4.3 Review

Alpha-glucosidase inhibitors 2012-cardiovascular considerations and trial evaluation

期刊

DIABETES & VASCULAR DISEASE RESEARCH
卷 9, 期 3, 页码 163-169

出版社

SAGE PUBLICATIONS LTD
DOI: 10.1177/1479164112441524

关键词

Alpha-glucosidase inhibitors; postprandial hyperglycaemia; glycaemic variability; myocardial infarction; STOP-NIDDM Trial; Acarbose Evaluation Trial

资金

  1. Association for the Support of International Scientific Communication in Diabetology e.V., Munich, Germany
  2. Astra Zenica
  3. Bayer
  4. BMS
  5. GSK
  6. Johnson Johnson
  7. Lilly
  8. Menarini
  9. Merck-Serono
  10. MSD/Merck
  11. Novartis
  12. NovoNordisk
  13. Rambaxi
  14. Roche
  15. Sanofi-Aventis
  16. Servier
  17. Takeda
  18. Bayer Schering Pharma

向作者/读者索取更多资源

Alpha-glucosidase inhibitors have been available for clinical use for about 20 years. They have shown reasonably good efficacy comparable to other oral blood glucose lowering drugs and in some parts of the world are the most commonly prescribed oral diabetes medication, especially in Asian countries. Unlike as has been observed with some other blood glucose lowering agents, however, no adverse signals of potential cardiovascular harm have emerged in relation to their use. On the contrary, significant beneficial cardiovascular outcome results have been observed in the post-hoc analyses of randomised placebo-controlled trials with the alpha-glucosidase inhibitor acarbose. Targeting mainly postprandial hyperglycaemia, alpha-glucosidase inhibitors favourably affect several cardiovascular risk factors, such as obesity, hypertension and high glycaemic variability with little to no risk for hypoglycaemia. Furthermore, acarbose favourably affects endothelial dysfunction and carotid intima media thickening in humans and, in animal models, improves cardiac interstitial fibrosis and hypertrophy of cardiomyocytes. The ultimate determination of the cardiovascular effects of alpha-glucosidase inhibitors in terms of clinical outcomes awaits the results of ongoing long-term, randomised, placebo-controlled trials.

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