Evidence map›Paper›PMID 32828613›Full record

ArticleSchizophrenia research2020

Common mechanisms for type 2 diabetes and psychosis: Findings from a prospective birth cohort.

Benjamin I Perry, Hannah J Jones, Tom G Richardson, Stan Zammit, Nicholas J Wareham, Glyn Lewis, Peter B Jones, Golam M Khandaker

Open access · hybridAbstract read
In one paragraph

Article in Schizophrenia research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 16% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
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  3. Article
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  5. Article
  6. Genomic insights into the comorbidity between type 2 diabetes and schizophrenia.medRxiv : the preprint server for health sciences · 2023
    Article
  7. 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

8 authors at 4 institutions in 1 country.

Benjamin I PerryDepartment of Psychiatry, University of Cambridge School of Clinical Medicine, Cambridge, England, UK; Cambridgeshire and Peterborough NHS Foundation Trust, Cambridge, England, UK. Electronic address: bip20@medschl.cam.ac.uk.
Hannah J JonesCentre for Academic Mental Health, Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, England, UK; NIHR Biomedical Research Centre, University Hospitals Bristol NHS Foundation Trust and University of Bristol, Bristol, UK.
Tom G RichardsonMRC Integrative Epidemiology Unit, Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, England, UK.
Stan ZammitCentre for Academic Mental Health, Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, England, UK; NIHR Biomedical Research Centre, University Hospitals Bristol NHS Foundation Trust and University of Bristol, Bristol, UK; MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, Wales, UK.
Nicholas J WarehamMRC Epidemiology Unit, University of Cambridge School of Clinical Medicine, Cambridge, England, UK.
Glyn LewisDivision of Psychiatry, University College London, London, England, UK.
Peter B JonesDepartment of Psychiatry, University of Cambridge School of Clinical Medicine, Cambridge, England, UK; Cambridgeshire and Peterborough NHS Foundation Trust, Cambridge, England, UK.
Golam M KhandakerDepartment of Psychiatry, University of Cambridge School of Clinical Medicine, Cambridge, England, UK; Cambridgeshire and Peterborough NHS Foundation Trust, Cambridge, England, UK.
University of Cambridge · GBUniversity Hospitals Bristol NHS Foundation Trust · GBUniversity College London · GBUniversity of Bristol · GB

Funding

Department of Health DRF-2018-11-ST2-018Medical Research Council G0701503Medical Research Council G9815508Medical Research Council MC_PC_15018Medical Research Council MC_PC_17213Medical Research Council MC_PC_19009Medical Research Council MC_UU_12015/1Medical Research Council MR/L010305/1Medical Research Council MR/M006727/1Medical Research Council MR/S003886/1Wellcome Trust 201486/Z/16/Z
6 · The paper itself

Abstract

backgroundPsychosis and type 2 diabetes mellitus (T2DM) are commonly comorbid and may share pathophysiologic mechanisms. To investigate shared genetic variation and inflammation as potential common mechanisms, we tested: (i) associations between genetic predisposition for T2DM and psychotic experiences and psychotic disorder in young adults; (ii) the association between genetic predisposition for schizophrenia and insulin resistance (IR), a precursor of T2DM; and (iii) whether these associations are mediated by childhood inflammation.

methodsPsychotic experiences (PEs), psychotic disorder and IR were assessed at age 18. Polygenic risk scores (PRS) for T2DM and schizophrenia were derived based on large genome-wide association studies. Associations between PRS and psychotic/IR outcomes were assessed using regression analysis based on 3768 ALSPAC birth cohort participants with complete data. Inflammatory markers C-reactive protein (CRP) and interleukin 6 (IL-6) measured at age 9 were used in regression and mediation analyses.

resultsGenetic predisposition for T2DM was associated with PEs (adjusted OR = 1.21; 95% CI, 1.01-1.45) and psychotic disorder (adjusted OR = 1.51; 95% CI, 1.04-2.03) at age 18 in a linear dose-response fashion. Genetic predisposition for schizophrenia was weakly associated with IR (adjusted OR = 1.10; 95% C·I, 0.99-1.22) at age 18. The association between genetic risk for T2DM and PEs was partly mediated by childhood CRP (p = .040).

conclusionsComorbidity between psychosis and T2DM may be partly underpinned by shared genes and inflammation. A summation of minor genetic variation representing lifetime risk for T2DM at conception may predispose individuals to psychosis in adulthood by influencing physiologic changes, such as low-grade inflammation, detectable as early as childhood.

Indexed as

Diabetes Mellitus, Type 2Psychotic DisordersSchizophreniaAdolescentAdultChildGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansProspective StudiesYoung AdultALSPACDiabetes mellitusPolygenic riskPsychosisSchizophrenia

Identifiers

PMID32828613
PMCPMC7758839
OpenAlexW3061292538

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.