Evidence map›Paper›PMID 25881118›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2015

Cortisol Stress Response in Men and Women Modulated Differentially by the Mu-Opioid Receptor Gene Polymorphism OPRM1 A118G.

William R Lovallo, Mary-Anne Enoch, Ashley Acheson, Andrew J Cohoon, Kristen H Sorocco, Colin A Hodgkinson, Andrea S Vincent, David C Glahn, David Goldman

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05142267 (Stress and Opioid Misuse Risk), which is not on this map. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 14% 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.

NCT05142267 narecruitingnot on this mapstarted 2022, after this paper: background citation

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

39 citing papers in PubMed, 1 synthesis or guideline pooled it, 55 citations in OpenAlex.

  1. Pooled it
  2. Opioid-blunted cortisol response to stress is associated with increased negative mood and wanting of social reward.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2022
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  18. Association Between the A118G Polymorphism of theNeuropsychiatric disease and treatment · 2021
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  19. Review
  20. Progress and Research Trends onFrontiers in pharmacology · 2021
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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

9 authors at 8 institutions in 1 country.

William R LovalloVA Medical Center, Oklahoma City, OK, USA.
Mary-Anne EnochLaboratory of Neurogenetics, NIH, NIAAA, Bethesda, MD, USA.
Ashley AchesonDepartment of Psychiatry, University of Texas Health Sciences Center at San Antonio, San Antonio, TX, USA.
Andrew J CohoonVA Medical Center, Oklahoma City, OK, USA.
Kristen H SoroccoVA Medical Center, Oklahoma City, OK, USA.
Colin A HodgkinsonLaboratory of Neurogenetics, NIH, NIAAA, Bethesda, MD, USA.
Andrea S VincentCognitive Science Research Center, University of Oklahoma, Norman, OK, USA.
David C GlahnOlin Neuropsychiatry Research Center, Institute of Living, Hartford Hospital, Hartford, CT, USA.
David GoldmanLaboratory of Neurogenetics, NIH, NIAAA, Bethesda, MD, USA.
National Institute on Alcohol Abuse and Alcoholism · USDonald W. Reynolds Foundation · USNational Institutes of Health · USOklahoma City VA Medical Center · USThe University of Texas Health Science Center at San Antonio · USUniversity of Oklahoma · USUniversity of Oklahoma Health Sciences Center · USYale University · US

Funding

Integrative genetics of behavior with high throughput technologiesZIAAA000301 · NIAAA · NATIONAL INSTITUTE ON ALCOHOL ABUSE AND ALCOHOLISM · PI GOLDMAN, DAVID · 2009 to 2025
$68.6M
Institute for Integration of Medicine & Science: A Partnership to Improve HealthUL1TR001120 · NCATS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CLARK, ROBERT A, HARGREAVES, KENNETH M · 2013 to 2017
$16.5M
Trt. of Primary Hyperaldosteronism w/ACE Inhibitors &Angiotension Rec. BlockersM01RR014467 · NCRR · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI SOROCCO, KRISTEN H · 2001 to 2007
$10.4M
Psychophysiological Precursors of AlcoholismR01AA012207 · NIAAA · UNIV OF ARKANSAS FOR MED SCIS · PI ACHESON, ASHLEY, KOCHUNOV, PETER V. · 2001 to 2025
$9.0M
Institute for Integration of Medicine & Science: A Partnership to Improve HealthKL2TR001118 · NCATS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CLARK, ROBERT A, DOUGHERTY, DONALD M · 2013 to 2017
$3.4M
Gene-Environment Interations Underlying Alcoholism Vulnerability DisordersZIAAA000306 · NIAAA · NATIONAL INSTITUTE ON ALCOHOL ABUSE AND ALCOHOLISM · PI GOLDMAN, DAVID · 2009 to 2016
$839k
Neuroimaging in the Oklahoma Family Health Patterns ProjectR01AA019691 · NIAAA · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI LOVALLO, WILLIAM R · 2011 to 2013
$555k
Intramural NIH HHSNCATS NIH HHS KL2 TR001118NCATS NIH HHS UL1 TR001120NCRR NIH HHS M01 RR014467NIAAA NIH HHS R01 AA012207NIAAA NIH HHS R01AA019691
6 · The paper itself

Abstract

Differences in stress reactivity may affect long-term health outcomes, but there is little information on how these differences arise. The stress axis is regulated by, in part, the endogenous opioid, beta-endorphin, acting on mu-opioid receptors. Persons carrying one or two copies of the G allele of the mu-opioid receptor gene (OPRM1 A118G) may have higher receptor binding for beta-endorphin compared with AA homozygotes that may contribute to individual differences in cortisol reactivity to stress, leading to a relative blunting of cortisol stress reactivity in G allele genotypes. We measured cortisol in 251 young adults (69 GA/GG vs 182 AA genotypes) exposed to mental arithmetic plus public speaking stress relative to a resting control day. Women had smaller cortisol responses than men (F=10.2, p=0.002), and women with GA or GG genotypes (N=39) had an absence of cortisol response relative to AA carriers (N=110) (F=18.4, p<0.0001). Male genotypes had no such difference in response (F=0.29). Cortisol response following mu-opioid receptor blockade using naltrexone in 119 of these subjects unmasked a greater tonic opioid inhibition of cortisol secretion in women (N=64), consistent with their blunted stress reactivity. Compared with men, women may have cortisol stress responses that are more heavily regulated by endogenous opioid mechanisms, and the OPRM1 GA/GG genotypes may affect females differentially relative to males. Diminished cortisol responses to stress may have consequences for health behaviors in women with GA/GG genotypes.

Indexed as

Polymorphism, Single NucleotideAdolescentAdultDouble-Blind MethodFemaleGenotypeHeart RateHumansHydrocortisoneMaleMathematical ConceptsNaltrexoneNarcotic AntagonistsRandom AllocationReceptors, Opioid, muSalivaHydrocortisoneNaltrexoneNarcotic AntagonistsOPRM1 protein, humanReceptors, Opioid, mu

Identifiers

PMID25881118
PMCPMC4569944
OpenAlexW2062079462

What OpenQuestion holds

Textmetadata
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.