Alter Benedict J, Maurer Maya, O'Connell Brian, Sanchez Andrea Gomez, Kaynar A Murat, DiGioia Anthony M, Huppert Theodore, Wasan Ajay D
Department of Anesthesiology and Perioperative Medicine, University of Pittsburgh, Pittsburgh, PA, United States.
Department of Critical Care Medicine, University of Pittsburgh, Pittsburgh, PA, United States.
Pain. 2025 Jun 19. doi: 10.1097/j.pain.0000000000003648.
Offset analgesia reflects time-dependent, central nervous system pain inhibition and refers to a dramatic drop in pain intensity after an offset of noxious stimulus intensity. Neuropathic and nociplastic pain conditions with strong central nervous system pathophysiologic mechanisms show deficits in offset analgesia. Whether offset analgesia is altered in more peripherally driven chronic nociceptive pain was unknown. Therefore, the primary goal of the current study was to determine whether chronic nociceptive pain is associated with changes in offset analgesia. We measured offset analgesia and sensory function using quantitative sensory tests, patient-reported pain and function, and walking and stair climbing performance using standardized tasks in knee osteoarthritis patients with equivalent joint degeneration but Moderate-to-Severe (n = 36) or Mild pain intensity (n = 36) and Pain-free controls without knee osteoarthritis (n = 30) matching for age, gender, and body mass index. Offset analgesia was significantly reduced in knee osteoarthritis groups compared with the Pain-free controls, with deficits occurring at both the nonpainful forearm and painful knee and in both genders. Greater deficits in offset analgesia were associated with more impairment in walking and stair climbing. Onset hyperalgesia, a novel measure of time-dependent pain facilitation, was reduced in women with Mild knee pain but not in men. These results suggest that deficits in temporal pain inhibition and gender-specific changes in temporal pain facilitation may contribute to pain and functional impairment in knee osteoarthritis, supporting further study of central pain modulation as a clinically relevant mechanism of chronic nociceptive pain.
消退性镇痛反映了时间依赖性的中枢神经系统疼痛抑制,指的是有害刺激强度消退后疼痛强度的显著下降。具有强烈中枢神经系统病理生理机制的神经性和伤害性感受性疼痛状况表现出消退性镇痛缺陷。在更多由外周驱动的慢性伤害性疼痛中,消退性镇痛是否改变尚不清楚。因此,本研究的主要目的是确定慢性伤害性疼痛是否与消退性镇痛的变化有关。我们使用定量感觉测试、患者报告的疼痛和功能,以及在年龄、性别和体重指数相匹配的无膝骨关节炎的无痛对照组(n = 30)、关节退变程度相当但疼痛强度为中度至重度(n = 36)或轻度(n = 36)的膝骨关节炎患者中使用标准化任务测量行走和爬楼梯表现,来测量消退性镇痛和感觉功能。与无痛对照组相比,膝骨关节炎组的消退性镇痛显著降低,在无痛的前臂和疼痛的膝盖以及男女两性中均出现缺陷。消退性镇痛方面更大的缺陷与行走和爬楼梯方面更多的损伤相关。起始痛觉过敏是一种新的时间依赖性疼痛易化测量指标,在轻度膝痛的女性中降低,但在男性中未降低。这些结果表明,时间性疼痛抑制缺陷和时间性疼痛易化的性别特异性变化可能导致膝骨关节炎的疼痛和功能损害,支持将中枢性疼痛调制作为慢性伤害性疼痛的一种临床相关机制进行进一步研究。