Evidence map›Paper›PMID 41320189›Full record

ArticleJournal of intellectual disability research : JIDR2026

Antipsychotic Use Among Intellectually Disabled Individuals With Rare Genetic Variants That Confer Risk for Schizophrenia.

Mark Ainsley Colijn

Abstract read
In one paragraph

Article in Journal of intellectual disability research : JIDR, 2026. 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

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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

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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

1 author.

Mark Ainsley ColijnDepartment of Psychiatry, Hotchkiss Brain Institute, Mathison Centre for Mental Health Research and Education, University of Calgary, Calgary, Alberta, Canada.ORCID 0000-0002-8151-1173

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRare genetic variation can predispose individuals to the development of schizophrenia, with certain genes and copy number variants (CNVs) conferring risk at the exome/genome-wide level. Despite this strong association, little is known about antipsychotic effectiveness and tolerability among individuals with most of these disorders. As such, this retrospective chart review sought to gather more data regarding the real-world use of antipsychotics in this context.

methodsThis largely descriptive, cross-sectional and retrospective chart review took place at a developmental disabilities mental health clinic. Clinical information was primarily derived from electronic medical records. Individuals with a history of psychosis and antipsychotic exposure identified as having a genetic variant known to confer exome/genome-wide risk for schizophrenia were included in the study.

resultsOf the 1196 charts reviewed, 24 individuals with a relevant genetic variant were identified, 11 of whom had experienced psychotic symptoms that were treated with antipsychotic medication. Six have 22q11.2 deletion syndrome, two have 15q11-q13 duplication syndrome and one individual each has a 16p11.2 duplication, a 7q11.23 duplication and a missense variant in TRIO. Overall, antipsychotic therapy tended to be reasonably effective and well tolerated (particularly among those individuals who do not have 22q11.2 deletion syndrome), despite side effects of some kind occurring in most cases.

conclusionWhile this study had numerous limitations that prevent firm conclusions from being drawn, it provides preliminary evidence that antipsychotics may be relatively safe and effective in at least some of the genetic disorders most strongly associated with schizophrenia.

Indexed as

Antipsychotic AgentsIntellectual DisabilityPsychotic DisordersSchizophreniaAdolescentAdultChildCross-Sectional StudiesDNA Copy Number VariationsFemaleGenetic Predisposition to DiseaseHumansMaleMiddle AgedRetrospective StudiesYoung AdultAntipsychotic Agentsantipsychoticgenetic disordersgeneticsintellectual disabilityneuropsychiatrypsychosisschizophrenia

Identifiers

PMID41320189
PMCPMC12950631

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