Arthritis Research UK Pain Centre, University of Nottingham, Medical School, Queen's Medical Centre, Nottingham, United Kingdom.
School of Life Sciences, University of Nottingham, Nottingham, United Kingdom.
Pain. 2019 Mar;160(3):658-669. doi: 10.1097/j.pain.0000000000001445.
Anxiety and depression are associated with increased pain responses in chronic pain states. The extent to which anxiety drives chronic pain, or vice versa, remains an important question that has implications for analgesic treatment strategies. Here, the effect of existing anxiety on future osteoarthritis (OA) pain was investigated, and potential mechanisms were studied in an animal model. Pressure pain detection thresholds, anxiety, and depression were assessed in people with (n = 130) or without (n = 100) painful knee OA. Separately, knee pain and anxiety scores were also measured twice over 12 months in 4730 individuals recruited from the general population. A preclinical investigation of a model of OA pain in normo-anxiety Sprague-Dawley (SD) and high-anxiety Wistar Kyoto (WKY) rats assessed underlying neurobiological mechanisms. Higher anxiety, independently from depression, was associated with significantly lower pressure pain detection thresholds at sites local to (P < 0.01) and distant from (P < 0.05) the painful knee in patients with OA. Separately, high anxiety scores predicted increased risk of knee pain onset in 3274 originally pain-free people over the 1-year period (odds ratio = 1.71; 95% confidence interval = 1.25-2.34, P < 0.00083). Similarly, WKY rats developed significantly lower ipsilateral and contralateral hind paw withdrawal thresholds in the monosodium iodoacetate model of OA pain, compared with SD rats (P = 0.0005). Linear regressions revealed that baseline anxiety-like behaviour was predictive of lowered paw withdrawal thresholds in WKY rats, mirroring the human data. This augmented pain phenotype was significantly associated with increased glial fibrillary acidic protein immunofluorescence in pain-associated brain regions, identifying supraspinal astrocyte activation as a significant mechanism underlying anxiety-augmented pain behaviour.
焦虑和抑郁与慢性疼痛状态下的疼痛反应增加有关。焦虑是导致慢性疼痛的原因,还是反之亦然,这仍然是一个重要的问题,对镇痛治疗策略有影响。在这里,研究了现有的焦虑对未来骨关节炎 (OA) 疼痛的影响,并在动物模型中研究了潜在的机制。在有(n = 130)或没有(n = 100)膝关节 OA 疼痛的人群中评估了压痛检测阈值、焦虑和抑郁。此外,在从普通人群中招募的 4730 名个体中,还在 12 个月内两次测量了膝关节疼痛和焦虑评分。在正常焦虑 Sprague-Dawley (SD) 和高焦虑 Wistar Kyoto (WKY) 大鼠的 OA 疼痛模型中进行了一项临床前研究,评估了潜在的神经生物学机制。在有 OA 的患者中,独立于抑郁,较高的焦虑与局部(P < 0.01)和远处(P < 0.05)疼痛膝关节处的压痛检测阈值明显降低有关。另外,在最初无痛的 3274 人中,高焦虑评分预测了 1 年内膝关节疼痛发作的风险增加(优势比=1.71;95%置信区间=1.25-2.34,P < 0.00083)。同样,与 SD 大鼠相比,WKY 大鼠在碘乙酸单钠诱导的 OA 疼痛模型中对同侧和对侧后爪撤回阈值的降低更明显(P = 0.0005)。线性回归显示,基线焦虑样行为可预测 WKY 大鼠的爪撤回阈值降低,与人类数据相吻合。这种增强的疼痛表型与疼痛相关脑区中胶质纤维酸性蛋白免疫荧光的增加显著相关,表明脊髓星形胶质细胞激活是焦虑增强疼痛行为的一个重要机制。
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