Evidence map›Paper›PMID 37540905›Full record

Trial reportPsychoneuroendocrinology2023

Hormone sensitivity predicts the beneficial effects of transdermal estradiol on reward-seeking behaviors in perimenopausal women: A randomized controlled trial.

Danielle A Swales, Serena Lozza-Fiacco, Elizabeth Helen Andersen, Jessica A Cooper, Michael T Treadway, Kai Xia, Crystal Edler Schiller, Susan S Girdler, Gabriel S Dichter

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Psychoneuroendocrinology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.8field-weighted citation impact, top 13% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Anhedonia: Current and future treatments.PCN reports : psychiatry and clinical neurosciences · 2025
    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

9 authors at 2 institutions in 2 countries.

Danielle A SwalesDepartment of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA. Electronic address: danielle_swales@med.unc.edu.
Serena Lozza-FiaccoDepartment of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA; Department of Psychology, University of Zurich, Zurich, Switzerland.
Elizabeth Helen AndersenDepartment of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Jessica A CooperDepartment of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, GA, USA.
Michael T TreadwayDepartment of Psychology, Emory University, Atlanta, GA, USA.
Kai XiaDepartment of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Crystal Edler SchillerDepartment of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Susan S GirdlerDepartment of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Gabriel S DichterDepartment of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
University of North Carolina at Chapel Hill · USEmory University · US

Funding

Examining the Effects of Estradiol on Neural and Molecular Response to Rewards in Perimenopausal-Onset Anhedonia and PsychosisR01MH128238 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI GABRIEL S DICHTER, DAVID S LALUSH · 2022 to 2026
$3.6M
The Menopause Transition: Estrogen Variability, HPA axis and Affective SymptomsR01MH108690 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI GIRDLER, SUSAN S. · 2016 to 2020
$3.2M
Postdoctoral Training in Reproductive Mood DisordersT32MH093315 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SUSAN Scott GIRDLER, David R. Rubinow · 2012 to 2026
$2.8M
From stress to anhedonia: examining inflammation and altered glutamate function as distinct or common etiological pathwaysK01MH126308 · NIMH · EMORY UNIVERSITY · PI Jessica Cooper Robinson · 2022 to 2026
$900k
Defining the Neuropathophysiological Mechanisms Linking Ovarian Hormone Variability with Depression Risk in Peripubertal GirlsK01MH121575 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ANDERSEN, ELIZABETH HELEN · 2020 to 2024
$790k
NIMH NIH HHS K01 MH121575NIMH NIH HHS K01 MH126308NIMH NIH HHS R01 MH108690NIMH NIH HHS R01 MH128238NIMH NIH HHS T32 MH093315
6 · The paper itself

Abstract

Depression is highly prevalent during the menopause transition (perimenopause), and often presents with anxious and anhedonic features. This increased vulnerability for mood symptoms is likely driven in part by the dramatic hormonal changes that are characteristic of the menopause transition, as prior research has linked fluctuations in estradiol (E2) to emergence of depressed mood in at risk perimenopausal women. Transdermal estradiol (TE2) has been shown to reduce the severity of depression in clinically symptomatic women, particularly in those with recent stressful life events. This research extends prior work by examining the relation between E2 and reward seeking behaviors, a precise behavioral indicator of depression. Specifically, the current study utilizes a randomized, double blind, placebo-controlled design to investigate whether mood sensitivity to E2 flux ("hormone sensitivity") predicts the beneficial effects of TE2 interventions on reward seeking behaviors in perimenopausal women, and whether recent stressful life events moderate any observed associations.

methodParticipants were 66 women who met standardized criteria for being early or late perimenopausal based on bleeding patterns. Participants were recruited from a community sample; therefore, mood symptoms varied across the continuum and the majority of participants did not meet diagnostic criteria for a depressive or anxiety disorder at the time of enrollment. Hormone sensitivity was quantified over an 8-week baseline period, using within-subjects correlations between repeated weekly measures of E2 serum concentrations and weekly anxiety (State Trait Anxiety Inventory) and anhedonia ratings (Snaith-Hamilton Pleasure Scale). Women were then randomized to receive 8 weeks of TE2 (0.1 mg) or transdermal placebo, and reward-seeking behaviors were assessed using the Effort-Expenditure for Rewards Task (EEfRT).

resultsParticipants who were randomized to receive transdermal estradiol and who demonstrated greater anxiety sensitivity to E2 fluctuations at baseline, demonstrated more reward seeking behaviors on the EEfRT task. Notably, the strength of the association between E2-anxiety sensitivity and post-randomization EEfRT for TE2 participants increased when women experienced more recent stressful life events and rated those events as more stressful. E2-anhedonia sensitivity was not associated with reward-seeking behaviors.

conclusionPerimenopausal women who are more sensitive to E2 fluctuations and experienced more recent life stress may experience a greater benefit of TE2 as evidenced by an increase in reward seeking behaviors.

Indexed as

EstradiolPerimenopauseAffectAnhedoniaFemaleHumansMenopauseEstradiolAnhedoniaAnxietyEstradiolHormone sensitivityPerimenopauseReward seeking behaviors

Identifiers

PMID37540905
PMCPMC10568486
OpenAlexW4384938266

What OpenQuestion holds

Textmetadata
LicenceTDM
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.