2015
DOI: 10.1016/j.jevs.2015.03.197
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Effect of Diet on Haflinger Horses With GYS1 Mutation (Polysaccharide Storage Myopathy Type 1)

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Cited by 6 publications
(13 citation statements)
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“…Haflinger mares heterozygous positive (polysaccharide storage myopathy type 1, n = 7) and negative (control, n = 7) for glycogen synthase (GYS1) mutation were included. As a part of the preceding study using the same data collections [ 16 ], the effect of diet was investigated; horses received 6 weeks of carbohydrate rich diet followed by hay only or vice versa, with a wash out period of two weeks between diets. The results of that study have been published [ 16 ], and no effect of diet or GYS1 was found; therefore, this factor is not further investigated in the present study.…”
Section: Methodsmentioning
confidence: 99%
“…Haflinger mares heterozygous positive (polysaccharide storage myopathy type 1, n = 7) and negative (control, n = 7) for glycogen synthase (GYS1) mutation were included. As a part of the preceding study using the same data collections [ 16 ], the effect of diet was investigated; horses received 6 weeks of carbohydrate rich diet followed by hay only or vice versa, with a wash out period of two weeks between diets. The results of that study have been published [ 16 ], and no effect of diet or GYS1 was found; therefore, this factor is not further investigated in the present study.…”
Section: Methodsmentioning
confidence: 99%
“…clinical symptoms such as training intolerance and/or exertional rhabdomyolysis throughout the 15-year testing period (supervision commission ARGE Noriker, personal communication, 2015). The absence of clinical signs (weakness, training intolerance, muscle atrophy, rhabdomyolysis) was also mentioned by studies performing and evaluating submaximal exercise tests in draft horses (Naylor et al, 2012) and draft-horse-related breeds (Schwarz et al, 2011;Schröder et al, 2015). Naylor et al (2012), who studied 125 Belgian and Percheron horses, argued that the low level of work demanded in their study was the reason for the absence of clinical signs in 54 GSY1-mutation-carrying animals.…”
Section: Disciplinesmentioning
confidence: 96%
“…Schwarz et al (2011), who conducted a submaximal exercise test in 50 Haflinger horses consisting of 5 min of walk, followed by 20 min trotting on the lunge, also did not detect clinical signs in nine R / H animals, which the authors attributed to the horses' management. Schröder et al (2015) conducted a submaximal treadmill exercise test (2 min of walk, 13 min of trot) in seven R / R and seven R / H Haflinger horses. In this study no horse showed PSSMrelated clinical signs.…”
Section: Disciplinesmentioning
confidence: 99%
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“…More work is required to confirm whether such measures are optimal for those with type 2 PSSM and other breeds. Recent work, for example, apparently showed that for a small group of Haflingers (heterozygous positive for the GYS1 mutation but with no known history or clinical signs of any muscle problem) receiving free paddock as well as regular structured exercise, feeding a cereal based feed (providing~30% of daily DE) and hay for 6 weeks did not induce clinical signs (even after a standardised exercise test) or increase complex periodic acid Schiff-positive amylaseresistant inclusions (Schr€ oder et al 2015).…”
Section: Nutritional Management: All Affected Individualsmentioning
confidence: 99%