Estimated prevalence of the Type 1 Polysaccharide Storage Myopathy mutation in selected North American and European breeds

被引:20
作者
McCue, M. E. [1 ]
Anderson, S. M. [2 ]
Valberg, S. J. [1 ]
Piercy, R. J. [3 ]
Barakzai, S. Z. [4 ]
Binns, M. M. [5 ]
Distl, O. [6 ]
Penedo, M. C. T. [7 ]
Wagner, M. L. [2 ]
Mickelson, J. R. [2 ]
机构
[1] Univ Minnesota, Coll Vet Med, Dept Vet Populat Med, St Paul, MN 55108 USA
[2] Univ Minnesota, Coll Vet Med, Dept Vet & Biomed Sci, St Paul, MN 55108 USA
[3] Royal Vet Coll, Dept Vet Clin Sci, Comparat Neuromuscular Dis Lab, Hatfield AL9 7TA, Herts, England
[4] Univ Edinburgh, Easter Bush Vet Ctr, Royal Dick Sch Vet Studies, Roslin EH25 9RG, Midlothian, Scotland
[5] Equine Anal Syst Inc, Midway, KY 40347 USA
[6] Univ Vet Med Hannover, Inst Genet & Anim Breeding, D-30559 Hannover, Germany
[7] Univ Calif Davis, Vet Genet Lab, Davis, CA 95616 USA
关键词
glycogen storage disease; glycogen synthase; PSSM; EXERTIONAL RHABDOMYOLYSIS; GYS1; MUTATION; WILD HORSES; ALLELE;
D O I
10.1111/j.1365-2052.2010.02124.x
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
P>The GYS1 gene mutation that is causative of Type 1 Polysaccharide Storage Myopathy (PSSM) has been identified in more than 20 breeds of horses. However, the GYS1 mutation frequency or Type 1 PSSM prevalence within any given breed is unknown. The purpose of this study was to determine the frequency of the GYS1 mutation and prevalence of genetic susceptibility to Type 1 PSSM in selected breeds from Europe and North America. The GYS1 mutation was detected in 11 breeds, including, in order of increasing allele frequency, Shires, Morgans, Appaloosas, Quarter Horses, Paints, Exmoor Ponies, Saxon-Thuringian Coldbloods, South German Coldbloods, Belgians, Rhenish German Coldbloods and Percherons. The prevalence of genetic susceptibility to Type 1 PSSM in these breeds varied from 0.5% to 62.4%. The GYS1 mutation was not found in the sampled Thoroughbreds, Akhal-Tekes, Connemaras, Clydesdales, Norwegian Fjords, Welsh Ponies, Icelandics, Schleswig Coldbloods or Hanoverians, but failure to detect the mutation does not guarantee its absence. This knowledge will help breed associations determine whether they should screen for the GYS1 mutation and will alert veterinarians to a possible differential diagnosis for muscle pain, rhabdomyolysis or gait abnormalities.
引用
收藏
页码:145 / 149
页数:5
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