Evidence map›Paper›PMID 27481827›Full record

ArticleSchizophrenia bulletin2017

Testing the Validity of Taxonic Schizotypy Using Genetic and Environmental Risk Variables.

Sarah E Morton, Kirstie J M O'Hare, Jaimee L K Maha, Max P Nicolson, Liana Machado, Ruth Topless, Tony R Merriman, Richard J Linscott

Open access · bronzeAbstract read
In one paragraph

Article in Schizophrenia bulletin, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

17 citing papers in PubMed, 38 citations in OpenAlex.

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  8. Annales medico-psychologiques · 2021
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  12. Review
  13. Progress in achieving quantitative classification of psychopathology.World psychiatry : official journal of the World Psychiatric Association (WPA) · 2018
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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

8 authors at 1 institution in 2 countries.

Sarah E MortonDepartment of Psychology, University of Otago, Dunedin, New Zealand.
Kirstie J M O'HareDepartment of Psychology, University of Otago, Dunedin, New Zealand.
Jaimee L K MahaDepartment of Psychology, University of Otago, Dunedin, New Zealand.
Max P NicolsonDepartment of Psychology, University of Otago, Dunedin, New Zealand.
Liana MachadoDepartment of Psychology, University of Otago, Dunedin, New Zealand.
Ruth ToplessDepartment of Biochemistry, University of Otago, Dunedin, New Zealand.
Tony R MerrimanDepartment of Biochemistry, University of Otago, Dunedin, New Zealand.
Richard J LinscottDepartment of Psychology, University of Otago, Dunedin, New Zealand.
University of Otago · NZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Meehl regarded schizotypy as a categorial liability for schizophrenia that is the product of genes, environment, and gene-environment interactions. We sought to test whether schizophrenia-related genotypes and environmental risk factors predict membership in classes defined by taxometric analyses of positive (cognitive-perceptual), negative (interpersonal), and disorganized schizotypy. Methods: Participants (n = 500) completed the Schizotypal Personality Questionnaire (SPQ) and provided information on the following risk factors: cannabis use, pregnancy and obstetric complications, social adjustment, and family history of psychosis. Saliva samples were obtained so that the frequency of single-nucleotide polymorphism (SNP) alleles associated with risk for developing schizophrenia could be determined. Genotyped SNPs were rs1625579 (MIR137), rs7004633 (MMP16), rs7914558 (CNNM2), and rs12966547 (CCDC68). Sets of SPQ items were subject to multiple coherent cut kinetic (CCK) analyses, including mean-above-minus-below-a-cut, maximum covariance, maximum eigenvalue, and latent modes analyses. Results: CCK analyses indicated latent taxonicity of schizotypy across the 3 item sets. The cognitive-perceptual class had a base rate of 25%, and membership was predicted by the rs7004633 SNP (odds ratio = 2.33, 95% confidence interval = 1.15-4.72 in adjusted analyses). Poor social adjustment predicted memberships in the interpersonal (16%) and disorganized (21%) classes. Classes were found not to be mutually exclusive. Conclusions: Schizotypy is taxonic and schizotypy class membership is predicted by genetic and environmental factors that predict schizophrenia. The findings hold the promise that a more complete understanding of schizotypy as a schizophrenia liability state will come from investigation of other genes and environmental factors associated with schizophrenia.

Indexed as

Interpersonal RelationsSocial AdjustmentAdultCation Transport ProteinsCyclinsFemaleHumansMaleMatrix Metalloproteinase 16MicroRNAsPsychotic DisordersRisk FactorsSchizophreniaSchizotypal Personality DisorderTumor Suppressor ProteinsYoung AdultCation Transport ProteinsCCDC68 protein, humanCNNM2 protein, humanCyclinsMatrix Metalloproteinase 16MicroRNAsMIRN137 microRNA, humanMMP16 protein, humanTumor Suppressor Proteinsclass structuremaximum covariance analysisMMP16psychosisschizophreniasocial adjustmenttaxometrics

Identifiers

PMID27481827
PMCPMC5464059
OpenAlexW2501818423

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.