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Degeneration alters structure-function relationships at multiple length-scales and across interfaces in human intervertebral discs.
Ashinsky, Beth G; Gullbrand, Sarah E; Wang, Chao; Bonnevie, Edward D; Han, Lin; Mauck, Robert L; Smith, Harvey E.
Afiliação
  • Ashinsky BG; McKay Orthopaedic Research Laboratory, Department of Orthopaedic Surgery, University of Pennsylvania, Philadelphia, PA, USA.
  • Gullbrand SE; Drexel University School of Biomedical Engineering, Science and Health Systems, Philadelphia, PA, USA.
  • Wang C; Translational Musculoskeletal Research Center, Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA, USA.
  • Bonnevie ED; McKay Orthopaedic Research Laboratory, Department of Orthopaedic Surgery, University of Pennsylvania, Philadelphia, PA, USA.
  • Han L; Translational Musculoskeletal Research Center, Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA, USA.
  • Mauck RL; Drexel University School of Biomedical Engineering, Science and Health Systems, Philadelphia, PA, USA.
  • Smith HE; McKay Orthopaedic Research Laboratory, Department of Orthopaedic Surgery, University of Pennsylvania, Philadelphia, PA, USA.
J Anat ; 238(4): 986-998, 2021 04.
Article em En | MEDLINE | ID: mdl-33205444
ABSTRACT
Intervertebral disc (IVD) degeneration and associated back pain place a significant burden on the population. IVD degeneration is a progressive cascade of cellular, compositional, and structural changes, which results in a loss of disc height, disorganization of extracellular matrix architecture, tears in the annulus fibrosus which may involve herniation of the nucleus pulposus, and remodeling of the bony and cartilaginous endplates (CEP). These changes to the IVD often occur concomitantly, across the entire motion segment from the disc subcomponents to the CEP and vertebral bone, making it difficult to determine the causal initiating factor of degeneration. Furthermore, assessments of the subcomponents of the IVD have been largely qualitative, with most studies focusing on a single attribute, rather than multiple adjacent IVD substructures. The objective of this study was to perform a multiscale and multimodal analysis of human lumbar motion segments across various length scales and degrees of degeneration. We performed multiple assays on every sample and identified several correlations between structural and functional measurements of disc subcomponents. Our results demonstrate that with increasing Pfirrmann grade there is a reduction in disc height and nucleus pulposus T2 relaxation time, in addition to alterations in motion segment macromechanical function, disc matrix composition and cellular morphology. At the cartilage endplate-vertebral bone interface, substantial remodeling was observed coinciding with alterations in micromechanical properties. Finally, we report significant relationships between vertebral bone and nucleus pulposus metrics, as well as between micromechanical properties of the endplate and whole motion segment biomechanical parameters, indicating the importance of studying IVD degeneration as a whole organ.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Degeneração do Disco Intervertebral / Disco Intervertebral / Vértebras Lombares Tipo de estudo: Prognostic_studies / Qualitative_research Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: J Anat Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Degeneração do Disco Intervertebral / Disco Intervertebral / Vértebras Lombares Tipo de estudo: Prognostic_studies / Qualitative_research Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: J Anat Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos