A similar 24-h blood pressure control is obtained by zofenopril and candesartan in primary hypertensive patients

Objective. To compare the antihypertensive effect of treatment with zofenopril vs candesartan by office and ambulatory blood pressure (BP). Design and methods. Following a 2-week wash-out from previous treatment, 236 grade I-II primary hypertensive patients were randomized double-blind to 12 weeks treatment with zofenopril 30 mg or candesartan 8 mg od. After 4 weeks, treatment was doubled in responder non-normalized (office systolic BP≥140 mmHg and office diastolic BP reduction ≥10 mmHg) or non-responder patients (office systolic BP≥140 mmHg and office diastolic BP reduction <10 mmHg). Following a further 4 weeks, non-responder non-normalized patients were withdrawn. Results. In the intention-to-treat population, office systolic BP and diastolic BP reductions after 12 weeks of treatment were similar between the two groups (zofenopril: 21±11/15±8 mmHg, n=114 vs C: 20±11/15±7 mmHg (candesartan; p=NS). Also 24-h ambulatory BPs were equally reduced by zofenopril and candesartan (7±13/ 5±8 mmHg vs 7±12/5±8 mmHg; p=NS). The trough-to-peak ratio and smoothness index were not sigficantly different between zofenopril and candesartan. Tolerability of both drugs was good. Conclusions. Monotherapy with zofenopril and candesartan similary reduced office and 24-h BPs. Since almost 90% of patiens were normalized by either zofenopril or candesartan, this result suppots the importance of considering low- or high-dose monotherapies as initial for most hypertensive patients of mild degree.