Effect of Fimasartan versus Valsartan and Olmesartan on Office and Ambulatory Blood Pressure in Korean Patients with Mild-to-Moderate Essential Hypertension: A Randomized, Double-Blind, Active Control, Three-Parallel Group, Forced Titration, Multicenter, Phase IV Study (Fimasartan Achieving Systolic Blood Pressure Target (FAST) Study)

被引:7
|
作者
Chung, Woo-Baek [1 ]
Ihm, Sang-Hyun [2 ]
Jang, Sung-Won [3 ]
Her, Sung-Ho [4 ]
Park, Chul Soo [5 ]
Lee, Jong-Min [6 ]
Chang, Kiyuk [1 ]
Jeon, Doo-Soo [7 ]
Yoo, Ki-Dong [8 ]
Seung, Ki-Bae [1 ]
机构
[1] Catholic Univ Korea, Seoul St Mais Hosp, Dept Internal Med, Div Cardiol, 222 Banpo Daero, Seoul 06591, South Korea
[2] Catholic Univ Korea, Bucheon St Marys Hosp, Dept Internal Med, Div Cardiol, Seoul, South Korea
[3] Catholic Univ Korea, Div Cardiol, Dept Internal Med, St Pauls Hosp, Seoul, South Korea
[4] Catholic Univ Korea, Daejeon St Marys Hosp, Seoul, South Korea
[5] Catholic Univ Korea, Yeouido St Marys Hosp, Dept Internal Med, Div Cardiol, Seoul, South Korea
[6] Catholic Univ Korea, Uijeongbu St Marys Hosp, Dept Internal Med, Div Cardiol, Seoul, South Korea
[7] Catholic Univ Korea, In Cheon St Marys Hosp, Dept Internal Med, Div Cardiol, Seoul, South Korea
[8] Catholic Univ Korea, St Vincents Hosp, Dept Internal Med, Div Cardiol, Seoul, South Korea
来源
关键词
24 hr ambulatory blood pressure monitoring; angiotensin receptor blocker; essential hypertension; antihypertensive; ANGIOTENSIN RECEPTOR BLOCKERS; COMPARATIVE EFFICACY; PARALLEL-GROUP; NETWORK METAANALYSIS; II ANTAGONISTS; CLINICAL-TRIAL; SAFETY; MANAGEMENT; LOSARTAN; 8-WEEK;
D O I
10.2147/DDDT.S231293
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Purpose: Head-to-head comparison of the blood pressure (BP) lowering effect of fimasartan versus valsartan, with olmesartan as a reference, on office blood pressure and ambulatory BP. Patients and Methods: Of the 369 randomly assigned patients in this study, 365 hypertensive patients were referred as the full analysis set and divided into 3 groups with a 3:3:1 ratio (fimasartan group: 155, valsartan group: 157, olmesartan group: 53). After the 2-week single-blind placebo run-in period, initial standard doses of 60-mg fimasartan, 80-mg valsartan, and 10-mg olmesartan were administered for 2 weeks, then forcibly up-titrated higher doses (fimasartan 120 mg, valsartan 160 mg, olmesartan 20 mg) were given for 4 weeks. ABP was measured before and after the 6-week treatment. Primary endpoint was reduction of sitting office systolic BP (SiSBP) of fimasartan compared to valsartan after 6 weeks. Secondary endpoints were reduction of sitting office diastolic BP (SiDBP) and 24 hrs, daytime, and night-time mean systolic and diastolic ABP (ASBP, ADBP) after 6 weeks. Results: Patients' mean age was 58.34+7.68 years, and 289 patients were male (79.18%). After the 6-week treatment, SiSBP reduction of fimasartan and valsartan were -16.26+15.07 and -12.81+13.87 (p=0.0298) and SiDBP were -7.63+9.67 and -5.14+8.52 (p=0.0211). Reductions in 24 hrs mean ASBP were -15.22+13.33 and -9.45+12.37 (p=0.0009), and ADBPs were -8.74+7.55 and -5.98+7.85 (p=0.0140). Reductions of night-time ASBPs were -16.80+15.81 and -10.32+14.88 (p=0.0012), and those of night-time ADBPs were -8.89 +9.93 and -5.55+9.70 (p=0.0152). Reduction of BP in olmesartan group did not demonstrate significant difference with fimasartan group in all end-points. Conclusion: Fimasartan 120-mg treatment demonstrated superior efficacy in reduction of SiSBP, SiDBP, and 24 hrs ASBP and ADBP compared to valsartan 160 mg. Reduction of night-time ASBP from baseline was largest in fimasartan group, suggesting that fimasartan may be effective for recovering dipping pattern.
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收藏
页码:347 / 360
页数:14
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