J 2024

Identification of Plasmatic microRNA-206 as New Predictor of Early Recurrence of Atrial Fibrillation after Catheter Ablation Using Next-generation Sequencing

ŠUSTR, Filip; Táňa MACHÁČKOVÁ; Martin PEŠL; Jana SVAČINOVÁ; Karolína TRACHTOVÁ et al.

Basic information

Original name

Identification of Plasmatic microRNA-206 as New Predictor of Early Recurrence of Atrial Fibrillation after Catheter Ablation Using Next-generation Sequencing

Authors

ŠUSTR, Filip; Táňa MACHÁČKOVÁ; Martin PEŠL; Jana SVAČINOVÁ; Karolína TRACHTOVÁ; Zdeněk STÁREK; Bohuslav KIANIČKA; Ondřej SLABÝ and Jan NOVÁK

Edition

THERAPY, AUCKLAND, ADIS INT LTD, 2024, 1177-1062

Other information

Language

English

Type of outcome

Article in a journal

Country of publisher

New Zealand

Confidentiality degree

is not subject to a state or trade secret

References:

URL

Marked to be transferred to RIV

Yes

RIV identification code

RIV/00216224:14110/24:00135395

Organization

Lékařská fakulta – Repository – Repository

DOI

https://doi.org/10.1007/s40291-024-00698-x

UT WoS

001177382100001

EID Scopus

2-s2.0-85186885685

Keywords in English

Plasmatic MicroRNA-206; Atrial Fibrillation; Catheter Ablation

Links

LX22NPO5104, research and development project. MUNI/A/1156/2021, interní kód Repo. MUNI/A/1377/2022, interní kód Repo. MUNI/A/1555/2023, interní kód Repo.
Changed: 4/9/2025 00:49, RNDr. Daniel Jakubík

Abstract

In the original language

Background Catheter ablation (CA) of atrial fibrillation (AF) is indicated in patients with recurrent and symptomatic AF episodes. Despite the strict inclusion/exclusion criteria, AF recurrence after CA remains high. Identification of a novel biomarker that would predict AF recurrence would help to stratify the patients. The aim of the study was to seek novel biomarkers among the plasmatic microRNAs (miRNAs, miRs). Methods A prospective monocentric study was conducted. A total of 49 consecutive AF patients indicated for CA were included. Blood sampling was performed prior to CA. RNA was isolated from plasma using commercial kits. In the exploration phase, small RNA sequencing was performed in ten AF patients (five with and five without AF recurrence) using Illumina instrument. In the validation phase, levels of selected miRNAs were determined using quantitative reverse transcription polymerase chain reaction (qRT-PCR) in all participants. Results Altogether, 22 miRNAs were identified as altered between the groups by next-generation sequencing (using the DESeq2 algorithm). Using qRT-PCR, levels of the five most altered miRNAs (miR-190b/206/326/505-5p/1296-5p) were verified in the whole cohort. Plasma levels of hsa-miR-206 were significantly higher in patients with early (within 6 months) AF recurrence and showed an increase of risk recurrence,2.65 times by every increase in its level by 1 unit in the binary logistic regression. Conclusion We have identified a set of 22 plasmatic miRNAs that differ between the patients with and without AF recurrence after CA and confirmed hsa-miR-206 as a novel miRNA associated with early AF recurrence. Results shall be verified in a larger independent cohort.
Displayed: 2/5/2026 19:08