Evidence map›Paper›PMID 36833311›Full record

ArticleGenes2023

Multiple Genetic Loci Associated with Pug Dog Thoracolumbar Myelopathy.

Gustaf Brander, Cecilia Rohdin, Matteo Bianchi, Kerstin Bergvall, Göran Andersson, Ingrid Ljungvall, Karin Hultin Jäderlund, Jens Häggström, Åke Hedhammar, Kerstin Lindblad-Toh and 1 more

Open access · goldAbstract read
In one paragraph

Article in Genes, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Review
  3. Genomic analyses identify 15 risk loci and revealProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Article
  5. 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

11 authors at 4 institutions in 3 countries.

Gustaf BranderScience for Life Laboratory, Department of Medical Biochemistry and Microbiology, Uppsala University, 751 23 Uppsala, Sweden.ORCID 0000-0002-9549-4909
Cecilia RohdinDepartment of Clinical Sciences, Swedish University of Agricultural Sciences, 750 07 Uppsala, Sweden.
Matteo BianchiScience for Life Laboratory, Department of Medical Biochemistry and Microbiology, Uppsala University, 751 23 Uppsala, Sweden.
Kerstin BergvallDepartment of Clinical Sciences, Swedish University of Agricultural Sciences, 750 07 Uppsala, Sweden.
Göran AnderssonDepartment of Animal Breeding and Genetics, Swedish University of Agricultural Sciences, 750 07 Uppsala, Sweden.ORCID 0000-0001-5131-3144
Ingrid LjungvallDepartment of Clinical Sciences, Swedish University of Agricultural Sciences, 750 07 Uppsala, Sweden.
Karin Hultin JäderlundDepartment of Companion Animal Clinical Sciences, Norwegian University of Life Sciences, N-1432 Ås, Norway.
Jens HäggströmDepartment of Clinical Sciences, Swedish University of Agricultural Sciences, 750 07 Uppsala, Sweden.ORCID 0000-0003-3402-023X
Åke HedhammarDepartment of Clinical Sciences, Swedish University of Agricultural Sciences, 750 07 Uppsala, Sweden.
Kerstin Lindblad-TohScience for Life Laboratory, Department of Medical Biochemistry and Microbiology, Uppsala University, 751 23 Uppsala, Sweden.ORCID 0000-0001-8338-0253
Katarina TengvallScience for Life Laboratory, Department of Medical Biochemistry and Microbiology, Uppsala University, 751 23 Uppsala, Sweden.
Swedish University of Agricultural Sciences · SEBroad Institute · USUppsala University · SENorwegian University of Life Sciences · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pug dogs with thoracolumbar myelopathy (PDM) present with a specific clinical phenotype that includes progressive pelvic limb ataxia and paresis, commonly accompanied by incontinence. Vertebral column malformations and lesions, excessive scar tissue of the meninges, and central nervous system inflammation have been described. PDM has a late onset and affects more male than female dogs. The breed-specific presentation of the disorder suggests that genetic risk factors are involved in the disease development. To perform a genome-wide search for PDM-associated loci, we applied a Bayesian model adapted for mapping complex traits (BayesR) and a cross-population extended haplotype homozygosity test (XP-EHH) in 51 affected and 38 control pugs. Nineteen associated loci (harboring 67 genes in total, including 34 potential candidate genes) and three candidate regions under selection (with four genes within or next to the signal) were identified. The multiple candidate genes identified have implicated functions in bone homeostasis, fibrotic scar tissue, inflammatory responses, or the formation, regulation, and differentiation of cartilage, suggesting the potential relevance of these processes to the pathogenesis of PDM.

Indexed as

Bone Diseases, DevelopmentalSpinal Cord DiseasesAnimalsBayes TheoremCicatrixDogsFemaleGenetic LociMaleThoracic VertebraebayesianBayesRbone homeostasiscartilagedog geneticsfibrotic scar tissueGWASinflammatory responsemyelopathypugselectionXP-EHH

Identifiers

PMID36833311
PMCPMC9957375
OpenAlexW4318778060

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.