(Editor’s Note: Please consider participating in this study if you have a senior horse diagnosed with pituitary pars intermedia dysfunction—PPID. See below for further details.)

About the Research

Researchers from the  University of Minnesota (UMN) College of Veterinary Medicine are conducting a pioneering research initiative aimed at advancing the understanding and treatment of PPID in horses. PPID, commonly known as equine Cushing’s disease, is the most prevalent endocrine disorder in aging horses. It affects up to 30% of horses over the age of 15.

The disease leads to a range of clinical signs and serious health complications. These include abnormal hair coat shedding, muscle wasting, laminitis, and increased susceptibility to infections.

Despite its prevalence, significant challenges exist in accurate diagnosis, especially early in the disease process. In addition, treatment is lifelong and not effective in all horses.

Dr. Molly McCue  and Dr. Lauren Hughes from the UMN Equine Genetics and Genomics Laboratory, in collaboration with Dr. Dianne McFarlane from the University of Florida, are conducting the research. The study is a critical step forward in understanding and managing this challenging disease. 

Genetics and PPID

The current standard treatment for PPID is a drug called pergolide, which can have variable efficacy. Less than 75% of cases fully respond. Additionally, the drug can cause adverse effects that impact both quality of life and the outcomes of treatment. 

Genetics may play a key role in disease progression and treatment response. This study aims to better understand these factors and optimize long-term management strategies for affected horses.

The key objective of the study is to understand the genetic variants (mutations) that contribute to the effectiveness and adverse effects of pergolide in managing PPID symptoms. The long-term goal is enhancing treatment protocols to improve the quality of life for horses affected by PPID.

“As a veterinarian, I understand just how devastating PPID can be for horses and the owners that love them,” said Hughes. “I am very excited about the potential outcomes of this study and improving our understanding of how genetics impacts pergolide response. Our research team is dedicated to learning more about this very important equine disease with the goal of improving the way we screen, diagnose, treat, and manage these horses.” 

How You Can Participate

Horse owners and veterinarians are invited to enroll equine participants in this important study. By enrolling your horse in this study, you play a crucial role in shaping the future of PPID treatment, helping to unlock new insights into this prevalent disease, and improve the lives of horses worldwide.

To enroll, horses must meet the following criteria:

  • Over the age of 15 at the time of PPID diagnosis;
  • Diagnosis made by veterinarian and diagnosis included bloodwork (ACTH levels);
  • Horse has/had clinical signs consistent with PPID (long shaggy haircoat, muscle atrophy, changes in mentation, or recurrent infections);
  • Horse has been on pergolide therapy for a minimum of 6 months and has had rechecked blood values (ACTH, TRH stim, or dexamethasone suppression).

Study participation requires the following:

  1. Taking an enrollment survey (15-30 minutes);
  2. Submitting a hair or blood sample by mail (detailed instructions provided); and,
  3. Sharing pertinent medical records and photos via email.

To learn more about the study or to enroll, please visit the UMN College of Veterinary Medicine website or watch this video.

About the UMN Equine Genetics and Genomics Laboratory

The University of Minnesota Equine Genetics and Genomics Laboratory is at the forefront of equine health research. It is dedicated to advancing veterinary medicine through innovative genetic studies and clinical trials.

Further Reading