Diagnostic value of standardized assays for anti-neutrophil cytoplasmic antibodies in idiopathic systemic vasculitis

Autor: E. Christiaan Hagen, Mohamed R. Daha, Jo Hermans, Konrad Andrassy, Elena Csernok, Gillian Gaskin, Phillippe Lesavre, Jens Lüdemann, Niels Rasmussen, R. Alberto Sinico, Allan Wiik, Fokko J. van der Woude, null for the EC/BCR Project for ANCA Assay Standardization
Přispěvatelé: Hagen, E, Daha, M, Hermans, J, Andrassy, K, Csernok, E, Gaskin, G, Lesavre, P, Lüdemann, J, Rasmussen, N, Sinico, R, Wiik, A, Van Der Woude, F
Rok vydání: 1998
Předmět:
Male
Pathology
Proteinase 3
Rapidly progressive glomerulonephritis
Microscopic polyangiiti
Child
Fluorescent Antibody Technique
Indirect

Aged
80 and over

Myeloperoxidase
microscopic polyangiitis
biology
Panca
Wegener’s granulomatosis
Proteinase- 3
IIf
Middle Aged
Serine Endopeptidase
Anti-neutrophil cytoplasmic antibodie
Nephrology
anti-neutrophil cytoplasmic antibodies
ELISA
Systemic vasculiti
Female
systemic vasculitis
Case-Control Studie
Microscopic polyangiitis
Vasculitis
Human
Systemic vasculitis
Adult
Vasculiti
medicine.medical_specialty
Adolescent
Myeloblastin
Churg-Strauss syndrome
Enzyme-Linked Immunosorbent Assay
Sensitivity and Specificity
Antibodies
Antineutrophil Cytoplasmic

Rapidly progressive glomerulonephriti
medicine
cardiovascular diseases
Glomerulonephriti
rapidly progressive glomerulonephritis
Aged
Peroxidase
Anti-neutrophil cytoplasmic antibody
Churg- Strauss syndrome
business.industry
Biomarker
medicine.disease
biology.organism_classification
Immunofluorescence test
Wegener's granulomatosi
Reference Standard
proteinase-3
business
Zdroj: Kidney International. 53:743-753
ISSN: 0085-2538
Popis: Diagnostic value of standardized assays for anti-neutrophil cytoplasmic antibodies in idiopathic systemic vasculitis. Anti-neutrophil cytoplasmic antibodies (ANCA) are widely used as diagnostic markers for Wegener’s granulomatosis (WG), microscopic polyangiitis (MPA), Churg-Strauss syndrome (CSS) and idiopathic rapidly progressive glomerulonephritis (iRPGN). The objective of this study was to evaluate the diagnostic value of ANCA measurement by the indirect immunofluorescence (IIF) test, and by anti-PR3 and anti-MPO ELISA performed in different locations, in patients with idiopathic small vessel vasculitis. Fourteen centers participated in a standardization study of ANCA assays, and entered a total number of 169 newly diagnosed and 189 historical patients with idiopathic systemic vasculitis or iRPGN. Patients were classified according to a pre-defined diagnostic classification system. Results were compared with those of 184 disease controls and 740 healthy controls. The IIF test was performed according to standard methodology; ELISAs had been standardized among the participants in a previous phase of the study. The sensitivities of assays in patients were as follows. The sensitivity in WG was: cANCA 64%, pANCA 21%, anti-PR3 66%, anti-MPO 24%. In MPA the sensitivity was: cANCA 23%, pANCA 58%, anti-PR3 26%, anti-MPO 58%. Sensitivity in iRPGN was: cANCA 36%, pANCA 45%, anti-PR3 50%, anti-MPO 64%. The specificity of assays (related to disease controls) was: cANCA 95%, pANCA 81%, anti-PR3 87%, anti-MPO 91%. When the results of the IIF test were combined with those of the ELISAs (cANCA/anti-PR3 positive, pANCA/anti-MPO positive), the diagnostic specificity increased to 99%. The sensitivity of the combination of cANCA + anti-PR3 or pANCA + anti-MPO for WG, MPA or iRPGN was 73%, 67% and 82%, respectively. From this study we conclude that the value of the IIF test for ANCA detection can be greatly increased by the addition of a well standardized antigen-specific ELISA. In a significant number of patients with idiopathic small vessel vasculitis, however, the ANCA test results (either in IIF or ELISA) are negative.
Databáze: OpenAIRE