Evidence map›Paper›PMID 23671631›Full record

ArticlePloS one2013

Healthy volunteers can be phenotyped using cutaneous sensitization pain models.

Mads U Werner, Karin L Petersen, Michael C Rowbotham, Jørgen B Dahl

2 registry-linked trialsAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 22 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 2 pooled it
–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.

NCT02442726 nacompletednot on this mapstarted 2015, after this paper: background citation

Activation of A-delta-fibres and C-fibres in a First Degree Thermal Injury in Volunteers

TypeinterventionalSponsorUniversity of CopenhagenRan2015 to 2015Enrolled18ConditionsHealthy SubjectsArmsCO2-Laser stimulation (Laser Stimulation Device, SIFEC)
NCT02684669 phase2completednot on this mapstarted 2016, after this paper: background citation

Effect of High-dose Target-controlled Naloxone Infusion on Pain and Hyperalgesia During a Burn Injury. A Randomized, Placebo-controlled, Double-blind Crossover Study

TypeinterventionalSponsormads u wernerRan2016 to 2017Enrolled80ConditionsHealthy SubjectsArmsNaloxone, Normal saline
3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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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

4 authors.

Mads U WernerMultidisciplinary Pain Center, Neuroscience Center, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark. mads.u.werner@gmail.com
Karin L Petersen
Michael C Rowbotham
Jørgen B Dahl

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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' (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.

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.

Indexed as

AntipruriticsBurnsCapsaicinHealthy VolunteersHot TemperatureHumansHyperalgesiaModels, BiologicalPainPain MeasurementReproducibility of ResultsSkinAntipruriticsCapsaicin

Identifiers

PMID23671631
PMCPMC3650051

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Registered trials

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.