Exosomal miRNA Changes Associated with Restoration to Sinus Rhythm in Atrial Fibrillation Patients

Author:

Tsai Pei-Chien123,Ko Albert Min-Shan124,Chen Yu-Lin1,Chiu Cheng-Hsun35,Yeh Yung-Hsin46,Tsai Feng-Chun78

Affiliation:

1. Department of Biomedical Sciences, Chang Gung University, Taoyuan City 33302, Taiwan

2. Healthy Aging Research Center, Chang Gung University, Taoyuan City 33302, Taiwan

3. Molecular Infectious Disease Research Center, Chang Gung Memorial Hospital, Taoyuan City 33305, Taiwan

4. Cardiovascular Department, Chang Gung Memorial Hospital, Taoyuan City 33305, Taiwan

5. Division of Pediatric Infectious Diseases, Department of Pediatrics, Chang Gung Memorial Hospital, Taoyuan City 33305, Taiwan

6. School of Medicine, Chang Gung University, Taoyuan City 33302, Taiwan

7. Department of Surgery, College of Medicine, Kaohsiung Medical University, Kaohsiung City 80708, Taiwan

8. Division of Cardiovascular Surgery, Department of Surgery, Kaohsiung Medical University Hospital, Kaohsiung City 80708, Taiwan

Abstract

We aimed to identify serum exosomal microRNAs (miRNAs) associated with the transition from atrial fibrillation (AF) to sinus rhythm (SR) and investigate their potential as biomarkers for the early recurrence of AF within three months post-treatment. We collected blood samples from eight AF patients at Chang Gung Memorial Hospital in Taiwan both immediately before and within 14 days following rhythm control treatment. Exosomes were isolated from these samples, and small RNA sequencing was performed. Using DESeq2 analysis, we identified nine miRNAs (16-2-3p, 22-3p, 23a-3p, 23b-3p, 125a-5p, 328-3p, 423-5p, 504-5p, and 582-3p) associated with restoration to SR. Further analysis using the DIABLO model revealed a correlation between the decreased expression of miR-125a-5p and miR-328-3p and the early recurrence of AF. Furthermore, early recurrence is associated with a longer duration of AF, presumably indicating a more extensive state of underlying cardiac remodeling. In addition, the reads were mapped to mRNA sequences, leading to the identification of 14 mRNAs (AC005041.1, ARHGEF12, AMT, ANO8, BCL11A, DIO3OS, EIF4ENIF1, G2E3-AS1, HERC3, LARS, NT5E, PITX1, SLC16A12, and ZBTB21) associated with restoration to SR. Monitoring these serum exosomal miRNA and mRNA expression patterns may be beneficial for optimizing treatment outcomes in AF patients.

Funder

Chang Gung Memorial Hospital

Ministry of Science and Technology, Taiwan

Publisher

MDPI AG

Reference46 articles.

1. Zheng, D., Huo, M., Li, B., Wang, W., Piao, H., Wang, Y., Zhu, Z., Li, D., Wang, T., and Liu, K. (2021). The Role of Exosomes and Exosomal MicroRNA in Cardiovascular Disease. Front. Cell Dev. Biol., 8.

2. The Role of Exosomes and Their Cargos in the Mechanism, Diagnosis, and Treatment of Atrial Fibrillation;Huang;Front. Cardiovasc. Med.,2021

3. Quality of life in patients with atrial fibrillation: How to assess it and how to improve it;Aliot;EP Eur.,2014

4. Revisiting Antiarrhythmic Drug Therapy for Atrial Fibrillation: Reviewing Lessons Learned and Redefining Therapeutic Paradigms;Geng;Front. Pharmacol.,2020

5. Techniques improving electrical cardioversion success for patients with atrial fibrillation: A systematic review and meta-analysis;Nguyen;EP Eur.,2023

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