Evidence map›Paper›PMID 29204916›Full record

ArticleJournal of endocrinological investigation2018

RNASEH1 gene variants are associated with autoimmune type 1 diabetes in Colombia.

N Pineda-Trujillo, A Rodríguez-Acevedo, A Rodríguez, A Ruíz-Linares, G Bedoya, A Rivera, J-M Alfaro

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of endocrinological investigation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 26% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. 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

7 authors at 2 institutions in 2 countries.

N Pineda-TrujilloGrupo Mapeo Genetico, Departamento de Pediatria, Facultad de Medicina, Universidad de Antioquia, Medellín, 050010470, Colombia. nicolas.pineda@udea.edu.co.
A Rodríguez-AcevedoGrupo Mapeo Genetico, Departamento de Pediatria, Facultad de Medicina, Universidad de Antioquia, Medellín, 050010470, Colombia.
A RodríguezGrupo Mapeo Genetico, Departamento de Pediatria, Facultad de Medicina, Universidad de Antioquia, Medellín, 050010470, Colombia.
A Ruíz-LinaresDepartment of Biology, University College London, London, WC1E 6BT, UK.
G BedoyaGENMOL, Instituto de Biologia, Universidad de Antioquia, Medellín, 1226, Colombia.
A RiveraGrupo Mapeo Genetico, Departamento de Pediatria, Facultad de Medicina, Universidad de Antioquia, Medellín, 050010470, Colombia.
J-M AlfaroGrupo Mapeo Genetico, Departamento de Pediatria, Facultad de Medicina, Universidad de Antioquia, Medellín, 050010470, Colombia.
Universidad de Antioquia · COUniversity College London · GB

Funding

CODI-Universidad de Antioquia 8704-2449COLCIENCIAS 1115-343-19156
6 · The paper itself

Abstract

backgroundIn a previous work, we found linkage and association of type 1 diabetes (T1D) to a 12 known gene region at chromosome 2p25 in Colombian families. Here, we present further work on this candidate region. MATERIALS AND

methodsSeventeen SNPs located on the 12 candidate genes, in 100 familial trios set, were tested by ARMS-tetraprimer-PCR or PCR-RFLP. Five extra SNPs in the vicinity of rs10186193 were typed. A replica phase included 97 novel familial trios, in whom diabetes-related auto-antibodies (AABs) were tested in sera of the patients. In addition to transmission disequilibrium tests, haplotype analyses were carried out using the unphased software.

resultsSNP rs10186193 (at RNASEH1 gene) showed association with T1D (P = 0.005). The additional five SNPs revealed that rs7607888 (P = 2.03 × 10

conclusionIn conclusion, our analyses suggest that RNASEH1 gene variants associate with susceptibility/protection to T1D in Colombia.

Indexed as

Polymorphism, Single NucleotideAdultChildColombiaDiabetes Mellitus, Type 1FamilyFemaleGene FrequencyGenetic Association StudiesGenetic Predisposition to DiseaseHaplotypesHumansLinkage DisequilibriumMalePolymorphism, Restriction Fragment LengthRibonuclease HRibonuclease Hribonuclease HIAssociation studyColombiaNovel locusRNASEH1 geneSpecial populationT1D

Identifiers

PMID29204916
OpenAlexW2771143358

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.