Evidence map›Paper›PMID 40692375›Full record

ArticleEuropean journal of pain (London, England)2025

Conditioned Pain Modulation, Placebo and Offset Analgesia: Rates of Behavioural Expression of Inhibitory, Nonresponse and Facilitatory Pain Modulatory Effects.

Lewis S Crawford, Ashleigh Wake, Rebecca V Robertson, Allan Peng, Noemi Meylakh, Damien C Boorman, Leana Sattarov, Alister Ramachandran, Vaughan G Macefield, Kevin A Keay and 1 more

Abstract read
In one paragraph

Article in European journal of pain (London, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
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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

11 authors.

Lewis S CrawfordSchool of Medical Sciences (Neuroscience), Brain and Mind Centre, University of Sydney, Sydney, New South Wales, Australia.ORCID https://orcid.org/0000-0003-2231-5196
Ashleigh WakeSchool of Medical Sciences (Neuroscience), Brain and Mind Centre, University of Sydney, Sydney, New South Wales, Australia.
Rebecca V RobertsonSchool of Medical Sciences (Neuroscience), Brain and Mind Centre, University of Sydney, Sydney, New South Wales, Australia.ORCID https://orcid.org/0009-0005-0795-1532
Allan PengSchool of Medical Sciences (Neuroscience), Brain and Mind Centre, University of Sydney, Sydney, New South Wales, Australia.
Noemi MeylakhSchool of Medical Sciences (Neuroscience), Brain and Mind Centre, University of Sydney, Sydney, New South Wales, Australia.
Damien C BoormanSchool of Medical Sciences (Neuroscience), Brain and Mind Centre, University of Sydney, Sydney, New South Wales, Australia.ORCID https://orcid.org/0000-0003-2819-1948
Leana SattarovSchool of Medical Sciences (Neuroscience), Brain and Mind Centre, University of Sydney, Sydney, New South Wales, Australia.ORCID https://orcid.org/0009-0000-1125-4266
Alister RamachandranWestmead Hospital Pain Management Centre, Sydney, New South Wales, Australia.
Vaughan G MacefieldDepartment of Neuroscience, Monash University, Melbourne, Victoria, Australia.ORCID https://orcid.org/0000-0003-3325-6566
Kevin A KeaySchool of Medical Sciences (Neuroscience), Brain and Mind Centre, University of Sydney, Sydney, New South Wales, Australia.ORCID https://orcid.org/0000-0003-3934-4380
Luke A HendersonSchool of Medical Sciences (Neuroscience), Brain and Mind Centre, University of Sydney, Sydney, New South Wales, Australia.ORCID https://orcid.org/0000-0002-1026-0151

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe brain is capable of powerfully inhibiting perceived pain intensity. Experimentally, three pain modulating phenomena have been well explored: placebo analgesia (PA), offset analgesia (OA) and conditioned pain modulation (CPM). While all three can reduce pain intensity, these paradigms are not often compared behaviourally, nor are their potentially common psychological or physiological mechanisms considered.

methodsHere, we present retrospective behavioural pain rating, psychological and demographic data in 273 pain-free control participants who underwent either PA (n = 100), OA (n = 37) or CPM (n = 136). Significant changes in pain intensities were assessed using permutation testing to derive cohorts where pain was significantly inhibited (inhibitory responders), unchanged (nonresponder) or increased (facilitatory responder) during the expression of each phenomenon. Psychological questionnaire scores, demography and pain perception variability were compared between response cohorts to all three phenomena.

resultsWe identified largely similar proportions of individuals categorised as either inhibitory responders, nonresponders or facilitatory responders to each of PA, OA and CPM-with no sex differences identified in any phenomena nor response category. Dispositional optimism and calibrated noxious temperature demonstrated a significant effect in PA and CPM responses, respectively-with inhibitory responders recording higher scores than facilitatory responders in PA, and inhibitory responders possessing lower thermal sensitivity to nonresponders in CPM.

conclusionA shared mechanism was identified between PA and OA, such that perceived pain variability to repeated identical noxious stimuli related to both phenomena's expression. This warrants further investigation given the suggested neural circuit differences between these two phenomena, and only PA is presently linked with Bayesian theorem. SIGNIFICANCE STATEMENT: Humans are capable of inhibiting their own pain in several ways; however, the brain systems driving these analgesic mechanisms are complex and are known to diverge despite producing similar outcomes. Here we show core behavioural similarities between different forms of endogenous analgesic phenomena, with differences in psychological and physiological correlates.

Indexed as

AnalgesiaConditioning, PsychologicalPainPain ManagementPain PerceptionAdultFemaleHumansMaleMiddle AgedPain MeasurementPlacebo EffectRetrospective StudiesYoung Adult

Identifiers

PMID40692375
PMCPMC12281077

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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.