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What Is Systemic Lupus Erythematosus (SLE)?

Systemic lupus erythematosus (SLE), also called lupus, is a disease that causes inflammation in connective tissue and can damage several organs. It can affect joints, skin, lungs, heart, blood vessels, kidneys, nervous system, and blood cells. Some people also have Raynaud’s phenomenon, which causes spasms in blood vessels, and pain and discoloration in the fingers, toes, ears, and nose.

SLE affects about 1 in 2000 people, five times more women than men; it is most often diagnosed in people 15 to 40 years old. African Americans and people of Asian and Hispanic ancestry get SLE more often than Caucasians.

What Causes SLE?

The cause is unknown, but hereditary and environmental factors may increase the risk of having SLE. SLE isn’t contagious or transmitted from parent to offspring.

What Are the Symptoms of SLE?

The disease is characterized by intervals of active disease (flares) and remissions. Symptoms depend on which organ is involved. The first ones may be fatigue and joint pain, and swelling or stiffness, usually in hands, wrists, and knees. Joint pain can be severe and interfere with activities and work. People may have a rash on sun exposed parts of the body, often the face (cheeks and nose). This is called a butterfly rash. Raynaud’s phenomenon makes fingers change color and become painful when exposed to cold. Some people have pleurisy (inflammation of the lining of lungs), which can make breathing painful, with shortness of breath. Affected kidneys may lead to high blood pressure and kidney failure. SLE may affect memory and mood and cause stress or confusion.

How Is SLE Diagnosed?

The health care provider makes a diagnosis from a medical history, physical examination, and laboratory tests. X-rays may be done. Laboratory tests include an erythrocyte sedimentation rate (ESR), complete blood cell count (CBC), antinuclear anti-body (ANA), and urinalysis. The ESR measures inflammation. The CBC counts blood cells and platelets. The health care provider may order an anti-DNA test, which is more specific for SLE. The health care provider may suggest seeing a rheumatologist (specialist in joint problems).

How Is SLE Treated?

Treatment depends on symptoms and which organs are involved. Medicines help reduce inflammation. Nonsteroidal anti-inflammatory drugs (NSAIDs) are often given first. The health care provider may also prescribe prednisone, which works quickly. If they don’t help enough, disease-modifying medicines can slow the disease. These include hydroxychloroquine, methotrexate, azathioprine, and cyclophosphamide.

Exercise is important for joint movement and muscle strength.

DOs and DON’Ts in Managing SLE:

  • DO tell your health care provider if you’re pregnant or plan to get pregnant.
  • DO have your blood pressure checked and blood tested for diabetes while you’re taking prednisone.
  • DO see your eye health care provider yearly.
  • DO get sleep and exercise. Alternating rest and activity helps manage fatigue.
  • DO take your medicines as prescribed. Call your health care provider if you have medicine side effects.
  • DO call your health care provider if you have a temperature higher than 101° F, blood in urine or stool, shortness of breath, chest pain, or severe stomach pain.
  • DON’T stop taking your medicine or change your dosage because you feel better unless your health care provider tells you to.
  • DON’T give up. If one medicine doesn’t work, talk to your health care provider about others.
FOR MORE INFORMATION

Contact the following sources:

  • The Arthritis Foundation
    Tel: (800) 283-7800
    Website: http://www.arthritis.org
  • Lupus Foundation of America
    Tel: (301) 670-9292, (800) 558-0121
    Website: http://www.lupus.org
  • American College of Rheumatology
    Tel: (404) 633-3777
    Website: http://www.rheumatology.org

Copyright © 2016 by Saunders, an imprint of Elsevier, Inc.

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