Evidence map›Paper›PMID 40420218›Full record

ArticleActa veterinaria Scandinavica2025

Genetic analyses of lumbosacral transitional vertebra and hip dysplasia in nine dog breeds in Norway.

Jon Andre Berg, Bente Kristin Sævik, Cathrine Trangerud, Per Madsen, Frode Lingaas

Abstract read
In one paragraph

Article in Acta veterinaria Scandinavica, 2025. 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
–field-weighted citation impact
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

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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.

  1. 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

5 authors.

Jon Andre BergDepartment of Preclinical Sciences and Pathology, Faculty of Veterinary Medicine, Norwegian University of Life Sciences, Oluf Thesens Vei 30, Ås, 1432, Norway. jon.andre.berg@nmbu.no.ORCID http://orcid.org/0000-0001-5344-755X
Bente Kristin SævikAniCura Jeløy Dyresykehus, Varnaveien 43d, Moss, 1526, Norway.
Cathrine TrangerudDepartment of Companion Animal Clinical Sciences, Faculty of Veterinary Medicine, Norwegian University of Life Sciences, Oluf Thesens Vei 30, Ås, Norway.
Per MadsenCenter for Quantitative Genetics and Genomics, Aarhus University, Aarhus, DK-8000, Denmark.
Frode LingaasDepartment of Preclinical Sciences and Pathology, Faculty of Veterinary Medicine, Norwegian University of Life Sciences, Oluf Thesens Vei 30, Ås, 1432, Norway.

Funding

Norges Forskningsråd 310847
6 · The paper itself

Abstract

backgroundA lumbosacral transitional vertebra (LTV) is a congenital anomaly with reported prevalences ranging from 0 to 67% in different dog breeds, implying possible genetic differences. LTV has been associated with canine hip dysplasia (CHD) and degenerative lumbosacral stenosis (DLSS). Genetic parameters, including heritability estimates, are important for understanding the genetic influence on specific traits and for evaluating the effectiveness of possible genetic selection in reducing the prevalence of disorders. This study aimed to determine the heritability of LTV in nine dog breeds in Norway and estimate the genetic correlation with CHD.

resultsThe heritability estimates for LTV across the nine breeds ranged from low to moderate (0.056-0.314), while the heritability estimates for CHD were moderate to high (0.254-0.580). The estimates of genetic correlations between the two traits were mostly non-significant and varied strongly among breeds in size and direction.

conclusionsThis study indicated that genetic factors influence LTV in several breeds and that there is a potential to reduce the prevalence by genetic selection, even if the heritability estimates of LTV ranged from low to moderate. The heritability estimates of CHD were within the range reported earlier, ranging from moderate to high. There was no general indication of a genetic correlation between LTV and CHD across breeds.

Indexed as

Dog DiseasesHip Dysplasia, CanineLumbar VertebraeAnimalsDogsFemaleLumbosacral RegionMaleNorwayCanineCHDHeritabilityInheritanceLTVTransitional vertebra

Identifiers

PMID40420218
PMCPMC12107804

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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.