1. Family aggregation analysis shows a possible heritable background of equine grass sickness (dysautonomia) in a Hungarian stud population
- Author
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Boglárka Vincze, Marta Varga, Ottó Szenci, Orsolya Kutasi, Petra Zenke, Norbert Solymosi, Sándor Spisák, Sándor Cseh, Alan Bartels, and Ferenc Baska
- Subjects
Male ,040301 veterinary sciences ,Population ,Disease ,Primary Dysautonomias ,Biology ,030308 mycology & parasitology ,0403 veterinary science ,03 medical and health sciences ,medicine ,Prevalence ,Animals ,Grass sickness ,Horses ,education ,Retrospective Studies ,0303 health sciences ,education.field_of_study ,Hungary ,General Veterinary ,Incidence ,Dysautonomia ,Retrospective cohort study ,04 agricultural and veterinary sciences ,Increased risk ,Intestinal Microbiome ,Etiology ,Female ,Horse Diseases ,medicine.symptom ,Demography - Abstract
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.
- Published
- 2020