Evidence map›Paper›PMID 25459893›Full record

Trial reportPsychoneuroendocrinology2015

Sex differences in acute hormonal and subjective response to naltrexone: The impact of menstrual cycle phase.

Daniel J O Roche, Andrea C King

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Psychoneuroendocrinology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 4 pooled it
1.3field-weighted citation impact, top 26% 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

29 citing papers in PubMed, 4 syntheses or guidelines pooled it, 46 citations in OpenAlex.

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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

2 authors at 2 institutions in 1 country.

Daniel J O RocheDepartment of Psychology, University of California Los Angeles, Los Angeles, CA 90095, USA. Electronic address: droche@ucla.edu.
Andrea C KingDepartment of Psychiatry and Behavioral Neuroscience, University of Chicago, Chicago, IL 60637, USA.
University of California, Los Angeles · USUniversity of Chicago · US

Funding

TRANSLATIONAL RESEARCH UNIVERSITY OF CHICAGO: CLINICAL TRIALSUL1RR024999 · NCRR · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2007 to 2011
$25.3M
Re-Engineering Translational Research at the University of ChicagoUL1TR000430 · NCATS · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2012 to 2016
$20.2M
Efficacy of Naltrexone in Women's Smoking CessationR01DA016834 · NIDA · UNIVERSITY OF CHICAGO · PI KING, ANDREA C · 2005 to 2009
$3.0M
Role of estradiol in women smokers' acute HPA axis hormone response to naltrexoneF31DA030073 · NIDA · UNIVERSITY OF CHICAGO · PI ROCHE, DANIEL · 2011 to 2012
$65k
NCATS NIH HHS UL1 TR000430NCRR NIH HHS UL1 RR024999NIDA NIH HHS 1F31DA030073NIDA NIH HHS F31 DA030073NIDA NIH HHS R01 DA016834NIDA NIH HHS R01-DA016834
6 · The paper itself

Abstract

Women often exhibit larger hormonal and subjective responses to opioid receptor antagonists than men, but the biological mechanisms mediating this effect remain unclear. Among women, fluctuations in estradiol (E2) and progesterone (P4) across the menstrual cycle (MC) affect the endogenous opioid system. Therefore, the goal of the current study was to compare acute naltrexone response between women in the early follicular phase of the MC (low E2 and P4), women in the luteal phase of the MC (high E2 and P4), and men. Seventy healthy controls (n=46 women) participated in two morning sessions in which they received 50mg naltrexone or placebo in a randomized, counterbalanced order. Women were randomized to complete both sessions in either the early follicular (n=23) or luteal phase of the MC. Serum cortisol, salivary cortisol, prolactin, luteinizing hormone (LH), and subjective response were assessed upon arrival to the laboratory and at regular intervals after pill administration. In luteal and early follicular women but not men, naltrexone (vs. placebo) increased serum cortisol and prolactin levels from baseline; however, the naltrexone-induced increases in these hormones were significantly greater in luteal women than early follicular women. Additionally, only luteal women demonstrated an increase from baseline in salivary cortisol levels and the severity of adverse drug effects in response to naltrexone. In sum, the results indicate that luteal phase women are more sensitive to acute hormonal and subjective effects of naltrexone than early follicular women and men. These findings may have important implications for the use of naltrexone in women.

Indexed as

AdultFemaleFollicular PhaseHumansHydrocortisoneLuteal PhaseMaleNaltrexoneNarcotic AntagonistsProlactinSex FactorsYoung AdultHydrocortisoneNaltrexoneNarcotic AntagonistsProlactinCortisolEndogenous opioid systemLuteinizing hormoneMenstrual cycleNaltrexoneProlactinSex differencesSubjective response

Identifiers

PMID25459893
PMCPMC4482338
OpenAlexW2108961806

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.