Impact of microRNAs on cardiovascular diseases and aging.

J Int Med Res

Department of Gynecology and Obstetrics, College of Medicine, Jouf University, Sakaka, Kingdom of Saudi Arabia.

Published: October 2024

AI Article Synopsis

  • * MicroRNAs (miRNAs) play a crucial role in regulating heart health, as their abnormal expression is linked to various CVDs and they show promise as both diagnostic markers and therapeutic targets.
  • * Aging negatively affects body functions and is a major, unchangeable risk factor for CVDs, with new research highlighting how miRNAs also influence the aging process and related diseases.

Article Abstract

Cardiovascular disease (CVD) is the leading cause of morbidity and mortality for both men and women among all ethnicities worldwide. Although significant improvements in the management of CVD occurred in the 20th century, non-invasive, universal, early diagnostic biomarkers and newer therapeutic drugs are needed for clinical treatment by physicians. MicroRNAs (miRNAs) are a class of endogenous, non-coding, single-stranded, small RNA molecules that are critically controlled by all human biological processes. Moreover, dysregulated miRNA expression is directly involved in various CVDs, including stable coronary artery disease and acute coronary syndrome. Several miRNAs that are enriched in the plasma of CVD patients have potential as clinical biomarkers, and overexpression or inhibition of specific miRNAs has novel therapeutic significance in the management of CVD. Aging is a multifactorial physiological process that gradually deteriorates tissue and organ function and is considered a non-modifiable major risk factor for CVDs. Recently, several studies established that various miRNAs essentially regulate aging and aging-related disease processes. This narrative review briefly discusses the recently updated molecular involvement of miRNAs in CVDs, their possible diagnostic, prognostic, and therapeutic value, and their relationship to the aging process.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11459564PMC
http://dx.doi.org/10.1177/03000605241279190DOI Listing

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