» Articles » PMID: 38255639

Traditional Therapeutics and Potential Epidrugs for CVD: Why Not Both?

Overview
Journal Life (Basel)
Specialty Biology
Date 2024 Jan 23
PMID 38255639
Authors
Affiliations
Soon will be listed here.
Abstract

Cardiovascular disease (CVD) is the leading cause of death worldwide. In addition to the high mortality rate, people suffering from CVD often endure difficulties with physical activities and productivity that significantly affect their quality of life. The high prevalence of debilitating risk factors such as obesity, type 2 diabetes mellitus, smoking, hypertension, and hyperlipidemia only predicts a bleak future. Current traditional CVD interventions offer temporary respite; however, they compound the severe economic strain of health-related expenditures. Furthermore, these therapeutics can be prescribed indefinitely. Recent advances in the field of epigenetics have generated new treatment options by confronting CVD at an epigenetic level. This involves modulating gene expression by altering the organization of our genome rather than altering the DNA sequence itself. Epigenetic changes are heritable, reversible, and influenced by environmental factors such as medications. As CVD is physiologically and pathologically diverse in nature, epigenetic interventions can offer a ray of hope to replace or be combined with traditional therapeutics to provide the prospect of addressing more than just the symptoms of CVD. This review discusses various risk factors contributing to CVD, perspectives of current traditional medications in practice, and a focus on potential epigenetic therapeutics to be used as alternatives.

References
1.
Bubna A . Vorinostat-An Overview. Indian J Dermatol. 2015; 60(4):419. PMC: 4533557. DOI: 10.4103/0019-5154.160511. View

2.
Bays H, Kulkarni A, German C, Satish P, Iluyomade A, Dudum R . Ten things to know about ten cardiovascular disease risk factors - 2022. Am J Prev Cardiol. 2022; 10:100342. PMC: 9061634. DOI: 10.1016/j.ajpc.2022.100342. View

3.
Morimoto T, Sunagawa Y, Kawamura T, Takaya T, Wada H, Nagasawa A . The dietary compound curcumin inhibits p300 histone acetyltransferase activity and prevents heart failure in rats. J Clin Invest. 2008; 118(3):868-78. PMC: 2248328. DOI: 10.1172/JCI33160. View

4.
Borgerding M, Klus H . Analysis of complex mixtures--cigarette smoke. Exp Toxicol Pathol. 2005; 57 Suppl 1:43-73. DOI: 10.1016/j.etp.2005.05.010. View

5.
Saltzman B, Weiss N, Sieh W, Fitzpatrick A, McTiernan A, Daling J . Use of antihypertensive medications and breast cancer risk. Cancer Causes Control. 2012; 24(2):365-71. DOI: 10.1007/s10552-012-0122-8. View