Evidence map›Paper›PMID 40690541›Full record

ArticleRevista brasileira de psiquiatria (Sao Paulo, Brazil : 1999)2025

Neurocognitive and neurobiological features of early-stage, unmedicated patients with bipolar disorder.

Signem Oztekin, Fatma Akdeniz Usakli, Arzu Oran, Fatma Taneli, Sophia Frangou, Omer Aydemir

Abstract read
In one paragraph

Article in Revista brasileira de psiquiatria (Sao Paulo, Brazil : 1999), 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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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

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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

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5 · Who and what money

Authors and funding

6 authors.

Signem OztekinDepartment of Psychiatry and Psychotherapy, Klinikum Nurnberg, Nurnberg, Germany.
Fatma Akdeniz UsakliPrivate Practice, Afyon, Turkey.
Arzu OranEskisehir Hospital, Acibadem Healthcare Group, Eskisehir, Turkey.
Fatma TaneliDepartment of Clinical Biochemistry, Celal Bayar University Medical Faculty, Manisa, Turkey.
Sophia FrangouDepartment of Psychiatry, Mount Sinai School of Medicine, New York, NY, USA.
Omer AydemirDepartment of Psychiatry, Celal Bayar University Medical Faculty, Manisa, Turkey.

Funding

Incentive Award for Research Project of the Turkish Psychiatric Association; 18th Annual Meeting and Clinical Education Symposium of the Turkish Psychiatric Association, April 2014Research Award of the Turkish Psychiatric Association; 52nd National Psychiatry Congress of Turkish Psychiatric Association, November 2016
6 · The paper itself

Abstract

objectiveThis study aimed to identify young adults who met the criteria for bipolar disorder (BD) but had not yet been diagnosed or treated. It also aimed to evaluate their neurocognitive and neurobiological changes compared to healthy controls (HC).

methodsIndividuals at high risk for BD were identified by using the Hypomania Checklist 32 items (HCL-32R). Participants were then assessed with the Structured Clinical Interview for DSM-IV Axis I Disorders (SCID-I) to identify previously undiagnosed and drug-naive patients (DNP) (n=27). A matched HC group (n=27) was included for comparison. All participants completed a cognitive battery assessing executive function, attention, working memory, and verbal learning. Magnetic resonance imaging (MRI) was used to assess cortical thickness. Oxidative stress markers - including thiobarbituric acid reactive substances (TBARS), nitric oxide (NO), and the antioxidant enzymes superoxide dismutase (SOD) and catalase (CAT) - were measured.

resultsThe DNP group underperformed across all the tests administered but group differences were significant in the Wisconsin Card Sorting Test (WCST) and Rey Auditory Verbal Learning Test (RVALT). Among oxidative stress markers, only CAT levels were significantly higher in the DNP group. Additionally, patients exhibited significant cortical thinning in several brain regions.

conclusionNeurobiological alterations and neurocognitive dysfunction are present in the earlystage, unmedicated stages of BD. However, longitudinal studies are needed to better understand the progression of these changes.

Indexed as

Bipolar DisorderAdultBiomarkersCase-Control StudiesExecutive FunctionFemaleHumansMagnetic Resonance ImagingMaleNeuropsychological TestsOxidative StressThiobarbituric Acid Reactive SubstancesYoung AdultBiomarkersThiobarbituric Acid Reactive Substancesaffective disorderscortical thicknessMRIoxidative stress

Identifiers

PMID40690541
PMCPMC12815405

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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.