RETRACTED: Effects of valsartan on morbidity and mortality in uncontrolled hypertensive patients with high cardiovascular risks: KYOTO HEART Study (Retracted Article)

被引:118
作者
Sawada, Takahisa [1 ]
Yamada, Hiroyuki [1 ]
Dahlof, Bjorn [2 ]
Matsubara, Hiroaki [1 ]
机构
[1] Kyoto Prefectural Univ, Sch Med, Dept Cardiovasc Med, Kamigyo Ku, Kyoto 6028566, Japan
[2] Sahlgrens Univ Hosp, Dept Med, Gothenburg, Sweden
关键词
High-risk hypertension; Angiotensin receptor blockers; Cardiovascular mortality-morbidity; Valsartan; RANDOMIZED-TRIAL; DISEASE; AMLODIPINE; POPULATION; OUTCOMES; MASS;
D O I
10.1093/eurheartj/ehp363
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims The objective was to assess the add-on effect of valsartan on top of the conventional treatment for high-risk hypertension in terms of the morbidity and mortality. Methods and results The KYOTO HEART Study was of a multicentre, Prospective Randomised Open Blinded Endpoint (PROBE) design, and the primary endpoint was a composite of fatal and non-fatal cardiovascular events (clintrials.gov NCT00149227). A total of 3031 Japanese patients (43% female, mean 66 years) with uncontrolled hypertension were randomized to either valsartan add-on or non-ARB treatment. Median follow-up period was 3.27 years. In both groups, blood pressure at baseline was 157/88 and 133/76 mmHg at the end of study. Compared with non-ARB arm, valsartan add-on arm had fewer primary endpoints (83 vs. 155; HR 0.55, 95% Cl 0.42-0.72, P = 0.00001). Conclusion Vatsartan add-on treatment to improve blood pressure control prevented more cardiovascular events than conventional non-ARB treatment in high-risk hypertensive patients in Japan. These benefits cannot be entirely explained by a difference in blood pressure control.
引用
收藏
页码:2461 / 2469
页数:9
相关论文
共 27 条
[1]   World Heart Day 2002 - The international burden of cardiovascular disease: Responding to the emerging global epidemic [J].
Bonow, RO ;
Smaha, LA ;
Smith, SC ;
Mensah, GA ;
Lenfant, C .
CIRCULATION, 2002, 106 (13) :1602-1605
[2]   Angiotensin-converting enzyme inhibitors [J].
Brown, NJ ;
Vaughan, DE .
CIRCULATION, 1998, 97 (14) :1411-1420
[3]   Body-mass index and mortality in a prospective cohort of US adults [J].
Calle, EE ;
Thun, MJ ;
Petrelli, JM ;
Rodriguez, C ;
Heath, CW .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (15) :1097-1105
[4]   A randomized trial of the angiotensin-receptor blocker valsartan in chronic heart failure [J].
Cohn, JN ;
Tognoni, G .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 345 (23) :1667-1675
[5]   Cardiovascular morbidity and mortality in the Losartan Intervention For Endpoint reduction in hypertension study (LIFE):: a randomised trial against atenolol [J].
Dahlöf, B ;
Devereux, RB ;
Kjeldsen, SE ;
Julius, S ;
Beevers, G ;
de Faire, U ;
Fyhrquist, F ;
Ibsen, H ;
Kristiansson, K ;
Lederballe-Pedersen, O ;
Lindholm, LH ;
Nieminen, MS ;
Omvik, P ;
Oparil, S ;
Wedel, H .
LANCET, 2002, 359 (9311) :995-1003
[6]   Hyperch olesterolemia stimulates angiotensin peptide synthesis and contributes to atherosclerosis through the AT1A receptor [J].
Daugherty, A ;
Rateri, DL ;
Lu, H ;
Inagami, T ;
Cassis, LA .
CIRCULATION, 2004, 110 (25) :3849-3857
[7]   The cardiovascular disease continuum validated: Clinical evidence of improved patient outcomes - Part II: Clinical trial evidence (acute coronary syndromes through renal disease) and future directions [J].
Dzau, Victor J. ;
Antman, Elliott M. ;
Black, Henry R. ;
Hayes, David L. ;
Manson, JoAnn E. ;
Plutzky, Jorge ;
Popma, Jeffrey J. ;
Stevenson, William .
CIRCULATION, 2006, 114 (25) :2871-2891
[8]  
Hansson L, 1992, Blood Press, V1, P113, DOI 10.3109/08037059209077502
[9]  
Hollenberg NK, 1998, AM J MANAG CARE, V4, pS384
[10]   Outcomes in hypertensive patients at high cardiovascular risk treated with regimens based on valsartan or amlodipine: the VALUE randomised trial [J].
Julius, S ;
Kjeldsen, SE ;
Weber, M ;
Brunner, HR ;
Ekman, S ;
Hansson, L ;
Hua, TS ;
Laragh, J ;
McInnes, GT ;
Mitchell, L ;
Plat, F ;
Schork, A ;
Smith, B ;
Zanchetti, A .
LANCET, 2004, 363 (9426) :2022-2031