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Chronic angina: new medical options for treatment
1Department of Medicine, Divisions of Cardiology, Nutrition and Preventive Medicine, William Beaumont Hospital, Royal Oak, Michigan, USA.
Insights
New antianginal medications, trimetazidine and ranolazine, offer improved treatment for coronary artery disease. Ranolazine is highlighted as a significant advancement for patients and clinicians in the US.
Area of Science:
- Cardiology
- Pharmacology
Background:
- The aging US population faces a growing prevalence of coronary artery disease and stable angina.
- Current treatments for stable angina have limitations including reduced work capacity, orthostasis, and drug interactions.
Purpose of the Study:
- To review current medical approaches for chronic stable angina.
- To highlight ranolazine as a novel therapeutic option in the US market.
Main Methods:
- Review of existing randomized trials for trimetazidine (16 trials) and ranolazine (6 trials in the US).
- Analysis of the pharmacological mechanisms of trimetazidine and ranolazine.
Main Results:
- Trimetazidine partially inhibits fatty acid oxidation, shifting myocardial metabolism to a lower oxygen-consuming state.
- Ranolazine functions as a late sodium channel inhibitor, impacting cardiac action potentials and ventricular tachycardia.
- Ranolazine exhibits some fatty acid oxidation properties, but this is not its primary mechanism.
Conclusions:
- Ranolazine represents an important advancement in managing chronic stable angina for US patients and clinicians.
- Piperazine derivatives like trimetazidine and ranolazine offer new therapeutic avenues beyond conventional antianginal therapies.
Abstract:
As the US population ages, the pool of patients with coronary artery disease and stable angina is projected to grow. Conventional approaches with mechanical and pharmacological therapies have made inroads toward curbing this trend, reducing the risk of future myocardial infarction and cardiac death. However, the potential benefits of currently available antianginal medications are limited by reduced work capacity, orthostasis, and important drug-drug interactions. A new approach is represented by the piperazine derivatives trimetazidine (TMZ) and ranolazine (RNZ). TMZ acts to partially inhibit fatty acid oxidation, thus shifting myocardial energy metabolism to a lower oxygen-consuming state. A total of 16 randomized trials have been completed with TMZ. In the US market, 6 trials have been completed with RNZ. RNZ has been separately classified as a late sodium channel inhibitor, which reverses action potential prolongation, suppresses early after-depolarizations, and terminates resultant ventricular tachycardia. Though it has some of the same fatty acid oxidation properties as TMZ, this is not considered its primary mechanism of action. This paper reviews medical approaches to chronic stable angina and highlights RNZ as an important advance for patients and clinicians in the US market.
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