Evidence map›Paper›PMID 36411452›Full record

ArticleActa veterinaria Scandinavica2022

Heritability estimates of distichiasis in Staffordshire bull terriers using pedigrees and genome-wide SNP data.

Dina Joergensen, Per Madsen, Ernst-Otto Ropstad, Frode Lingaas

Open access · goldAbstract read
In one paragraph

Article in Acta veterinaria Scandinavica, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 27% 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.

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

4 authors at 3 institutions in 2 countries.

Dina JoergensenDepartment of Preclinical Sciences and Pathology, Faculty of Veterinary Medicine, Norwegian University of Life Sciences, NMBU Veterinærhøgskolen, Oluf Thesens Vei 22, 1433, Ås, Norway. dijo@nmbu.no.ORCID http://orcid.org/0000-0002-8215-3355
Per MadsenCenter for Quantitative Genetics and Genomics, Aarhus University, 8830, Tjele, Denmark.
Ernst-Otto RopstadEvidensia, Oslo Dyresykehus, Ensjøveien 14, 0655, Oslo, Norway.
Frode LingaasDepartment of Preclinical Sciences and Pathology, Faculty of Veterinary Medicine, Norwegian University of Life Sciences, NMBU Veterinærhøgskolen, Oluf Thesens Vei 22, 1433, Ås, Norway.
Norwegian University of Life Sciences · NOAarhus University · DKEvidensia Oslo dyresykehus · NO

Funding

Agria Djurförsäkring/SKK N2021-0020
6 · The paper itself

Abstract

backgroundDistichiasis is the most frequently recorded eye disorder in the Norwegian Staffordshire bull terrier (SBT). The condition is often mild but can, in severe cases, lead to pain and blindness. The current study's main purpose was to estimate the heritability based on pedigree information as well as single nucleotide polymorphisms (SNPs) to evaluate whether it is realistic to reduce the frequency by systematic breeding. The majority of the dogs had only one examination as a young puppy. To evaluate whether this early screening gave a reliable representation of the disease burden in the population, we compared the diagnosis in puppies and adult dogs.

resultsOur material consisted of data from 4177 dogs with an overall prevalence of distichiasis of 8.38% (CI 7.56-9.26). The prevalence in puppies examined around eight weeks of age was significantly lower than in dogs examined after 52 weeks (2.87%, CI 2.29-3.54 versus 18.72%, CI 16.71-20.87). The heritability was estimated in dogs examined after 52 weeks. We used both pedigree (1391 dogs) and genotype (498 dogs) information for the estimates. The pedigree-based heritability was ~ 0.22 (on the underlying scale ~ 0.48), while the genomic-based heritability (on the underlying scale) was ~ 0.47, and ~ 0.37 when excluding close relatives with equal affection status.

conclusionsScreening for distichiasis in puppies before eight weeks of age is not sufficient to give an accurate estimate of the prevalence, and an additional examination after one year is recommended. The heritability of distichiasis is medium to high, showing that it should be possible to reduce the prevalence by selective breeding.

Indexed as

Polymorphism, Single NucleotideAnimalsDogsPedigreeAberrant eyelashCanineGenomic heritabilityOcular disorderSNP-based heritability

Identifiers

PMID36411452
PMCPMC9677626
OpenAlexW4309662817

What OpenQuestion holds

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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.