Evidence map›Paper›PMID 42371207›Full record

ArticleInternational journal of bipolar disorders2026

Objective sleep parameters and cognitive performance in euthymic bipolar disorder: a cross-sectional 21-day actigraphy study.

Candice Libourel, Mathilde Charron, Victoire Martinot, Mathilde Carminati, Bruno Etain, Vincent Hennion

Registry-linked trialAbstract read
In one paragraph

Article in International journal of bipolar disorders, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02627404 (Study of the Genetic and Environmental Factors of Vulnerability in Bipolar Disorders), which is not on this map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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.

NCT02627404 naunknown statusnot on this map

Study of the Genetic and Environmental Factors of Vulnerability in Bipolar Disorders

TypeinterventionalSponsorAssistance Publique - Hôpitaux de ParisRan2013 to 2018Enrolled400ConditionsBipolar DisorderArmsBlood sample, actometer
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Candice LibourelOptimisation Thérapeutique en Neuropharmacologie, UMR-S 1144, Université Paris Cité, Inserm, Paris, 75006, France.
Mathilde CharronOptimisation Thérapeutique en Neuropharmacologie, UMR-S 1144, Université Paris Cité, Inserm, Paris, 75006, France.
Victoire MartinotOptimisation Thérapeutique en Neuropharmacologie, UMR-S 1144, Université Paris Cité, Inserm, Paris, 75006, France.
Mathilde CarminatiDépartement de Psychiatrie et de Médecine Addictologique, Hôpitaux Lariboisière- Fernand Widal, GHU-APHP Nord, Paris, 75010, France.
Bruno EtainOptimisation Thérapeutique en Neuropharmacologie, UMR-S 1144, Université Paris Cité, Inserm, Paris, 75006, France.
Vincent HennionOptimisation Thérapeutique en Neuropharmacologie, UMR-S 1144, Université Paris Cité, Inserm, Paris, 75006, France. vincent.hennion@aphp.fr.

Funding

Assistance Publique - Hôpitaux de Paris GAN12Institut National de la Santé et de la Recherche Médicale C0829
6 · The paper itself

Abstract

backgroundSleep disturbances persist during euthymia in bipolar disorder (BD) and may contribute to cognitive impairment. While subjective sleep complaints have been linked to cognition, associations between objective sleep parameters and objective cognitive performance are under-explored.

methodsIn this exploratory cross-sectional study, 40 euthymic individuals with BD underwent 21 days of actigraphy to assess objective sleep parameters, including sleep duration, sleep onset latency, sleep efficiency, wake time after sleep onset (WASO), and fragmentation index. Cognitive performance was assessed using the Screen for Cognitive Impairment in Psychiatry (SCIP). Associations between sleep parameters and cognitive outcomes were examined using Spearman correlations, then using multivariable linear regression models, including a stepwise selection of potential confounding factors and a false discovery rate correction for multiple testing.

resultsAssumed sleep duration was negatively associated with the SCIP total score (β = -0.38, p = 0.011), with age retained as a covariate (p = 0.011). Total sleep time was negatively associated with delayed verbal learning (β = -0.48, p = 0.003), with no covariate retained. Sleep onset latency was negatively associated with working memory (β = -0.41, p = 0.014), with no covariate retained. Sleep onset latency was negatively associated with processing speed (β = -0.38, p = 0.002), with age (p < 0.001) and sex (p = 0.022) retained as covariates. WASO was negatively associated with verbal fluency (β = -0.39, p = 0.016), with no covariate retained.

conclusionsIn euthymic individuals with BD, objective measures of sleep duration, sleep initiation, and sleep continuity were associated with distinct cognitive domains. These findings highlight the relevance of sleep continuity and sleep initiation, beyond sleep duration alone, as correlates of cognitive functioning in BD. Due to methodological limitations, these results should be considered hypothesis-generating and require replication in larger, longitudinal cohorts. CLINICAL

trial registrationThis study was conducted as part of a larger research protocol entitled GAN (Genetics, Actimetry, and Neuropsychology in Bipolar Disorders). The protocol has been registered on ClinicalTrials.gov on November 13, 2015 (NCT02627404).

Indexed as

ActigraphyBipolar disorderCognitionMemorySleep

Identifiers

PMID42371207
PMCPMC13582676

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