Skip Main Navigation
outline goes here
The Lancet, Volume 369, Issue 9571, Pages 1431 - 1439, 28 April 2007
doi:10.1016/S0140-6736(07)60669-2Cite or Link Using DOI
This article can be found in the following collections: Cardiology & Vascular Medicine (Hypertension)

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

Summary

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% CI 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.
To read this article in full you will need to login or make a payment

Already Registered?  Please Login

Payment Options

Purchase this article for $31.50
Online access for 24 hours. The PDF version can be downloaded as your permanent record.

Visit SciVerse ScienceDirect to see if you have access via your institution.

Already a Print Subscriber?

Claim online access
Renew your print subscription

Have a Free Trial Code?

Activate your free trial
a Division of Cardiology, Department of Internal Medicine, Jikei University School of Medicine, Tokyo, Japan
b Division of Diabetes, Metabolism, and Endocrinology, Department of Internal Medicine, Jikei University School of Medicine, Tokyo, Japan
c Institute of Medicine, Department of Emergency and Cardiovascular Medicine, Sahlgrenska University Hospital/Östra, Göteborg, Sweden
Corresponding Author Information Correspondence to: Prof Seibu Mochizuki, Division of Cardiology, Department of Internal Medicine, The Jikei University School of Medicine, 3-25-8 Nishi-shinbashi, Minato-ku, Tokyo, Japan
Members listed at end of article
Access this article on SciVerse ScienceDirect
Visit SciVerse ScienceDirect to see if you have access via your institution.
Article Options
Summary
Full Text
PDF (198 KB)
Cited by in Scopus (250)
Printer Friendly Version
Download images
Request permission
Export Citation
Create Citation Alert
Please login above or register to use this functionality. Registration is free, takes no more than two minutes, and offers you many benefits.
Bookmark