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Circulating miRNA Expression Profiling in Primary Aldosteronism.

Authors :
Decmann, Abel
Nyírö, Gábor
Darvasi, Ottó
Turai, Péter
Bancos, Irina
Kaur, Ravinder Jeet
Pezzani, Raffaele
Iacobone, Maurizio
Kraljevic, Ivana
Kastelan, Darko
Parasiliti-Caprino, Mirko
Maccario, Mauro
Nirschl, Nina
Heinrich, Daniel
Reincke, Martin
Patócs, Attila
Igaz, Peter
Source :
Frontiers in Endocrinology; 10/29/2019, Vol. 10, p1-12, 12p
Publication Year :
2019

Abstract

Objective: Primary aldosteronism is a major cause of secondary hypertension. Its two principal forms are bilateral adrenal hyperplasia (BAH) and aldosterone-producing adenoma (APA) whose differentiation is clinically pivotal. There is a major clinical need for a reliable and easily accessible diagnostic biomarker for case identification and subtyping. Circulating microRNAs were shown to be useful as minimally invasive diagnostic markers. Our aim was to determine and compare the circulating microRNA expression profiles of adenoma and hyperplasia plasma samples, and to evaluate their applicability as minimally invasive markers. Methods: One hundred and twenty-three samples from primary aldosteronism patients were included. Next-generation sequencing was performed on 30 EDTA-anticoagulated plasma samples (discovery cohort). Significantly differently expressed miRNAs were validated by real-time reverse transcription-qPCR in an independent validation cohort (93 samples). Results: We have found relative overexpression of miR-30e-5p, miR-30d-5p, miR-223-3p , and miR-7-5p in hyperplasia compared to adenoma by next-generation sequencing. Validation by qRT-PCR confirmed significant overexpression of hsa-miR-30e-5p, hsa-miR-30d-5p , and hsa-miR-7-5p in hyperplasia samples. Regarding the microRNA expressional variations, adenoma is more heterogeneous at the miRNA level compared to hyperplasia. Conclusion: Three microRNAs were significantly overexpressed in hyperplasia samples compared to adenoma samples, but their sensitivity and specificity values are not good enough for introduction to clinical practice. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16642392
Volume :
10
Database :
Complementary Index
Journal :
Frontiers in Endocrinology
Publication Type :
Academic Journal
Accession number :
139649037
Full Text :
https://doi.org/10.3389/fendo.2019.00739