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Treating postprandial hyperglycemia does not appear to delay progression of early type 2 diabetes: the Early Diabetes Intervention Program.

AbstractOBJECTIVE:
Postprandial hyperglycemia characterizes early type 2 diabetes. We investigated whether ameliorating postprandial hyperglycemia with acarbose would prevent or delay progression of diabetes, defined as progression to frank fasting hyperglycemia, in subjects with early diabetes (fasting plasma glucose [FPG] <140 mg/dl and 2-h plasma glucose > or =200 mg/dl).
RESEARCH DESIGN AND METHODS:
Two hundred nineteen subjects with early diabetes were randomly assigned to 100 mg acarbose t.i.d. or identical placebo and followed for 5 years or until they reached the primary outcome (two consecutive quarterly FPG measurements of > or =140 mg/dl). Secondary outcomes included measures of glycemia (meal tolerance tests, HbA(1c), annual oral glucose tolerance tests [OGTTs]), measures of insulin resistance (homeostasis model assessment [HOMA] of insulin resistance and insulin sensitivity index from hyperglycemic clamps), and secondary measures of beta-cell function (HOMA-beta, early- and late-phase insulin secretion, and proinsulin-to-insulin ratio).
RESULTS:
Acarbose significantly reduced postprandial hyperglycemia. However, there was no difference in the cumulative rate of frank fasting hyperglycemia (29% with acarbose and 34% with placebo; P = 0.65 for survival analysis). There were no significant differences between groups in OGTT values, measures of insulin resistance, or secondary measures of beta-cell function. In a post hoc analysis of subjects with initial FPG <126 mg/dl, acarbose reduced the rate of development of FPG > or =126 mg/dl (27 vs. 50%; P = 0.04).
CONCLUSIONS:
Ameliorating postprandial hyperglycemia did not appear to delay progression of early type 2 diabetes. Factors other than postprandial hyperglycemia may be greater determinants of progression of diabetes. Alternatively, once FPG exceeds 126 mg/dl, beta-cell failure may no longer be remediable.
AuthorsM Sue Kirkman, R Ravi Shankar, Sudha Shankar, Changyu Shen, Edward Brizendine, Alain Baron, Janet McGill
JournalDiabetes care (Diabetes Care) Vol. 29 Issue 9 Pg. 2095-101 (Sep 2006) ISSN: 0149-5992 [Print] United States
PMID16936159 (Publication Type: Journal Article, Randomized Controlled Trial, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Chemical References
  • Blood Glucose
  • Hypoglycemic Agents
  • Acarbose
Topics
  • Acarbose (administration & dosage, therapeutic use)
  • Adult
  • Blood Glucose (analysis)
  • Diabetes Mellitus, Type 2 (blood, drug therapy, pathology)
  • Disease Progression
  • Female
  • Humans
  • Hyperglycemia (blood, drug therapy)
  • Hypoglycemic Agents (administration & dosage, therapeutic use)
  • Kaplan-Meier Estimate
  • Male
  • Middle Aged
  • Postprandial Period
  • Treatment Outcome

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