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  • Meeting abstract
  • Open Access

Presence of anti-RNP-A and anti-RNP-C antibodies is inversely associated with renal symptoms of systemic lupus erythematosus

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Arthritis Res Ther20035 (Suppl 1) :9

  • Received: 14 January 2003
  • Published:


  • Confidence Interval
  • Systemic Lupus Erythematosus
  • Proteinuria
  • Systemic Lupus Erythematosus Patient
  • Glomerulonephritis


Systemic lupus erythematosus (SLE) is an autoimmune rheumatic disease characterised by the production of autoantibodies. The most common serious feature of SLE is renal involvement. An association with anti-RNP antibodies remains controversial.


To identify associations of autoantibodies and renal symptoms in a consecutive cohort of SLE patients.


Sera and clinical data from 235 consecutive SLE patients, fulfilling the ACR criteria for SLE, were collected in four centres. The presence of renal disease was defined as the presence of cellular casts in the urine, proteinuria (>0.5 g/day), or glomerulonephritis during the course of the disease. Autoantibody profiles were determined by the INNO-LIA™ ANA Update (a line immunoassay with recombinant and/or native antigens, including SmB, SmD, RNP-70, RNP-A, RNP-C, Ro52, Ro60, SSB, and ribosomal P) and anti-dsDNA antibodies by indirect immunofluorescence on Crithidia luciliae. Odds ratios (ORs) and their 95% confidence intervals (CI) were computed to determine the associations between antibodies and renal symptoms. No correction was made for multiple testing.


The presence of anti-RNP-A and anti-RNP-C appeared to be protective against renal involvement (OR = 0.445, CI = 0.210–0.942 and OR = 0.484, CI = 0.243–0.964, respectively). Concerning the individual symptoms, anti-RNP-C was associated with a lower occurrence of proteinuria (OR = 0.470, CI = 0.230–6.938), cellular casts (OR = 0.324, CI = 0.150–0.696) and glomerulonephritis (OR = 0.460, CI = 0.226–0.934), whereas anti-RNP-A was only significantly associated with a lower occurrence of cellular casts (OR = 0.303, CI = 0.129–0.716). In contrast, antibodies to dsDNA were associated with a higher risk for cellular casts (OR = 2.014, CI = 1.057–3.839). We found no associations between renal symptoms and other specific antinuclear reactivities. More specifically, for anti-RNP-70 a trend was only detected for the association with the presence of cellular casts (OR = 0.411, CI = 0.153–1.106).


Anti-RNP-A and anti-RNP-C antibodies appear to be associated with a lower risk for renal disease.

Authors’ Affiliations

UZG, Ghent, Belgium
Innogenetics, Ghent, Belgium
Leiden University Medical Center, Leiden, The Netherlands
Research Institute for Rheumatic Diseases, Piestany, Slovakia
University College London, London, UK


© The Author(s) 2003