Evidence map›Paper›PMID 21668741›Full record

Trial reportPain medicine (Malden, Mass.)2011

Individual differences in morphine and butorphanol analgesia: a laboratory pain study.

Kimberly T Sibille, Lindsay L Kindler, Toni L Glover, Ricardo D Gonzalez, Roland Staud, Joseph L Riley, Roger B Fillingim

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Pain medicine (Malden, Mass.), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Trial
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  5. An intronic variant in OPRD1 predicts treatment outcome for opioid dependence in African-Americans.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2013
    Trial
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  10. Strategies for DevelopingThe Journal of pharmacology and experimental therapeutics · 2020
    Review
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  14. Review
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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

7 authors.

Kimberly T SibilleCommunity Dentistry and Behavioral Science, College of Dentistry, University of Florida, Gainesville, FL 32610-3629, USA. ksibille@ufl.edu
Lindsay L Kindler
Toni L Glover
Ricardo D Gonzalez
Roland Staud
Joseph L Riley
Roger B Fillingim

Funding

University of Florida Older Americans Independence Center (OAIC)P30AG028740 · NIA · UNIVERSITY OF FLORIDA · PI CHRISTIAAN LEEUWENBURGH · 2007 to 2026
$22.8M
UF CLINICAL AND TRANSLATIONAL SCIENCE AWARDUL1RR029890 · NCRR · UNIVERSITY OF FLORIDA · PI NELSON, DAVID R · 2009 to 2011
$14.4M
Sex-Related Genetic Influences on Pain and AnalgesiaR01NS041670 · NINDS · UNIVERSITY OF FLORIDA · PI FILLINGIM, ROGER B · 2000 to 2009
$4.4M
Integrative and translational training in pain researchT32NS045551 · NINDS · UNIVERSITY OF FLORIDA · PI YEZIERSKI, ROBERT P. · 2005 to 2014
$1.8M
NCRR NIH HHS RR029890NCRR NIH HHS UL1 RR029890NIA NIH HHS P30 AG028740NINDS NIH HHS NS041670NINDS NIH HHS NS045551NINDS NIH HHS R01 NS041670NINDS NIH HHS T32 NS045551
6 · The paper itself

Abstract

objectiveResponses to opioid analgesics are highly variable, and the understanding of contributing factors is limited. This laboratory study was designed to examine the contributions of sex and race to inter-individual variability in response to opioids.

designA randomized, double-blind, mixed design was implemented in the evaluation of analgesic response to a µ-opioid agonist and mixed agonist-antagonist, using three well-validated experimental pain assays (thermal, pressure, and ischemic). SUBJECTS: Participants included a total of 142 healthy subjects (76 men/66 women), 119 non-Hispanic whites and 23 African Americans.

interventionThree sessions of pain testing were completed prior to and following an intravenous administration of morphine (0.08 mg/kg), butorphanol (0.016 mg/kg), and placebo (saline) in counterbalanced order. OUTCOME MEASURES: A change score was calculated from the difference between the pre-drug and postdrug values. Three separate change scores (morphine, saline, and butorphanol) were computed for each experimental pain variable. Mixed-model analyses of covariance were performed on analgesic change scores.

resultsSignificant sex differences emerged for predrug pain measures with minimal differences for race. Sex differences in opioid analgesia were not demonstrated. However, significant race differences and race X drug interactions emerged for thermal, pressure, and ischemic pain measures. The pattern of results generally indicated that for pressure and ischemic pain, African American subjects showed greater analgesic responses to both medications compared with non-Hispanic whites. For thermal pain threshold, butorphanol but not morphine analgesia was greater for African American vs non-Hispanic whites.

conclusionsFindings are among the first to demonstrate race differences in a laboratory study of opioid analgesia.

Indexed as

EthnicityIndividualityAdolescentAdultAnalgesics, OpioidButorphanolDouble-Blind MethodFemaleHumansMaleMiddle AgedMorphinePainPain MeasurementPlacebosYoung AdultAnalgesics, OpioidButorphanolMorphinePlacebos

Identifiers

PMID21668741
PMCPMC3155877

What OpenQuestion holds

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Read underepoch 390

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.