Evidence map›Paper›PMID 41257974›Full record

ArticleTranslational psychiatry2025

A study on electroretinography as a biomarker for seasonal vulnerability in depression.

Julia Maruani, Lily Vissouze, Héloise Rach, Marc Hébert, Michel Lejoyeux, Patrice Bourgin, Pierre A Geoffroy

Abstract read
In one paragraph

Article in Translational psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

7 authors.

Julia MaruaniDépartement de psychiatrie et d'addictologie, AP-HP, GHU Paris Nord, DMU Neurosciences, Hôpital Bichat - Claude Bernard, F-75018, Paris, France. julia.maruani@aphp.fr.ORCID http://orcid.org/0000-0002-2002-6051
Lily VissouzeDépartement de psychiatrie et d'addictologie, AP-HP, GHU Paris Nord, DMU Neurosciences, Hôpital Bichat - Claude Bernard, F-75018, Paris, France.ORCID http://orcid.org/0000-0002-2779-6403
Héloise RachDépartement de psychiatrie et d'addictologie, AP-HP, GHU Paris Nord, DMU Neurosciences, Hôpital Bichat - Claude Bernard, F-75018, Paris, France.
Marc HébertCERVO Brain Research Centre, Centre Intégré Universitaire de Santé et des Services Sociaux de la Capitale Nationale, Québec, QC, Canada.ORCID http://orcid.org/0000-0002-6635-8369
Michel LejoyeuxDépartement de psychiatrie et d'addictologie, AP-HP, GHU Paris Nord, DMU Neurosciences, Hôpital Bichat - Claude Bernard, F-75018, Paris, France.
Patrice BourginSleep Disorders Center - CIRCSom (International Research Center for ChronoSomnology), University Hospital of Strasbourg 1, place de l'hôpital, 67000, Strasbourg, France.
Pierre A GeoffroyDépartement de psychiatrie et d'addictologie, AP-HP, GHU Paris Nord, DMU Neurosciences, Hôpital Bichat - Claude Bernard, F-75018, Paris, France. pierre.a.geoffroy@gmail.com.ORCID http://orcid.org/0000-0001-9121-209X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Depressive disorders involve disruptions in light signal processing. Seasonal Affective Disorder (SAD) has been linked to abnormalities in phototransduction, including impaired retinal responses and sleep disturbances. Similar retinal anomalies have been observed in Major Depressive Episode (MDE) patients without seasonal pattern. However, no study has directly compared light-signaling biomarkers between SAD and non-seasonal MDE using sleep assessments and electroretinography (ERG) measures. This study aims to develop a model combining clinical and ERG markers to predict seasonality in MDE patients. Patients with MDE (N = 320) were classified based on their vulnerability to seasonality using the Global Seasonality Score (GSS) from the Seasonal Pattern Assessment Questionnaire (SPAQ), with a threshold of ≥ 11 indicating seasonal vulnerability. This dimensional approach provides a more nuanced reflection of underlying pathophysiological mechanisms than the categorical DSM-5-TR classification of SAD. Subjective sleep, psychiatric, and ERG biomarkers were analyzed. Significant variables were entered into a Backward Stepwise Logistic Regression (N = 35, subset of participants who had all available data including ERG measures), and model performance was assessed using sensitivity, specificity, accuracy, AUC, ROC curve, and Youden's index. The model retained six predictors: reduced bipolar cell amplitude (rods), increased cone response amplitude at 7 cd·s⁻¹·m⁻², increased daytime sleepiness, higher depression severity, younger age, and female gender. It demonstrated good discriminative power (AUC = 0.861, sensitivity = 0.905, specificity = 0.714, Youden's index = 0.619). The model effectively distinguishes seasonal from non-seasonal MDE, explaining 30.5% of the variance. ERG is a promising tool for identifying biomarkers of Seasonal Vulnerability in depression. Enhancing predictive approaches with multimodal diagnostic and longitudinal data could further improve early detection and personalized interventions.

Indexed as

ElectroretinographyMajor Depressive DisorderSeasonal Affective DisorderAdultBiomarkersFemaleHumansMaleMiddle AgedSeasonsBiomarkers

Identifiers

PMID41257974
PMCPMC12789525

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Registered trials

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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.