Asymptomatic Autoantibodies Associate with Future Anti-glomerular Basement Membrane Disease

• Published in: Journal of the American Society of Nephrology Vol. 22; no. 10; pp. 1946 - 1952
• Main Authors: Olson, Stephen W., Arbogast, Charles B., Baker, Thomas P., Owshalimpur, David, Oliver, David K., Abbott, Kevin C., Yuan, Christina M.
• Format: Journal Article
• Language: English
• Published: Washington, DC American Society of Nephrology 01.10.2011
• Subjects: Adolescent; Adult; Age Factors; Anti-Glomerular Basement Membrane Disease - immunology; Autoantibodies - blood; Biological and medical sciences; Case-Control Studies; Clinical Research; Female; Glomerulonephritis; Humans; Male; Medical sciences; Middle Aged; Myeloblastin - immunology; Nephrology. Urinary tract diseases; Nephropathies. Renovascular diseases. Renal failure; Peroxidase - immunology; Sex Factors; Time Factors; Young Adult; Kidney disease; Autoimmunity; Glomerulonephritis; Nephrology; Urinary system disease; Antibody; Autoantibody; Asymptomatic; Urology; Basement membrane
• ISSN: 1046-6673; 1533-3450; 1533-3450
• DOI: 10.1681/ASN.2010090928

The pathophysiology of anti-glomerular basement membrane (anti-GBM) disease before clinical presentation is unknown. The presence of anti-GBM, anti-proteinase 3 (PR3), and anti-myeloperoxidase (MPO) antibodies associate with the disease at the time of diagnosis, but little is known about the presence of these autoantibodies before diagnosis. We used serum samples from the Department of Defense Serum Repository to conduct a case-control study involving 30 patients diagnosed with anti-GBM disease and 30 healthy controls matched for the age, gender, race, and age of the serum samples. We analyzed a maximum of three samples from each subject: the most recent sample before diagnosis, the penultimate sample before diagnosis, and the oldest sample available; the average time between the most recent sample and diagnosis was 195 days (range, 4 to 1346 days). Elevated anti-GBM levels (≥3 U/ml) were present in four patients, all less than 1 year before diagnosis but in no controls. Detectable anti-GBM antibody levels (≥1 U/ml but <3 U/ml) in a single serum sample before diagnosis were more frequent in cases than controls (70% versus 17%, P < 0.001). Only study patients had detectable anti-GBM levels in multiple samples before diagnosis (50% versus 0%, P < 0.001). Almost all patients had detectable anti-PR3 and/or anti-MPO that preceded the onset of disease. Among patients with a clear antecedent antibody, anti-PR3 or anti-MPO always became detectable before the anti-GBM antibody. In summary, our data describe the subclinical formation of autoantibodies, which improves our understanding of the pathophysiology of anti-GBM disease.