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March is National Kidney Month

From the National Kidney Foundation®

Lupus and Kidney Disease

Lupus can harm your kidneys as well as other organs and tissues in your body. This fact sheet will give you information about lupus in general and about how it can affect your kidneys. It also offers suggestions about how you can live with lupus and keep feeling your best.

What is lupus?

Lupus is a short name for a disease called "lupus erythematosus." Lupus is called an "autoimmune" disease because the immune system, which usually protects the body from disease, turns against the body, causing harm to organs and tissues.

There are two types of lupus. “Systemic” lupus erythematosus (SLE) can harm your skin, joints, kidneys and brain and may be fatal if untreated. The other type, called "discoid" lupus erythematosus, affects only your skin.

What causes lupus?

No one knows what causes the disease. Your family history is important. People with family members who have SLE are much more likely to develop the disease. Infections, viruses and certain medications may also play a role in causing the disease.

People of all ages, races and both sexes can get lupus. However, it is about ten times more common in women than men. About 500,000 Americans have lupus.

What are the symptoms of lupus?

Different people get different symptoms. These may include: skin rashes, joint pain and swelling, hair loss, sun sensitivity, tiredness, weight loss, fever, swelling of lymph glands, chest pain, nerve involvement and ankle swelling.

How can lupus harm the kidneys?

Lupus causes an inflammation of the filtering units (glomeruli) of the kidney. Since these filtering units clear your blood of waste, damage to them can cause your kidneys to work poorly or not at all. About 90 percent of lupus patients will have some kidney damage but only a small percentage actually develop kidney disease severe enough to require treatment.

The kidney disease may be "silent" and not cause any symptoms. However, you may have dark urine, pain in your side, high blood pressure, weight gain from extra fluid, and swelling around your eyes, hands and feet.

How do I know if I have lupus?

Your doctor will do a physical examination, look at your medical history and take x-rays and a blood test for "antinuclear" antibodies and other markers of SLE.

How is lupus treated?

Lupus is treated with anti-inflammatory drugs that block your body's immune system. Some of these are prednisone, azathioprine, cyclophosphamide or cyclosporine and mycophenolate.

Do these treatments have side effects?

Yes. These drugs have some side effects. Some cause cosmetic changes such as hair thinning and weight gain. All cause an increased susceptibility to infections and tumors. Fortunately, with modern treatment regimens, these side effects are usually easily manageable for most patients.

Do I need to follow a special diet?

Sometimes. All patients should follow a well- balanced diet. When the disease is active, you may have to follow some restrictions. You need to talk with your doctor or dietitian about the best diet for you.

If you have kidney disease, you may need to eat less protein and sodium (salt). If you have high blood pressure, you should be sure to take the drugs prescribed by your kidney doctor to control your pressure. If you are overweight, losing weight may help to control your blood pressure.

How can I tell if the disease has hurt my kidneys?

The doctor can tell if lupus has harmed your kidneys by testing for protein or blood in your urine. Also, the levels of urea and creatinine in your blood will be high if your kidneys are not getting rid of these waste products as well as usual. Your doctor may estimate your level of kidney function from the results of your blood creatinine test and your age, size and gender. This is called you glomerular fitration rate, or GFR.

What happens if my kidneys fail?

If your kidneys fail, you can be treated with dialysis or a kidney transplant. Lupus patients do as well with these treatments as people who have other types of kidney disease.

Many patients with lupus kidney disease have received a kidney transplant. The drugs used to prevent your body from rejecting the new kidney are the same or like those used to treat lupus. It is unusual for lupus to come back in the new kidney. Most of the time, the lupus stays inactive. Lupus patients with new kidneys do as well as any other patients with transplanted kidneys.

What is my long-term outlook?

Most patients do well long-term. You may need to take medication over many years. Even patients who have less involvement should have periodic checkups.

What can I do to help myself?

You should learn more about the disease and the factors that cause it to flare up. One of these factors is sun exposure. You should avoid outdoor activities between 10 a.m. and 4 p.m. when the sun exposure is greatest. If you must go out, you should apply strong sunscreens and wear wide-brimmed hats and long-sleeved shirts. You need to follow your doctor's orders carefully and take your medications as directed.

Fatigue (tiredness) also can cause the disease to flare up. You should plan your physical activities carefully and schedule rest periods. Planned exercise is also helpful.

Chronic illness requires coping as well as understanding and support from family members. When the disease is active, lupus patients may have decreased ability to handle household or job-related tasks. The ability to cope and to be flexible will go a long way toward learning to live with lupus.

What If I have more questions?

If you have additional questions, you should speak to your doctor. You may also be interested in the following publications available from the National Kidney Foundation:

  • Warning Signs of Kidney and Urinary Tract Disease
  • Your Kidneys: Master Chemists of the Body
  • Are You at Increased Risk for Chronic Kidney Disease
  • About Chronic Kidney Disease: A Guide for Patients and their Families
  • What You Need to Know About Urinalysis

 


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