Clinical Exposures: Copper-associated hepatitis in a Doberman pinscher - Veterinary Medicine
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Clinical Exposures: Copper-associated hepatitis in a Doberman pinscher


Diagnostic findings

The first and most consistent laboratory abnormality reported in Bedlington terriers with copper-associated hepatitis is elevated alanine transaminase (ALT) activity.1,5 In Doberman pinschers, the first sign can be elevated ALT activity in a young (1 to 3 years) usually female dog.1 Other laboratory findings include elevations in other liver enzyme activities (alkaline phosphatase and gamma-glutamyl transferase) or evidence of loss of liver functions (decreased BUN, cholesterol, albumin, or glucose concentrations).

Radiographic findings are usually nonspecific, such as microhepatia and ascites.1 An ultrasonographic examination is helpful in ruling out other liver diseases.1 The liver size is usually normal but can be decreased if the disease has progressed to cirrhosis. The liver echogenicity is either normal, increased, decreased, or irregular.1

The only method for definitive diagnosis is histologic examination of a liver biopsy sample. Findings are consistent with chronic active hepatitis, cholestasis, and cirrhosis in later stages. The earliest changes are infiltration by inflammatory cells (macrophages, lymphocytes and plasma cells) and collagen deposition (scar tissue formation). These changes begin around the small hepatic vein branches. Progression of the disease leads to further fibrosis, inflammation, and hepatocyte loss beginning among zone 3 hepatocytes around the terminal hepatic vein branches.8

The copper concentrations in liver tissue can be assessed quantitatively or by spectrophotometric methods.1 The limitation of the quantitative methods is that a large amount of tissue is required. Alternatively, histochemical stains can be used for semiquantitative assessment, which may give a subjective result.2

Treatment options

Common treatments for copper-associated hepatitis include chelation with penicillamine or trientine, administration of zinc, antioxidant supplementation, and dietary modification. Penicillamine mobilizes copper from tissues and promotes copper excretion in urine. It also has anti-inflammatory, immunosuppressive, and antifibrotic effects and may increase the synthesis of metallothionein (a copper-binding protein). Penicillamine is administered at a dosage of 10 to 15 mg/kg b.i.d. orally.9 This drug should not be given with any other medications or supplements and is potentially teratogenic, so inform owners about safe handling practices.

Copper chelator therapy with penicillamine in subclinical dogs can normalize the copper concentrations and reverse histologic damage.10 One study showed that in dogs treated with D-penicillamine, copper retention was effectively reduced and the histologic appearance of hepatic lesions improved.4

Trientine hydrochloride (10 to 15 mg/kg orally b.i.d.)9 is used when penicillamine is not tolerated. This drug can also have a teratogenic effect in animals, so owners should be informed about safe handling practices.

Zinc (100 mg orally divided b.i.d.)9 orally reduces copper absorption from the diet by inducing metallothionein production by the intestinal mucosal cells. The removal of hepatic copper resulting from zinc administration is relatively slow, so it should not be used as sole therapy and can be used as maintenance treatment. In people, it has been used as first-line therapy in asymptomatic patients.

Diet changes should be made to reduce the absorption of copper from the intestinal tract.1,6 Foods that contain a high amount of copper include eggs, liver, shellfish, organ meats, beans, mushrooms, chocolate, nuts, and cereals and should be avoided.1 Commercial diets low in copper are available (e.g. Veterinary Diet canine HEPATIC LS—ROYAL CANIN; Prescription Diet l/d Canine Hepatic Health—Hill's Pet Nutrition). A study in Labrador retrievers demonstrated that a low-copper diet can stabilize the liver copper concentration in the high normal range.6 The dogs in the study were not at the clinical stage of the disease, so it has not been determined whether dietary management improves the clinical signs.

Since chronic inflammatory liver diseases and cholestatic liver diseases result in reduced protection against oxidative stress, the use of antioxidants could be helpful.3,5 Common antioxidants used in animals with liver diseases are S-adenosylmethionine (SAMe) (20 mg/kg orally once a day), milk thistle (20 to 50 mg/kg orally once a day), and N-acetylcysteine (70 mg/kg orally t.i.d.),11 which help replenish glutathione, and certain vitamins such as vitamin E.

Unfortunately, the prognosis for dogs with cirrhosis or decompensated liver function at presentation is poor,12-14 and once clinical signs of chronic hepatitis in Dobermans are seen, the response to treatment is poor. Diagnosing and managing the disease in the early stages results in a better prognosis. Early detection, by regularly measuring ALT activity in dog breeds at risk of developing copper-associated hepatitis, can help identify patients that would benefit from early intervention. The exact cause of chronic hepatitis is still unclear, and clinical trials are still necessary for understanding the best treatment approach.

Michal O. Hess, DVM
50 Greenway N
Forest Hills, NY 11375


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