Ev. Ostchepkova et al., Efficacy of 8-week monotherapy with losartan and its combination with hydrochlorothiazide in patients with hypertensive disease, KARDIOLOGIY, 41(6), 2001, pp. 18-24
Effect of 8 weeks of monotherapy with losartan (50 mg/day) on 24-hour blood
pressure (BP) profile was studied in 28 patients with stage I-III hyperten
sive disease. in 16 patients who did not reach target blood pressure hydroc
hlorothiazide was added to losartan for 4 more weeks. Decreases of the foll
owing parameters were observed during monotherapy with losartan: diurnal BP
(by 10.5/6.6+/-2.3/1.8 mm Hg p<0.001), nocturnal BP (by 10.3/5.8+/-2.5/2.0
mm Hg, p<0.01), pulse pressure (p<0.05), rate of morning diastolic BP elev
ation (p<0.002). BP and heart rate (HR) variability, degree of nocturnal lo
wering of systolic BP did not change. Trough/peak ratio was equal to 75 and
64.5% for systolic and diastolic BP, respectively, indicating that losarta
n taken once daily produced sufficient and steady hypotensive effect throug
hout 24 hours. Antihypertensive effect of therapy with losartan was observe
d in 50%, complete normalization of BP - in 33% of patients. In 16 patients
hypotensive effect of losartan was insufficient during day and especially
night time. After addition of hydrochlorothiazide nocturnal systolic BP was
lowered by 11.2+/-2.5 mm Hg (p<0.02), diurnal systolic BP - by 7.0+/-3.7 m
m Hg (p<0.1). Twenty four hour BP rhythm remained normal in dippers and imp
roved in nondipppers and night peakers. BP and HR variability did not chang
e. Target level of BP was achieved in 50% of patients with insufficient eff
ect of losartan. Thus in nonresponders to losartan monotherapy addition of
hydrochlorothiazide led to further lowering of BP and correction of 24-hour
BP profile.