4.7 Article

Differential expression of microRNA miR-150-5p in IgA nephropathy as a potential mediator and marker of disease progression

Journal

KIDNEY INTERNATIONAL
Volume 99, Issue 5, Pages 1127-1139

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.kint.2020.12.028

Keywords

IgAN; kidney biopsy; microRNA (miR)

Funding

  1. Kidney Research UK
  2. Mayer Family Foundation
  3. European Rare Kidney Disease Network (ERKNet) by Deutsche Forschungsgemeinschaft [BE-3801]
  4. University Hospital of Cologne, Germany

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The study identified four microRNAs that are differentially expressed in IgA nephropathy progressors compared to non-progressors, and correlated with kidney function and histological scores. MiR-150-5p showed the best discrimination ability between progressors and nonprogressors, indicating a potential role in kidney fibrosis.
Understanding why certain patients with IgA nephropathy progress to kidney failure while others maintain normal kidney function remains a major unanswered question. To help answer this, we performed miRNome profiling by next generation sequencing of kidney biopsies in order to identify microRNAs specifically associated with the risk of IgA nephropathy progression. Following sequencing and validation in independent cohorts, four microRNAs (-1505p,-155-5p, -146b-5p, -135a-5p) were found to be differentially expressed in IgA nephropathy progressors compared to non-progressors, and patients with thin membrane nephropathy, lupus nephritis and membranous nephropathy, and correlated with estimated glomerular filtration rate, proteinuria, and the Oxford MEST-C scores (five histological features that are independent predictors of clinical outcome). Each individual microRNA increased the discrimination score of the International IgAN Prediction Tool, although due to the small number of samples the results did not reach statistical significance. miR-150-5p exhibited the largest amplitude of expression between cohorts and displayed the best discrimination between IgA nephropathy progressors and nonprogressors by receiver operating curve analysis (AUC: 0.8). However, expression was similarly upregulated in kidneys with established fibrosis and low estimated glomerular filtration rates at the time of biopsy. Consistent with a more generic role in kidney fibrosis, in situ hybridization revealed that miR-150-5p was found in lymphoid infiltrates, and areas of proliferation and fibrosis consistent with the known drivers of progression. Thus, miR-150-5p may be a potential functional mediator of kidney fibrosis that may add value in predicting risk of progression in IgA nephropathy and other kidney diseases.

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