Evidence map›Paper›PMID 32495635›Full record

ArticleCanadian journal of psychiatry. Revue canadienne de psychiatrie2020

High Rates of Genetic Diagnosis in Psychiatric Patients with and without Neurodevelopmental Disorders: Toward Improved Genetic Diagnosis in Psychiatric Populations.

Joyce So, Venuja Sriretnakumar, Jessica Suddaby, Brianna Barsanti-Innes, Hanna Faghfoury, Timothy Gofine

Open access · greenAbstract read
In one paragraph

Article in Canadian journal of psychiatry. Revue canadienne de psychiatrie, 2020. 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, top 94% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Review
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 at 3 institutions in 1 country.

Joyce SoThe Fred A. Litwin Family Centre in Genetic Medicine, 7989University Health Network and Mount Sinai Hospital, Toronto, Ontario, Canada.
Venuja Sriretnakumar7978Centre for Addiction and Mental Health, Toronto, Ontario, Canada.
Jessica SuddabyThe Fred A. Litwin Family Centre in Genetic Medicine, 7989University Health Network and Mount Sinai Hospital, Toronto, Ontario, Canada.ORCID 0000-0002-9693-5323
Brianna Barsanti-Innes7978Centre for Addiction and Mental Health, Toronto, Ontario, Canada.
Hanna FaghfouryThe Fred A. Litwin Family Centre in Genetic Medicine, 7989University Health Network and Mount Sinai Hospital, Toronto, Ontario, Canada.
Timothy GofineOntario Shores Centre for Mental Health Sciences, Whitby, Ontario, Canada.
Mount Sinai Hospital · CACentre for Addiction and Mental Health · CAUniversity of Toronto · CA

Funding

CIHR
6 · The paper itself

Abstract

objectiveThere is a paucity of literature on genetic diagnosis in psychiatric populations, particularly the vulnerable population of patients with concomitant neurodevelopmental disorder (NDD). In this cross-sectional study, we investigated the genetic diagnostic rate in 151 adult psychiatric patients from two centers in Ontario, Canada, including a large subset (73.5%) with concurrent NDD, and performed phenotypic analysis to determine the strongest predictors for the presence of a genetic diagnosis.

methodPatients 16 years of age or older and affected with a psychiatric disorder plus at least one of NDD, neurological disorder, congenital anomaly, dysmorphic features, or family history of NDD were recruited through the genetics clinics between 2012 and 2016. Patients underwent genetic assessment and testing according to clinical standards. Chi-squared test was used for phenotypic comparisons. Multivariate logistic regression analysis was performed to determine which phenotypic features were predictive of genetic diagnosis types.

resultsOverall, 45.7% of patients in the total cohort were diagnosed with genetic disorders with the vast majority of diagnoses (89.9%) comprising single gene and chromosomal disorders. There were management and treatment implications for almost two-thirds (63.8%) of diagnosed patients. Presence of a single gene disorder or chromosomal diagnosis was predicted by differing combinations of neurological, NDD, and psychiatric phenotypes.

conclusionThe results of this study highlight the frequency and impact of genetic diagnosis in psychiatric populations, particularly those with concomitant NDD. Genetic assessment should be considered in psychiatric patients, particularly those with multiple brain phenotypes (psychiatric, neurodevelopmental, neurological).

Indexed as

Mental DisordersNeurodevelopmental DisordersAdultCross-Sectional StudiesDiagnosis, Dual (Psychiatry)FemaleGenetic Predisposition to DiseaseHumansMaleMiddle AgedOntarioPhenotypeadult psychiatrydual diagnosisgeneticsscreening

Identifiers

PMID32495635
PMCPMC7658423
OpenAlexW3030942456

What OpenQuestion holds

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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.