Evidence map›Paper›PMID 24553304›Full record

Trial reportRegional anesthesia and pain medicine

Endogenous opioid inhibition of chronic low-back pain influences degree of back pain relief after morphine administration.

Stephen Bruehl, John W Burns, Rajnish Gupta, Asokumar Buvanendran, Melissa Chont, Erik Schuster, Christopher R France

3 registry-linked trialsAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Regional anesthesia and pain medicine. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.7field-weighted citation impact, top 16% 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.

NCT02469077 nacompletednot on this map

Reduced Opioid Analgesic Requirements Via Improved Endogenous Opioid Function

TypeinterventionalSponsorVanderbilt University Medical CenterRan2015 to 2019Enrolled117ConditionsChronic PainArms6 week aerobic exercise intervention, Placebo, Morphine, naloxone
NCT04744883 early_phase1active not recruitingnot on this map

Evaluating Specific and Non-Specific Mechanisms in Two Distinct Complementary/Integrative Interventions for Chronic Pain

TypeinterventionalSponsorRush University Medical CenterRan2020 to 2026Enrolled140ConditionsChronic Low-back PainArmsSpinal Manipulation Therapy (SMT), Naloxone, Placebo, Mindfulness Based Stress Reduction Therapy (MT)
NCT05142267 narecruitingnot on this map

Stress and Opioid Misuse Risk: The Role of Endogenous Opioid and Endocannabinoid Mechanisms

TypeinterventionalSponsorVanderbilt University Medical CenterRan2022 to 2026Enrolled120ConditionsOpioid Use Disorder, Back Pain, StressArmsPlacebo, Oxycodone, Naloxone
3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 23 citations in OpenAlex.

  1. Trial
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  6. Article
  7. Predicting Extent of Opioid Use Following Cardiac Surgery: A Pilot Study.Journal of cardiothoracic and vascular anesthesia · 2025
    Observational
  8. Review
  9. Review
  10. Article
  11. [Diagnostic value of endogenous morphine in childhood sepsis].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2018
    Article
  12. Article
  13. Article
  14. Article
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  16. Article
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

7 authors at 3 institutions in 1 country.

Stephen BruehlFrom the *Department of Anesthesiology, Vanderbilt University School of Medicine, Nashville, TN; †Department of Behavioral Science, Rush University, Chicago, IL; ‡Department of Anesthesiology, Rush University, Chicago, IL; and §Department of Psychology, Ohio University, Athens, OH.
John W Burns
Rajnish Gupta
Asokumar Buvanendran
Melissa Chont
Erik Schuster
Christopher R France
Rush University · USVanderbilt University · USOhio University · US

Funding

The Vanderbilt Institute for Clinical and Translational Research (VICTR)UL1TR000445 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BERNARD, GORDON RAPHAEL · 2012 to 2016
$41.4M
Predictors of Opioid Analgesic Responses and Common Endogenous Opioid MechanismsR01DA031726 · NIDA · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BRUEHL, STEPHEN, BURNS, JOHN W. · 2011 to 2015
$2.7M
NCATS NIH HHS UL1 TR000445NCATS NIH HHS UL1TR000445NIDA NIH HHS R01 DA031726NIDA NIH HHS R01- DA031726
6 · The paper itself

Abstract

BACKGROUND AND

objectivesFactors underlying differential responsiveness to opioid analgesic medications used in chronic pain management are poorly understood. We tested whether individual differences in endogenous opioid inhibition of chronic low-back pain were associated with the magnitude of acute reductions in back pain ratings after morphine administration.

methodsIn randomized counterbalanced order over three sessions, 50 chronic low-back pain patients received intravenous naloxone (8 mg), morphine (0.08 mg/kg), or placebo. Back pain intensity was rated predrug and again after peak drug activity was achieved using the McGill Pain Questionnaire-Short Form (Sensory and Affective subscales, VAS Intensity measure). Opioid blockade effect measures to index degree of endogenous opioid inhibition of back pain intensity were derived as the difference between predrug to postdrug changes in pain intensity across placebo and naloxone conditions, with similar morphine responsiveness measures derived across placebo and morphine conditions.

resultsMorphine significantly reduced back pain compared with placebo (McGill Pain Questionnaire-Short Form Sensory, VAS; P < 0.01). There were no overall effects of opioid blockade on back pain intensity. However, individual differences in opioid blockade effects were significantly associated with the degree of acute morphine-related reductions in back pain on all measures, even after controlling for effects of age, sex, and chronic pain duration (P < 0.03). Individuals exhibiting greater endogenous opioid inhibition of chronic back pain intensity reported less acute relief of back pain with morphine.

conclusionsMorphine appears to provide better acute relief of chronic back pain in individuals with lower natural opioidergic inhibition of chronic pain intensity. Possible implications for personalized medicine are discussed.

Indexed as

AdultCross-Over StudiesDouble-Blind MethodFemaleHumansLow Back PainMaleMiddle AgedMorphineOpioid PeptidesPain MeasurementMorphineOpioid Peptides

Identifiers

PMID24553304
PMCPMC3933525
OpenAlexW2037570965

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.