Relationship between facet joint osteoarthritis and lumbar paraspinal muscle atrophy: a cross-sectional study.

IF 2.9 2区 医学 Q2 CLINICAL NEUROLOGY
Journal of neurosurgery. Spine Pub Date : 2024-06-14 Print Date: 2024-09-01 DOI:10.3171/2024.4.SPINE231018
Ali E Guven, Lukas Schönnagel, Gaston Camino-Willhuber, Erika Chiapparelli, Krizia Amoroso, Jiaqi Zhu, Soji Tani, Thomas Caffard, Artine Arzani, Arman T Zadeh, Jennifer Shue, Ek Tsoon Tan, Andrew A Sama, Federico P Girardi, Frank P Cammisa, Alexander P Hughes
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引用次数: 0

Abstract

Objective: The paraspinal muscles play an essential role in the stabilization of the lumbar spine. Lumbar paraspinal muscle atrophy has been linked to chronic back pain and degenerative processes within the spinal motion segment. However, the relationship between the different paraspinal muscle groups and facet joint osteoarthritis (FJOA) has not been fully explored.

Methods: In this cross-sectional study, the authors analyzed adult patients who underwent lumbar spinal surgery between December 2014 and March 2023 for degenerative spinal conditions and had preoperative MRI and CT scans. The fatty infiltration (FI) and functional cross-sectional area (fCSA) of the psoas, erector spinae, and multifidus muscles were assessed on axial T2-weighted MR images at the level of the upper endplate of L4 based on established studies and calculated using custom-made software. Intervertebral disc degeneration at each lumbar level was evaluated using the Pfirrmann grading system. The grades from each level were summed to report the cumulative lumbar Pfirrmann grade. Weishaupt classification (0-3) was used to assess FJOA at all lumbar levels (L1 to S1) on preoperative CT scans. The total lumbar FJOA score was determined by adding the Weishaupt grades of both sides at all 5 levels. Correlation and linear regression analyses were conducted to assess the relationship between FJOA and paraspinal muscle parameters.

Results: A total of 225 patients (49.7% female) with a median age of 61 (IQR 54-70) years and a median BMI of 28.3 (IQR 25.1-33.1) kg/m2 were included. After adjustment for age, sex, BMI, and the cumulative lumbar Pfirrmann grade, only multifidus muscle fCSA (estimate -4.69, 95% CI -6.91 to -2.46; p < 0.001) and FI (estimate 0.64, 95% CI 0.33-0.94; p < 0.001) were independently predicted by the total FJOA score. A similar relation was seen with individual Weishaupt grades of each lumbar level after controlling for age, sex, BMI, and the Pfirrmann grade of the corresponding level.

Conclusions: Atrophy of the multifidus muscle is significantly associated with FJOA in the lumbar spine. The absence of such correlation for the erector spinae and psoas muscles highlights the unique link between multifidus muscle quality and the degeneration of the spinal motion segment. Further research is necessary to establish the causal link and the clinical implications of these findings.

面关节骨关节炎与腰椎旁肌肉萎缩之间的关系:一项横断面研究。
目的腰椎旁肌肉在稳定腰椎方面起着至关重要的作用。腰椎旁肌肉萎缩与慢性背痛和脊柱运动区段内的退行性过程有关。然而,不同脊柱旁肌群与面关节骨关节炎(FJOA)之间的关系尚未得到充分探讨:在这项横断面研究中,作者分析了在 2014 年 12 月至 2023 年 3 月期间因脊柱退行性病变而接受腰椎手术并进行术前 MRI 和 CT 扫描的成年患者。根据既有研究,在L4上终板水平的轴向T2加权MR图像上评估了腰肌、竖脊肌和多侧肌的脂肪浸润(FI)和功能横截面积(fCSA),并使用定制软件进行了计算。使用 Pfirrmann 分级系统对每个腰椎级别的椎间盘退变进行评估。将每个级别的分级相加,得出累计的腰椎 Pfirrmann 分级。魏氏分级(0-3)用于评估术前 CT 扫描中所有腰椎级别(L1 至 S1)的 FJOA。腰椎 FJOA 总分由两侧所有 5 个级别的 Weishaupt 分级相加得出。对 FJOA 和脊柱旁肌肉参数之间的关系进行了相关性和线性回归分析:共纳入 225 名患者(49.7% 为女性),中位年龄为 61(IQR 54-70)岁,中位体重指数为 28.3(IQR 25.1-33.1)kg/m2。在对年龄、性别、体重指数和累积腰椎 Pfirrmann 分级进行调整后,只有多裂肌 fCSA(估计值 -4.69,95% CI -6.91 至 -2.46;p <0.001)和 FI(估计值 0.64,95% CI 0.33 至 0.94;p <0.001)可由 FJOA 总分独立预测。在控制了年龄、性别、体重指数和相应腰椎水平的 Pfirrmann 分级后,每个腰椎水平的 Weishaupt 分级也有类似的关系:结论:腰椎多裂肌萎缩与 FJOA 有显著相关性。结论:腰椎多裂肌萎缩与 FJOA 有明显相关性,而竖脊肌和腰方肌没有这种相关性,这凸显了多裂肌质量与脊柱运动节段退化之间的独特联系。要确定这些发现的因果关系和临床意义,还需要进一步的研究。
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来源期刊
Journal of neurosurgery. Spine
Journal of neurosurgery. Spine 医学-临床神经学
CiteScore
5.10
自引率
10.70%
发文量
396
审稿时长
6 months
期刊介绍: Primarily publish original works in neurosurgery but also include studies in clinical neurophysiology, organic neurology, ophthalmology, radiology, pathology, and molecular biology.
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