ACE Phenotyping as a Guide Toward Personalized Therapy With ACE Inhibitors

J Cardiovasc Pharmacol Ther. 2017 Jul;22(4):374-386. doi: 10.1177/1074248416686188. Epub 2017 Jan 10.

Abstract

Background: Angiotensin-converting enzyme (ACE) inhibitors (ACEI) are widely used in the management of cardiovascular diseases but with significant interindividual variability in the patient's response.

Objectives: To investigate whether interindividual variability in the response to ACE inhibitors is explained by the "ACE phenotype"-for example, variability in plasma ACE concentration, activity, and conformation and/or the degree of ACE inhibition in each individual.

Methods: The ACE phenotype was determined in plasma of 14 patients with hypertension treated chronically for 4 weeks with 40 mg enalapril (E) or 20 mg E + 16 mg candesartan (EC) and in 20 patients with hypertension treated acutely with a single dose (20 mg) of E with or without pretreatment with hydrochlorothiazide. The ACE phenotyping included (1) plasma ACE concentration; (2) ACE activity (with 2 substrates: Hip-His-Leu and Z-Phe-His-Leu and calculation of their ratio); (3) detection of ACE inhibitors in patient's blood (indicator of patient compliance) and the degree of ACE inhibition (ie, adherence); and (4) ACE conformation.

Results: Enalapril reduced systolic and diastolic blood pressure in most patients; however, 20% of patients were considered nonresponders. Chronic treatment results in 40% increase in serum ACE concentrations, with the exception of 1 patient. There was a trend toward better response to ACEI among patients who had a higher plasma ACE concentration.

Conclusion: Due to the fact that "20% of patients do not respond to ACEI by blood pressure drop," the initial blood ACE level could not be a predictor of blood pressure reduction in an individual patient. However, ACE phenotyping provides important information about conformational and kinetic changes in ACE of individual patients, and this could be a reason for resistance to ACE inhibitors in some nonresponders.

Keywords: ACE conformation; ACE inhibitor; ACE phenotyping; angiotensin-converting enzyme; blood pressure; hypertension; nonresponders.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Angiotensin II Type 1 Receptor Blockers / therapeutic use
  • Angiotensin-Converting Enzyme Inhibitors / adverse effects
  • Angiotensin-Converting Enzyme Inhibitors / pharmacokinetics
  • Angiotensin-Converting Enzyme Inhibitors / therapeutic use*
  • Antihypertensive Agents / adverse effects
  • Antihypertensive Agents / pharmacokinetics
  • Antihypertensive Agents / therapeutic use*
  • Benzimidazoles / therapeutic use
  • Biphenyl Compounds
  • Blood Pressure / drug effects*
  • Cross-Over Studies
  • Double-Blind Method
  • Drug Monitoring
  • Drug Resistance / genetics
  • Drug Therapy, Combination
  • Enalapril / adverse effects
  • Enalapril / pharmacokinetics
  • Enalapril / therapeutic use*
  • Genotype
  • Humans
  • Hydrochlorothiazide / therapeutic use
  • Hypertension / drug therapy*
  • Hypertension / enzymology
  • Hypertension / genetics
  • Hypertension / physiopathology
  • Patient Selection
  • Peptidyl-Dipeptidase A / genetics*
  • Peptidyl-Dipeptidase A / metabolism
  • Pharmacogenetics
  • Pharmacogenomic Testing
  • Pharmacogenomic Variants*
  • Phenotype
  • Precision Medicine*
  • Predictive Value of Tests
  • Sodium Chloride Symporter Inhibitors / therapeutic use
  • Tetrazoles / therapeutic use
  • Treatment Outcome

Substances

  • Angiotensin II Type 1 Receptor Blockers
  • Angiotensin-Converting Enzyme Inhibitors
  • Antihypertensive Agents
  • Benzimidazoles
  • Biphenyl Compounds
  • Sodium Chloride Symporter Inhibitors
  • Tetrazoles
  • Hydrochlorothiazide
  • Enalapril
  • ACE protein, human
  • Peptidyl-Dipeptidase A
  • candesartan