Abstract

BackgroundHuman 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.MethodsWe 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.ResultsWithin-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’ (1st quartile [<25%]) and ‘large area’ (4th 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.ConclusionSecondary 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.

Highlights

  • It has been hypothesized that the propensity for developing central sensitization in response to noxious events is a heritable trait and may explain differences in susceptibility to developing chronic pain [1]

  • It has been recognized that areas of secondary hyperalgesia varies substantially between subjects, but there is a scarcity of information in the literature about the within-subject and between-subject variability

  • We aimed to examine the robustness of cutaneous secondary hyperalgesia induced by one or more of three different human experimental models: the heat/capsaicin sensitization model (H/ C), the brief thermal sensitization model (BTS), and the burn injury model (BI)

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Summary

Introduction

It has been hypothesized that the propensity for developing central sensitization in response to noxious events is a heritable trait and may explain differences in susceptibility to developing chronic pain [1]. The area of secondary hyperalgesia is experimentally induced with either chemical, electrical or heat stimuli. This phenomenon is inducible in most subjects and thought to be due, at least in part, to central neuronal sensitization [1]. A recent study of human twins showed that familial effects accounted for 24–32% of observed variances in heat and cold pressor pain thresholds, and, opioidmediated elevations in cold pressor pain tolerance [10]. 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

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