Feller Daniel, van den Berg Roxanne, Enthoven Wendy T M, Oei Edwin H G, Bierma-Zeinstra Sita M, Koes Bart W, Chiarotto Alessandro
Department of General Practice, Erasmus MC, University Medical Center, Rotterdam, the Netherlands.
ConsultAssistent, Rotterdam, the Netherlands.
Osteoarthr Cartil Open. 2024 Oct 18;6(4):100535. doi: 10.1016/j.ocarto.2024.100535. eCollection 2024 Dec.
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).
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.
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.
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.
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退变(LDD)以及通过C反应蛋白(CRP)测量的全身炎症之间的关联。最终目标是帮助形成未来脊柱骨关节炎(OA)的定义。
使用了荷兰“老年人背部疼痛”(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(即多节段椎间盘间隙狭窄和多节段骨赘)与CRP之间的关系。进行了针对混杂变量进行调整的回归模型。
纳入675例患者。平均年龄为66.52岁(标准差7.69),平均CRP为3.20mg/L(标准差7.61)。脊柱晨僵的严重程度与多节段椎间盘间隙狭窄相关:“轻度”晨僵的比值比(OR)为2.89(95%置信区间:1.24至6.74),“中度”为2.97(95%置信区间:1.18至7.44),“重度”为3.23(95%置信区间:1.17至8.90),“极重度”晨僵严重程度的OR为5.62(95%置信区间:1.70至18.60)。然而,脊柱晨僵严重程度与多节段骨赘无关,LDD的两个多节段特征均与脊柱晨僵的持续时间无关。未发现脊柱晨僵严重程度或持续时间与CRP水平之间存在关联。
我们的结果表明,在未来有症状脊柱OA的定义中可能需要考虑患者报告的脊柱晨僵的严重程度,并且脊柱晨僵可能是脊柱退变过程的症状,而不是背痛患者全身炎症的症状。