Abstract

IgA nephropathy (IgAN), the most frequent primary glomerulonephritis, affects young patients and is associated with a high risk of progression to end-stage renal disease. Consequently, patients with IgAN constitute an important proportion of candidates for kidney transplantation. Several studies showed a significant risk of IgAN recurrence on kidney graft, but the risks factors for recurrence remain to be accurately evaluated. Indeed, early identification of at risk patients may allow the optimization of treatment and the reduction of recurrence rate on the graft. In the present work, we studied the relationship between post-transplant serum IgA (sIgA) levels and the risk of IgAN recurrence after kidney transplantation. Recipients with IgAN had higher levels of sIgA as compared to patients with other nephropathies (p<0.05). The prevalence of IgAN recurrence was 20.8% during the period of analysis (mean follow-up of 6 ± 3.2 years). Serum IgA levels at M6, M12 and M24 post-transplant were significantly higher in patients with IgAN recurrence as compared to those without (p = 0.009, p = 0.035 and p = 0.029, respectively). Using receiver operating curve (ROC), sIgA at M6 and M12 post-transplant were significantly associated with IgAN recurrence (AUC = 0.771, p = 0.004 and AUC = 0.767, p = 0.016, respectively), while serum creatinine and proteinuria were not. Serum IgA level at month 6 was significantly associated with the occurrence of post-transplant IgA recurrence, whether it was analyzed as a continuous or a categorical variable. After successive adjustment on age, gender and proteinuria, sIgA remained a significant risk factor of post-transplant IgAN recurrence. Finally, survival free of IgAN recurrence was significantly better in patients with sIgA<222 mg/dL at month 6 as compare to IgAN patients with sIgA≥222 mg/dL (p = 0.03). Thus, the present work supports a link between post-transplant sIgA levels and IgAN recurrence and suggests that sIgA may be a valuable predictive biomarker of IgAN recurrence in kidney transplant recipients.

Highlights

  • IgA nephropathy (IgAN), the most frequent primary glomerulonephritis, is characterized by immune deposition of polymeric IgA in the glomerular mesangium [1]

  • We analyzed the relationship between serum IgA (sIgA) levels and the occurrence of IgAN recurrence after kidney transplantation

  • Our results support a link between sIgA and the risk of post-transplant IgAN recurrence

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Summary

Introduction

IgA nephropathy (IgAN), the most frequent primary glomerulonephritis, is characterized by immune deposition of polymeric IgA in the glomerular mesangium [1]. Clinical presentations of IgAN are heterogeneous, going from macroscopic hematuria with or without acute kidney disease to microscopic hematuria with or without proteinuria and hypertension [2]. Several studies showed a high incidence of IgAN recurrence on kidney graft at variable rates, depending on length of posttransplant follow-up and indication for biopsy [4]. The diagnosis of IgAN recurrence associates a compatible clinical context (proteinuria, macroscopic or microscopic hematuria and/or kidney failure) and histological criteria, mainly the presence of mesangial IgA deposition on the graft biopsy. Thereby, identification of biomarkers to predict IgAN recurrence on kidney graft are needed to identify at risk patients. Such biomarkers may allow optimizing treatment and decreasing the rate of IgAN recurrence

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