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有限元模型揭示了软骨终板在椎间盘退变准静态生物力学中的作用。

Finite element model reveals the involvement of cartilage endplate in quasi-static biomechanics of intervertebral disc degeneration.

作者信息

Zhang Yujun, Pan Yanli, Mao Xinning, He Du, Zhang Liangping, Cheng Wei, Zhu Chengyue, Zhu Hang, Zhang Wei, Jin HongTing, Pan Hao, Wang Dong

机构信息

Department of Orthopaedics, Hangzhou TCM Hospital Affiliated to Zhejiang Chinese Medical University (Hangzhou Hospital of Traditional Chinese Medicine), Hangzhou 310000, Zhejiang Province, China.

Department of Orthopaedics, Hangzhou Dingqiao Hospital, Huanding Road NO 1630, Hangzhou 310021, Zhejiang Province, China.

出版信息

Heliyon. 2024 Sep 5;10(18):e37524. doi: 10.1016/j.heliyon.2024.e37524. eCollection 2024 Sep 30.

DOI:10.1016/j.heliyon.2024.e37524
PMID:39309961
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11414571/
Abstract

BACKGROUND AND OBJECTIVE

The intrinsic link between the compositional and structural attributes and the biomechanical functionality is evident in intervertebral discs. However, it remains unclear from a biomechanical perspective whether cartilage endplate (CEP) degeneration exacerbates intervertebral disc degeneration.

METHODS

This study developed and quantitatively validated four biphasic swelling-based finite element models. We then applied four quasi-static tests and simulated daily loading scenarios to examine the effects of CEP degradation.

RESULTS

Under free-swelling conditions, short-term responses were prevalent, with CEP performance changes not significantly impacting response proportionality. The creep test results showed the more than 50 % of the strain was attributed to long-term responses. Stress-relaxation testing indicated that all responses increased with disc degeneration, yet CEP degeneration's impact was minimal. Daily load analyses revealed that disc degeneration significantly reduces nucleus pulposus pressure and disc height, whereas CEP degeneration marginally increases nucleus pressure and slightly decreases disc height.

CONCLUSIONS

Glycosaminoglycan content and CEP permeability are critical to the fluid-dependent viscoelastic response of intervertebral discs. Our findings suggest that CEP contributes to disc degeneration under daily loading conditions.

摘要

背景与目的

椎间盘的成分和结构属性与生物力学功能之间存在内在联系。然而,从生物力学角度来看,软骨终板(CEP)退变是否会加剧椎间盘退变仍不清楚。

方法

本研究开发并定量验证了四个基于双相肿胀的有限元模型。然后,我们应用四个准静态测试并模拟日常负荷情况来研究CEP退变的影响。

结果

在自由肿胀条件下,短期反应普遍存在,CEP性能变化对反应比例性影响不显著。蠕变测试结果表明,超过50%的应变归因于长期反应。应力松弛测试表明,所有反应均随椎间盘退变而增加,但CEP退变的影响最小。日常负荷分析显示,椎间盘退变显著降低髓核压力和椎间盘高度,而CEP退变仅略微增加髓核压力并略微降低椎间盘高度。

结论

糖胺聚糖含量和CEP通透性对于椎间盘依赖流体的粘弹性反应至关重要。我们的研究结果表明,在日常负荷条件下,CEP会导致椎间盘退变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d29/11414571/7326c91892f7/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d29/11414571/7d9df61f5139/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d29/11414571/14daf1287a4a/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d29/11414571/d78ee305c4dc/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d29/11414571/30fe07a013ee/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d29/11414571/7326c91892f7/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d29/11414571/7d9df61f5139/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d29/11414571/14daf1287a4a/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d29/11414571/d78ee305c4dc/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d29/11414571/30fe07a013ee/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d29/11414571/7326c91892f7/gr5.jpg

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