腰椎终板Modic变化中脂质代谢及软骨退变相关因子的表达。

IF 1.9 Q2 ORTHOPEDICS Joint diseases and related surgery Pub Date : 2025-01-02 Epub Date: 2024-12-18 DOI:10.52312/jdrs.2025.1870
Congjie Li, Di Li, Xiaowei Yao, Shaosong Sun, Bao Ren, Ye Han
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引用次数: 0

摘要

目的:探讨脂质代谢及软骨退行性变相关因子的表达与腰椎modc变化的关系。患者和方法:本前瞻性研究共纳入10例患者(男性6例,女性4例;平均年龄:60.4±8.7岁;51 - 82岁),因腰椎退行性疾病行腰椎椎间融合术(MC组),对照组10例(男4例,女6例;平均年龄49.7±9.8岁;范围,42至76岁),在2020年1月至2022年12月期间发生腰椎爆裂骨折(非mc组)。收集临床影像学资料及软骨组织,观察软骨特征及病理改变。采用定量聚合酶链式反应(qPCR)检测软骨组织中脂质代谢相关炎症因子基质金属蛋白酶-1 (MMP-1)、带血栓反应蛋白基元的崩解素和金属蛋白酶-5 (ADAMTS-5)、聚集蛋白的相对表达水平。Western blotting检测软骨组织中MMP-1和ADAMTS-5蛋白的相对表达水平。结果:两组患者的基线特征无显著差异。对照组终板软骨颜色及透明度均明显优于MCs组。x线片和苏木素-伊红染色显示,对照组终板软骨组织细胞外基质高于MCs组(p结论:退行性腰椎疾病患者椎终板存在脂质代谢和软骨退变相关炎症因子,MMP-1和ADAMTS-5的上调可能与MCs和终板退变有关。
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Expression of lipid metabolism and cartilage degeneration-related factors in lumbar vertebral endplate Modic changes.

Objectives: This study aims to investigate the relationship between the expression of lipid metabolism and cartilage degeneration-related factors and Modic changes (MCs) of lumbar vertebral.

Patients and methods: This prospective study included a total of 10 patients (6 males, 4 females; mean age: 60.4±8.7 years; range 51 to 82 years) who underwent lumbar interbody fusion surgery due to degenerative lumbar diseases (MC group), and 10 control patients (4 males, 6 females; mean age: 49.7±9.8 years; range, 42 to 76 years) with lumbar burst fractures (nonMC group) between January 2020 and December 2022. Clinical imaging data and cartilage tissues were collected to observe cartilage characteristics and pathological changes. The relative expression levels of lipid metabolism-related inflammatory factors matrix metalloproteinase-1 (MMP-1), a disintegrin and metalloproteinase with thromboSpondin motifs-5 (ADAMTS-5), and aggrecan in cartilage were detected by quantitative polymerase chain reaction (qPCR). The relative expression levels of MMP-1 and ADAMTS-5 proteins in cartilage tissues were detected by Western blotting.

Results: There were no significant differences in the baseline characteristics between the two groups. The color and transparency of the endplate cartilage in the control group were significantly better than those in the MCs group. Radiographic and hematoxylin-eosin staining of the endplate cartilage tissues showed that the extracellular matrix was higher in the control group than in the MCs group (p<0.05). Compared to the control group, qPCR analysis showed higher expression of MMP-1 and ADAMTS-5 in the MCs group, while aggrecan expression was lower (p<0.05). Western blot analysis showed that both MMP-1 and ADAMTS-5 expression were higher in the MCs group than in the control group (p<0.05).

Conclusion: Lipid metabolism and cartilage degeneration-related inflammatory factors exist in the vertebral endplate of the patients with degenerative lumbar diseases, and the upregulation of MMP-1 and ADAMTS-5 may be related to MCs and endplate degeneration.

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