Department of Psychology, The University of Tulsa, Tulsa, Oklahoma.
Department of Psychology, The University of Tulsa, Tulsa, Oklahoma.
J Pain. 2019 Aug;20(8):941-955. doi: 10.1016/j.jpain.2019.02.006. Epub 2019 Feb 15.
Adverse life experiences (ALEs) are associated with hyperalgesia and chronic pain, but the underlying mechanisms are poorly understood. One potential mechanism is hyperexcitability of spinal neurons (ie, central sensitization). Given that Native Americans (NAs) are more likely to have ALEs and to have a higher prevalence of chronic pain, the relationship between ALEs and spinal hyperexcitability might contribute to their pain risk. The present study assessed temporal summation of the nociceptive flexion reflex (TS-NFR; a correlate of spinal hyperexcitability) and pain (TS-Pain) in 246 healthy, pain-free non-Hispanic whites and NAs. The Life Events Checklist was used to assess the number of ALEs. Multilevel growth models were used to predict TS-NFR and TS-Pain, after controlling for age, perceived stress, psychological problems, negative and positive affect, and painful stimulus intensity. ALEs and negative affect were significantly associated with greater pain, but not enhanced TS-Pain. By contrast, ALEs were associated with enhanced TS-NFR. Race did not moderate these relationships. This finding implies that ALEs promote hyperalgesia as a result of increased spinal neuron excitability. Although relationships between ALEs and the nociceptive flexion reflex/pain were not stronger in NAs, given prior evidence that NAs experience more ALEs, this factor might contribute to the higher prevalence of chronic pain in NAs. PERSPECTIVE: This study found a dose-dependent relationship between ALEs and spinal neuron excitability. Although the relationship was not stronger in NAs than non-Hispanic whites, given prior evidence that NAs experience more ALEs, this could contribute to the higher prevalence of chronic pain in NAs.
不良生活经历(ALEs)与痛觉过敏和慢性疼痛有关,但潜在机制尚不清楚。一个潜在的机制是脊髓神经元的过度兴奋(即中枢敏化)。鉴于美洲原住民(NAs)更有可能经历 ALEs 并具有更高的慢性疼痛患病率,ALE 与脊髓过度兴奋之间的关系可能导致他们面临更高的疼痛风险。本研究评估了 246 名健康、无痛的非西班牙裔白人和 NAs 中的伤害性屈肌反射的时间总和(TS-NFR;脊髓过度兴奋的相关指标)和疼痛(TS-Pain)。使用生活事件检查表评估 ALE 的数量。使用多层次增长模型,在控制年龄、感知压力、心理问题、消极和积极影响以及疼痛刺激强度后,预测 TS-NFR 和 TS-Pain。ALE 和消极情绪与更大的疼痛显著相关,但与增强的 TS-Pain 无关。相比之下,ALE 与增强的 TS-NFR 相关。种族并没有调节这些关系。这一发现意味着 ALEs 通过增加脊髓神经元兴奋性而促进痛觉过敏。尽管 NAs 中 ALEs 和伤害性屈肌反射/疼痛之间的关系并不比非西班牙裔白人更强,但考虑到之前的证据表明 NAs 经历了更多的 ALEs,这一因素可能导致 NAs 慢性疼痛的患病率更高。观点:本研究发现 ALEs 与脊髓神经元兴奋性之间存在剂量依赖性关系。尽管 NAs 与非西班牙裔白人之间的关系并不比非西班牙裔白人更强,但考虑到之前的证据表明 NAs 经历了更多的 ALEs,这可能导致 NAs 慢性疼痛的患病率更高。