Exploring the role of non-coding RNAs in atrial septal defect pathogenesis: A systematic review

Author:

AmiRsardari ZahraORCID,Gholipour Akram,Khajali Zahra,Maleki Majid,Malakootian MahshidORCID

Abstract

Background Extensive research has recognized the significant roles of non-coding RNAs (ncRNAs) in various cellular pathophysiological processes and their association with diverse diseases, including atrial septal defect (ASD), one of the most prevalent congenital heart diseases. This systematic review aims to explore the intricate involvement and significance of ncRNAs in the pathogenesis and progression of ASD. Methods Four databases (PubMed, Embase, Scopus, and the Web of Science) were searched systematically up to June 19, 2023, with no year restriction. The risk of bias assessment was evaluated using the Newcastle-Ottawa scale. Results The present systematic review included thirteen studies with a collective study population of 874 individuals diagnosed with ASD, 21 parents of ASD patients, and 22 pregnant women carrying ASD fetuses. Our analysis revealed evidence linking five long ncRNAs (STX18-AS1, HOTAIR, AA709223, BX478947, and Moshe) and several microRNAs (hsa-miR-19a, hsa-miR-19b, hsa-miR-375, hsa-miR-29c, miR-29, miR-143/145, miR-17-92, miR-106b-25, and miR-503/424, miR-9, miR-30a, miR-196a2, miR-139-5p, hsa-let-7a, hsa-let-7b, and hsa-miR-486) to ASD progression, corresponding to previous studies. Conclusions NcRNAs play a crucial role in unraveling the underlying mechanisms of ASD, contributing to both biomarker discovery and therapeutic advancements. This systematic review sheds light on the mechanisms of action of key ncRNAs involved in ASD progression, providing valuable insights for future research in this field.

Publisher

Public Library of Science (PLoS)

Reference79 articles.

1. Atrial septal defects;T. Geva;The Lancet,2014

2. Long-term outcomes after atrial septal defect transcatheter closure by age and against population controls;L. Abrahamyan;Cardiovascular Interventions,2021

3. Atrial septal defect;E.A. Bradley;Cardiology clinics,2020

4. Phenotypes with GATA4 or NKX2. 5 mutations in familial atrial septal defect;K. Hirayama‐Yamada;American journal of medical genetics Part A,2005

5. Identification and functional study of GATA4 gene regulatory variants in atrial septal defects;D. Fan;BMC Cardiovascular Disorders,2021

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