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Anti-Neutrophil Cytoplasmic Antibodies (C-ANCA, P-ANCA)

Specimen Required

3-5cc Clotted Blood or Serum

Fasting Required

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Purpose of the Test

To test for certain autoimmune disorders, specifically small vessel vasculitities such as as Granulomatosis with polyangitis (GPA formerly known as Wegners Granulomatosis [WG]), microscopic polyangitis (MPA), Churg-Strauss Syndrome (CSS) and a few others

When this test is required

An ANCA test and/or tests for MPO and PR3 are requested when a person is suspected of having a systemic autoimmune vasculitis, especially when symptoms suggest Granulomatosis with polyangitis (GPA ) or microscopic polyangiitis. Early in the disease, symptoms may be vague or nonspecific, such as fever, fatigue, weight loss, muscle and/or joint aches, and night sweats.As the disease progresses, damage to small blood vessels throughout the body may cause signs and symptoms associated with complications involving various tissues and organs. A few examples include: Eyes — red, itchy eyes or “pink eye” (conjunctivitis); problems with sight (blurry vision, loss of vision) Ears — hearing loss Nose — runny nose or other upper respiratory symptoms that do not go away Skin — rashes and/or granulomas Lungs — cough and/or difficulty breathing Kidneys — abnormal amounts of protein in the urineSome laboratories will perform all three tests, ANCA, MPO and PR3, as a panel while others will perform MPO and PR3 only if an initial ANCA test is positive.Testing may also be performed periodically to monitor a person who has been diagnosed with an autoimmune vasculitis.

What the Test Detects

Antineutrophil cytoplasmic antibodies (ANCA) are a group of autoantibodies produced when a person’s immune system mistakenly targets and attacks its own neutrophil proteins. Two of the most commonly targeted proteins are myeloperoxidase (MPO) and proteinase 3 (PR3). This results in the production of antibodies to MPO and/or PR3. The ANCA blood test detects the presence or absence of these autoantibodies by looking at the pattern…Antineutrophil cytoplasmic antibodies (ANCA) are a group of autoantibodies produced when a person’s immune system mistakenly targets and attacks its own neutrophil proteins. Two of the most commonly targeted proteins are myeloperoxidase (MPO) and proteinase 3 (PR3). This results in the production of antibodies to MPO and/or PR3. The ANCA blood test detects the presence or absence of these autoantibodies by looking at the pattern of fluorescence on a slide under a microscope. Antineutrophil cytoplasmic antibodies may be present in a variety of autoimmune disorders that cause inflammation and damage to blood vessels, predominantly small blood vessels, throughout the body (systemic vasculitis). Vasculitis can cause tissue and organ damage due to the narrowing and obstruction of these small blood vessels and the subsequent loss of blood supply. It can also produce areas of weakness in blood vessel walls, known as aneurysms, which have the potential to rupture. The symptoms experienced by a person with small vessel systemic vasculitis depend upon the degree of autoimmune activity and the parts of the body involved. Early in the disease process, symptoms are often nonspecific – they include fatigue, fever, weight loss, muscle aches, and night sweats. As the disorder progresses, vascular damage may affect the functioning of the kidneys, eyes, skin, lungs, and liver. This can cause a wide range of symptoms related to these organ systems. PR3 antibodies are most frequently seen in Granulomatosis with polyangitis (GPA). MPO antibodies are most often associated with microscopic polyangitis but may also be seen in people with pauci-immune necrotising glomerulonephritis, Churg-Strauss syndrome, and GPA.For more about these conditions, visit the Vasculitis UK. See MoreSee Less

Preparation for the Test

None

Sample Requirements

A blood sample taken from a vein in your arm

Additional Notes

In most cases, a biopsy of an affected blood vessel is necessary to confirm a diagnosis of autoimmune vasculitis.