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DOI | 10.1186/1745-6215-12-13 |
Main results of the Ouabain and Adducin for Specific Intervention on Sodium in Hypertension Trial (OASIS-HT): a randomized placebo-controlled phase-2 dose-finding study of rostafuroxin | |
Staessen, Jan A.1,2; Thijs, Lutgarde1; Stolarz-Skrzypek, Katarzyna3; Bacchieri, Antonella4; Barton, John5; degli Espositi, Ezio6; de Leeuw, Peter W.7; Dluzniewski, Miroslaw8; Glorioso, Nicola9; Januszewicz, Andrzej10; Manunta, Paolo11; Milyagin, Viktor12; Nikitin, Yuri13; Soucek, Miroslav14; Lanzani, Chiara11; Citterio, Lorena11; Timio, Mario15; Tykarski, Andrzej16; Ferrari, Patrizia17; Valentini, Giovanni4; Kawecka-Jaszcz, Kalina3; Bianchi, Giuseppe11 | |
通讯作者 | Staessen, Jan A. |
来源期刊 | TRIALS
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ISSN | 1745-6215 |
出版年 | 2011 |
卷号 | 12 |
英文摘要 | Background: The Ouabain and Adducin for Specific Intervention on Sodium in Hypertension (OASIS-HT) Trial was a phase-2 dose-finding study of rostafuroxin, a digitoxygenin derivative, which selectively antagonizes the effects of endogenous ouabain (EO) on Na(+),K(+)-ATPase and mutated adducin. Rostafuroxin lowered blood pressure (BP) in some animal models and in humans. Methods: OASIS-HT consisted of 5 concurrently running double-blind cross-over studies. After 4 weeks without treatment, 435 patients with uncomplicated systolic hypertension (140-169 mm Hg) were randomized to rostafuroxin (0.05, 0.15, 0.5, 1.5 or 5.0 mg/d) or matching placebo, each treatment period lasting 5 weeks. The primary endpoint was the reduction in systolic office BP. Among the secondary endpoints were diastolic office BP, 24-h ambulatory BP, plasma EO concentration and renin activity, 24-h urinary sodium and aldosterone excretion, and safety. ANOVA considered treatment sequence (fixed effect), subjects nested within sequence (random), period (fixed), and treatment (fixed). Results: Among 410 analyzable patients (40.5% women; mean age, 48.4 years), the differences in the primary endpoint (rostafuroxin minus placebo) ranged from -0.18 mm Hg (P = 0.90) on 0.15 mg/d rostafuroxin to 2.72 mm Hg (P = 0.04) on 0.05 mg/d. In the 5 dosage arms combined, the treatment effects averaged 1.30 mm Hg (P = 0.03) for systolic office BP; 0.70 mm Hg (P = 0.08) for diastolic office BP; 0.36 mm Hg (P = 0.49) for 24-h systolic BP; and 0.05 mm Hg (P = 0.88) for 24-h diastolic BP. In the 2 treatment groups combined, systolic (-1.36 mm Hg) and diastolic (-0.97 mm Hg) office BPs decreased from week 5 to 10 (P for period effect <= 0.028), but carry-over effects were not significant (P >= 0.11). All other endpoints were not different on rostafuroxin and placebo. Minor side-effects occurred with similarly low frequency on rostafuroxin and placebo. Conclusions: In 5 concurrently running double-blind cross-over studies rostafuroxin did not reduce BP at any dose. |
类型 | Article |
语种 | 英语 |
国家 | Belgium ; Netherlands ; Poland ; Italy ; Ireland ; Russia ; Czech Republic |
收录类别 | SCI-E |
WOS记录号 | WOS:000286896900001 |
WOS关键词 | ENDOGENOUS OUABAIN ; BLOOD-PRESSURE ; ANTIHYPERTENSIVE COMPOUND ; PST 2238 ; EXCRETION ; GENES |
WOS类目 | Medicine, Research & Experimental |
WOS研究方向 | Research & Experimental Medicine |
资源类型 | 期刊论文 |
条目标识符 | http://119.78.100.177/qdio/handle/2XILL650/170744 |
作者单位 | 1.Katholieke Univ Leuven, Studies Coordinating Ctr, Div Hypertens & Cardiovasc Rehabil, Dept Cardiovasc Res, Louvain, Belgium; 2.Maastricht Univ, Dept Epidemiol, Maastricht, Netherlands; 3.Jagiellonian Univ, Dept Cardiol & Hypertens 1, Coll Med, Krakow, Poland; 4.Sigma Tau Ind Farmaceut Riunite, Pomezia, Italy; 5.Portiuncula Hosp, Cardiac Res Dept, Galway, Ireland; 6.Osped San Maria delle Croci, Unita Valutaz Efficacia Clin, Ravenna, Italy; 7.Maastricht Univ, Dept Internal Med, Med Ctr, Maastricht, Netherlands; 8.Postgrad Med Sch, Dept Cardiol, Warsaw, Poland; 9.Univ Sassari, Hypertens Ctr, I-07100 Sassari, Italy; 10.Med Acad Warsaw, Dept Internal Med & Hypertens, Warsaw, Poland; 11.Univ Vita Salute, Osped San Raffaele, Div Nefrol Dialisi & Ipertens, Dipartimento Sci & Techol Biomed, Milan, Italy; 12.Smolensk State Med Acad, Dept Internal Med, Smolensk, Russia; 13.Russian Acad Med Sci, Inst Internal Med, Siberian Branch, Novosibirsk, Russia; 14.Univ Brno, St Anna Hosp, Dept Internal Med 2, Brno, Czech Republic; 15.Hosp San Giovanni Battista, Dept Internal Med Nephrol & Dialysis, Perugia, Italy; 16.Sch Med, Dept Hypertens, Poznan, Poland; 17.Prassis Res Inst, Milan, Italy |
推荐引用方式 GB/T 7714 | Staessen, Jan A.,Thijs, Lutgarde,Stolarz-Skrzypek, Katarzyna,et al. Main results of the Ouabain and Adducin for Specific Intervention on Sodium in Hypertension Trial (OASIS-HT): a randomized placebo-controlled phase-2 dose-finding study of rostafuroxin[J],2011,12. |
APA | Staessen, Jan A..,Thijs, Lutgarde.,Stolarz-Skrzypek, Katarzyna.,Bacchieri, Antonella.,Barton, John.,...&Bianchi, Giuseppe.(2011).Main results of the Ouabain and Adducin for Specific Intervention on Sodium in Hypertension Trial (OASIS-HT): a randomized placebo-controlled phase-2 dose-finding study of rostafuroxin.TRIALS,12. |
MLA | Staessen, Jan A.,et al."Main results of the Ouabain and Adducin for Specific Intervention on Sodium in Hypertension Trial (OASIS-HT): a randomized placebo-controlled phase-2 dose-finding study of rostafuroxin".TRIALS 12(2011). |
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