1Department of Obstetrics and Food Animal Medicine Clinic, University of Veterinary Medicine, István u. 2, H-1078 Budapest, Hungary.
2Department of Animal Breeding, Nutrition and Laboratory Animal Science, Laboratory of Genetics, University of Veterinary Medicine, Budapest, Hungary.
Acta Vet Hung. 2020 Sep 30;68(3):263-268. doi: 10.1556/004.2020.00038.
Equine grass sickness (also known as dysautonomia) is a life-threatening polyneuropathic disease affecting horses with approx. 80% mortality. Since its first description over a century ago, several factors, such as the phenotype, intestinal microbiome, environment, management and climate, have been supposed to be associated with the increased risk of dysautonomia. In this retrospective study, we examined the possible involvement of genetic factors. Medical and pedigree datasets regarding 1,233 horses with 49 affected animals born during a 23-year period were used in the analysis. Among the descendants of some stallions, the proportion of animals diagnosed with dysautonomia was unexpectedly high. Among males, the odds of dysautonomia were found to be higher, albeit not significantly, than among females. Significant familial clustering (genealogical index of familiality, P = 0.001) was observed among the affected animals. Further subgroups were identified with significant (P < 0.001) aggregation among close relatives using kinship-based methods. Our analysis, along with the slightly higher disease frequency in males, suggests that dysautonomia may have a genetic causal factor with an X-linked recessive inheritance pattern. This is the first study providing ancestry data and suggesting a heritable component in the likely multifactorial aetiology of the disease.
马属植物性疾病(也称为自主神经功能紊乱)是一种危及生命的多神经病,影响约 80%死亡率的马匹。自一个多世纪前首次描述以来,一些因素,如表型、肠道微生物群、环境、管理和气候,被认为与自主神经功能紊乱的风险增加有关。在这项回顾性研究中,我们检查了遗传因素的可能参与。在分析中使用了涉及 1233 匹马的医疗和系谱数据集,其中 49 只患病动物在 23 年期间出生。在一些种马的后代中,被诊断患有自主神经功能紊乱的动物比例出乎意料地高。在雄性中,自主神经功能紊乱的几率虽然没有显著增加,但高于雌性。在受影响的动物中观察到显著的家族聚集(家族亲密度的遗传指数,P = 0.001)。使用基于亲属关系的方法,进一步确定了具有显著聚集(P < 0.001)的亚组。我们的分析以及雄性中略高的疾病频率表明,自主神经功能紊乱可能具有遗传原因,其遗传模式为 X 连锁隐性遗传。这是第一项提供祖先数据并提示疾病的可能多因素病因中存在遗传性成分的研究。