Antineutrophil cytoplasmic antibodies and the Churg-Strauss syndrome
- PMID: 16263885
- DOI: 10.7326/0003-4819-143-9-200511010-00006
Antineutrophil cytoplasmic antibodies and the Churg-Strauss syndrome
Abstract
Background: Since testing for antineutrophil cytoplasmic antibodies (ANCA) became available for routine evaluation, no large homogeneous cohort of patients with the Churg-Strauss syndrome has been studied.
Objective: To define the clinical and biological characteristics of newly diagnosed Churg-Strauss syndrome, according to the presence or absence of ANCA.
Design: Cross-sectional analysis of manifestations of participants who were enrolled in treatment trials between December 1995 and December 2002.
Setting: Multicenter study in 63 clinical centers in France, Belgium, Latvia, and the United Kingdom, coordinated by the French Vasculitis Study Group.
Participants: 112 patients with Churg-Strauss syndrome that was recently diagnosed on the basis of current classifications.
Measurements: The authors compared principal demographic, clinical, and laboratory features according to ANCA status at diagnosis.
Results: The authors detected ANCA in 43 (38%) patients. Positive ANCA status at diagnosis was associated with renal involvement, peripheral neuropathy, and biopsy-proven vasculitis, whereas negative ANCA status was associated with heart disease and fever.
Limitations: The authors assessed ANCA by immunofluorescence, but they did not assess ANCA centrally or systematically retest if ANCA was undetected at diagnosis.
Conclusions: Phenotypically, ANCA-positive and ANCA-negative Churg-Strauss syndrome might differ. The association of ANCA positivity with clinical symptoms that indicate inflammation and necrosis of small vessels might characterize a predominantly vasculitic pattern of the Churg-Strauss syndrome.
Comment in
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Are there different forms of life in the antineutrophil cytoplasmic antibody universe?Ann Intern Med. 2005 Nov 1;143(9):683-5. doi: 10.7326/0003-4819-143-9-200511010-00012. Ann Intern Med. 2005. PMID: 16263891 No abstract available.
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