Evidence map›Paper›PMID 42387906›Full record

SynthesisBipolar disorders2026

Biofluid Biomarkers of Cognitive Functioning in Bipolar Disorder: A Systematic Review by the Targeting Cognition and Older-Age Bipolar Disorder ISBD Task Forces.

Alexandra J M Beunders, Sigfried N T M Schouws, Andrew T Olagunju, Vicent Balanzá-Martínez, Nicole C M Korten, Ralph W Kupka, Katherine E Burdick, Andre F Carvalho, Ariel G Gildengers, Lars V Kessing and 12 more

Abstract readSystematic Review
In one paragraph

Synthesis in Bipolar disorders, 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

22 authors.

Alexandra J M BeundersGGZ inGeest, Specialized Mental Health Care, Amsterdam, the Netherlands.ORCID 0000-0001-9620-2579
Sigfried N T M SchouwsGGZ inGeest, Specialized Mental Health Care, Amsterdam, the Netherlands.ORCID 0000-0003-0591-5405
Andrew T OlagunjuDepartment of Psychiatry and Behavioural Neurosciences, McMaster University/St. Joseph's Healthcare, Hamilton, Ontario, Canada.ORCID 0000-0003-1736-9886
Vicent Balanzá-MartínezDepartment of Medicine, Universitat de València, Hospital Clínic Universitari de València, INCLIVA, CIBERSAM, Valencia, Spain.
Nicole C M KortenDepartment of Medical Psychology, Northwest Clinics, Alkmaar, the Netherlands.
Ralph W KupkaGGZ inGeest, Specialized Mental Health Care, Amsterdam, the Netherlands.
Katherine E BurdickDepartment of Psychiatry, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.ORCID 0000-0003-4417-4988
Andre F CarvalhoIMPACT (Innovation in Mental and Physical Health and Clinical Treatment), strategic Research Centre, School of Medicine, Barwon Health, Deakin University, Geelong, Victoria, Australia.
Ariel G GildengersDepartment of Psychiatry, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Lars V KessingCopenhagen Affective Disorder Research Center (CADIC), Psychiatric Center, Copenhagen, Denmark.ORCID 0000-0001-9377-9436
Roger S McIntyreDepartment of Psychiatry, Department of Pharmacology and Toxicology, University of Toronto, Toronto, Ontario, Canada.ORCID 0000-0003-4733-2523
Paula V NunesBipolar Disorder Program (PROMAN), Department of Psychiatry, University of São Paulo Medical School, Sao Paulo, Brazil.
Ayal SchafferDepartment of Psychiatry, Department of Pharmacology and Toxicology, University of Toronto, Toronto, Ontario, Canada.ORCID 0000-0001-6220-5042
Ivan J TorresDepartment of Psychiatry, University of British Columbia, Vancouver, British Columbia, Canada.
Shang-Ying TsaiDepartment of Psychiatry, Taipei Medical University and Hospital, Taipei, Taiwan.
Tamsyn E Van RheenenDepartment of Psychiatry, Faculty of Medicine Dentistry and Health Sciences, University of Melbourne, Melbourne, Australia.
Eduard VietaBipolar and Depressive Disorders Unit, Institute of Neuroscience, Hospital Clinic, University of Barcelona, IDIBAPS, CIBERSAM, Barcelona, Catalonia, Spain.ORCID 0000-0002-0548-0053
Lakshmi N YathamDepartment of Psychiatry, University of British Columbia, Vancouver, British Columbia, Canada.
Allan H YoungDepartment of Psychological Medicine, Institue Psychiatry, King's College London, London, UK.
Lisa T EylerDepartment of Psychiatry, University of California San Diego, San Diego, California, USA.
Kamilla W MiskowiakNeurocognition and Emotion in Affective Disorders (NEAD) Centre, Department of Psychology, University of Copenhagen, and Mental Health Services, Capital Region of Denmark, Copenhagen, Denmark.
Annemiek DolsAmsterdam Public Health Research Institute, Amsterdam UMC, location VUmc, Amsterdam, the Netherlands.ORCID 0000-0003-1964-0318

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCognitive impairment is common in bipolar disorder (BD), but the underlying pathophysiology remains unclear. This systematic review aimed to (1) summarize all literature describing relationships of biofluid biomarkers and cognition in BD and (2) identify which biofluid biomarkers correlate most consistently with cognition in BD.

methodsThis systematic review followed procedures of the PRISMA statement. PubMed, EMBASE, and PsycINFO were searched from inception until July 2023. Original studies assessing the relationships between biofluid biomarkers and cognitive functioning in adults with BD were included. Studies on neuroimaging markers and genetic biomarkers were excluded.

resultsWe identified 60 studies, together describing 184 biofluid biomarkers that were measured in relation to cognitive functioning in BD. Biomarkers were organized into ten categories: oxidative stress markers (n = 14); growth factors (n = 13); neurotransmitters (n = 14); neuropeptides and hormones (n = 14); neurodegenerative markers (n = 11); inflammatory/immune markers (n = 59); serostatus to infectious agents (n = 11); amino acids, vitamins, and minerals (n = 7); metabolic factors (n = 23); hemogram, coagulation, and fibrinolysis markers (n = 18). Preliminary evidence for a significant relationship with cognition appeared for HSV-1 IgG, CRP, and homocysteine (Hcy); higher biomarker levels were associated with worse cognition. DISCUSSION: Included studies were heterogeneous and many were deemed to be of low quality following risk of bias assessment. The identified three biofluid biomarkers represent history of previous infections, current inflammation, and/or physical or psychological stress. Poor physical health, possibly represented by a broad range of biomarker aberrations, may play a role in the pathophysiology of cognitive impairment in BD.

trial registrationPROSPERO registration number: CRD42021224226.

Indexed as

BiomarkersBipolar DisorderCognitive DysfunctionHumansBiomarkersbiomarkerbipolar disordercognitioncognitive impairmentelderlyolder age bipolar disordersystematic review

Identifiers

PMID42387906
PMCPMC13324234

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.