Department of Anesthesiology, Harvard Medical School, Brigham & Women's Hospital, Boston, Massachusetts, USA.
Pain Med. 2013 Nov;14(11):1757-68. doi: 10.1111/pme.12220. Epub 2013 Aug 7.
To examine the temporal stability of conditioned pain modulation (CPM), formerly termed diffuse noxious inhibitory controls, among a sample of patients with chronic pain. The study also examined the factors that might be responsible for the stability of CPM.
DESIGN, SUBJECTS, AND METHODS: In this test-retest study, patients underwent a series of standardized psychophysical pain-testing procedures designed to assess CPM on two separate occasions (i.e., baseline and follow up). Patients also completed self-report measures of catastrophizing (Pain Catastrophizing Scale [PCS] and negative affect [NA]).
Overall, results provided evidence for the stability of CPM among patients with chronic pain. Results, however, revealed considerable sex differences in the stability of CPM. For women, results revealed a significant test-retest correlation between baseline and follow-up CPM scores. For men, however, the test-retest correlation between baseline and follow-up CPM scores was not significant. Results of a Fisher's Z-test revealed that the stability of CPM was significantly greater for women than for men. Follow-up analyses revealed that the difference between men and women in the stability of CPM could not be accounted for by any demographic (e.g., age) and/or psychological factors (PCS and NA).
Our findings suggest that CPM paradigms possess sufficient reliability to be incorporated into bedside clinical evaluation of patients with chronic pain, but only among women. The lack of CPM reproducibility/stability observed among men places limits on the potential use of CPM paradigms in clinical settings for the assessment of men's endogenous pain-inhibitory function.
在慢性疼痛患者样本中,考察条件性疼痛调制(CPM),即以前称为弥散性抑制控制,的时间稳定性。本研究还考察了导致 CPM 稳定性的因素。
设计、对象和方法:在这项测试-再测试研究中,患者接受了一系列标准化的心理物理疼痛测试程序,旨在两次(即基线和随访)分别评估 CPM。患者还完成了灾难化(疼痛灾难化量表[PCS]和负性情绪[NA])的自我报告测量。
总体而言,结果提供了慢性疼痛患者 CPM 稳定性的证据。然而,结果显示 CPM 的稳定性存在明显的性别差异。对于女性,基线和随访 CPM 评分之间存在显著的测试-再测试相关性。然而,对于男性,基线和随访 CPM 评分之间的测试-再测试相关性不显著。Fisher Z 检验的结果表明,女性 CPM 的稳定性明显大于男性。随访分析表明,男性和女性 CPM 稳定性之间的差异不能用任何人口统计学(例如年龄)和/或心理因素(PCS 和 NA)来解释。
我们的发现表明,CPM 范式具有足够的可靠性,可以纳入慢性疼痛患者的床边临床评估,但仅适用于女性。在男性中观察到的 CPM 可重复性/稳定性缺乏限制了 CPM 范式在临床环境中评估男性内源性疼痛抑制功能的潜在用途。