Abstract

Background/aims: Previous studies showed that two microRNAs, let-7b and miR-148, which regulate the O-glycosylation process of IgA1, may predict diagnosis of primary IgA nephropathy (IgAN). The combined analysis of their serum levels in calculated statistical models may act as serum biomarkers for the diagnosis of primary IgAN. In the present study, we aimed to assess their impact not only on clinical and histological findings at onset but also on renal function after a long-term follow-up. Patients and methods: We enrolled 61 Caucasian patients with biopsy-proven IgAN. Serum levels of miR-148b, let-7b, and galactose-deficient IgA1 (Gd-IgA1) at the time of diagnosis were measured using real-time quantitative PCR and enzyme-linked immunosorbent assay using the monoclonal antibody KM55, respectively. Their values along with calculated Models 1 and 2 were correlated with histologic scoring system (Oxford classification system) and with renal function at diagnosis and after 11.9 ± 6.6 years. Fifty-five healthy volunteers were enrolled as controls. Results: No significant correlation was found between miRNA and Gd-IgA1 levels and eGFR and proteinuria at diagnosis. A significant negative association was detected between the presence of crescents and serum levels of let-7b (p = 0.002), miR-148b (p = 0.01), and Models 1 and 2 (p = 0.02 and p = 0.007, respectively). At the end of follow-up, eGFR correlated with let-7b levels (p = 0.01), Model 1 (p = 0.002), and Model 2 (p = 0.004). Patients with fast progression of the renal damage had significantly increased levels of let-7b (p = 0.01), Model 1 (p = 0.003), and Model 2 (p = 0.005) compared to slow progressors, as did those who reached ESKD (p = 0.002, p = 0.001, and p = 0.001, respectively). Results were most prominent in those treated with corticosteroids. Finally, cut off levels in Models 1 and 2 could also predict the renal function outcome after long-term follow-up. Conclusions: Serum levels of let-7b and miR-148b and their combination, may serve as predictors for long-term renal function outcomes, particularly in patients treated with corticosteroids.

Highlights

  • Immunoglobulin A nephropathy (IgAN) is the most common glomerulonephritis worldwide even though its true incidence might be underestimated since many cases are thought to remain undiagnosed

  • In the present study we evaluated the possible correlation between serum Galactose-deficient IgA1 (Gd-IgA1) levels, together with two miRNAs, which regulate the glycosylation process of IgA1 molecule, miR-148, and let-7b, with clinical and kidney biopsy findings at presentation

  • The present study is based on previously estimated miRNA serum levels, and calculated models based on the above measurements, which established their significant role in the diagnosis of primary IgAN [9]

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Summary

Introduction

Immunoglobulin A nephropathy (IgAN) is the most common glomerulonephritis worldwide even though its true incidence might be underestimated since many cases are thought to remain undiagnosed. Several attempts have been made to predict the course of the disease based on clinical [1] or histological [2] score systems but additional criteria reflecting the major players involved in the pathogenesis of IgAN could be very helpful. They could identify patients at high risk for deterioration of renal function and allow a more aggressive and targeted treatment in these cases. This assay is easier to perform and more reliable than the previous assays for Gd-IgA1 detection using lectins

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