Faculty of Health Sciences, The University of Sydney, Sydney, New South Wales, Australia Neuroscience Research Australia and The University of New South Wales, Sydney, New South Wales, Australia.
Pain. 2013 Sep;154(9):1497-1504. doi: 10.1016/j.pain.2013.05.031. Epub 2013 May 24.
Sensitization of the nervous system can present as pain hypersensitivity that may contribute to clinical pain. In spinal pain, however, the relationship between sensory hypersensitivity and clinical pain remains unclear. This systematic review examined the relationship between pain sensitivity measured via quantitative sensory testing (QST) and self-reported pain or pain-related disability in people with spinal pain. Electronic databases and reference lists were searched. Correlation coefficients for the relationship between QST and pain intensity or disability were pooled using random effects models. Subgroup analyses and mixed effects meta-regression were used to assess whether the strength of the relationship was moderated by variables related to the QST method or pain condition. One hundred and forty-five effect sizes from 40 studies were included in the meta-analysis. Pooled estimates for the correlation between pain threshold and pain intensity were -0.15 (95% confidence interval [CI]: -0.18 to -0.11) and for disability -0.16 (95% CI: -0.22 to -0.10). Subgroup analyses and meta-regression did not provide evidence that these relationships were moderated by the QST testing site (primary pain/remote), pain condition (back/neck pain), pain type (acute/chronic), or type of pain induction stimulus (eg, mechanical/thermal). Fair correlations were found for the relationship between pain intensity and thermal temporal summation (0.26, 95% CI: 0.09 to 0.42) or pain tolerance (-0.30, 95% CI: -0.45 to -0.13), but only a few studies were available. Our study indicates either that pain threshold is a poor marker of central sensitization or that sensitization does not play a major role in patients' reporting of pain and disability. Future research prospects are discussed.
神经系统敏化可表现为痛觉过敏,可能导致临床疼痛。然而,在脊柱疼痛中,感觉过敏与临床疼痛之间的关系尚不清楚。本系统评价研究了通过定量感觉测试(QST)测量的疼痛敏感性与脊柱疼痛患者自我报告的疼痛或与疼痛相关的残疾之间的关系。检索了电子数据库和参考文献列表。使用随机效应模型汇总 QST 与疼痛强度或残疾之间关系的相关系数。使用混合效应荟萃回归进行亚组分析,以评估 QST 方法或疼痛状况相关变量是否调节了关系的强度。荟萃分析纳入了 40 项研究的 145 个效应量。疼痛阈值与疼痛强度之间的相关性的汇总估计值为-0.15(95%置信区间[CI]:-0.18 至-0.11),与残疾的相关性为-0.16(95%CI:-0.22 至-0.10)。亚组分析和荟萃回归没有提供证据表明这些关系受到 QST 测试部位(主要疼痛/远处)、疼痛状况(背部/颈部疼痛)、疼痛类型(急性/慢性)或疼痛诱发刺激类型(例如机械/热)的调节。在疼痛强度与热时间总和(0.26,95%CI:0.09 至 0.42)或疼痛耐受力(-0.30,95%CI:-0.45 至-0.13)之间的关系中,发现了适度的相关性,但只有少数研究可用。我们的研究表明,疼痛阈值要么是中枢敏化的不良标志物,要么是敏化在患者对疼痛和残疾的报告中没有起主要作用。讨论了未来的研究前景。