Evidence map›Paper›PMID 42127997›Full record

ArticleJournal of animal science2026

Unraveling the genomic architecture of hock conformation defects in Pura Raza Española horses.

Nora Laseca, Antonio Molina, Chiraz Ziadi, Davinia I Perdomo-Gonzalez, Mercedes Valera

Abstract read
In one paragraph

Article in Journal of animal science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Nora LasecaDepartment of Agronomy, School of Agricultural Engineering, University of Seville, Seville, 41013, Spain.ORCID 0000-0003-3753-6725
Antonio MolinaDepartment of Genetics, University of Cordoba, Córdoba, 14014, Spain.ORCID 0000-0002-9566-6600
Chiraz ZiadiDepartment of Genetics, University of Cordoba, Córdoba, 14014, Spain.ORCID 0000-0002-1866-7028
Davinia I Perdomo-GonzalezDepartment of Animal Production, Faculty of Veterinary Medicine, Complutense University of Madrid, Madrid, 28040, Spain.ORCID 0000-0003-2618-105X
Mercedes ValeraDepartment of Agronomy, School of Agricultural Engineering, University of Seville, Seville, 41013, Spain.ORCID 0000-0003-1742-550X

Funding

COFINANC. RRHH JDC2023-051241-IEuropean Social Fund Plus (FSE+)Fundaciónde Investigación de la Universidad de Sevilla and the Real Asociación Nacional de Criadores de Caballos de Pura Raza Española)Genetic evaluation of Pura Raza EspañolaPR202304988Universidad de Sevilla/CBUA
6 · The paper itself

Abstract

Conformational traits define a horse's shape and morphology, heavily influencing its functionality, sport performance, health, and appearance, making conformation a critical selection criterion in horse breeding. However, the genomic basis of conformational defects, specifically those affecting the hock, remains largely unexplored. This research aimed to identify the genomic regions associated with hock defects using a large cohort of Pura Raza Española (PRE) horses. A total of 58,930 horses were evaluated for hock angle, with 4,122 genotyped on high- or medium-density arrays. For this purpose, weighed single-step genomic REML analysis methodology was used with the hock evaluation assessed as a continuous variable (lateral view hock defect, LVHD, and rear-view hock defect, RVHD) and divided into two different opposite defects: closed and open and convergent and divergent, respectively (multinomial approach). Some deviation from the optimum hock angle was observed in 49,386 horses, of which 10.1% were evaluated as having a severe or very severe defect. The most prevalent hock defect in the PRE population evaluated was open hock (6.67% considered severe or very severe), while the least prevalent was closed hock (0.2%). The estimated heritability for the continuously evaluated traits was 0.18 for LVHD and 0.25 for RVHD, while the estimated heritability of the traits evaluated with a multinomial approach ranged from 0.25 to 0.42 for open and divergent defects, respectively. A genome-wide association study revealed eight genomic regions associated with hock defects. In these, 17 genes related to musculoskeletal diseases, bone malformations, joint disorders, cartilage defects, or bone fragility were identified. These findings could support the development of selective breeding strategies aimed at reducing conformational defects in the hock of the PRE and related breeds. Furthermore, they provide insight into the genetic and molecular mechanisms involved in the occurrence of conformation defects. However, further studies are needed to shed further light on these conformational defects in the equine species.

Indexed as

Horse DiseasesAnimalsBreedingFemaleGenotypeHorsesMaleequineGWASlimbsmorphological defectswssGREML

Identifiers

PMID42127997
PMCPMC13220149

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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.