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CCP

Also known as: Citrulline antibody, Anti-citrulline antibody, anti-cyclic citrullinated peptide antibody, anti-CCP
Formally known as: Cyclic Citrullinated Peptide Antibody
Related tests: Rheumatoid Factor
The Test
 
How is it used?
When is it requested?
What does the test result mean?
Is there anything else I should know?

How is it used?
Rheumatoid arthritis (RA) is a chronic systemic autoimmune disease that causes inflammation, pain, stiffness, and destructive changes in the hands, feet, and other joints throughout the body. There are a variety of treatments available to minimize the complications of RA, but they depend on making an accurate diagnosis and on beginning treatment before the development of significant joint damage.

Rheumatoid factor (RF) has been the main autoantibody test used to help in the diagnosis of RA and distinguish it from other types of arthritis and other inflammatory processes. However, RF test is not ideal; it can be negative in patients who have clinical signs of RA and positive in patients who do not e.g. in patients with infections, or in the elderly.

CCP antibodies are much more specific for diagnosis of RA, meaning that if present they are more likely to indicate the presence of RA.

 

However, CCP may be less sensitive than RF, resulting in more false negatives, and hence RF remains the first-line autoantibody test.

  

CCP can be also be useful in helping to diagnose early RA. An elevated CCP can be found in a significant number of patients who have a negative RF, and therefore can help to make a diagnosis. According to the American College of Rheumatology, CCP antibodies may be detected in about 50-60% of patients with early RA (as early as 3-6 months after the beginning of symptoms). Anti-CCP positive early RA patients may develop a more erosive disease than those without anti-CCP. Early detection and diagnosis of RA allows doctors to begin aggressive treatment of the condition, minimizing the associated complications and tissue damage.

CCP may also be requested to help evaluate the likely development of RA in patients with an undifferentiated polyarthritis (those whose symptoms might suggest but do not yet meet the full criteria of RA). The reason it is useful in difficult clinical presentations is that CCP is a more specific test for RA then the traditional RF. According to American College of Rheumatology, approximately 95% of patients with a positive CCP will develop RA in the future.




When is it requested?

CCP can be requested along with an RF test when a patient has symptoms suggestive of RA, or has been diagnosed with an undifferentiated polyarthritis. In many cases, it may be used as a follow-up test to a negative RF test when clinical signs, such as symmetrical joint pain and inflammation, lead the doctor to suspect RA.




What does the test result mean?

As a rule, test results on their own, outside the context of clinical symptoms and signs, cannot be assessed. Nonetheless, if a patient is positive for both CCP and RF, it is very likely that they have RA and it is possible that they may develop a more severe form of the disease. If a patient is positive for CCP but not RF and clinical signs suggest RA, then it is likely that they have early RA or that they will develop RA in the future.

If a patient is negative for CCP but has a positive RF, then the clinical symptoms and signs are more vital in determining whether a patient has RA versus some other inflammatory condition. Remember that RF, particularly weak RF results, can be found in patients with infections, and in the elderly.

If a patient is negative for both CCP and RF, then it is less likely that they have RA. It must be emphasized, however, that RA is a clinical diagnosis based on patient’s symptoms, examination, and radiology, and may be made in the absence of positive autoantibodies.



Is there anything else I should know?

The CCP test is promising but not yet widely used. Its ultimate clinical usefulness and the ways in which it will be used have yet to be determined.

 

The CCP test is not useful for disease monitoring in RA.





This page was last modified on August 20, 2007.
 

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