Evidence map›Paper›PMID 34094888›Full record

ArticleSchizophrenia research. Cognition2021

Neurocognition in Kenyan youth at clinical high risk for psychosis.

Daniel Mamah, Victoria N Mutiso, David M Ndetei

Open access · goldAbstract read
In one paragraph

Article in Schizophrenia research. Cognition, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 23% 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

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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
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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

3 authors at 3 institutions in 2 countries.

Daniel MamahDepartment of Psychiatry, Washington University Medical School, St. Louis, MO, United States of America.
Victoria N MutisoAfrica Mental Health Research and Training Foundation, Nairobi, Kenya.
David M NdeteiAfrica Mental Health Research and Training Foundation, Nairobi, Kenya.
Africa Mental Health Foundation · KEUniversity of Nairobi · KEWashington University in St. Louis · US

Funding

Clinical and Biomarker-Based Trajectories of Psychosis-Risk Populations in KenyaR01MH127571 · NIMH · WASHINGTON UNIVERSITY · PI MAMAH, DANIEL · 2021 to 2025
$3.3M
Genes, Behavior and Psychosis Risk in KenyaR56MH111300 · NIMH · WASHINGTON UNIVERSITY · PI MAMAH, DANIEL · 2016 to 2016
$640k
IDENTIFICATION OF PSYCHOSIS-RISK TRAITS IN AFRICAR21MH095645 · NIMH · WASHINGTON UNIVERSITY · PI MAMAH, DANIEL · 2013 to 2014
$270k
NIMH NIH HHS R01 MH127571NIMH NIH HHS R21 MH095645NIMH NIH HHS R56 MH111300
6 · The paper itself

Abstract

introductionCognitive deficits are typically seen in schizophrenia and in the prodrome, and are a major predictor of functional outcomes in patients. In Africa, few studies have investigated neurocognition in psychosis, which presents a gap in our understanding of the heterogeneity of the illness. In this study, we assessed neurocognition among the largest sample of psychosis-risk participants recruited in the continent to date.

methodsThe study was conducted in Kenya, and involved 295 psychiatric medication-naïve participants at clinical high-risk (CHR) for psychosis and healthy controls, aged 15-25 yrs. Psychosis-risk status was determined separately using the Structured Interview of Psychosis-Risk Syndromes (i.e. CHR) and by self-report with the Washington Early Recognition Center Affectivity and Psychosis Screen. Eleven tests were administered using the University of Pennsylvania Computerized Neurocognitive Battery. Test performance across groups were investigated, as well as demographic and clinical effects.

resultsFewer participants were designated as being at psychosis-risk with structured interview (

conclusionDeficits across multiple cognitive domains are present in Kenyan psychosis-risk youth, most significantly in verbal intelligence. The pattern of cognitive deficits and an absence of gender effects may represent ethnicity-specific phenotypes of the psychosis-risk state. Longitudinal studies of neurocognition in Kenyan patients who convert to psychosis may enhance risk prediction in this population, and facilitate targeted interventions.

Indexed as

AfricaCognitionKenyaNeurocognitionPsychosisRiskSIPSWERCAP

Identifiers

PMID34094888
PMCPMC8167199
OpenAlexW3164333941

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.