Evidence map›Paper›PMID 19399358›Full record

ArticleEuropean archives of psychiatry and clinical neuroscience2009

Heritability of Trail Making Test performance in multiplex schizophrenia families: implications for the search for an endophenotype.

Raúl Mendoza Quiñones, Yuranny Cabral Calderín, Mayelin Domínguez, Tania M Bravo, Adnelys Reyes Berazaín, Alexander García, Antonio Caballero, Migdyrai Martín Reyes

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Article in European archives of psychiatry and clinical neuroscience, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.9field-weighted citation impact, top 16% of its field
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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3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 17 citations in OpenAlex.

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4 · The record

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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

8 authors at 2 institutions in 2 countries.

Raúl Mendoza QuiñonesDepartment of Biological Psychiatry, Cuban Neurosciences Center, Cubanacán, Havana City, Cuba.
Yuranny Cabral Calderín
Mayelin Domínguez
Tania M Bravo
Adnelys Reyes Berazaín
Alexander García
Antonio Caballero
Migdyrai Martín Reyes
Cuban Neuroscience Center · CUHospital Tobar García · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The impairment of the Trail Making Test (TMT) performance as a measure of executive function deficits has been found both in patients with schizophrenia and in their unaffected first-degree relatives, suggesting that it might be considered as a familial vulnerability marker, but its heritability estimates are not well known. This study investigated the genetic heritability of impairments in TMT performance using a sample of 80 schizophrenia patients, 145 unaffected first-degree relatives and 127 healthy controls from families with multiple members with schizophrenia. Consistent with previous reports in the literature, relatives performed in between healthy controls and schizophrenia patients. Based on these results, a variance component-analysis provided small, but significant additive heritability estimates for performance indices relating performance in TMT-version A to TMT-version B. These results showed that this significant but small evidence of heritability on the one hand suggests an association with genetic predisposition to schizophrenia, but that TMT performance is also associated with epigenetic or environmental factors.

Indexed as

PhenotypeSchizophrenic PsychologyAdolescentAdultAgedAnalysis of VarianceCognition DisordersExecutive FunctionFamilyFemaleHumansMaleMiddle AgedSchizophreniaTrail Making TestYoung Adult

Identifiers

PMID19399358
OpenAlexW1985312681

What OpenQuestion holds

Textmetadata
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Registered trials

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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.