Angiotensin converting enzyme gene polymorphism predicts blood pressure response to angiotensin II receptor type 1 antagonist treatment in hypertensive patientsShow others and affiliations
2001 (English)In: Journal of Hypertension, ISSN 0263-6352, E-ISSN 1473-5598, Vol. 19, no 10, p. 1783-1787Article in journal (Refereed) Published
Abstract [en]
OBJECTIVES: To determine whether polymorphisms in the renin-angiotensin system can predict blood pressure-lowering response to antihypertensive treatment; more specifically, in response to treatment with irbesartan or atenolol.
DESIGN AND METHODS: Eighty-six patients with hypertension were randomized to double-blind treatment with either the angiotensin II type 1 receptor antagonist irbesartan or the beta1 adrenergic receptor blocker atenolol and followed for 3 months. We analysed angiotensinogen T174M and M235T, angiotensin converting enzyme (ACE) I/D and angiotensin II type 1 receptor A1166C polymorphisms and related them to blood pressure reduction.
RESULTS: The mean reductions in blood pressure were similar for both treatments. In the irbesartan group, individuals homozygous for the ACE gene I allele showed a greater reduction in diastolic blood pressure, exceeding those with the D allele (-18 +/- 11 SD versus -7 +/- 10 mmHg, P = 0.0096). This was not the case during treatment with atenolol, and the interaction term between type of treatment and ACE II genotype was significant (P = 0.0176). The angiotensinogen and angiotensin II type 1 receptor polymorhisms were not related to the response to treatment.
CONCLUSIONS: ACE genotyping predicted the blood pressure-lowering response to antihypertensive treatment with irbesartan but not atenolol. Thus, specific genotypes might predict the response to specific antihypertensive treatment.
Place, publisher, year, edition, pages
Lippincott Williams & Wilkins, 2001. Vol. 19, no 10, p. 1783-1787
Keywords [en]
genes, pharmacology, treatment, renin-angiotensin system
National Category
Medical and Health Sciences Cardiac and Cardiovascular Systems Pharmacology and Toxicology
Identifiers
URN: urn:nbn:se:oru:diva-69695DOI: 10.1097/00004872-200110000-00012ISI: 000171341200012PubMedID: 11593098OAI: oai:DiVA.org:oru-69695DiVA, id: diva2:1257328
2018-10-192018-10-192018-10-19Bibliographically approved