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Effect of Acarbose on the 24-Hour Blood Glucose Profile and Pattern of Carbohydrate Absorption

  1. Rodney H Taylor,
  2. David J A Jenkins,
  3. Helen M Barker,
  4. Hashmein Fielden,
  5. David V Goff,
  6. J J Misiewicz,
  7. Donald A Lee,
  8. H Brian Allen,
  9. Garry MacDonald and
  10. Horst Wallrabe
  1. Department of Gastroenterology and Nutrition, Central Middlesex Hospital London NW10
  2. Department of Nutritional Sciences, Faculty of Medicine, University of Toronto
  3. University Laboratory of Physiology Oxford
  4. Bayer UK Limited, Pharmaceutical Division, Haywards Heath Sussex
  1. Address reprint requests to Rodney H. Taylor, Department of Gastroenterology and Nutrition, Central Middlesex Hospital, Park Royal, London NW10, England.

Abstract

Acarbose (Bay g 5421) is a powerful α-glucoside hydrolase inhibitor of potential value in the treatment of diabetes and hypoglycemic dumping syndrome after gastric surgery. The extent of its use may be limited by symptoms produced by carbohydrate malabsorption. To minimize these, the action of low doses of acarbose on 24-h blood glucose profiles and hydrogen evolution have been studied on four ambulant volunteers on control diets, after exclusion of sucrose and also after addition of guar in an attempt to enhance the therapeutic effect. Replacement of dietary sucrose by starch abolished significant hydrogen evolution in the morning after low doses of acarbose but did not reduce its effectiveness in decreasing the mean three-meal blood glucose area by 41% (P < 0.002). Addition of hydrated guar to this diet reduced the mean three-meal glucose area after acarbose further by 72% (P < 0.001) but increased hydrogen evolution. The results suggest that acarbose will be both effective and acceptable given at low dose when the dietary carbohydrate is starch.

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