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A genome-wide association study demonstrates significant genetic variation for fracture risk in Thoroughbred racehorses

BACKGROUND: Thoroughbred racehorses are subject to non-traumatic distal limb bone fractures that occur during racing and exercise. Susceptibility to fracture may be due to underlying disturbances in bone metabolism which have a genetic cause. Fracture risk has been shown to be heritable in several s...

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Autores principales: Blott, Sarah C, Swinburne, June E, Sibbons, Charlene, Fox-Clipsham, Laura Y, Helwegen, Maud, Hillyer, Lynn, Parkin, Tim DH, Newton, J Richard, Vaudin, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4008154/
https://www.ncbi.nlm.nih.gov/pubmed/24559379
http://dx.doi.org/10.1186/1471-2164-15-147
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author Blott, Sarah C
Swinburne, June E
Sibbons, Charlene
Fox-Clipsham, Laura Y
Helwegen, Maud
Hillyer, Lynn
Parkin, Tim DH
Newton, J Richard
Vaudin, Mark
author_facet Blott, Sarah C
Swinburne, June E
Sibbons, Charlene
Fox-Clipsham, Laura Y
Helwegen, Maud
Hillyer, Lynn
Parkin, Tim DH
Newton, J Richard
Vaudin, Mark
author_sort Blott, Sarah C
collection PubMed
description BACKGROUND: Thoroughbred racehorses are subject to non-traumatic distal limb bone fractures that occur during racing and exercise. Susceptibility to fracture may be due to underlying disturbances in bone metabolism which have a genetic cause. Fracture risk has been shown to be heritable in several species but this study is the first genetic analysis of fracture risk in the horse. RESULTS: Fracture cases (n = 269) were horses that sustained catastrophic distal limb fractures while racing on UK racecourses, necessitating euthanasia. Control horses (n = 253) were over 4 years of age, were racing during the same time period as the cases, and had no history of fracture at the time the study was carried out. The horses sampled were bred for both flat and National Hunt (NH) jump racing. 43,417 SNPs were employed to perform a genome-wide association analysis and to estimate the proportion of genetic variance attributable to the SNPs on each chromosome using restricted maximum likelihood (REML). Significant genetic variation associated with fracture risk was found on chromosomes 9, 18, 22 and 31. Three SNPs on chromosome 18 (62.05 Mb – 62.15 Mb) and one SNP on chromosome 1 (14.17 Mb) reached genome-wide significance (p < 0.05) in a genome-wide association study (GWAS). Two of the SNPs on ECA 18 were located in a haplotype block containing the gene zinc finger protein 804A (ZNF804A). One haplotype within this block has a protective effect (controls at 1.95 times less risk of fracture than cases, p = 1 × 10(-4)), while a second haplotype increases fracture risk (cases at 3.39 times higher risk of fracture than controls, p = 0.042). CONCLUSIONS: Fracture risk in the Thoroughbred horse is a complex condition with an underlying genetic basis. Multiple genomic regions contribute to susceptibility to fracture risk. This suggests there is the potential to develop SNP-based estimators for genetic risk of fracture in the Thoroughbred racehorse, using methods pioneered in livestock genetics such as genomic selection. This information would be useful to racehorse breeders and owners, enabling them to reduce the risk of injury in their horses.
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spelling pubmed-40081542014-05-03 A genome-wide association study demonstrates significant genetic variation for fracture risk in Thoroughbred racehorses Blott, Sarah C Swinburne, June E Sibbons, Charlene Fox-Clipsham, Laura Y Helwegen, Maud Hillyer, Lynn Parkin, Tim DH Newton, J Richard Vaudin, Mark BMC Genomics Research Article BACKGROUND: Thoroughbred racehorses are subject to non-traumatic distal limb bone fractures that occur during racing and exercise. Susceptibility to fracture may be due to underlying disturbances in bone metabolism which have a genetic cause. Fracture risk has been shown to be heritable in several species but this study is the first genetic analysis of fracture risk in the horse. RESULTS: Fracture cases (n = 269) were horses that sustained catastrophic distal limb fractures while racing on UK racecourses, necessitating euthanasia. Control horses (n = 253) were over 4 years of age, were racing during the same time period as the cases, and had no history of fracture at the time the study was carried out. The horses sampled were bred for both flat and National Hunt (NH) jump racing. 43,417 SNPs were employed to perform a genome-wide association analysis and to estimate the proportion of genetic variance attributable to the SNPs on each chromosome using restricted maximum likelihood (REML). Significant genetic variation associated with fracture risk was found on chromosomes 9, 18, 22 and 31. Three SNPs on chromosome 18 (62.05 Mb – 62.15 Mb) and one SNP on chromosome 1 (14.17 Mb) reached genome-wide significance (p < 0.05) in a genome-wide association study (GWAS). Two of the SNPs on ECA 18 were located in a haplotype block containing the gene zinc finger protein 804A (ZNF804A). One haplotype within this block has a protective effect (controls at 1.95 times less risk of fracture than cases, p = 1 × 10(-4)), while a second haplotype increases fracture risk (cases at 3.39 times higher risk of fracture than controls, p = 0.042). CONCLUSIONS: Fracture risk in the Thoroughbred horse is a complex condition with an underlying genetic basis. Multiple genomic regions contribute to susceptibility to fracture risk. This suggests there is the potential to develop SNP-based estimators for genetic risk of fracture in the Thoroughbred racehorse, using methods pioneered in livestock genetics such as genomic selection. This information would be useful to racehorse breeders and owners, enabling them to reduce the risk of injury in their horses. BioMed Central 2014-02-21 /pmc/articles/PMC4008154/ /pubmed/24559379 http://dx.doi.org/10.1186/1471-2164-15-147 Text en Copyright © 2014 Blott et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Research Article
Blott, Sarah C
Swinburne, June E
Sibbons, Charlene
Fox-Clipsham, Laura Y
Helwegen, Maud
Hillyer, Lynn
Parkin, Tim DH
Newton, J Richard
Vaudin, Mark
A genome-wide association study demonstrates significant genetic variation for fracture risk in Thoroughbred racehorses
title A genome-wide association study demonstrates significant genetic variation for fracture risk in Thoroughbred racehorses
title_full A genome-wide association study demonstrates significant genetic variation for fracture risk in Thoroughbred racehorses
title_fullStr A genome-wide association study demonstrates significant genetic variation for fracture risk in Thoroughbred racehorses
title_full_unstemmed A genome-wide association study demonstrates significant genetic variation for fracture risk in Thoroughbred racehorses
title_short A genome-wide association study demonstrates significant genetic variation for fracture risk in Thoroughbred racehorses
title_sort genome-wide association study demonstrates significant genetic variation for fracture risk in thoroughbred racehorses
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4008154/
https://www.ncbi.nlm.nih.gov/pubmed/24559379
http://dx.doi.org/10.1186/1471-2164-15-147
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