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Abstract
Background: Stevioside, a natural glycoside isolated from the plant Stevia rebaudiana Bertoni, has been used as a commercial sweetening agent in Japan and Brazil for >20 years.
Previous animal and human studies have indicated that stevioside has an antihypertensive
effect.
Objectives: This study was undertaken to investigate the long-term (2-year) efficacy and tolerability
of stevioside in patients with mild essential hypertension. Secondary objectives were
to determine the effects of stevioside on left ventricular mass index (LVMI) and quality
of life (QOL).
Methods: This was a multicenter, randomized, double-blind, placebo-controlled trial in Chinese
men and women aged between 20 and 75 years with mild essential hypertension (systolic
blood pressure [SBP] 140–159 mm Hg and diastolic blood pressure [DBP] 90–99 mm Hg).
Patients took capsules containing 500 mg stevioside powder or placebo 3 times daily
for 2 years. Blood pressure was measured at monthly clinic visits; patients were also
encouraged to monitor blood pressure at home using an automated device. LVMI was determined
by 2-dimensional echocardiography at baseline and after 1 and 2 years of treatment.
QOL was assessed using the Medical Outcomes Study 36-Item Short-Form Health Survey.
Electrocardiographic, laboratory, and QOL parameters were assessed at the beginning
of treatment, and at 6 months, 1 year, and 2 years.
Results: One hundred seventy-four patients (87 men, 87 women) were enrolled in the study,
and 168 completed it: 82 (42 men, 40 women; mean [SD] age, 52 [7] years) in the stevioside
group and 86 (44 women, 42 men; mean age, 53 [7] years) in the placebo group. After
2 years, the stevioside group had significant decreases in mean (SD) SBP and DBP compared
with baseline (SBP, from 150 [7.3] to 140 [6.8] mm Hg; DBP, from 95 [4.2] to 89 [3.2]
mm Hg; P < 0.05) and compared with placebo (P < 0.05). Based on patients' records of self-monitored blood pressure, these effects
were noted beginning ∼1 week after the start of treatment and persisted throughout
the study. There were no significant changes in body mass index or blood biochemistry,
and the results of laboratory tests were similar in the 2 groups throughout the study.
No significant difference in the incidence of adverse effects was noted between groups,
and QOL scores were significantly improved overall with stevioside compared with placebo
(P < 0.001). Neither group had a significant change in mean LVMI. However, after 2 years,
6 of 52 patients (11.5%) in the stevioside group had left ventricular hypertrophy
(LVH), compared with 17 of 50 patients (34.0%) in the placebo group (P < 0.001). Of those who did not have LVH at baseline, 3 of 46 patients (6.5%) in the
stevioside group had developed LVH after 2 years, compared with 9 of 37 patients (24.3%)
in the placebo group (P < 0.001).
Conclusions: In this 2-year study in Chinese patients with mild hypertension, oral stevioside
significantly decreased SBP and DBP compared with placebo. QOL was improved, and no
significant adverse effects were noted.
Keywords
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Article info
Publication history
Accepted:
September 11,
2003
Identification
Copyright
© 2003 Published by Elsevier Inc.