Evidence map›Paper›PMID 36302227›Full record

ArticleSchizophrenia bulletin2023

Cumulative Environmental Risk in Early Life: Associations With Schizotypy in Childhood.

Kirstie O'Hare, Oliver Watkeys, Tyson Whitten, Kimberlie Dean, Kristin R Laurens, Stacy Tzoumakis, Felicity Harris, Vaughan J Carr, Melissa J Green

Abstract read
In one paragraph

Article in Schizophrenia bulletin, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Kirstie O'HareDiscipline of Psychiatry and Mental Health, University of New South Wales, Sydney, Australia.
Oliver WatkeysDiscipline of Psychiatry and Mental Health, University of New South Wales, Sydney, Australia.
Tyson WhittenDiscipline of Psychiatry and Mental Health, University of New South Wales, Sydney, Australia.
Kimberlie DeanDiscipline of Psychiatry and Mental Health, University of New South Wales, Sydney, Australia.
Kristin R LaurensDiscipline of Psychiatry and Mental Health, University of New South Wales, Sydney, Australia.ORCID 0000-0002-3987-6486
Stacy TzoumakisSchool of Criminology and Criminal Justice, Griffith University, Southport, Australia.
Felicity HarrisDiscipline of Psychiatry and Mental Health, University of New South Wales, Sydney, Australia.
Vaughan J CarrDiscipline of Psychiatry and Mental Health, University of New South Wales, Sydney, Australia.
Melissa J GreenDiscipline of Psychiatry and Mental Health, University of New South Wales, Sydney, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and hypothesisPsychotic disorders are associated with a growing number of recognized environmental exposures. Cumulative exposure to multiple environmental risk factors in childhood may contribute to the development of different patterns of schizotypy evident in early life. Hypotheses were that distinct profiles of schizotypy would have differential associations with a cumulative score of environmental risk factors. STUDY

designWe prospectively examined the relationship between 19 environmental exposures (which had demonstrated replicated associations with psychosis) measured from the prenatal period through to age 11 years, and 3 profiles of schizotypy in children (mean age = 11.9 years, n = 20 599) that have been established in population data from the New South Wales-Child Development Study. Multinomial logistic regression was used to examine associations between membership in each of 3 schizotypy profiles (true schizotypy, introverted schizotypy, and affective schizotypy) and exposure to a range of 19 environmental risk factors for psychosis (both individually and summed as a cumulative environmental risk score [ERS]), relative to children showing no risk.

resultsAlmost all environmental factors were associated with at least 1 schizotypy profile. The cumulative ERS was most strongly associated with the true schizotypy profile (OR = 1.61, 95% CI = 1.52-1.70), followed by the affective (OR = 1.33, 95% CI = 1.28-1.38), and introverted (OR = 1.32, 95% CI = 1.28-1.37) schizotypy profiles.

conclusionsConsistent with the cumulative risk hypothesis, results indicate that an increased number of risk exposures is associated with an increased likelihood of membership in the 3 schizotypy profiles identified in middle childhood, relative to children with no schizotypy profile.

Indexed as

Psychotic DisordersSchizotypal Personality DisorderChildHumansLogistic ModelsPersonalityRisk Factorsenvironmentlatent profile analysispsychosisrisk scoreschizophrenia-spectrum disorders

Identifiers

PMID36302227
PMCPMC10016419

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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.