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A panel of serum biomarkers differentiates IgA nephropathy from other renal diseases

There is increasing evidence that galactose-deficient IgA1 (Gd-IgA1) and Gd-IgA1-containing immune complexes are important for the pathogenesis of IgA nephropathy (IgAN). In the present study, we assessed a novel noninvasive multi-biomarker approach in the diagnostic test for IgAN. We compared serum...

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Bibliographic Details
Published in:PloS one 2014-05, Vol.9 (5), p.e98081
Main Authors: Yanagawa, Hiroyuki, Suzuki, Hitoshi, Suzuki, Yusuke, Kiryluk, Krzysztof, Gharavi, Ali G, Matsuoka, Kiyoshi, Makita, Yuko, Julian, Bruce A, Novak, Jan, Tomino, Yasuhiko
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Language:English
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Summary:There is increasing evidence that galactose-deficient IgA1 (Gd-IgA1) and Gd-IgA1-containing immune complexes are important for the pathogenesis of IgA nephropathy (IgAN). In the present study, we assessed a novel noninvasive multi-biomarker approach in the diagnostic test for IgAN. We compared serum levels of IgA, IgG, Gd-IgA1, Gd-IgA1-specific IgG and Gd-IgA1-specific IgA in 135 IgAN patients, 79 patients with non-IgAN chronic kidney disease (CKD) controls and 106 healthy controls. Serum was collected at the time of kidney biopsy from all IgAN and CKD patients. Each serum marker was significantly elevated in IgAN patients compared to CKD (P
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0098081