In the past 15 years, a form of Pulmonary Fibrosis (lung scarring) has been recognized in dogs, almost exclusively in West Highland white terriers (WHWT). Signs of Pulmonary Fibrosis (PF) in dogs include cyanosis (bluish coloring and/or pale gums), lethargy, cough (nonproductive), shortness of breath, increased respiratory rate and effort, open-mouthed breathing, and exercise intolerance. The prognosis is guarded, with many dogs dying from progressive lung failure within 12–18 months. Currently, the underlying cause and genetics of PF in dogs is poorly understood, with only one published report investigating the possible causes. A genetic predisposition is strongly suspected because of the preponderance of WHWT reported to have confirmed PF.
The diagnosis in dogs is usually made based on clinical signs, arterial blood gas analysis, and chest radiographs. The diagnosis is greatly improved by using High Resolution Computed Tomography (HR-CT). Currently there is no known specific treatment, and therapy is at best to relieve the symptoms but does not affect the progression of the disease.
The purpose of this study is to obtain blood DNA samples, and blood gas samples from dogs affected with pulmonary fibrosis, as well as from dogs aged 8 years and older that are not affected. We will obtain chest x-rays from dogs that have low blood oxygen and might be affected with pulmonary fibrosis. We will use the DNA samples to sequence the whole genome (all the DNA sequence) of some of the dogs, and later possibly to get DNA marker data for all the dogs enrolled. We will compare the DNA of affected dogs versus unaffected dogs to see if we can detect gene mutations that predispose dogs to develop pulmonary fibrosis. If gene mutations are found, and verified, they could be used as a test to diagnosis pulmonary fibrosis and also as a test to help breeding decisions to decrease the number of WHWT with pulmonary fibrosis. In addition, knowledge of the genes involved will hopefully lead to specific treatments being developed.
How to Participate
You can participate in our genetic study by sending a completed Pulmonary Fibrosis Submission Form along with a small blood sample for DNA isolation. No financial compensation is currently available for dogs submitted from outside of the University of Minnesota Small Animal Hospital.
Your dog may be able to help if he/she:
Your dog has a diagnosis of Pulmonary Fibrosis (any breed, any age); or WHWT with unexplained cough for 3 month or more
Your dog is a purebred West Highland white terrier who is at least 8 years old and has no history of persistent cough or other persistent respiratory signs
Canine Genetic Testing
- 2,8- Dihydroxyadenine Urinary Stones
- Alaskan Malamute Polyneuropathy
- Exercise Induced Collapse
- Hereditary Calcium Oxalate Urolithiasis, Type 1
- Inflammatory Myopathy (Myositis)
- Leonberger Health Panel
- Neuronal Degeneration
- Persistent Müllerian Duct Syndrome
- Saint Bernard Laryngeal Paralysis & Polyneuropathy
- Sarcoglycan Deficient Muscular Dystrophy
- Toy Manchester Terrier / English Toy Terrier Health Panel
- Ullrich Congenital Muscular Dystrophy
Canine Genetic Research
- Addison's Disease - Autoantibody Study
- Addison’s Disease – Genetics Study in Portuguese Water Dogs
- Addison’s Disease – Standard Poodle MHC Study
- Atypical Seizures / Paroxysmal Dyskinesia
- Border Collie Collapse
- Calcium Oxalate Urinary Stones
- Idiopathic Epilepsy
- Immune-Mediated Hemolytic Anemia (IMHA)
- Leonberger Polyneuropathy / Laryngeal Paralysis
- Pulmonary Fibrosis
- Whippet Exercise Induced Hyperthermia