Acarbose treatment and the risk of cardiovascular disease and hypertension in patients with impaired glucose tolerance: the STOP-NIDDM trial
- PMID: 12876091
- DOI: 10.1001/jama.290.4.486
Acarbose treatment and the risk of cardiovascular disease and hypertension in patients with impaired glucose tolerance: the STOP-NIDDM trial
Abstract
Context: The worldwide explosive increase in type 2 diabetes mellitus and its cardiovascular morbidity are becoming major health concerns.
Objective: To evaluate the effect of decreasing postprandial hyperglycemia with acarbose, an alpha-glucosidase inhibitor, on the risk of cardiovascular disease and hypertension in patients with impaired glucose tolerance (IGT).
Design, setting, and participants: International, multicenter double-blind, placebo-controlled, randomized trial, undertaken in hospitals in Canada, Germany, Austria, Norway, Denmark, Sweden, Finland, Israel, and Spain from July 1998 through August 2001. A total of 1429 patients with IGT were randomized with 61 patients (4%) excluded because they did not have IGT or had no postrandomization data, leaving 1368 patients for a modified intent-to-treat analysis. Both men (49%) and women (51%) participated with a mean (SD) age of 54.5 (7.9) years and body mass index of 30.9 (4.2). These patients were followed up for a mean (SD) of 3.3 (1.2) years.
Intervention: Patients with IGT were randomized to receive either placebo (n = 715) or 100 mg of acarbose 3 times a day (n = 714).
Main outcome measures: The development of major cardiovascular events (coronary heart disease, cardiovascular death, congestive heart failure, cerebrovascular event, and peripheral vascular disease) and hypertension (> or =140/90 mm Hg).
Results: Three hundred forty-one patients (24%) discontinued their participation prematurely, 211 in the acarbose-treated group and 130 in the placebo group; these patients were also followed up for outcome parameters. Decreasing postprandial hyperglycemia with acarbose was associated with a 49% relative risk reduction in the development of cardiovascular events (hazard ratio [HR], 0.51; 95% confidence interval [CI]; 0.28-0.95; P =.03) and a 2.5% absolute risk reduction. Among cardiovascular events, the major reduction was in the risk of myocardial infarction (HR, 0.09; 95% CI, 0.01-0.72; P =.02). Acarbose was also associated with a 34% relative risk reduction in the incidence of new cases of hypertension (HR, 0.66; 95% CI, 0.49-0.89; P =.006) and a 5.3% absolute risk reduction. Even after adjusting for major risk factors, the reduction in the risk of cardiovascular events (HR, 0.47; 95% CI, 0.24-0.90; P =.02) and hypertension (HR, 0.62; 95% CI, 0.45-0.86; P =.004) associated with acarbose treatment was still statistically significant.
Conclusion: This study suggests that treating IGT patients with acarbose is associated with a significant reduction in the risk of cardiovascular disease and hypertension.
Comment in
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Acarbose for patients with hypertension and impaired glucose tolerance.JAMA. 2003 Dec 17;290(23):3066; author reply 3067-9. doi: 10.1001/jama.290.23.3066-b. JAMA. 2003. PMID: 14679260 No abstract available.
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Acarbose for patients with hypertension and impaired glucose tolerance.JAMA. 2003 Dec 17;290(23):3066-7; author reply 3067-9. doi: 10.1001/jama.290.23.3066-c. JAMA. 2003. PMID: 14679261 No abstract available.
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Acarbose for patients with hypertension and impaired glucose tolerance.JAMA. 2003 Dec 17;290(23):3066; author reply 3067-9. doi: 10.1001/jama.290.23.3066-a. JAMA. 2003. PMID: 14679262 No abstract available.
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Acarbose for patients with hypertension and impaired glucose tolerance.JAMA. 2003 Dec 17;290(23):3067; author reply 3067-9. doi: 10.1001/jama.290.23.3067-a. JAMA. 2003. PMID: 14679263 No abstract available.
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Acarbose reduced the risk for cardiovascular disease and hypertension in impaired glucose tolerance.ACP J Club. 2004 Jan-Feb;140(1):2. ACP J Club. 2004. PMID: 14711273 No abstract available.
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Acarbose and the risk of cardiovascular disease and hypertension.Curr Diab Rep. 2004 Feb;4(1):11. Curr Diab Rep. 2004. PMID: 14764272 No abstract available.
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