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炎症生物标志物与非特异性下腰痛的关联:系统评价。

Association Between Inflammatory Biomarkers and Nonspecific Low Back Pain: A Systematic Review.

机构信息

Department of Epidemiology and Preventive Medicine, School of Public Health and Preventive Medicine, Monash University.

Alfred Hospital, Melbourne, Vic., Australia.

出版信息

Clin J Pain. 2020 May;36(5):379-389. doi: 10.1097/AJP.0000000000000810.

Abstract

OBJECTIVES

Chronic inflammation increases the production of cytokines and activates proinflammatory pathways which may lead to nonspecific low back pain (LBP). We systematically reviewed the literature to investigate whether inflammatory biomarkers are associated with nonspecific LBP.

MATERIALS AND METHODS

CINAHL, Medline, and Embase were searched between January 1946 and May 2018. MeSH terms and key words were used to identify studies examining the association between inflammatory biomarkers and LBP. Two reviewers performed the risk of bias assessment and 3 reviewers extracted data independently. Qualitative evidence synthesis was performed.

RESULTS

Thirteen studies, ranging from fair to low quality, were included. Five studies examined the association between C-reactive protein (CRP)/high-sensitivity CRP and LBP; 6 studies assessed tumor necrosis factors (TNFs); 8 studies assessed interleukins (ILs); and 2 studies assessed fibrinogen. There was evidence for an association of elevated levels of CRP, TNFs, and IL-6 with LBP. There was conflicting evidence for an association between IL-1β, fibrinogen, and LBP.

DISCUSSION

Our findings support the notion of a positive association between inflammatory biomarkers and nonspecific LBP, specifically for CRP, TNFs, and IL-6. Although further high quality longitudinal studies are needed to confirm these findings and evaluate the magnitude of these associations, our findings suggest a role of inflammation in the pathogenesis of nonspecific LBP.

摘要

目的

慢性炎症会增加细胞因子的产生,并激活促炎途径,从而可能导致非特异性下腰痛(LBP)。我们系统地回顾了文献,以调查炎症生物标志物是否与非特异性 LBP 相关。

材料和方法

在 1946 年 1 月至 2018 年 5 月期间,我们在 CINAHL、Medline 和 Embase 上进行了搜索。使用 MeSH 术语和关键词来确定研究炎症生物标志物与 LBP 之间关联的研究。两名审查员进行了偏倚风险评估,3 名审查员独立提取数据。进行了定性证据综合分析。

结果

共纳入了 13 项研究,质量从一般到低不等。五项研究检查了 C-反应蛋白(CRP)/高敏 CRP 与 LBP 的关系;6 项研究评估了肿瘤坏死因子(TNFs);8 项研究评估了白细胞介素(ILs);两项研究评估了纤维蛋白原。CRP、TNFs 和 IL-6 水平升高与 LBP 相关有证据支持。IL-1β、纤维蛋白原和 LBP 之间存在关联的证据存在冲突。

讨论

我们的研究结果支持炎症生物标志物与非特异性 LBP 之间存在正相关的观点,特别是 CRP、TNFs 和 IL-6。尽管需要进一步的高质量纵向研究来证实这些发现并评估这些关联的程度,但我们的研究结果表明炎症在非特异性 LBP 的发病机制中起作用。

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