Demetriou Lysia, Perro Danielle, Coxon Lydia, Krassowski Michal, Lunde Claire E, Ferreira-Gomes Joana, Charrua Ana, Abreu-Mendes Pedro, Arendt-Nielsen Lars, Aziz Qasim, Birch Judy, Garbutt Kurtis, Horne Andrew, Hoffman Anja, Hummelshoj Lone, Meijlink Jane, Obendorf Maik, Pogatzki-Zahn Esther, Sasamoto Naoko, Terry Kathryn, Treede Rolf-Detlef, Vitonis Allison, Vollert Jan, Rahmioglu Nilufer, Becker Christian M, Cruz Francisco, Missmer Stacey A, Zondervan Krina, Sieberg Christine B, Nagel Jens, Vincent Katy
Nuffield Department of Women's and Reproductive Health, Oxford Endometriosis Centre, University of Oxford, Oxforfd, United Kingdom.
Division of Adolescent & Young Adult Medicine, Department of Pediatrics, Boston Children's Hospital, Boston, MA, United States.
Front Pain Res (Lausanne). 2025 Mar 12;6:1439563. doi: 10.3389/fpain.2025.1439563. eCollection 2025.
Conditioned pain modulation (CPM) is considered a human proxy for descending inhibitory pain pathways. However, there is wide variation in the CPM response described in the literature and ongoing debate about its utility.
Here we explored CPM in women with ( = 59) and without ( = 26) chronic pelvic pain (CPP), aiming to determine the magnitude of effect and factors influencing variability in the CPM response.
Using a pressure pain threshold test stimulus and ischaemic pressure cuff conditioning stimulus (CS), we found no significant difference in the mean CPM effect between CPP and control participants. Using a robust statistical method (+/-2 standard error of measurement) to further investigate CPM, there was no significant difference in the proportion exhibiting inhibition between controls and CPP participants ( = 0.003, = 0.96). Notably, only 23.1% of our healthy controls demonstrated a "true" CPM effect ( = 4 inhibitory, = 2 facilitatory). Despite a rich data set, we were unable to identify any single questionnaire, clinical or psychophysical covariate correlating with the CPM effect.
Despite using one of the recommended CPM paradigms we were only able to demonstrate "true" CPM in 23.1% of control participants. Thus, the absence of differences between women with and without chronic pelvic pain must be interpreted with caution. Future studies using different CPM paradigms or larger sample sizes may find different results. Although CPM in chronic pain populations is of major theoretical mechanistic interest, the lack of an established assessment standard led us to question its added value in current clinical research.
条件性疼痛调制(CPM)被认为是下行抑制性疼痛通路的一种人体替代指标。然而,文献中描述的CPM反应存在很大差异,并且关于其效用的争论仍在继续。
在此,我们对患有慢性盆腔疼痛(CPP,n = 59)和未患慢性盆腔疼痛(n = 26)的女性进行了CPM研究,旨在确定CPM反应的效应大小以及影响其变异性的因素。
使用压力疼痛阈值测试刺激和缺血性压力袖带条件刺激(CS),我们发现CPP患者和对照参与者之间的平均CPM效应无显著差异。使用稳健的统计方法(测量的±2标准误)进一步研究CPM,对照参与者和CPP参与者之间表现出抑制的比例无显著差异(P = 0.003,r = 0.96)。值得注意的是,我们的健康对照中只有23.1%表现出“真正的”CPM效应(n = 4例抑制,n = 2例易化)。尽管有丰富的数据集,但我们无法确定任何与CPM效应相关的单一问卷、临床或心理物理学协变量。
尽管使用了推荐的CPM范式之一,但我们仅在23.1%的对照参与者中证明了“真正的”CPM。因此,对于患有和未患有慢性盆腔疼痛的女性之间没有差异这一结果必须谨慎解释。未来使用不同CPM范式或更大样本量的研究可能会得出不同的结果。虽然慢性疼痛人群中的CPM在主要理论机制方面具有重要意义,但缺乏既定的评估标准使我们对其在当前临床研究中的附加价值产生质疑。