Acarbose treatment and the risk of cardiovascular disease and hypertension in patients with impaired glucose tolerance: the STOP-NIDDM trial - PubMed (original) (raw)
Clinical Trial
. 2003 Jul 23;290(4):486-94.
doi: 10.1001/jama.290.4.486.
Affiliations
- PMID: 12876091
- DOI: 10.1001/jama.290.4.486
Clinical Trial
Acarbose treatment and the risk of cardiovascular disease and hypertension in patients with impaired glucose tolerance: the STOP-NIDDM trial
Jean-Louis Chiasson et al. JAMA. 2003.
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
- Acarbose for patients with hypertension and impaired glucose tolerance.
Kaiser T, Sawicki PT. Kaiser T, et al. 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. - Acarbose for patients with hypertension and impaired glucose tolerance.
Bridges CM. Bridges CM. 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. - Acarbose for patients with hypertension and impaired glucose tolerance.
Rosenthal JH. Rosenthal JH. 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. - Acarbose for patients with hypertension and impaired glucose tolerance.
González-Clemente JM, Ortega-Martínez de Victoria E, Giménez-Palop O, Mauricio D. González-Clemente JM, et al. 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. - Acarbose reduced the risk for cardiovascular disease and hypertension in impaired glucose tolerance.
Hackam DG. Hackam DG. ACP J Club. 2004 Jan-Feb;140(1):2. ACP J Club. 2004. PMID: 14711273 No abstract available. - Acarbose and the risk of cardiovascular disease and hypertension.
Barrett EJ. Barrett EJ. Curr Diab Rep. 2004 Feb;4(1):11. Curr Diab Rep. 2004. PMID: 14764272 No abstract available.
Similar articles
- Effects of acarbose on cardiovascular and diabetes outcomes in patients with coronary heart disease and impaired glucose tolerance (ACE): a randomised, double-blind, placebo-controlled trial.
Holman RR, Coleman RL, Chan JCN, Chiasson JL, Feng H, Ge J, Gerstein HC, Gray R, Huo Y, Lang Z, McMurray JJ, Rydén L, Schröder S, Sun Y, Theodorakis MJ, Tendera M, Tucker L, Tuomilehto J, Wei Y, Yang W, Wang D, Hu D, Pan C; ACE Study Group. Holman RR, et al. Lancet Diabetes Endocrinol. 2017 Nov;5(11):877-886. doi: 10.1016/S2213-8587(17)30309-1. Epub 2017 Sep 13. Lancet Diabetes Endocrinol. 2017. PMID: 28917545 Clinical Trial. - Acarbose for the prevention of Type 2 diabetes, hypertension and cardiovascular disease in subjects with impaired glucose tolerance: facts and interpretations concerning the critical analysis of the STOP-NIDDM Trial data.
Chiasson JL, Josse RG, Gomis R, Hanefeld M, Karasik A, Laakso M; STOP-NIDDM Trial Research Group. Chiasson JL, et al. Diabetologia. 2004 Jun;47(6):969-75; discussion 976-7. doi: 10.1007/s00125-004-1409-4. Epub 2004 May 26. Diabetologia. 2004. PMID: 15164169 Clinical Trial. - Inhibition of postprandial hyperglycemia by acarbose is a promising therapeutic strategy for the treatment of patients with the metabolic syndrome.
Yamagishi S, Nakamura K, Takeuchi M. Yamagishi S, et al. Med Hypotheses. 2005;65(1):152-4. doi: 10.1016/j.mehy.2004.12.008. Epub 2005 Jan 28. Med Hypotheses. 2005. PMID: 15893133 - Acarbose in the prevention of cardiovascular disease in subjects with impaired glucose tolerance and type 2 diabetes mellitus.
Delorme S, Chiasson JL. Delorme S, et al. Curr Opin Pharmacol. 2005 Apr;5(2):184-9. doi: 10.1016/j.coph.2004.11.005. Curr Opin Pharmacol. 2005. PMID: 15780829 Review.
Cited by
- Yellow pea-based pasta's impacts on the salt intake, glycemic parameters and oxidative stress in healthy individuals: a randomized clinical trial.
Ito M, Yoshimoto J, Ishii S, Maeda T, Wada Y, Yonei Y, Kishi M, Ono T. Ito M, et al. Sci Rep. 2024 Oct 7;14(1):23333. doi: 10.1038/s41598-024-72290-6. Sci Rep. 2024. PMID: 39375402 Free PMC article. Clinical Trial. - Perspective on the health value of carbohydrate-rich foods: glycemic index and load; fiber and whole grains.
Jenkins DJ, Willett WC. Jenkins DJ, et al. Am J Clin Nutr. 2024 Sep;120(3):468-470. doi: 10.1016/j.ajcnut.2024.07.004. Am J Clin Nutr. 2024. PMID: 39232600 Free PMC article. - Prediabetes: A Benign Intermediate Stage or a Risk Factor in Itself?
Mulla IG, Anjankar A, Pratinidhi S, Agrawal SV, Gundpatil D, Lambe SD. Mulla IG, et al. Cureus. 2024 Jun 26;16(6):e63186. doi: 10.7759/cureus.63186. eCollection 2024 Jun. Cureus. 2024. PMID: 39070421 Free PMC article. Review. - Semaglutide and Cardiovascular Outcomes by Baseline HbA1c and Change in HbA1c in People With Overweight or Obesity but Without Diabetes in SELECT.
Lingvay I, Deanfield J, Kahn SE, Weeke PE, Toplak H, Scirica BM, Rydén L, Rathor N, Plutzky J, Morales C, Lincoff AM, Lehrke M, Jeppesen OK, Gajos G, Colhoun HM, Cariou B, Ryan D; SELECT Trial Investigators. Lingvay I, et al. Diabetes Care. 2024 Aug 1;47(8):1360-1369. doi: 10.2337/dc24-0764. Diabetes Care. 2024. PMID: 38907684 Free PMC article. Clinical Trial. - Two weeks of acarbose treatment shows no effect on gut microbiome composition in patients with type 2 diabetes: a randomised, placebo-controlled, double-blind, crossover study.
Dalsgaard NB, Gasbjerg LS, Hansen LS, Nielsen DS, Rasmussen TS, Knop FK. Dalsgaard NB, et al. Endocr Connect. 2024 Jun 28;13(7):e240052. doi: 10.1530/EC-24-0052. Print 2024 Jul 1. Endocr Connect. 2024. PMID: 38842918 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical