Atenolol versus losartan in children and young adults with Marfan's syndrome
Publication year
2014Author(s)
Source
The New England Journal of Medicine, 371, 22, (2014), pp. 2061-71ISSN
Publication type
Article / Letter to editor
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Organization
Human Genetics
Journal title
The New England Journal of Medicine
Volume
vol. 371
Issue
iss. 22
Page start
p. 2061
Page end
p. 71
Subject
Radboudumc 0: Other Research RIMLS: Radboud Institute for Molecular Life SciencesAbstract
BACKGROUND: Aortic-root dissection is the leading cause of death in Marfan's syndrome. Studies suggest that with regard to slowing aortic-root enlargement, losartan may be more effective than beta-blockers, the current standard therapy in most centers. METHODS: We conducted a randomized trial comparing losartan with atenolol in children and young adults with Marfan's syndrome. The primary outcome was the rate of aortic-root enlargement, expressed as the change in the maximum aortic-root-diameter z score indexed to body-surface area (hereafter, aortic-root z score) over a 3-year period. Secondary outcomes included the rate of change in the absolute diameter of the aortic root; the rate of change in aortic regurgitation; the time to aortic dissection, aortic-root surgery, or death; somatic growth; and the incidence of adverse events. RESULTS: From January 2007 through February 2011, a total of 21 clinical centers enrolled 608 participants, 6 months to 25 years of age (mean [+/-SD] age, 11.5+/-6.5 years in the atenolol group and 11.0+/-6.2 years in the losartan group), who had an aortic-root z score greater than 3.0. The baseline-adjusted rate of change in the mean (+/-SE) aortic-root z score did not differ significantly between the atenolol group and the losartan group (-0.139+/-0.013 and -0.107+/-0.013 standard-deviation units per year, respectively; P=0.08). Both slopes were significantly less than zero, indicating a decrease in the aortic-root diameter relative to body-surface area with either treatment. The 3-year rates of aortic-root surgery, aortic dissection, death, and a composite of these events did not differ significantly between the two treatment groups. CONCLUSIONS: Among children and young adults with Marfan's syndrome who were randomly assigned to losartan or atenolol, we found no significant difference in the rate of aortic-root dilatation between the two treatment groups over a 3-year period. (Funded by the National Heart, Lung, and Blood Institute and others; ClinicalTrials.gov number, NCT00429364.).
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