Identification of Plasmatic MicroRNA-206 as New Predictor of Early Recurrence of Atrial Fibrillation After Catheter Ablation Using Next-generation Sequencing
Language English Country New Zealand Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
Grant support
Institutional support project
Fakultni Nemocnice u Svaté Anny v Brně
Specific research of the Masaryk University MUNI/A/1156/2021
Ministerstvo Školství, Mládeže a Tělovýchovy
"National Institute for Research of Metabolic
European Union Next Generation
Cardiovascular Diseases" (Programme EXCELES
European Union Next Generation
No. LX22NPO5104)
European Union Next Generation
PubMed
38459249
PubMed Central
PMC11068688
DOI
10.1007/s40291-024-00698-x
PII: 10.1007/s40291-024-00698-x
Knihovny.cz E-resources
- MeSH
- Biomarkers * blood MeSH
- Atrial Fibrillation * genetics blood diagnosis surgery MeSH
- Catheter Ablation * adverse effects MeSH
- Middle Aged MeSH
- Humans MeSH
- MicroRNAs * blood genetics MeSH
- Prognosis MeSH
- Prospective Studies MeSH
- Recurrence * MeSH
- Aged MeSH
- High-Throughput Nucleotide Sequencing * MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Biomarkers * MeSH
- MicroRNAs * MeSH
- MIRN206 microRNA, human MeSH Browser
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.
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