4.7 Article

Circulating miRNAs in extracellular vesicles related to treatment response in patients with idiopathic membranous nephropathy

Journal

JOURNAL OF TRANSLATIONAL MEDICINE
Volume 20, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12967-022-03430-7

Keywords

Extracellular vesicles; microRNAs; Glomerulonephritis; Treatment outcome

Funding

  1. Engineering Research Center Program through the National Research Foundation of Korea (NRF) [2018R1A5A1025511]
  2. Ministry of Education through the National Research Foundation of Korea (NRF) [NRF-2020R1I1A3A04037367]
  3. Soonchunhyang University Research Fund
  4. Biobank of Seoul National University Hospital, a member of the Korea Biobank Network [KBN4_A03]
  5. Biobank of Soochunhyang University Seoul Hospital, a member of the Korea Biobank Network [KBN4_A03]

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This study identified circulating extracellular vesicle (EV) microRNAs (miRNAs) associated with idiopathic membranous nephropathy (IMN) and their association with therapeutic response. The results suggest that these EV-miRNAs have potential as markers for the diagnosis and prediction of treatment response in patients with IMN.
Background Extracellular vesicle (EV)-microRNAs (miRNAs) are potential biomarkers for various renal diseases. This study attempted to identify the circulating EV-miRNA signature not only for discriminating idiopathic membranous nephropathy (IMN) from idiopathic nephrotic syndrome (INS), but also to predict the treatment response of patients with IMN. Methods We prospectively enrolled 60 participants, including those with IMN (n = 19) and INS (n = 21) and healthy volunteers (HVs; n = 20) in this study. Using RNA sequencing, we assessed the serum EV-miRNA profiles of all participants. To identify the EV-miRNAs predictive of treatment response in IMN, we also analyzed EV-miRNAs among patients with IMN with and without clinical remission. Results The expression levels of 3 miRNAs differed between IMN patients, INS patients and HVs. In addition, compared to HVs, RNA sequencing revealed differential expression of 77 and 44 EV-miRNAs in patients with IMN without and with remission, respectively. We also identified statistically significant (|fold change >= 2, p < 0.05) differences in the expression levels of 23 miRNAs in IMN without remission. Biological pathway analysis of miRNAs in IMN without remission indicated that they are likely involved in various pathways, including renal fibrosis. Conclusion Our study identified EV-miRNAs associated with IMN as well as those associations with therapeutic response. Therefore, these circulating EV-miRNAs may be used as potential markers for the diagnosis and prediction of treatment response in patients with IMN.

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