Source: American College of RheumatologyRelated MedlinePlus Pages: Fever, Genetic Disorders
Patient Education - CAPS (Pediatric)
Cryopyrin-Associated Autoinflammatory Syndromes (CAPS)
Cryopyrin-Associated Autoinflammatory Syndromes (CAPS)
WHO GETS IT?
All the CAPS are very rare, found in about one in a million people. Familial cold autoinflammatory syndrome is more common in the Unites States, and Muckle-Wells syndrome is more common in Europe. NOMID is present around the world, and usually starts shortly after birth. Muckle-Wells syndrome may start later in life. Males and females are both affected, and all ethnic groups can be affected.WHAT CAUSES THE DISEASE?
CAPS are genetic diseases. CAPS is inherited as an autosomal dominant disease (in which a mutation in only one copy of the gene inherited from one parent is sufficient to cause disease). That means that one of the parents may be ill with CAPS, or that the gene mutation developed in the sick child. A genetic defect is found in only 50-60% of patients with NOMID, 65-75% in patients with Muckle-Wells syndrome and in nearly all patients with familial cold autoinflammatory syndrome. The gene mutation causes a defect in a protein called cryopyrin, which has an important role in controlling inflammation.HOW IS IT DIAGNOSED?
CAPS is suspected by the symptoms and signs found by the physician on physical examination. The diagnosis may be confirmed by a genetic test, although occasionally the genetic test may be normal. Other tests may include skin biopsy (examining a small sample of the skin) of the rash, an eye examination, hearing tests and imaging of the brain and inner ears by magnetic resonance imaging (MRI).HOW IS CAPS TREATED?
Until recently there was no effective treatment. Patients were treated with medications such as nonsteroidal anti-inflammatory drugs (ibuprofen or naproxen), steroids or methotrexate to reduce symptoms. Exciting recent research has shown that medications that target interleukin-1 are very effective in treating CAPS. These medications include anakinra (Kineret), rilonacept (Arcalyst) and canakinumab (Ilaris). Treatment must continue throughout life, as there is no known cure.Other treatments include physical therapy, splints and other aids to treat joint deformities if they occur. Surgery is occasionally needed. Hearing aids are needed for children with deafness.
LIVING WITH THE DISEASE
Untreated patients suffer from frequent attacks, decreasing the quality of life. Families experience emotional and financial stress taking care of a chronically ill child, and patients can miss a lot of school. Patients with familial cold autoinflammatory syndrome usually need to live in a place with mild weather, a place that is not too cold but also not so hot that there is a constant need for air-conditioning.The outcome of NOMID used to be such that many patients developed severe joint deformities and neurologic damage, mainly to the ears and eyes. There also were cases of death from brain damage. New treatments may allow children to lead near-normal lives.
Untreated patients may develop a complication of inflammation called amyloidosis. Amyloid is a protein that deposits in certain organs in children with chronic inflammatory disease. The most common organ involved is the kidney, but amyloid can deposit in the intestines, skin and heart. Eventually, amyloid causes a loss of function, especially of the kidneys. This is another reason to continue life-long treatment, even when the child is feeling better.
POINTS TO REMEMBER
- CAPS includes three very rare diseases related to a defect in the same protein: cryopyrin.
- The major symptoms include fever; hive-like rash; joint pain and swelling; red eyes; and symptoms of the nervous system, including headaches and deafness.
- Treatments to block interleukin-1 are very effective, and, if started early, may prevent organ damage.
TO FIND A RHEUMATOLOGIST
For a listing of rheumatologists in your area, click here. Learn more about rheumatologists and rheumatology health professionals.
FOR MORE INFORMATION
The American College of Rheumatology has compiled this list to give you a starting point for your own additional research. The ACR does not endorse or maintain these websites, and is not responsible for any information or claims provided on them. It is always best to talk with your rheumatologist for more information and before making any decisions about your care.Muckle-Wells syndrome
www.ghr.nlm.nih.gov/condition=mucklewellssyndrome
www.ghr.nlm.nih.gov/condition=mucklewellssyndrome
Neonatal Onset Multi-system Inflammatory Disease
www.ghr.nlm.nih.gov/condition=neonatalonsetmultisysteminflammatorydisease
www.ghr.nlm.nih.gov/condition=neonatalonsetmultisysteminflammatorydisease
Familial Cold Auto-inflammatory Syndrome
www.ghr.nlm.nih.gov/condition=familialcoldautoinflammatorysyndrome
Updated May 2012www.ghr.nlm.nih.gov/condition=familialcoldautoinflammatorysyndrome
Written by Phil Hashkes, MD, Shaare Zedek Medical Center and the Hebrew University, Jerusalem, and reviewed by the American College of Rheumatology Communications and Marketing Committee.
This patient fact sheet is provided for general education only. Individuals should consult a qualified health care provider for professional medical advice, diagnosis and treatment of a medical or health condition.
© 2012 American College of Rheumatology
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