SAEVA Proceedings 2015 | Page 69

South African Equine Veterinary Association Congress 2015  Protea Hotel  Stellenbosch results? Finally, the ideal dosing interval and whether or not seasonal (fall) treatment can be an approach in some animals are unresolved questions. For researchers investigating PPID, challenges include better understanding of pathophysiology of the varied clinical syndromes of PPID. Specifically, might there be varying hormonal profiles in equids that are afflicted with diabetes or laminitis as compared to hypertrichosis and muscle wasting? Additional questions include: 1) why do some horses develop signs of PPID at a relatively early age; and 2) what is the role of insulin dysregulation in PPID? Next, although PPID affects many breeds, it has also been anecdotally recognized in several generations within certain families of equids. Consequently, the genetic basis for development of PPID needs to be explored. Finally, might environmental risk factors may also play a role in development of PPID? Answers for many of these questions will likely require longitudinal, multi-centre studies through which progression of PPID can be studied over a number of years. References General reviews van der Kolk JH. Equine Cushing‟s disease. Equine Vet Educ 1997;9:209. van der Kolk JH, Kalsbeek HC, van Garderen E, et al. Equine pituitary neoplasia: a clinical report of 21 cases (1990-1992). Vet Rec 1993;133:594. Schott HC. Pituitary pars intermedia dysfunction: equine Cushing‟s disease. Vet Clin North Amer: Equine Pract 2002;18:237. McFarlane D. Equine pituitary pars intermedia dysfunction. Vet Clin North Am: Equine Pract 2011;27:93. Prevalence McGowan TW, Pinchbeck GL, Phillips C, et al. A survey of aged horses in Queensland, Australia. Part 2: clinical signs and owner perceptions of health and welfare. Aust Vet J 2010;88:465. Ireland JL, Clegg PD, McGowan CM, et al. A cross-sectional study of geriatric horses in the United Kingdom. Part 2: health care and disease. Equine Vet J 2011;43:37. Pathophysiology van der Kolk JH, Heinrichs M, van Amerongen JD, et al. Evaluation of pituitary gland anatomy and histopathologic findings in clinically normal horses and horses and ponies with pituitary pars intermedia adenoma. Am J Vet Res 2004;65:1701. McFarlane D, Dybdal N, Donaldson MT, et al. Nitration and increased alpha-synuclein expression associated with dopaminergic neurodegeneration in equine pituitary pars intermedia dysfunction. J Neuroendocrinol 2005;17:73. Diagnostic testing Dybdal NO, Hargreaves KM, Madigan JE, et al. Diagnostic testing for pituitary pars intermedia dysfunction in horses. J Am Vet Med Assoc 1994;204:627. Couëtil L, Paradis MR, Knoll J. Plasma adrenocorticotropin concentration in healthy horses and in horses with clinical signs of hyperadrenocorticism. J Vet Int Med 1996;10:1. Donaldson MT, McDonnell SM, Schanbacher BJ, et al. Variation in plasma adrenocorticotropic hormone concentration and dexamethasone suppression test results with season, age, and sex in healthy ponies and horses. J Vet Int Med 2005: 19:217. 69