Blood pressure changes associated with sibutramine and weight management - an analysis from the 6-week lead-in period of the sibutramine cardiovascular outcomes trial (SCOUT)

被引:18
作者
Sharma, A. M. [1 ]
Caterson, I. D. [2 ]
Coutinho, W. [3 ]
Finer, N. [4 ]
Van Gaal, L. [5 ]
Maggioni, A. P. [6 ]
Torp-Pedersen, C. [8 ]
Bacher, H. P. [7 ]
Shepherd, G. M. [7 ]
James, W. P. T. [9 ]
机构
[1] Univ Alberta, Royal Alexandra Hosp, Edmonton, AB T5H 3V9, Canada
[2] Univ Sydney, Human Nutr Unit, Sydney, NSW 2006, Australia
[3] Pontificia Univ Catolica Rio de Janeiro, Endocrinol Obes & Eating Disorders Res Grp, Rio De Janeiro, Brazil
[4] Univ Cambridge, Sch Clin Med, Inst Metab Sci, Wellcome Clin Res Facil, Cambridge, England
[5] Univ Antwerp Hosp, Dept Diabetol Metab & Clin Nutr, Antwerp, Belgium
[6] ANMCO Res Ctr, Florence, Italy
[7] Abbott Labs, Abbott Pk, IL 60064 USA
[8] Univ Copenhagen, Gentofte Hosp, Dept Cardiol, Hellerup, Denmark
[9] London Sch Hyg & Trop Med, London WC1, England
关键词
antiobesity drugs; cardiovascular disease; CVD risk factors; hypertension; obesity; weight loss; HEART-RATE; FOLLOW-UP; HYPERTENSION; MORTALITY; OBESITY;
D O I
10.1111/j.1463-1326.2008.00930.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To explore vital sign changes among patient subgroups during the 6-week lead-in period of the sibutramine cardiovascular outcomes (SCOUT) trial. SCOUT is an ongoing, double-blind, randomized, placebo-controlled outcome trial in overweight/obese patients at high risk of a cardiovascular event. During the 6-week lead-in period, 10 742 patients received sibutramine and weight management. Vital sign changes were assessed post hoc by initial blood pressure (mmHg) categorized as normal (< 130/< 85), high-normal (130 to < 140/85 to < 90) or hypertensive (>= 140/>= 90); weight change categories (weight gain/no weight change, > 0 to 2.5% weight loss, > 2.5 to 5% weight loss and > 5% weight loss) and current antihypertensive medication class use (none, one, or two or more). To assess the impact of sibutramine on blood pressure and pulse rate, only patients (N = 10 025) who reported no change in the class of antihypertensive medication used and who did not report an increase in antihypertensive medication use were analysed. At entry, approximately 50% of patients were hypertensive and 26% were high-normal. In hypertensive patients, blood pressure changes (mmHg) decreased by median [5th, 95th percentile] of -6.5 systolic [-27.0, 8.0] and -2.0 diastolic [-15.0, 8.0] (p < 0.001). Hypertensive patients with no weight loss or with weight gain had median decreases of -3.5 systolic [-26.0, 10.0] and -1.5 diastolic [-16.0, 9.0] (p < 0.001). Normotensive patients had median increases of 1.5 systolic [-15.0, 19.5] and 1.0 diastolic [-10.5, 13.0] (p < 0.001) attenuated with increasing weight loss. Approximately 43% of patients initially categorized as hypertensive had a lower blood pressure category at end-point. Concomitant antihypertensive medication classes did not affect blood pressure reductions. Pulse rates were uniformly elevated (median 1-4 bpm, p < 0.001) across blood pressure and weight change categories. In hypertensive patients (>= 140/>= 90), blood pressure decreases were observed during 6-week treatment with sibutramine even when body weight was unchanged. In patients with normal blood pressure (< 130/< 85), weight loss of > 5% induced decreases in systolic blood pressure; otherwise, small increases were observed. Small pulse rate increases were observed regardless of blood pressure or weight change status.
引用
收藏
页码:239 / 250
页数:12
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