Pramlintide reduces postprandial glucose excursions when added to insulin lispro in subjects with type 2 diabetes: a dose‐timing study
暂无分享,去创建一个
C. Weyer | S. Schwartz | M. Fineman | J. Ruggles | D. Maggs | O. Kolterman | Yan Wang | Jonathan Kornstein | T. Burrell
[1] L. Bouter,et al. Hyperglycaemia is associated with all-cause and cardiovascular mortality in the Hoorn population: the Hoorn Study , 1999, Diabetologia.
[2] J. Buse,et al. Amylin Replacement With Pramlintide in Type 1 and Type 2 Diabetes: A Physiological Approach to Overcome Barriers With Insulin Therapy , 2002 .
[3] C. Weyer,et al. Amylin replacement with pramlintide as an adjunct to insulin therapy in type 1 and type 2 diabetes mellitus: a physiological approach toward improved metabolic control. , 2001, Current pharmaceutical design.
[4] O. Kolterman,et al. Pramlintide: A Human Amylin Analogue Reduced Postprandial Plasma Glucose, Insulin, and C‐peptide Concentrations in Patients with Type 2 Diabetes , 1997, Diabetic medicine : a journal of the British Diabetic Association.
[5] S. Del Prato. In search of normoglycaemia in diabetes: controlling postprandial glucose , 2002, International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity.
[6] J. Habener,et al. The glucagon-like peptides. , 1999, Endocrine reviews.
[7] W. Scherbaum. The role of amylin in the physiology of glycemic control , 2009, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.
[8] L. Want,et al. Adjunctive therapy with the amylin analogue pramlintide leads to a combined improvement in glycemic and weight control in insulin-treated subjects with type 2 diabetes. , 2002, Diabetes technology & therapeutics.
[9] A. Zinsmeister,et al. Effects of pramlintide, an amylin analogue, on gastric emptying in type 1 and 2 diabetes mellitus , 2002, Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society.
[10] C. Weyer,et al. Unresolved challenges with insulin therapy in type 1 and type 2 diabetes: potential benefit of replacing amylin, a second beta-cell hormone. , 2002, Diabetes technology & therapeutics.
[11] Richard Hellman,et al. The American Association of Clinical Endocrinologists Medical Guidelines for the Management of Diabetes Mellitus : The AACE System of Intensive Diabetes Self-Management — 2002 Update , 2002 .
[12] S. Edelman,et al. Pramlintide as an adjunct to insulin therapy , 2003, Current diabetes reports.
[13] M. Riddle. Evening Insulin Strategy , 1990, Diabetes Care.
[14] C. Weyer,et al. The Human Amylin Analog, Pramlintide, Reduces Postprandial Hyperglucagonemia in Patients with Type 2 Diabetes Mellitus , 2002, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme.
[15] E. Feskens,et al. Glucose tolerance and cardiovascular mortality: comparison of fasting and 2-hour diagnostic criteria. , 2001, Archives of internal medicine.
[16] D. Reed,et al. Postchallenge Glucose Concentration and Coronary Heart Disease in Men of Japanese Ancestry: Honolulu Heart Program , 1987, Diabetes.
[17] R. Rizza,et al. Lack of suppression of glucagon contributes to postprandial hyperglycemia in subjects with type 2 diabetes mellitus. , 2000, The Journal of clinical endocrinology and metabolism.
[18] Standards of Medical Care for Patients With Diabetes Mellitus , 1991, Diabetes Care.
[19] Dennis D. Kim,et al. Novel peptides under development for the treatment of type 1 and type 2 diabetes mellitus. , 2002, Current drug targets. Immune, endocrine and metabolic disorders.
[20] D. Roulin,et al. Effects of regular insulin or insulin LISPRO on glucose metabolism after an oral glucose load in patients with type 2 diabetes mellitus. , 1998, Diabetes & metabolism.
[21] D. Bruttomesso,et al. Restoration of early rise in plasma insulin levels improves the glucose tolerance of type 2 diabetic patients. , 1999, Diabetes.
[22] 1999 European Diabetes Policy Group. A desktop guide to Type 2 diabetes mellitus , 1999 .
[23] S. Schwartz,et al. Effect of 14 days' subcutaneous administration of the human amylin analogue, pramlintide (AC137), on an intravenous insulin challenge and response to a standard liquid meal in patients with IDDM , 1996, Diabetologia.
[24] O. Schmitz,et al. Amylin receptor agonists: a novel pharmacological approach in the management of insulin-treated diabetes mellitus , 2001, Expert opinion on investigational drugs.
[25] R. Unger. Glucagon physiology and pathophysiology. , 1971, The New England journal of medicine.