Evidence map›Paper›PMID 12956826›Full record

ArticleActa psychiatrica Scandinavica2003

Postmaturity in a genetic subtype of schizophrenia.

E W C Chow, J Husted, R Weksberg, A S Bassett

Open access · greenAbstract read
In one paragraph

Article in Acta psychiatrica Scandinavica, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.1field-weighted citation impact, top 52% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Fetal growth and gestational factors as predictors of schizophrenia in 22q11.2 deletion syndrome.Genetics in medicine : official journal of the American College of Medical Genetics · 2016
    Article
  2. Neonatal hypocalcemia, neonatal seizures, and intellectual disability in 22q11.2 deletion syndrome.Genetics in medicine : official journal of the American College of Medical Genetics · 2014
    Article
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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

4 authors at 3 institutions in 1 country.

E W C ChowClinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.
J Husted
R Weksberg
A S Bassett
Centre for Addiction and Mental Health · CAUniversity of Toronto · CAUniversity of Waterloo · CA

Funding

CIHR 97800
6 · The paper itself

Abstract

objectiveTo determine whether postmaturity (gestation > 41 weeks), small for gestational age (SGA), and other pregnancy and birth complications that may elevate risk for neurodevelopmental disorders, are associated with elevated risk for schizophrenia in 22q11 Deletion Syndrome (22qDS), a genetic subtype of schizophrenia.

methodAntepartum and intrapartum features were examined in 20 adults with 22qDS-schizophrenia and three comparison groups: newborn encephalopathy (n = 164) and healthy newborn controls (n = 400) from Badawi et al.'s (Br Med J 1998, 317: 1549) study, and 16 non-psychotic 22qDS adults (22qDS-NP).

resultsPostmaturity (OR 13.0, 95% CI 3.95, 42.77; P < 0.001) and SGA (OR 3.59, 95% CI 1.23, 10.5; P = 0.03) were more prevalent in 22qDS-SZ than controls. Postmaturity was non-significantly more prevalent in 22qDS-SZ than in newborn encephalopathy (P = 0.06) or 22qDS-NP (P = 0.2). SGA showed similar rates in the two 22qDS groups and newborn encephalopathy, but was more prevalent in 22qDS-NP than controls (P = 0.05).

conclusionThe results suggest that postmaturity may be associated with expression of schizophrenia in a 22qDS subtype of schizophrenia. SGA may be a non-specific marker of neurodevelopmental disturbance.

Indexed as

Chromosome DeletionInfant, PostmatureAdultBirth WeightBrain DiseasesCase-Control StudiesChromosomes, Human, Pair 22FemaleHumansInfant, NewbornMaleRisk FactorsSchizophrenia

Identifiers

PMID12956826
PMCPMC3152563
OpenAlexW2093881827

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.