RETRACTED: Valsartan in a Japanese population with hypertension and other cardiovascular disease (Jikei Heart Study): a randomised, open-label, blinded endpoint morbidity-mortality study (Retracted Article)

被引:253
作者
Mochizuki, Seibu [1 ]
Dahloef, Bjorn
Shimizu, Mitsuyuki
Ikewaki, Katsunori
Yoshikawa, Makoto
Taniguchi, Ikuo
Ohta, Makoto
Yamada, Taku
Ogawa, Kazuhiko
Kanae, Kiyoshi
Kawai, Makoto
Seki, Shingo
Okazaki, Fumiko
Taniguchi, Masayuki
Yoshida, Satoru
Tajima, Naoko
机构
[1] Jikei Univ, Sch Med, Dept Internal Med, Div Cardiol,Minato Ku, 3-25-8 Nishi Shinbashi, Tokyo, Japan
[2] Jikei Univ, Sch Med, Dept Internal Med, Div Endocrinol Diabet & Metab, Tokyo, Japan
[3] Sahlgrens Univ Hosp, Dept Emergency & Cardiovasc Med, Inst Med, Gothenburg, Sweden
关键词
D O I
10.1016/S0140-6736(07)60669-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Drugs that inhibit the renin-angiotensin-aldosterone system benefit patients at risk for or with existing cardiovascular disease. However, evidence for this effect in Asian populations is scarce. We aimed to investigate whether addition of an angiotensin receptor blocker, valsartan, to conventional cardiovascular treatment was effective in Japanese patients with cardiovascular disease. Methods We initiated a multicentre, prospective, randomised controlled trial of 3081 Japanese patients, aged 20-79 years, (mean 65 [SD 10] years) who were undergoing conventional treatment for hypertension, coronary heart disease, heart failure, or a combination of these disorders. In addition to conventional treatment, patients were assigned either to valsartan (40-160 mg per day) or to other treatment without angiotensin receptor blockers. Our primary endpoint was a composite of cardiovascular morbidity and mortality. Analysis was by intention to treat. The study was registered at clintrials.gov with the identifier NCT00133328. Findings After a median follow-up of 3.1 years (range 1-3.9) the primary endpoint was recorded in fewer individuals given valsartan than in controls (92 vs 149; absolute risk 21.3 vs 34.5 per 1000 patient years; hazard ratio 0.61, 95% Cl 0.47-0.79, p=0.0002). This difference was mainly attributable to fewer incidences of stroke and transient ischaemic attack (29 vs 48; 0.60, 0.38-0.95, p=0.028), angina pectoris (19 vs 53; 0.35, 0.20-0.58, p < 0.0001), and heart failure (19 vs 36; 0.53, 0.31-0.94, p=0.029) in those given valsartan than in the control group. Mortality or tolerability did not differ between groups. Interpretation The addition of valsartan to conventional treatment prevented more cardiovascular events than supplementary conventional treatment. These benefits cannot be entirely explained by a difference in blood pressure control.
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页码:1431 / 1439
页数:9
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