Inheritance of recurrent exertional rhabdomyolysis in thoroughbreds.

IF 1.8 2区 农林科学 Q2 VETERINARY SCIENCES Javma-journal of The American Veterinary Medical Association Pub Date : 2005-09-01 DOI:10.2460/javma.2005.227.762
Patricia K Dranchak, Stephanie J Valberg, Gary W Onan, Esther M Gallant, Jennifer M MacLeay, Erica C McKenzie, Flavio D De La Corte, Kari Ekenstedt, James R Mickelson
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引用次数: 37

Abstract

Objective: To develop a diagnostic test for recurrent exertional rhabdomyolysis (RER) in Thoroughbreds that relied on in vitro contracture of muscle biopsy specimens and determine whether the inheritance pattern of RER diagnosed on the basis of this contracture test was consistent with an autosomal dominant trait.

Design: Clinical trial.

Animals: 8 adult horses with RER and 16 control adult horses for development of the contracture test; 23 foals for inheritance of RER.

Procedure: External intercostal muscle biopsy specimens from the 24 adult horses were tested for contracture in response to halothane and caffeine, and criteria for a positive test result were determined. These criteria were then applied to results for the 23 foals to determine whether they had RER. Simple segregation analysis was performed to determine whether results were consistent with a dominant pattern of inheritance.

Results: Results of the contracture test were positive for 5 of the 12 colts and 4 of the 11 fillies. Results of segregation analysis were consistent with an auto-. somal dominant pattern of inheritance. Two sires with RER produced colts with RER, supporting the hypothesis that RER had an autosomal, rather than an X-linked, inheritance pattern. In addition, in 1 instance, an unaffected colt was produced by 2 affected parents, which was not consistent with a recessive mode of inheritance.

Conclusions and clinical relevance: Although the expression of the RER trait is influenced by sex, temperament, and diet, among other factors, results from the in vitro muscle contracture test and this breeding trial suggest that RER in Thoroughbreds can be modeled as a genetic trait with an autosomal dominant pattern of inheritance.

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纯种马复发性劳损性横纹肌溶解的遗传。
目的:建立一种依赖于肌肉活检标本体外挛缩的纯种马复发性劳损性横纹肌溶解(RER)的诊断方法,并确定基于该挛缩试验诊断的RER的遗传模式是否与常染色体显性性状相一致。设计:临床试验。动物:8匹患有RER的成年马和16匹对照成年马进行挛缩试验;23头小马驹RER遗传。程序:对24匹成年马的外肋间肌活检标本进行了氟烷和咖啡因反应的挛缩检测,并确定了阳性检测结果的标准。然后将这些标准应用于23匹马驹的结果,以确定它们是否患有RER。进行简单的分离分析以确定结果是否与显性遗传模式一致。结果:12匹小马中有5匹呈阳性,11匹母马中有4匹呈阳性。分离分析结果与一种自动分析相一致。染色体显性遗传模式。两个患有RER的母猪所生的小马都患有RER,这支持了RER是常染色体遗传模式而不是x连锁遗传模式的假设。此外,在1例中,2个受影响的亲本产生了一个未受影响的小驹,这与隐性遗传模式不一致。结论和临床意义:尽管内质网性状的表达受性别、气质和饮食等因素的影响,但体外肌肉挛缩试验和本育种试验的结果表明,纯种马内质网可以作为一种常染色体显性遗传模式的遗传性状建模。
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来源期刊
CiteScore
1.60
自引率
15.80%
发文量
539
审稿时长
6-16 weeks
期刊介绍: Published twice monthly, this peer-reviewed, general scientific journal provides reports of clinical research, feature articles and regular columns of interest to veterinarians in private and public practice. The News and Classified Ad sections are posted online 10 days to two weeks before they are delivered in print.
期刊最新文献
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