脊柱晨僵与腰椎间盘退变和 C 反应蛋白的关系:老年人背部不适(BACE)研究

Daniel Feller , Roxanne van den Berg , Wendy T.M. Enthoven , Edwin H.G. Oei , Sita M. Bierma-Zeinstra , Bart W. Koes , Alessandro Chiarotto
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引用次数: 0

摘要

目的确定非特异性背痛老年患者中患者报告的脊柱晨僵与腰椎间盘变性(LDD)和以C反应蛋白(CRP)测量的全身炎症之间的关联。设计使用荷兰 "老年人背部不适"(BACE)研究的基线数据。评估了患者报告的脊柱晨僵的严重程度和持续时间、LDD(即多层椎间盘间隙狭窄和多层骨质增生)和 CRP 之间的关系。结果共纳入六百七十五名患者。平均年龄为 66.52 岁(SD 7.69),平均 CRP 为 3.20 mg/L(SD 7.61)。脊柱晨僵的严重程度与多级椎间盘间隙狭窄有关:轻度 "的 OR 值为 2.89(95 % CI:1.24 至 6.74),"中度 "的 OR 值为 2.97(95 % CI:1.18 至 7.44),"重度 "的 OR 值为 3.23(95 % CI:1.17 至 8.90),"极重度 "的 OR 值为 5.62(95 % CI:1.70 至 18.60)。然而,脊柱晨僵的严重程度与多层次骨质增生无关,LDD的两个多层次特征与脊柱晨僵的持续时间无关。结论我们的研究结果表明,在未来对有症状的脊柱 OA 进行定义时,可以考虑患者报告的脊柱晨僵的严重程度,脊柱晨僵可能是脊柱退行性过程的症状,而不是背痛患者全身炎症的症状。
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The association of spinal morning stiffness with lumbar disc degeneration and C-reactive protein: The back complaints in older adults (BACE) study

Objective

To determine the association between patient-reported spinal morning stiffness and lumbar disc degeneration (LDD) and systemic inflammation, as measured by C-reactive protein (CRP), in older patients with non-specific back pain. The ultimate objective is to help shape a future definition of spinal osteoarthritis (OA).

Design

Baseline data from the Dutch “Back Complaints in the Older Adults” (BACE) study was used. The relationship between the severity and duration of patient-reported spinal morning stiffness, LDD (i.e., multilevel disc space narrowing and multilevel osteophytes), and CRP was assessed. Regression models adjusted for confounding variables were performed.

Results

Six hundred and seventy-five patients were included. The mean age was 66.52 years (SD 7.69), with a mean CRP of 3.20 ​mg/L (SD 7.61). The severity of spinal morning stiffness was associated with multilevel disc space narrowing: OR 2.89 (95 ​% CI: 1.24 to 6.74) for ‘mild’, OR 2.97 (95 ​% CI: 1.18 to 7.44) for ‘moderate’, OR 3.23 (95 ​% CI: 1.17 to 8.90) for ‘severe’, and OR 5.62 (95 ​% CI: 1.70 to 18.60) for ‘extreme’ morning stiffness severity. However, spinal morning stiffness severity was not associated with multilevel osteophytes, and both multilevel features of LDD showed no associations with the duration of spinal morning stiffness. No associations were found between spinal morning stiffness severity or duration, and CRP levels.

Conclusions

Our results suggest that the severity of patient-reported spinal morning stiffness might be considered in future definitions of symptomatic spinal OA and that spinal morning stiffness is probably a symptom of a degenerative process in the spine rather than a symptom of systemic inflammation in patients with back pain.
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来源期刊
Osteoarthritis and cartilage open
Osteoarthritis and cartilage open Orthopedics, Sports Medicine and Rehabilitation
CiteScore
3.30
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