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Autoimmune hepatitis

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Autoimmune hepatitis is a disease in which the body's immune system

attacks liver cells. This causes the liver to become inflamed

(hepatitis). Researchers think a genetic factor may predispose some

people to autoimmune diseases. About 70 percent of those with

autoimmune hepatitis are women, most between the ages of 15 and 40.

The disease is usually quite serious and, if not treated, gets worse

over time. It's usually chronic, meaning it can last for years, and

can lead to cirrhosis (scarring and hardening) of the liver and

eventually liver failure.

Autoimmune hepatitis is classified as either type I or II. Type I is

the most common form in North America. It occurs at any age and is

more common among women than men. About half of those with type I

have other autoimmune disorders, such as type 1 diabetes,

proliferative glomerulonephritis, thyroiditis, Graves' disease,

Sjögren's syndrome, autoimmune anemia, and ulcerative colitis. Type

II autoimmune hepatitis is less common, typically affecting girls

ages 2 to 14, although adults can have it too.

Autoimmune Disease

One job of the immune system is to protect the body from viruses,

bacteria, and other living organisms. Usually, the immune system

does not react against the body's own cells. However, sometimes it

mistakenly attacks the cells it is supposed to protect. This

response is called autoimmunity. Researchers speculate that certain

bacteria, viruses, toxins, and drugs trigger an autoimmune response

in people who are genetically susceptible to developing an

autoimmune disorder.

Symptoms

Fatigue is probably the most common symptom of autoimmune hepatitis.

Other symptoms include

enlarged liver

jaundice

itching

skin rashes

joint pain

abdominal discomfort

fatigue

spider angiomas (abnormal blood vessels) on the skin

nausea

vomiting

loss of appetite

dark urine

pale or gray colored stools

People in advanced stages of the disease are more likely to have

symptoms such as fluid in the abdomen (ascites) or mental confusion.

Women may stop having menstrual periods.

Symptoms of autoimmune hepatitis range from mild to severe. Because

severe viral hepatitis or hepatitis caused by a drug—for example,

certain antibiotics—has the same symptoms, tests may be needed for

an exact diagnosis. Your doctor should also review and rule out all

your medicines before diagnosing autoimmune hepatitis.

Diagnosis

Your doctor will make a diagnosis based on your symptoms, blood

tests, and liver biopsy.

Blood tests. A routine blood test for liver enzymes can help reveal

a pattern typical of hepatitis, but further tests, especially for

autoantibodies, are needed to diagnose autoimmune hepatitis.

Antibodies are proteins made by the immune system to fight off

bacteria and viruses. In autoimmune hepatitis, the immune system

makes antinuclear antibodies (ANA), antibodies against smooth muscle

cells (SMA), or liver and kidney microsomes (anti-LKM). The pattern

and level of these antibodies help define the type of autoimmune

hepatitis (type I or type II).

Blood tests also help distinguish autoimmune hepatitis from viral

hepatitis (such as hepatitis B or C) or a metabolic disease (such as

's disease).

Liver biopsy. A tiny sample of your liver tissue, examined under a

microscope, can help your doctor accurately diagnose autoimmune

hepatitis and tell how serious it is. You will go to a hospital or

outpatient surgical facility for this procedure.

Treatment

Treatment works best when autoimmune hepatitis is diagnosed early.

With proper treatment, autoimmune hepatitis can usually be

controlled. In fact, recent studies show that sustained response to

treatment not only stops the disease from getting worse, but also

may actually reverse some of the damage.

The primary treatment is medicine to suppress (slow down) an

overactive immune system.

Both types of autoimmune hepatitis are treated with daily doses of a

corticosteroid called prednisone. Your doctor may start you on a

high dose (20 to 60 mg per day) and lower the dose to 5 to 15 mg/day

as the disease is controlled. The goal is to find the lowest

possible dose that will control your disease.

Another medicine, azathioprine (Imuran) is also used to treat

autoimmune hepatitis. Like prednisone, azathioprine suppresses the

immune system, but in a different way. It helps lower the dose of

prednisone needed, thereby reducing its side effects. Your doctor

may prescribe azathioprine, in addition to prednisone, once your

disease is under control.

Most people will need to take prednisone, with or without

azathioprine, for years. Some people take it for life.

Corticosteroids may slow down the disease, but everyone is

different. In about one out of every three people, treatment can

eventually be stopped. After stopping, it is important to carefully

monitor your condition and promptly report any new symptoms to your

doctor because the disease may return and be even more severe,

especially during the first few months after stopping treatment.

In about 7 out of 10 people, the disease goes into remission, with a

lessening of severity of symptoms, within 2 years of starting

treatment. A portion of persons with a remission will see the

disease return within 3 years, so treatment may be necessary on and

off for years, if not for life.

Side Effects

Both prednisone and azathioprine have side effects. Because high

doses of prednisone are needed to control autoimmune hepatitis,

managing side effects is very important. However, most side effects

appear only after a long period of time.

Some possible side effects of prednisone are

weight gain

anxiety and confusion

thinning of the bones (osteoporosis)

thinning of the hair and skin

diabetes

high blood pressure

cataracts

glaucoma

Azathioprine can lower your white blood cell count and sometimes

causes nausea and poor appetite. Rare side effects are allergic

reaction, liver damage, and pancreatitis (inflammation of the

pancreas gland with severe stomach pain).

Other Treatments

People who do not respond to standard immune therapy or who have

severe side effects may benefit from other immunosuppressive agents

like mycophenylate mofetil, cyclosporine or tacrolimus. People who

progress to end stage liver disease (liver failure) and/or cirrhosis

may need a liver transplant. Transplantation has a 1-year survival

rate of 90 percent and a 5-year survival rate of 70 to 80 percent.

Hope Through Research

Scientists are studying various aspects of autoimmune hepatitis to

find out who gets it and why and to discover better ways to treat

it. Basic research on the immune system will expand knowledge of

autoimmune diseases in general. Epidemiologic research will help

doctors understand what triggers autoimmune hepatitis in some

people. Research on different steroids, alternatives to steroids,

and other immunosuppressants will eventually lead to more effective

treatments.

Points to Remember

Autoimmune hepatitis is a long-term disease in which your body's

immune system attacks liver cells.

The disease is diagnosed using various blood tests and a liver

biopsy.

With proper treatment, autoimmune hepatitis can usually be

controlled. The main treatment is medicine that suppresses the

body's overactive immune system.

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