Anti-proteinase 3 antibodies in diffuse systemic sclerosis (SSc) with normotensive renal impairment: is it suggestive for an overlapping between SSc and idiopathic vasculitis?

Bibliographic Details
Title: Anti-proteinase 3 antibodies in diffuse systemic sclerosis (SSc) with normotensive renal impairment: is it suggestive for an overlapping between SSc and idiopathic vasculitis?
Authors: F. Bellisai, G. Morozzi, M.R. Bacarelli, A. Radice, R.A. Sinico, J. Wieslander, G.D. Sebastiani, V. Campanella, R. Marcolongo, M. Galeazzi
Source: Reumatismo, Vol 53, Iss 1 (2001)
Publisher Information: PAGEPress Publications, 2001.
Publication Year: 2001
Collection: LCC:Medicine
LCC:Internal medicine
Subject Terms: Medicine, Internal medicine, RC31-1245
More Details: Objective. To test the prevalence of anti-neutrophil cytoplasmic antibodies (ANCA) in systemic sclerosis (SSc) and to verify a possible association of ANCA with normotensive renal involvement in SSc. Patients and methods: 51 patients affected by SSc, 35 with diffuse scleroderma (dSSc) and 16 with limited scleroderma (lSSc), were tested for ANCA by indirect immunofluorescence (IIF) on human ethanol and formalin-acetone-fixed granulocytes (before and after DNase treatment), by conventional enzyme linked immuno-sorbent assay (ELISA) and by capture-ELISA. Results. Six out of 51 selected SSc patients had ANCA by IIF (11.7%) and five presented a perinuclear/nuclear atypical ANCA pattern. In all cases we only found anti-proteinase3 (aPR3) antibodies. All ANCA positive patients had diffuse form of SSc (17.1%), all were anti-Scl70 positive (aScl70), five patients had proteinuria, three had microscopic haematuria. All ANCA positive patients were normotensive with normal renin plasma levels, the mean erythrocyte sedimentation rate (ESR) was higher in this group compared to the other SSc patients. Conclusions. Our study shows that aPR3 is not rare in dSSc. According to the clinical and serological findings and to the recent literature, we can hypothesise that when ANCA are found in SSc, an overlapping of scleroderma with systemic necrotizing vasculitis should be suspected.
Document Type: article
File Description: electronic resource
Language: English
Italian
ISSN: 0048-7449
2240-2683
Relation: https://reumatismo.org/index.php/reuma/article/view/6; https://doaj.org/toc/0048-7449; https://doaj.org/toc/2240-2683
DOI: 10.4081/reumatismo.2001.33
Access URL: https://doaj.org/article/5af40fe8174e40ba918882999a3612f0
Accession Number: edsdoj.5af40fe8174e40ba918882999a3612f0
Database: Directory of Open Access Journals
More Details
ISSN:00487449
22402683
DOI:10.4081/reumatismo.2001.33
Published in:Reumatismo
Language:English
Italian