Evidence map›Paper›PMID 30028859›Full record

ArticlePloS one2018

Genome-wide association studies of inflammatory bowel disease in German shepherd dogs.

Atiyeh Peiravan, Francesca Bertolini, Max F Rothschild, Kenneth W Simpson, Albert E Jergens, Karin Allenspach, Dirk Werling

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. 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, 44 citations in OpenAlex.

  1. Review
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  6. An initial genome-wide investigation of protein-losing enteropathy in Gordon setters: Exploratory observations.Canadian journal of veterinary research = Revue canadienne de recherche veterinaire · 2021
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  7. Article
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  9. Natural Infection withmSphere · 2020
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  12. Review
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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

7 authors at 3 institutions in 2 countries.

Atiyeh PeiravanDepartment of Pathology and Pathogen Biology, Royal Veterinary College, University of London, North Mymms, United Kingdom.ORCID 0000-0002-7846-6690
Francesca BertoliniDepartment of Animal Science, Iowa State University, Ames, Iowa, United States of America.
Max F RothschildDepartment of Animal Science, Iowa State University, Ames, Iowa, United States of America.
Kenneth W SimpsonCollege of Veterinary Medicine, Cornell University, Ithaca, NY, United States of America.
Albert E JergensCollege of Veterinary Medicine, Iowa State University, Ames, Iowa, United States of America.
Karin AllenspachCollege of Veterinary Medicine, Iowa State University, Ames, Iowa, United States of America.
Dirk WerlingDepartment of Pathology and Pathogen Biology, Royal Veterinary College, University of London, North Mymms, United Kingdom.
Iowa State University · USUniversity of London · GBCornell University · US

Funding

Biotechnology and Biological Sciences Research Council BB/J01236X/1
6 · The paper itself

Abstract

Canine Inflammatory Bowel Disease (IBD) is considered a multifactorial disease caused by complex interactions between the intestinal immune system, intestinal microbiota and environmental factors in genetically susceptible individuals. Although IBD can affect any breed, German shepherd dogs (GSD) in the UK are at increased risk of developing the disease. Based on previous evidence, the aim of the present study was to identify single nucleotide polymorphisms (SNPs), which may confer genetic susceptibility or resistance to IBD using a genome-wide association study (GWAS). Genomic DNA was extracted from EDTA blood or saliva samples of 96 cases and 98 controls. Genotyping of cases and controls was performed on the Canine Illumina HD SNP array and data generated was analyzed using PLINK. Several SNPs and regions on chromosomes 7,9,11 and 13 were detected to be associated with IBD using different SNP-by-SNP association methods and FST windows approach. Searching one Mb up-and down-stream of the most significant SNPs, as identified by single SNP analysis as well as 200Kb before and after the start and the end position of the associated regions identified by FST windows approach, we identified 63 genes. Using a combination of pathways analysis and a list of genes that have been reported to be involved in human IBD, we identified 16 candidate genes potentially associated with IBD in GSD.

Indexed as

Genetic Predisposition to DiseaseGenome-Wide Association StudyAnimalsBiopsyDogsGenotyping TechniquesInflammatory Bowel DiseasesIntestinal MucosaPolymorphism, Single NucleotideUnited Kingdom

Identifiers

PMID30028859
PMCPMC6054420
OpenAlexW2884795428

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.