Evidence map›Paper›PMID 38702455›Full record

Observational studyEuropean child & adolescent psychiatry2024

Functioning and neurocognition in very early and early-life onset bipolar disorders: the moderating role of bipolar disorder type.

D Sleurs, M Speranza, B Etain, B Aouizerate, V Aubin, F Bellivier, R Belzeaux, M Carminati, P Courtet, C Dubertret and 13 more

Abstract readMulticenter StudyObservational Study
PubMed Publisher
In one paragraph

Observational study in European child & adolescent psychiatry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. [Risk Prediction Performance of Blood Biomarkers for Bipolar Disorder With Psychotic Symptoms].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2025
    Article
  2. 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

23 authors.

D SleursFondation FondaMental, Créteil, France. david.sleurs@aphp.fr.
M SperanzaFondation FondaMental, Créteil, France.
B EtainFondation FondaMental, Créteil, France.
B AouizerateFondation FondaMental, Créteil, France.
V AubinFondation FondaMental, Créteil, France.
F BellivierFondation FondaMental, Créteil, France.
R BelzeauxFondation FondaMental, Créteil, France.
M CarminatiFondation FondaMental, Créteil, France.
P CourtetFondation FondaMental, Créteil, France.
C DubertretFondation FondaMental, Créteil, France.
B FredembachFondation FondaMental, Créteil, France.
E HaffenFondation FondaMental, Créteil, France.
F GroppiFondation FondaMental, Créteil, France.
P LaurentFondation FondaMental, Créteil, France.
M LeboyerFondation FondaMental, Créteil, France.
P M LlorcaFondation FondaMental, Créteil, France.
E OliéFondation FondaMental, Créteil, France.
M PolosanFondation FondaMental, Créteil, France.
R SchwanFondation FondaMental, Créteil, France.
D WeillFondation FondaMental, Créteil, France.
FACE-B. D. (FondaMental Academic Centers of Expertise for Bipolar Disorders) Group*
C PasserieuxFondation FondaMental, Créteil, France.
P RouxFondation FondaMental, Créteil, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Defining homogeneous subgroups of bipolar disorder (BD) is a major goal in personalized psychiatry and research. According to the neurodevelopmental theory, age at onset may be a key variable. As potential trait markers of neurodevelopment, cognitive and functional impairment should be greater in the early form of the disease, particularly type 1 BD (BD I). The age at onset was assessed in a multicenter, observational sample of 4190 outpatients with BD. We used a battery of neuropsychological tests to assess six domains of cognition. Functioning was measured using the Functioning Assessment Short Test (FAST). We studied the potential moderation of the type of BD on the associations between the age at onset and cognitive and functioning in a subsample of 2072 euthymic participants, controlling for potential clinical and socio-demographic covariates. Multivariable analyses showed cognition to not be impaired in individuals with early (21-30 years) and very early-life (before 14 years) onset of BD. Functioning was equivalent between individuals with early and midlife-onset of BD II and NOS but better for individuals with early onset of BD I. In contrast, functioning was not worse in individuals with very early-onset BD I but worse in those with very early-onset BD II and NOS. Early-life onset BDs were not characterized by poorer cognition and functioning. Our results do not support the neurodevelopmental view that a worse cognitive prognosis characterizes early-life onset BD. This study suggests that functional remediation may be prioritized for individuals with midlife-onset BD I and very early life onset BD 2 and NOS.

Indexed as

Age of OnsetBipolar DisorderNeuropsychological TestsAdolescentAdultCognitionCognitive DysfunctionFemaleHumansMaleMiddle AgedYoung AdultBipolar disorderCognitionEarly onsetFunctioning

Identifiers

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.