You are seeing this message because your Web browser does not support basic Web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.


ABOUT JAMA
Advanced Search

Welcome   | My Account | E-mail Alerts | Access Rights | Sign In


  Vol. 289 No. 1, January 1, 2003 TABLE OF CONTENTS
  JAMA
  •  Online Features
  Original Contribution
 This Article
 •Full text
 •PDF
 •Send to a friend
 • Save in My Folder
 •Save to citation manager
 •Permissions
 Citing Articles
 •Citation map
 •Citing articles on HighWire
 •Citing articles on ISI (54)
 •Contact me when this article is cited
 Related Content
 •Similar articles in JAMA
 Topic Collections
 •Neurology
 •Randomized Controlled Trial
 •Headache
 •Migraine
 •Alert me on articles by topic

Prophylactic Treatment of Migraine With an Angiotensin II Receptor Blocker

A Randomized Controlled Trial

Erling Tronvik, MD; Lars J. Stovner, PhD; Grethe Helde, RN; Trond Sand, PhD; Gunnar Bovim, PhD

JAMA. 2003;289:65-69.

Context  There is a paucity of effective, well-tolerated drugs available for migraine prophylaxis.

Objective  To determine whether treatment with the angiotensin II receptor blocker candesartan is effective as a migraine-prophylactic drug.

Design and Setting  Randomized, double-blind, placebo-controlled crossover study performed in a Norwegian neurological outpatient clinic from January 2001 to February 2002.

Patients  Sixty patients aged 18 to 65 years with 2 to 6 migraine attacks per month were recruited mainly from newspaper advertisements.

Interventions  A placebo run-in period of 4 weeks was followed by two 12-week treatment periods separated by 4 weeks of placebo washout. Thirty patients were randomly assigned to receive one 16-mg candesartan cilexetil tablet daily in the first treatment period followed by 1 placebo tablet daily in the second period. The remaining 30 received placebo followed by candesartan.

Main Outcome Measures  The primary end point was number of days with headache; secondary end points included hours with headache, days with migraine, hours with migraine, headache severity index, level of disability, doses of triptans, doses of analgesics, acceptability of treatment, days of sick leave, and quality-of-life variables on the Short Form 36 questionnaire.

Results  In a period of 12 weeks, the mean number of days with headache was 18.5 with placebo vs 13.6 with candesartan (P = .001) in the intention-to-treat analysis (n = 57). Some secondary end points also favored candesartan, including hours with headache (139 vs 95; P<.001), days with migraine (12.6 vs 9.0; P<.001), hours with migraine (92.2 vs 59.4; P<.001), headache severity index (293 vs 191; P<.001), level of disability (20.6 vs 14.1; P<.001) and days of sick leave (3.9 vs 1.4; P = .01), although there were no significant differences in health-related quality of life. The number of candesartan responders (reduction of >=50% compared with placebo) was 18 (31.6%) of 57 for days with headache and 23 (40.4%) of 57 for days with migraine. Adverse events were similar in the 2 periods.

Conclusion  In this study, the angiotensin II receptor blocker candesartan provided effective migraine prophylaxis, with a tolerability profile comparable with that of placebo.


Author Affiliations: Department of Neurology and Clinical Neurophysiology, Norwegian University of Science and Technology, Trondheim, Norway.



THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Migraine prevention
Dodick and Silberstein
PN 2007;7:383-393.
ABSTRACT | FULL TEXT  

Headaches and the Treatment of Blood Pressure: Results From a Meta-Analysis of 94 Randomized Placebo-Controlled Trials With 24 000 Participants
Law et al.
Circulation 2005;112:2301-2306.
ABSTRACT | FULL TEXT  

Topiramate for Migraine Prevention: A Randomized Controlled Trial
Brandes et al.
JAMA 2004;291:965-973.
ABSTRACT | FULL TEXT  

Angiotensin-Receptor Blockade to Prevent Migraines
JWatch General 2003;2003:7-7.
FULL TEXT  





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 2003 American Medical Association. All Rights Reserved.