Evidence map›Paper›PMID 27156239›Full record

ArticleSchizophrenia research2016

Parental type 2 diabetes in patients with non-affective psychosis.

Brian J Miller, David R Goldsmith, Nina Paletta, Joyce Wong, Prianka Kandhal, Carmen Black, Mark Hyman Rapaport, Peter F Buckley

Open access · greenAbstract read
In one paragraph

Article in Schizophrenia research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

3 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Co-shared genetics and possible risk gene pathway partially explain the comorbidity of schizophrenia, major depressive disorder, type 2 diabetes, and metabolic syndrome.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2019
    Review
  3. Article
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 2 institutions in 1 country.

Brian J MillerDepartment of Psychiatry and Health Behavior, Augusta University, Augusta, GA, USA. Electronic address: brmiller@augusta.edu.
David R GoldsmithDepartment of Psychiatry and Behavioral Sciences, Emory University, Atlanta, GA, USA.
Nina PalettaMedical College of Georgia, Augusta University, Augusta, GA, USA.
Joyce WongMedical College of Georgia, Augusta University, Augusta, GA, USA.
Prianka KandhalMedical College of Georgia, Augusta University, Augusta, GA, USA.
Carmen BlackMedical College of Georgia, Augusta University, Augusta, GA, USA.
Mark Hyman RapaportDepartment of Psychiatry and Behavioral Sciences, Emory University, Atlanta, GA, USA.
Peter F BuckleyMedical College of Georgia, Augusta University, Augusta, GA, USA.
Augusta University · USEmory University · US

Funding

A Potential State and Relapse Predictive Marker in SchizophreniaK23MH098014 · NIMH · AUGUSTA UNIVERSITY · PI MILLER, BRIAN JAMES · 2012 to 2016
$921k
NIMH NIH HHS K23 MH098014
6 · The paper itself

Abstract

objectivePeople with schizophrenia have an increased risk of diabetes that may be independent of antipsychotics. Previous studies have explored the prevalence of a family history of type 2 diabetes (DM2) in schizophrenia. We hypothesized that parental DM2 is increased in probands with non-affective psychosis (NAP) compared to controls, and parental DM2 predicts comorbid diabetes in NAP, after controlling for potential confounders.

methodN=217 patients with NAP and N=67 controls were interviewed for a history of parental DM2. NAP was investigated as a predictor of parental DM2 in binary logistic regression models, controlling for age, sex, race, smoking, body mass index, socioeconomic status, and parental psychiatric history.

resultsThere was an increased prevalence of DM2 in the mother (30.0% vs 13.8%, p=0.013) and in either the mother or father (44.5% vs 24.6%, p=0.006) in patients with NAP versus controls. After accounting for potential confounders, NAP was associated with significant increased odds of parental DM2 (OR=2.80, 95% CI 1.08-7.23, p=0.034). Parental DM2 was also associated with increased odds of comorbid DM2 in NAP (OR=3.67, 95% CI 1.58-8.56, p=0.003).

conclusionsWe replicated an association of an increased prevalence of parental DM2 in patients with NAP. Parental DM2 was also an independent predictor of comorbid DM2 in these patients. These associations may be due to shared environmental or genetic risk factors, or gene by environment interactions. Given risks of incident diabetes with antipsychotic treatment, screening for parental DM2 status is germane to the clinical care of patients with NAP.

Indexed as

ParentsAdultBody Mass IndexComorbidityDiabetes Mellitus, Type 2FemaleGenetic Predisposition to DiseaseHumansLogistic ModelsMalePsychotic DisordersSmokingSocioeconomic FactorsDiabetesEpidemiologyFamily historyNon-affective psychosisSchizophrenia

Identifiers

PMID27156239
PMCPMC4958496
OpenAlexW2346090570

What OpenQuestion holds

Textmetadata
LicenceTDM
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.