Evidence map›Paper›PMID 41355436›Full record

ArticleJournal of pineal research2026

Melatonin Circadian Phase Timing and Stability: Associations With Mood Symptoms Among a Clinically-Enriched Sample of Young Adults With Mood Disorders.

Rachel F L Walsh, Mackenzie A Maddox, Joshua Klugman, Namni Goel, Lauren B Alloy

Abstract read
In one paragraph

Article in Journal of pineal research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Rachel F L WalshDepartment of Psychology & Neuroscience, Temple University, Philadelphia, Pennsylvania, USA.ORCID https://orcid.org/0000-0002-0879-0612
Mackenzie A MaddoxDepartment of Psychology & Neuroscience, Temple University, Philadelphia, Pennsylvania, USA.ORCID https://orcid.org/0000-0002-1768-1434
Joshua KlugmanDepartment of Sociology, Temple University, Philadelphia, Pennsylvania, USA.
Namni GoelDepartment of Psychiatry and Behavioral Sciences, Rush University Medical Center, Chicago, Illinois, USA.ORCID https://orcid.org/0000-0003-2602-1996
Lauren B AlloyDepartment of Psychology & Neuroscience, Temple University, Philadelphia, Pennsylvania, USA.

Funding

Integrated Reward-Circadian Rhythm Model of First Onset of Bipolar Spectrum Disorders in Adolescence SupplementR01MH126911 · NIMH · TEMPLE UNIV OF THE COMMONWEALTH · PI ALLOY, LAUREN BERSH, NUSSLOCK, ROBIN · 2021 to 2025
$3.8M
Social and Circadian Rhythms, Reward Sensitivity, and Risk for Bipolar DisorderR01MH102310 · NIMH · TEMPLE UNIV OF THE COMMONWEALTH · PI ALLOY, LAUREN BERSH · 2014 to 2017
$1.6M
NIMH NIH HHS R01 MH102310NIMH NIH HHS R01 MH126911
6 · The paper itself

Abstract

Circadian rhythms regulate many aspects of human health, and disruptions in these rhythms have been implicated in mood disorders. Dim light melatonin onset (DLMO) provides a gold standard measure of circadian timing, yet few studies have examined its stability or relation to mood symptoms in psychiatric populations. This study examined DLMO across three time points over 20 days in a clinically-enriched sample of 124 young adults with and without mood disorders. Participants also reported mood symptom levels three times daily via ecological momentary assessments (EMA). Circadian timing and stability were quantified and their associations with mood symptoms and diurnal mood patterns were assessed. Overall, DLMO demonstrated substantial stability, and did not differ by diagnostic group. The mood disorder group had earlier circadian timing than healthy controls. Hypomanic, but not depressive, symptoms were consistently associated with later DLMO in both cross-sectional and prospective analyses. Moreover, hypomanic symptoms exhibited a diurnal pattern that differed for participants with earlier and later circadian timing. Future work should examine endogenous circadian rhythms in relation to mood disorder subtypes and mood episodes to determine whether circadian timing changes can be used to predict or intervene on psychiatric symptoms.

Indexed as

AffectCircadian RhythmMelatoninMood DisordersAdolescentAdultCross-Sectional StudiesFemaleHumansMaleYoung AdultMelatonincircadian rhythmhumanmelatoninmood disorders

Identifiers

PMID41355436
PMCPMC12912841

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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.