News

Treat Autoimmune Hepatitis Based on Natural History of Disease


 

FROM A SYMPOSIUM SPONSORED BY THE AMERICAN COLLEGE OF RHEUMATOLOGY

CHICAGO – A diagnosis of autoimmune hepatitis does not necessarily mandate therapy.

Rather, a decision about therapy should be based on the natural history of the disease, Dr. Bruce Luxon said at a symposium sponsored by the American College of Rheumatology.

Patients for whom treatment is mandatory are those with aspartate aminotransferase (AST) levels greater than 10 times the upper limit of normal, or 5 times the upper limit of normal plus gamma globulin levels greater than twice the upper limit of normal. Data from the 1970s showed that patients with these disease characteristics had a 6-month mortality of 60%, said Dr. Luxon, professor and chair of the department of internal medicine at Georgetown University, Washington.

Similarly, treatment is needed when a biopsy shows "bridging" – or multilobular – necrosis, as studies have shown that progression to cirrhosis occurs in more than 80% of such patients, and 5-year mortality is about 45%.

"In contrast, there is a group of patients whose AST and [alanine transaminase (ALT)] were quite normal or very close to normal [less than twice the normal value]. Those people had a 10-year life expectancy greater than 80%," he said, noting that these patients generally don’t require treatment.

Cirrhotic patients with significant inflammation, on the other hand, might benefit from a 3-6 month trial of therapy to slow down progression, he said adding: "That’s really a decision for a hepatologist to make."

In those who will be treated, prednisone remains the mainstay of therapy, as it has for 50 years, he noted.

It is given initially at a high dose of 60 mg for the first week (or 30 mg plus 50 mg of azathioprine, which is usually given to allow lowering of the prednisone dose). Prednisone is lowered to 40 mg for week 2 (or 20 mg and 50 mg of prednisone and azathioprine, respectively), and to 30 mg for weeks 3 and 4 (or 15 mg and 50 mg of prednisone and azathioprine, respectively).

After week 4, the dose remains 20 mg (or 10 mg and 50 mg of prednisone and azathioprine, respectively) until the clinical end point is reached.

Use of the combination therapy is associated with a much lower occurrence of corticosteroid-related side effects (10% vs. 44%), but not all patients can tolerate the azathioprine. It is fine to give prednisone monotherapy in such patients, he said.

The typical side effects of steroid therapy can occur, including weight gain, unwanted hair growth, acne, and – importantly – bone disease.

"You really want to make sure they are on calcium and vitamin D," he said, noting bisphosphonates, rather than controversial estrogen replacement, are usually prescribed as well.

Azathioprine side effects can include gastrointestinal upset, drug-induced hepatitis in rare cases, and cancer in very rare cases.

The efficacy of treatment should be evaluated on a biochemical or histological basis. But keep in mind that while a failure to normalize liver enzymes suggests residual disease, about half of those who do have normalization will still go on to have significant liver fibrosis and inflammation on biopsy. "So it’s not sufficient to just normalize transaminases," he said.

Since biopsy improvement lags behind biochemical improvement by about 6 months, a repeat biopsy at that time is warranted.

These serial biopsies, which are important in this disease, can also predict whether a patient can be taken off therapy, he said.

Patients with a normal liver biopsy at follow-up will have only about a 15%-20% risk of relapse, so it is reasonable to take them off treatment, he noted.

Conversely, those with interface hepatitis and inflammation on follow-up biopsy will relapse about 90% of the time and require ongoing treatment.

In most cases, autoimmune hepatitis can be controlled, although ongoing treatment might be required. About 65% of patients will remit within 18 months, while only about 10% of patients will fail treatment altogether – and those patients typically have other contributing factors, such as excessive alcohol use, concurrent viral infection such as hepatitis B or C, or an overlap syndrome.

Another 10% of patients won’t tolerate treatment.

Among those who require treatment indefinitely because of relapse, maintenance therapy with 7.5 mg/day of prednisone and 2 mg per kg/day of azathioprine can be effective for maintaining control. In one study, 85% of patients who relapsed were managed effectively with this strategy at a mean follow-up of 149 months, Dr. Luxon noted.

These patients generally have survival similar to age- and gender-matched controls, so although they have to stay on these low doses of treatment for life, the treatment is quite effective.

Pages

Recommended Reading

Disease Activity Higher in Obese RA Patients
MDedge Internal Medicine
RA Patients Taking Rituximab Are at Risk for PML
MDedge Internal Medicine
Updated ACR/EULAR Criteria May Result in Early RA Overdiagnosis, Overtreatment
MDedge Internal Medicine
AS Treatments May Relieve Symptoms But Not Halt Progression
MDedge Internal Medicine
Interstitial and Obstructive Lung Disease Risk, Mortality Increased in RA Patients
MDedge Internal Medicine
TRACTISS to Study Rituximab Effects in Sjögren's Syndrome
MDedge Internal Medicine
Diabetes-Induced Osteoarthritis Proposed as Possible Phenotype
MDedge Internal Medicine
Selenium Improves QOL, Slows Progression of Mild Graves’ Orbitopathy
MDedge Internal Medicine
Editorial: Compliments and Corrections
MDedge Internal Medicine
Rheumatoid Arthritis Confers Same Cardiovascular Risk as Diabetes
MDedge Internal Medicine