Evidence map›Paper›PMID 40646741›Full record

ArticleAnimals : an open access journal from MDPI2025

Two Cases of Chromosome 27 Trisomy in Horses Detected Using Illumina BeadChip Genotyping.

Cliona A Ryan, Donagh P Berry, Monika Bugno-Poniewierska, Mary-Kate Burke, Terje Raudsepp, Sonja Egan, Jennifer L Doyle

Abstract read
In one paragraph

Article in Animals : an open access journal from MDPI, 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

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.

  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.

Cliona A RyanTeagasc, Moorepark, Fermoy, P61 P302 Co. Cork, Ireland.ORCID 0000-0001-6708-9669
Donagh P BerryTeagasc, Moorepark, Fermoy, P61 P302 Co. Cork, Ireland.ORCID 0000-0003-4349-1447
Monika Bugno-PoniewierskaDepartment of Animal Reproduction, Anatomy and Genomics, University of Agriculture in Krakow, Mickiewicza 24/28 Av., 30-059 Kraków, Poland.ORCID 0000-0001-7537-6641
Mary-Kate BurkeDepartment of Veterinary Medicine, School of Science and Computing, SETU, X91 CF21 Co. Waterford, Ireland.ORCID 0009-0003-5322-3814
Terje RaudseppDepartment of Veterinary Integrative Biosciences, Texas A&M University, College Station, TX 77840, USA.ORCID 0000-0003-2276-475X
Sonja EganHorse Sport Ireland, Beech House, Millennium Park, Naas, W91 TK7N Co. Kildare, Ireland.ORCID 0000-0003-2503-2298
Jennifer L DoyleHorse Sport Ireland, Beech House, Millennium Park, Naas, W91 TK7N Co. Kildare, Ireland.ORCID 0000-0001-5247-4660

Funding

Department of Agriculture 21/RC/10303_P2 (VistaMilk)
6 · The paper itself

Abstract

Autosomal trisomy, a genetic disorder characterized by the presence of an extra autosome, is a rare but important chromosomal abnormality in horses, often associated with infertility, developmental abnormalities, and reduced life expectancy. This study represents the largest population-level screening for autosomal trisomy in horses; the analysis used single nucleotide polymorphism (SNP) panel genotype intensity data from 17,078 horses, 6601 of which were juveniles (i.e., ≤12 months of age) when genotyped. Using methodologies adapted from similar screening studies in cattle, the only aneuploidy detected was trisomy 27 in two juvenile male Irish Sport Horses (ISH) (0.03% prevalence among juveniles or 0.01% prevalence in the overall population). One ISH colt was cytogenetically confirmed and displayed no overt external phenotypic abnormalities, while cytogenetics was not undertaken on the other ISH colt, nor was it phenotypically assessed. Parentage analysis revealed that one ISH colt inherited two different copies of chr27 from the sire, demonstrating heterodisomy, likely due to a nondisjunction event during meiosis I in the sire. The other ISH colt inherited two different copies of chr27 from the dam, also indicating heterodisomy; the dam was 23 years of age when the colt was born. Based on the observed prevalence of autosomal trisomy, it can be estimated that at least 3 foals per 10,000 live births are likely to have autosomal trisomy. Though, given that only 74 (i.e., 0.004%) of horses were genotyped within a month of birth, this is likely an underestimate. The economic consequence of undiagnosed trisomy in high-value breeding horses that are potentially infertile could be substantial. As horse genotyping for parentage verification and discovery is transitioning to medium-density single nucleotide polymorphism panels, routine genomic screening for autosomal aneuploidy could be readily undertaken and potentially should form a standard screening prerequisite along with other genetic defects at horse sales. Currently, thoroughbred horses registered for racing are not genotyped, and only a limited number of sport horse studbooks are using SNP genotyping. This highlights an opportunity for those already genotyping to expand their support for breeders through low-cost, high-value chromosomal screening at the time of registration rather than incurring additional costs over the horse's life cycle to determine the root cause of certain phenotypes owing to the undiagnosed trisomy.

Indexed as

aneuploidycongenital abnormalitiesDown syndromeFISHhorseinfertilitykaryotypingneurologic disordersSNPtrisomy

Identifiers

PMID40646741
PMCPMC12248643

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Registered trials

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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.