Evidence map›Paper›PMID 37731476›Full record

ArticlePain reports

Responders and nonresponders to topical capsaicin display distinct temporal summation of pain profiles.

Felyx Wong, Aditi Reddy, Yeanuk Rho, Jan Vollert, Paul H Strutton, Sam W Hughes

Abstract read
In one paragraph

Article in Pain reports. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Felyx WongThe Nick Davey Laboratory, Department of Surgery and Cancer, Faculty of Medicine, Imperial College London, London, United Kingdom.
Aditi ReddyThe Nick Davey Laboratory, Department of Surgery and Cancer, Faculty of Medicine, Imperial College London, London, United Kingdom.
Yeanuk RhoThe Nick Davey Laboratory, Department of Surgery and Cancer, Faculty of Medicine, Imperial College London, London, United Kingdom.
Jan VollertPain Research, Department of Surgery and Cancer, Faculty of Medicine, Imperial College London, London, United Kingdom.
Paul H StruttonThe Nick Davey Laboratory, Department of Surgery and Cancer, Faculty of Medicine, Imperial College London, London, United Kingdom.
Sam W HughesThe Pain Modulation Laboratory, Brain Research and Imaging Centre (BRIC), School of Psychology, Faculty of Health, University of Plymouth, Plymouth, United Kingdom.ORCID https://orcid.org/0000-0002-3769-3803

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Topical application of capsaicin can produce an ongoing pain state in healthy participants. However, approximately one-third report no pain response (ie, nonresponders), and the reasons for this are poorly understood. Objectives: In this study, we investigated temporal summation of pain (TSP) profiles, pain ratings and secondary hyperalgesia responses in responders and nonresponders to 1% topical capsaicin cream. Methods: Assessments were made at baseline and then during an early (ie, 15 minutes) and late (ie, 45 minutes) time points post-capsaicin in 37 healthy participants. Results: Participants reporting a visual analogue scale (VAS) rating of >50 were defined as responders (n = 24) and those with <50 VAS rating were defined as nonresponders (n = 13). There was a facilitation of TSP during the transition from an early to the late time point post-capsaicin (P<0.001) and the development of secondary hyperalgesia (P<0.05) in the responder group. Nonresponders showed no changes in TSP or secondary hyperalgesia during the early and late time points. There was an association between baseline TSP scores and the later development of a responder or nonresponder phenotype (r = 0.36; P = 0.03). Receiver operating characteristic analysis revealed that baseline TSP works as a good response predictor at an individual level (area under the curve = 0.75). Conclusion: These data suggest that responders and nonresponders have different facilitatory pain mechanisms. The assessment of TSP may help to identify participants with stronger endogenous pain facilitation who may be more likely to respond to topical capsaicin.

Indexed as

CapsaicinFacilitationResponderTemporal summation

Identifiers

PMID37731476
PMCPMC10508395

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.