impact factor, citescore
logo
 

Full Papers

 

What is the clinical significance of anti-Sm antibodies in systemic lupus erythematosus? A comparison with anti-dsDNA antibodies and C3


1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11

 

  1. Department of Rheumatology and Clinical Immunology, Charité University Hospital Berlin, Germany.
  2. Department of Rheumatology and Clinical Immunology, Charité University Hospital Berlin, Germany.
  3. Department of Rheumatology and Clinical Immunology, Charité University Hospital Berlin, Germany.
  4. Department of Rheumatology and Clinical Immunology, Charité University Hospital Berlin, Germany.
  5. German Rheumatism Research Center Berlin-Leibniz Institute, Germany.
  6. EUROIMMUN Medizinische Labordiagnostika AG, Lübeck, Germany.
  7. EUROIMMUN Medizinische Labordiagnostika AG, Lübeck, Germany.
  8. Department of Nephrology and Intensive Care Medicine, Charité University Hospital Berlin, Germany.
  9. Department of Rheumatology and Clinical Immunology, Charité University Hospital Berlin, Germany.
  10. Department of Rheumatology and Clinical Immunology, Charité University Hospital Berlin, Germany.
  11. Department of Rheumatology and Clinical Immunology, Charité University Hospital Berlin, Germany. robert.biesen@charite.de

CER9757
2017 Vol.35, N°4
PI 0598, PF 0606
Full Papers

Free to view
(click on article PDF icon to read the article)

PMID: 28281463 [PubMed]

Received: 13/07/2016
Accepted : 20/12/2016
In Press: 03/03/2017
Published: 13/07/2017

Abstract

OBJECTIVES:
To investigate the clinical value of anti-Sm antibodies in diagnosis and monitoring of systemic lupus erythematosus (SLE) and their ability to predict lupus flares compared with that of anti-dsDNA antibody and complement (C3) assays.
METHODS:
Autoantibodies against Smith antigen (Sm) and double-stranded DNA (dsDNA) in sera from SLE (n=232), myositis (n=26), systemic sclerosis (n=81), Sjögren’s syndrome (n=88), and rheumatoid arthritis patients (n=165) and healthy donors (n=400) were determined by using enzyme-linked immunosorbent assays (both from Euroimmun). New thresholds for both autoantibodies were calculated by receiver operating characteristics (ROC) curve analysis. Cross-sectional, longitudinal and predictive analyses of anti-Sm and disease activity were also performed.
RESULTS:
Sensitivities of 25.9% for anti-Sm (cut-off: 3.6 relative units/ml) and 30.2% for anti-dsDNA (cut-off 157.4 international units/ml) were obtained at a specificity of 99%. 14.8% of anti-dsDNA-negative patients were positive for anti-Sm, and more than half (51.4%) of anti-dsDNA-positive patients were also positive for anti-Sm. Anti-Sm antibodies were associated with age (p=0.0174), the number of ACR criteria (p=0.0242), the ACR criteria renal (p=0.0350) and neurologic disorder (p=0.0239), the BILAG category constitutional symptoms (p=0.0227), fatigue (p=0.0311) and cross-sectional disease activity (r=0.2519, p=0.0224). Although no correlations with lupus activity were observed in the longitudinal and predictive analysis, a remarkable association was found between anti-Sm and proteinuria.
CONCLUSIONS:
Anti-Sm antibodies are essential for diagnosis of SLE, especially in anti-dsDNA-negative patients. However, our data suggest that anti-Sm monitoring is only helpful in SLE patients with active lupus nephritis.

Rheumatology Article

Rheumatology Addendum