AI Article Synopsis

  • The study aimed to assess the variation in secondary hyperalgesia, a heightened pain response, among healthy volunteers after brief exposure to high temperature (45°C for 3 minutes).
  • Fifty healthy participants were tested over four days to measure hyperalgesia areas, pain thresholds, and psychological factors, revealing a low consistency in individual responses but significant differences between individuals.
  • The findings suggest that while brief thermal sensitization is reproducible in eliciting secondary hyperalgesia, individual differences play a considerable role, indicating its potential for further research into pain responses in various populations.

Article Abstract

Introduction: Clinical pain models can be applied when investigating basic physiologic pain responses in healthy volunteers. Several pain models exist; however, only few have been adequately validated. Our primary aim with this prospective study was to investigate the intra- and inter-individual variation in secondary hyperalgesia elicited by brief thermal sensitization (45°C for 3 min) in healthy volunteers.

Material And Methods: Fifty healthy volunteers were included. Areas of secondary hyperalgesia following brief thermal sensitization were investigated by 2 observers on 4 experimental days, with a minimum interval of 7 days. Additionally, heat pain detection threshold and pain during thermal stimulation (45°C for 1 min.), and the psychological tests Pain Catastrophizing Scale and Hospital Anxiety and Depression Score were applied.

Results: For areas of secondary hyperalgesia, an intra-observer intra-person correlation of 0.85, 95% CI [0.78, 0.90], an intra-observer inter-person correlation of 0.03, 95% CI [0.00, 0.16], and a coefficient of variation of 0.17, 95% CI [0.14, 0.21] was demonstrated. Four percent of the study population had areas of secondary hyperalgesia both below the 1st and above the 3rd quartile considering all included participants. Heat pain detection threshold predicted area of secondary hyperalgesia with an adjusted R2 of 0.20 (P = 0.0006).

Conclusions: We have demonstrated a low intra-individual, and a high inter-individual variation in thermally induced secondary hyperalgesia. We conclude that brief thermal sensitization produce secondary hyperalgesia with a high level of reproducibility, which can be applied to investigate different phenotypes related to secondary hyperalgesia in healthy volunteers.

Trial Registration: clinicaltrials.gov NCT02166164.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4864410PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0155284PLOS

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