Comparison of patient-specific computational models vs. clinical follow-up, for adjacent segment disc degeneration and bone remodelling after spinal fusion

dc.contributor.authorvan Rijsbergen, Marc M.
dc.contributor.authorVan-Rietbergen, Bert
dc.contributor.authorBarthelemy, Veronique
dc.contributor.authorÉltes, Péter Endre
dc.contributor.authorLazàry, Áron
dc.contributor.authorLacroix, Damien
dc.contributor.authorNoailly, Jérôme
dc.contributor.authorTho, Marie Christine Ho Ba
dc.contributor.authorWilson, Wouter
dc.contributor.authorIto, Keita
dc.date.accessioned2020-03-18T16:13:22Z
dc.date.available2020-03-18T16:13:22Z
dc.date.issued2018
dc.description.abstractSpinal fusion is a standard surgical treatment for patients suffering from low back pain attributed to disc degeneration. However, results are somewhat variable and unpredictable. With fusion the kinematic behaviour of the spine is altered. Fusion and/or stabilizing implants carrying considerable load and prevent rotation of the fused segments. Associated with these changes, a risk for accelerated disc degeneration at the adjacent levels to fusion has been demonstrated. However, there is yet no method to predict the effect of fusion surgery on the adjacent tissue levels, i.e. bone and disc. The aim of this study was to develop a coupled and patient-specific mechanoregulated model to predict disc generation and changes in bone density after spinal fusion and to validate the results relative to patient follow-up data. To do so, a multiscale disc mechanoregulation adaptation framework was developed and coupled with a previously developed bone remodelling algorithm. This made it possible to determine extra cellular matrix changes in the intervertebral disc and bone density changes simultaneously based on changes in loading due to fusion surgery. It was shown that for 10 cases the predicted change in bone density and degeneration grade conforms reasonable well to clinical follow-up data. This approach helps us to understand the effect of surgical intervention on the adjacent tissue remodelling. Thereby, providing the first insight for a spine surgeon as to which patient could potentially be treated successfully by spinal fusion and in which patient has a high risk for adjacent tissue changes.en
dc.description.sponsorshipThe research leading to these results has received funding from the European Union Seventh Framework Programme (FP7-ICT-2009-6) under grant agreement n° 269909,
dc.format.mimetypeapplication/pdf
dc.identifier.citationVan Rijsbergen M, Van Rietbergen B, Barthelemy V, Eltes P, Lazáry A, Lacroix D, Noailly J, Tho MCHB, Wilson W, Ito K. Comparison of patient-specific computational models vs. clinical follow-up, for adjacent segment disc degeneration and bone remodelling after spinal fusion. PLoS ONE. 2018 Aug 30;13(8). DOI: 10.1371/journal.pone.0200899
dc.identifier.doihttp://dx.doi.org/10.1371/journal.pone.0200899
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/10230/43940
dc.language.isoeng
dc.publisherPublic Library of Science (PLoS)
dc.relation.ispartofPLoS ONE. 2018 Aug 30;13(8)
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/FP7/269909
dc.rights© 2018 Rijsbergen et al. This is an open access article distributed under the terms of the Creative Commons Attribution License https://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.subject.keywordBone densityen
dc.subject.keywordBone remodelingen
dc.subject.keywordCollagensen
dc.subject.keywordSpinal fusionen
dc.subject.keywordVertebraeen
dc.subject.keywordSurgical and invasive medical proceduresen
dc.subject.keywordChondrocytesen
dc.subject.keywordSpineen
dc.titleComparison of patient-specific computational models vs. clinical follow-up, for adjacent segment disc degeneration and bone remodelling after spinal fusionen
dc.typeinfo:eu-repo/semantics/article
dc.type.versioninfo:eu-repo/semantics/publishedVersion

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