Evidence map›Paper›PMID 28534863›Full record

ArticleGenes2017

The Clinical Course of Patients with Preschool Manifestation of Type 1 Diabetes Is Independent of the HLA DR-DQ Genotype.

Christina Reinauer, Joachim Rosenbauer, Christina Bächle, Christian Herder, Michael Roden, Sian Ellard, Elisa De Franco, Beate Karges, Reinhard W Holl, Jürgen Enczmann and 1 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Genes, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 24% 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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 2 countries.

Christina ReinauerDepartment of General Pediatrics, Neonatology and Pediatric Cardiology, University Children's Hospital, Heinrich Heine University Düsseldorf, 40225 Düsseldorf, Germany. Christina.reinauer@med.uni-duesseldorf.de.
Joachim RosenbauerInstitute for Biometrics and Epidemiology, German Diabetes Center, Leibniz Center for Diabetes Research at Heinrich Heine University Düsseldorf, 40225 Düsseldorf, Germany. Joachim.Rosenbauer@ddz.uni-duesseldorf.de.
Christina BächleInstitute for Biometrics and Epidemiology, German Diabetes Center, Leibniz Center for Diabetes Research at Heinrich Heine University Düsseldorf, 40225 Düsseldorf, Germany. Christina.Baechle@ddz.uni-duesseldorf.de.
Christian HerderGerman Center for Diabetes Research (DZD), 85764 München-Neuherberg, Germany. christian.herder@ddz.uni-duesseldorf.de.
Michael RodenGerman Center for Diabetes Research (DZD), 85764 München-Neuherberg, Germany. Michael.Roden@ddz.uni-duesseldorf.de.
Sian EllardInstitute of Biomedical and Clinical Science, University of Exeter Medical School, Exeter EX2 5DW, UK. sian.ellard@nhs.net.
Elisa De FrancoInstitute of Biomedical and Clinical Science, University of Exeter Medical School, Exeter EX2 5DW, UK. E.De-Franco@exeter.ac.uk.
Beate KargesGerman Center for Diabetes Research (DZD), 85764 München-Neuherberg, Germany. bkarges@ukaachen.de.
Reinhard W HollGerman Center for Diabetes Research (DZD), 85764 München-Neuherberg, Germany. reinhard.holl@uni-ulm.de.
Jürgen EnczmannInstitute for Transplantation Diagnostics and Cell Therapeutics, Heinrich Heine University Düsseldorf, 40225 Düsseldorf, Germany. Juergen.Enczmann@med.uni-duesseldorf.de.
Thomas MeissnerDepartment of General Pediatrics, Neonatology and Pediatric Cardiology, University Children's Hospital, Heinrich Heine University Düsseldorf, 40225 Düsseldorf, Germany. Thomas.meissner@med.uni-duesseldorf.de.
Deutsches Diabetes-Zentrum e.V. · DEHeinrich Heine University Düsseldorf · DEUniversity of Exeter · GBUniversität Ulm · DE

Funding

Wellcome Trust
6 · The paper itself

Abstract

introductionMajor histocompatibility complex class II genes are considered major genetic risk factors for autoimmune diabetes. We analysed Human Leukocyte Antigen (HLA)

methodsIntermediate resolution

resultsGenetic variability was low, 44.6% (104/233) of early-onset T1D patients carried the highest-risk genotype

conclusionIn this study, we saw no evidence for a different clinical course of early-onset T1D based on the HLA genotype within the first ten years after manifestation.

Indexed as

autoimmunityC-peptidediabetes mellitushuman leukocyte antigenMHC II

Identifiers

PMID28534863
PMCPMC5448020
OpenAlexW2615254379

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.