Evidence map›Paper›PMID 23570317›Full record

Trial reportMolecular pain2013

Gender, variation in opioid receptor genes and sensitivity to experimental pain.

Hiroe Sato, Joanne Droney, Joy Ross, Anne Estrup Olesen, Camilla Staahl, Trine Andresen, Ruth Branford, Julia Riley, Lars Arendt-Nielsen, Asbjørn Mohr Drewes

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in Molecular pain, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.8field-weighted citation impact, top 9% of its field
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

15 citing papers in PubMed, 53 citations in OpenAlex.

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  15. Is the experience of thermal pain genetics dependent?BioMed research international · 2015
    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

10 authors at 6 institutions in 2 countries.

Hiroe SatoClinical Genomics group, Imperial College London, London, UK. h.sato@imperial.ac.uk
Joanne Droney
Joy Ross
Anne Estrup Olesen
Camilla Staahl
Trine Andresen
Ruth Branford
Julia Riley
Lars Arendt-Nielsen
Asbjørn Mohr Drewes
Aalborg University Hospital · DKRoyal Marsden Hospital · GBAalborg University · DKGenomics England · GBImperial College London · GBMech-Sense · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPain tolerance is subject to considerable inter-individual variation, which may be influenced by a number of genetic and non-genetic factors. The mu, delta and kappa opioid receptors play a role in pain perception and are thought to mediate different pain modalities. The aim of this study was to explore associations between pain thresholds and gender and genetic variants in the three opioid receptor genes (OPRM, OPRD and OPRK). Experimental multi-modal pain data from previously published studies carried out in healthy Caucasian volunteers were used in order to limit the number of confounders to the study outcome. Data on thermal skin pain (n=36), muscle pressure pain (n=31) and mechanical visceral pain (n=50)) tolerance thresholds were included.

resultsNineteen genetic polymorphisms were included in linear regression modeling. Males were found to tolerate higher thermal and muscle pressure pain than females (p=0.003 and 0.02). Thirty four percent of variability in thermal skin pain was accounted for by a model consisting of OPRK rs6473799 and gender. This finding was just outside significance when correction for multiple testing was applied. Variability in muscle pressure pain tolerance was associated with OPRK rs7016778 and rs7824175. These SNPs accounted for 43% of variability in muscle pressure pain sensitivity and these findings remained significant after adjustment for multiple testing. No association was found with mechanical visceral pain.

conclusionThis is a preliminary and hypothesis generating study due to the relatively small study size. However, significant association between the opioid receptor genes and experimental pain sensitivity supports the influence of genetic variability in pain perception. These findings may be used to generate hypotheses for testing in larger clinical trials of patients with painful conditions.

Indexed as

Genetic VariationSex CharacteristicsAdultAgingFemaleGene FrequencyHumansMaleMiddle AgedMultivariate AnalysisMusclesPainPain ThresholdPolymorphism, Single NucleotideReceptors, OpioidRegression AnalysisReceptors, Opioid

Identifiers

PMID23570317
PMCPMC3635934
OpenAlexW2157616252

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.