Why the study?
Does pharmacogenetic profiling influence the response to ACE inhibitors in patients with stable coronary artery disease?
Does pharmacogenetic profiling influence the response to ACE inhibitors in patients with stable coronary artery disease?
Pharmacogenetic profiling of the renin-angiotensin-aldosterone system may enable personalized ACE inhibitor therapy in patients with stable coronary artery disease.
May support RAAS pharmacogenetic personalization of ACE inhibitors in stable CAD; leaves open need for prospective outcome trials.
The angiotensin-converting enzyme (ACE) inhibitors are a cornerstone drug therapy in the current treatment of patients with hypertension, stable coronary artery disease and heart failure. Individualizing therapy of ACE inhibitors with clinical risk factors in low-risk patients with stable coronary artery disease is not feasible. The concept of pharmacogenetics, by studying patient factors more individually, offers a first glimpse in the quest for the 'holy grail' of personalized medicine. As such, genetic targets in the direct pharmacodynamic pathway of ACE inhibitors, the renin-angiotensin-aldosterone system, is a plausible candidate for such an approach. In the past few decades, results of pharmacogenetic studies were scarce and inconsistent. However, recently the first reports of larger pharmacogenetic studies are now confirming that the 'pharmacogenetic approach' might be feasible in the future. The current review focuses on the recent developments in pharmacogenetic research in response to ACE inhibitors in patients with stable coronary artery disease.
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Brugts et al. (2012) studied this question.
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