Faculty of Health Sciences and Western's Bone and Joint Institute, Western University, London, ON, N6G1H1, Canada.
University of North Carolina, Chapel Hill, NC, USA.
Eur Spine J. 2021 Sep;30(9):2531-2548. doi: 10.1007/s00586-021-06865-6. Epub 2021 May 22.
To clarify the current state of knowledge on the association of endplate structural defects and back pain.
Five databases were searched for studies reporting on the association between endplate structural defects and back pain. Covidence and comprehensive meta-analysis software were used for article screening and selection and pooling of extracted data. Overall quality of evidence was assessed using GRADE.
Twenty-six studies comprised of 11,027 subjects met inclusion criteria. The presence of moderate heterogeneity (I = 73%; p = 0.001) prevented the pooling of estimates across all studies. However, it was possible to pool studies of specific endplate defect phenotypes, such as erosion (OR: 2.69; 95% CI: 1.35-5.50) and sclerosis (OR: 1.97; 95% CI: 1.50-2.58), which yielded significant associations with back pain. Schmorl's nodes were also associated with most individual back pain phenotypes (OR: 1.53-1326, I = 0-7.5%) and back pain overall (OR: 1.63, 95% CI: 1.37-1.94, I = 26%) in general population samples. The pooling of data from all studies of specific back pain phenotypes, such as frequent back pain (OR: 2.83; 95% CI: 1.77-4.52) and back pain incidence (OR: 1.65; 95% CI: 1.30-2.10), each yielded significant association with endplate structural defects and was supported by low heterogeneity (I = < 7.5.%).
Overall, there is moderate quality evidence of an association between back pain and endplate structural defects, which is most evident for erosion, sclerosis and Schmorl's nodes. Going forward, research on specific endplate defect phenotypes and back pain case definitions using strong study designs will be important in clarifying the extent of associations and underlying mechanisms. The study was prospectively registered in Prospero (CRD42020170835) on 02/24/2020.
阐明椎间盘终板结构缺陷与腰痛之间关联的现有知识状况。
检索了五个数据库,以查找报告椎间盘终板结构缺陷与腰痛之间关联的研究。使用 Covidence 和综合荟萃分析软件进行文章筛选和提取数据的选择和汇总。使用 GRADE 评估整体证据质量。
26 项研究共纳入 11027 名受试者,符合纳入标准。由于存在中度异质性(I = 73%;p = 0.001),无法对所有研究进行汇总估计。然而,可以对特定终板缺陷表型的研究进行汇总,例如侵蚀(OR:2.69;95%CI:1.35-5.50)和硬化(OR:1.97;95%CI:1.50-2.58),这些研究与腰痛有显著关联。Schmorl 结节也与大多数个体腰痛表型(OR:1.53-1326,I = 0-7.5%)和总体腰痛(OR:1.63,95%CI:1.37-1.94,I = 26%)相关在一般人群样本中。对特定腰痛表型(如频繁腰痛(OR:2.83;95%CI:1.77-4.52)和腰痛发生率(OR:1.65;95%CI:1.30-2.10))的所有研究数据进行汇总,每项研究都与椎间盘终板结构缺陷有显著关联,且异质性较低(I < 7.5%)。
总体而言,有中等质量证据表明腰痛与椎间盘终板结构缺陷之间存在关联,其中以侵蚀、硬化和 Schmorl 结节最为明显。未来,使用强有力的研究设计研究特定的终板缺陷表型和腰痛病例定义,将有助于阐明关联的程度和潜在机制。该研究于 2020 年 2 月 24 日在 Prospero(CRD42020170835)进行了前瞻性注册。