Evidence map›Paper›PMID 41138147›Full record

ArticleThe European journal of neuroscience2025

Differences in Performance in the Trail Making Test Part B Between Adoptees With High and Low Genetic Risk for Schizophrenia Spectrum Disorders: The Finnish Adoptive Family Study of Schizophrenia.

Toni Myllyaho, Mika Niemelä, Ritva Rauhala, Helinä Hakko, Karl-Erik Wahlberg, Sami Räsänen

Abstract read
In one paragraph

Article in The European journal of neuroscience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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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

1 citing paper in PubMed.

  1. Article
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

6 authors.

Toni MyllyahoDepartment of Psychiatry, Oulu University Hospital, Oulu, Finland.ORCID 0000-0001-5203-3339
Mika NiemeläFaculty of Medicine, Research Unit of Population Health, University of Oulu, Oulu, Finland.
Ritva RauhalaDepartment of Psychiatry, Oulu University Hospital, Oulu, Finland.
Helinä HakkoDepartment of Psychiatry, Oulu University Hospital, Oulu, Finland.
Karl-Erik WahlbergFaculty of Medicine, Research Unit of Clinical Medicine, Psychiatry, University of Oulu, Oulu, Finland.
Sami RäsänenDepartment of Psychiatry, Oulu University Hospital, Oulu, Finland.

Funding

Department of Psychiatry, Oulu University Hospital, Oulu, Finland (Researcher TM)Strategic Research Council (SRC) established within the Academy of Finland 352509
6 · The paper itself

Abstract

The current study uses data from the Finnish Adoptive Family Study of Schizophrenia to investigate the association of genetic risk status and diagnosed psychiatric disorders with executive functioning, measured by Trail Making Test Part B (TMT-B), in adoptees with high and low genetic risk for schizophrenia spectrum disorders. The results showed no statistically significant differences in TMT-B completion times between adoptees with high and low genetic risk for schizophrenia spectrum disorders, although adoptees with high genetic risk for schizophrenia spectrum disorders as a group exhibited slightly slower performance. This contradicts previous studies reporting poorer TMT-B performance in unaffected first-degree relatives of individuals with schizophrenia. However, it aligns with studies that did not find differences in TMT-B performance between first-degree relatives of individuals with schizophrenia and controls. Significant differences in TMT-B completion times were observed among adoptees with psychiatric disorders, indicating that psychiatric morbidity associates with TMT-B performance, regardless of genetic risk. These findings indicate that various forms of psychopathology may hinder TMT-B performance, potentially due to reduced processing speeds or increased propensity towards a higher error rate. This highlights the link between psychopathology and cognitive impairment, underscoring this relationship as a critical focus for neuroscience research. Although TMT-B performance did not differ between adoptees with high and low genetic risk for schizophrenia spectrum disorders, our results do not rule out the existence of other cognitive deficits in adoptees with high genetic risk for schizophrenia spectrum disorders.

Indexed as

AdoptionSchizophreniaTrail Making TestAdultExecutive FunctionFemaleFinlandGenetic Predisposition to DiseaseHumansMaleMiddle AgedYoung Adultadopted childrenadoptive familiesexecutive functioningpsychiatric disordersschizophrenia spectrum disordersTrail Making Test Part B (TMT‐B)

Identifiers

PMID41138147
PMCPMC12553483

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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 OpenQuestion graph.