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J Cardiovasc Pharmacol Ther ; 22(4): 374-386, 2017 07.
Artículo en Inglés | MEDLINE | ID: mdl-28587581

RESUMEN

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.


Asunto(s)
Inhibidores de la Enzima Convertidora de Angiotensina/uso terapéutico , Antihipertensivos/uso terapéutico , Presión Sanguínea/efectos de los fármacos , Enalapril/uso terapéutico , Hipertensión/tratamiento farmacológico , Peptidil-Dipeptidasa A/genética , Variantes Farmacogenómicas , Medicina de Precisión , Bloqueadores del Receptor Tipo 1 de Angiotensina II/uso terapéutico , Inhibidores de la Enzima Convertidora de Angiotensina/efectos adversos , Inhibidores de la Enzima Convertidora de Angiotensina/farmacocinética , Antihipertensivos/efectos adversos , Antihipertensivos/farmacocinética , Bencimidazoles/uso terapéutico , Compuestos de Bifenilo , Estudios Cruzados , Método Doble Ciego , Monitoreo de Drogas , Resistencia a Medicamentos/genética , Quimioterapia Combinada , Enalapril/efectos adversos , Enalapril/farmacocinética , Genotipo , Humanos , Hidroclorotiazida/uso terapéutico , Hipertensión/enzimología , Hipertensión/genética , Hipertensión/fisiopatología , Selección de Paciente , Peptidil-Dipeptidasa A/metabolismo , Farmacogenética , Pruebas de Farmacogenómica , Fenotipo , Valor Predictivo de las Pruebas , Inhibidores de los Simportadores del Cloruro de Sodio/uso terapéutico , Tetrazoles/uso terapéutico , Resultado del Tratamiento
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