Multidisciplinary Pain Center, Neuroscience Center, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
PLoS One. 2013 May 9;8(5):e62733. doi: 10.1371/journal.pone.0062733. Print 2013.
Human experimental pain models leading to development of secondary hyperalgesia are used to estimate efficacy of analgesics and antihyperalgesics. The ability to develop an area of secondary hyperalgesia varies substantially between subjects, but little is known about the agreement following repeated measurements. The aim of this study was to determine if the areas of secondary hyperalgesia were consistently robust to be useful for phenotyping subjects, based on their pattern of sensitization by the heat pain models.
We performed post-hoc analyses of 10 completed healthy volunteer studies (n = 342 [409 repeated measurements]). Three different models were used to induce secondary hyperalgesia to monofilament stimulation: the heat/capsaicin sensitization (H/C), the brief thermal sensitization (BTS), and the burn injury (BI) models. Three studies included both the H/C and BTS models.
Within-subject compared to between-subject variability was low, and there was substantial strength of agreement between repeated induction-sessions in most studies. The intraclass correlation coefficient (ICC) improved little with repeated testing beyond two sessions. There was good agreement in categorizing subjects into 'small area' (1(st) quartile [<25%]) and 'large area' (4(th) quartile [>75%]) responders: 56-76% of subjects consistently fell into same 'small-area' or 'large-area' category on two consecutive study days. There was moderate to substantial agreement between the areas of secondary hyperalgesia induced on the same day using the H/C (forearm) and BTS (thigh) models.
Secondary hyperalgesia induced by experimental heat pain models seem a consistent measure of sensitization in pharmacodynamic and physiological research. The analysis indicates that healthy volunteers can be phenotyped based on their pattern of sensitization by the heat [and heat plus capsaicin] pain models.
引发继发性痛觉过敏的人体实验性疼痛模型被用于评估镇痛药和抗痛觉过敏药物的疗效。不同个体发展继发性痛觉过敏的能力差异很大,但对于重复测量后的一致性知之甚少。本研究的目的是确定在基于热痛觉模型引起的敏化模式对受试者进行表型分析时,继发性痛觉过敏区域是否始终稳健且具有有用性。
我们对 10 项已完成的健康志愿者研究(n=342[409 次重复测量])进行了事后分析。使用三种不同的模型来诱导对单丝刺激的继发性痛觉过敏:热/辣椒素敏化(H/C)、短暂热敏化(BTS)和烧伤损伤(BI)模型。三项研究同时包括 H/C 和 BTS 模型。
与个体间变异性相比,个体内变异性较低,并且在大多数研究中,重复诱导期之间具有很强的一致性。在两次以上的测试中,组内相关系数(ICC)改善不大。将受试者分类为“小面积”(第 1 四分位数[<25%])和“大面积”(第 4 四分位数[>75%])应答者的一致性较好:56-76%的受试者在连续两天的研究中始终归入同一“小面积”或“大面积”类别。在同一天使用 H/C(前臂)和 BTS(大腿)模型诱导的继发性痛觉过敏区域之间存在中度至高度一致性。
实验性热痛觉模型引起的继发性痛觉过敏似乎是药物动力学和生理学研究中敏化的一致测量方法。分析表明,可以基于热[和热加辣椒素]痛觉模型引起的敏化模式对健康志愿者进行表型分析。