4.5 Article

Electrophoretic methods for analysis of urinary polypeptides in IgA-associated renal diseases

期刊

ELECTROPHORESIS
卷 28, 期 23, 页码 4469-4483

出版社

WILEY
DOI: 10.1002/elps.200700237

关键词

CE; IgA nephropathy; MS; urinary proteomics

资金

  1. NCRR NIH HHS [M01 RR00211, M01 RR00032] Funding Source: Medline
  2. NIDDK NIH HHS [DK64400, DK61525, DK78244, DK71802] Funding Source: Medline
  3. NIGMS NIH HHS [5 T32 GM08349, GM080148] Funding Source: Medline

向作者/读者索取更多资源

We evaluated the utility of SDS-PAGE/Western blot and CE coupled with NIS (CE-MS) for detection of urinary polypeptide biomarkers of renal disease in patients with IgA-associated glomerulonephritides. In a reference cohort of 402 patients with various renal disorders and 207 healthy controls, we defined CE-MS patterns of renal damage and IgA nephropathy (IgAN). In a blinded analysis of a separate cohort of patients with IgAN (n = 10), Henoch-Schoenlein purpura (HSP) with nephritis (n = 10), and IgA-associated glomerulonephritis due to hepatitis C virus (HCV)-induced cirrhosis (n = 9), and healthy controls (n = 12), we compared SDS-PAGE/Westem blot and CE-MS against clinical urinalysis for detection of urinary proteins/polypeptides. Urinalysis indicated proteinuria for 50, 90, and 33% of patients, respectively, and for none of the healthy controls. SDS-PAGE/Westem blot showed urinary polypeptides abnormality for 90, 80, and 67% of patients, respectively, and for none of the healthy controls. CE-MS indicated a Renal Damage Pattern in 80, 80, and 100 of patients, respectively, and in 17% of healthy controls, with the more specific IgAN Pattern in 90, 90, and 1%, respectively, and in none of the healthy controls. Based on differences in CE-MS patterns, the disease mechanisms may differ among various IgA-associated glomerulonephritides. These exploratory findings should be evaluated in a prospective study with contemporaneous renal biopsy and urinary testing. If validated, it may be feasible to adapt the CE-MS methodology to develop novel tests to detect renal injury at earlier stages., assess clinical manifestations, and monitor responses to therapy in patients with IgA-associated renal diseases.

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