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PMID: 7623902 Published · ppublish English Clinical Trial Clinical Trial, Phase I Clinical Trial, Phase II Clinical Trial, Phase III Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Efficacy of metformin in patients with non-insulin-dependent diabetes mellitus. The Multicenter Metformin Study Group.

The New England journal of medicine ·Vol. 333 ·No. 9 ·1995-08-31 ·Pages 541-9

DeFronzo RA, Goodman AM

Abstract

Sulfonylurea drugs have been the only oral therapy available for patients with non-insulin-dependent diabetes mellitus (NIDDM) in the United States. Recently, however, metformin has been approved for the treatment of NIDDM. We performed two large, randomized, parallel-group, double-blind, controlled studies in which metformin or another treatment was given for 29 weeks to moderately obese patients with NIDDM whose diabetes was inadequately controlled by diet (protocol 1: metformin vs. placebo; 289 patients), or diet plus glyburide (protocol 2: metformin and glyburide vs. metformin vs. glyburide; 632 patients). To determine efficacy we measured plasma glucose (while the patients were fasting and after the oral administration of glucose), lactate, lipids, insulin, and glycosylated hemoglobin before, during, and at the end of the study. In protocol 1, at the end of the study the 143 patients in the metformin group, as compared with the 146 patients in the placebo group, had lower mean (+/- SE) fasting plasma glucose concentrations (189 +/- 5 vs. 244 +/- 6 mg per deciliter [10.6 +/- 0.3 vs. 13.7 +/- 0.3 mmol per liter], P < 0.001) and glycosylated hemoglobin values (7.1 +/- 0.1 percent vs. 8.6 +/- 0.2 percent, P < 0.001). In protocol 2, the 213 patients given metformin and glyburide, as compared with the 210 patients treated with glyburide alone, had lower mean fasting plasma glucose concentrations (187 +/- 4 vs. 261 +/- 4 mg per deciliter [10.5 +/- 0.2 vs. 14.6 +/- 0.2 mmol per liter], P < 0.001) and glycosylated hemoglobin values (7.1 +/- 0.1 percent vs. 8.7 +/- 0.1 percent, P < 0.001). The effect of metformin alone was similar to that of glyburide alone. Eighteen percent of the patients given metformin and glyburide had symptoms compatible with hypoglycemia, as compared with 3 percent in the glyburide group and 2 percent in the metformin group. In both protocols the patients given metformin had statistically significant decreases in plasma total and low-density lipoprotein cholesterol and triglyceride concentrations, whereas the values in the respective control groups did not change. There were no significant changes in fasting plasma lactate concentrations in any of the groups. Metformin monotherapy and combination therapy with metformin and sulfonylurea are well tolerated and improve glycemic control and lipid concentrations in patients with NIDDM whose diabetes is poorly controlled with diet or sulfonylurea therapy alone.

MeSH Terms
Blood Glucose/analysis Body Weight/drug effects Cholesterol/blood Diabetes Mellitus/blood,drug therapy Diabetes Mellitus, Type 2/blood,drug therapy Double-Blind Method Drug Administration Schedule Drug Therapy, Combination Fasting/blood Female Folic Acid/blood Glucose Tolerance Test Glyburide/therapeutic use Glycated Hemoglobin A/analysis Humans Insulin/blood Lactates/blood Lactic Acid Male Metformin/therapeutic use Middle Aged Obesity Treatment Failure Vitamin B 12/blood
Chemicals
Blood Glucose Glycated Hemoglobin A Insulin Lactates Lactic Acid Metformin Folic Acid Cholesterol Vitamin B 12 Glyburide
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
DeFronzo R A
Diabetes Division, University of Texas Health Science Center, San Antonio, TX 78284, USA.
Goodman A M
Article Info
Journal
The New England journal of medicine
Abbr.
N Engl J Med
ISSN
0028-4793
Published
1995-08-31
Pages
541-9
Language
English
Region
United States
NLM ID
0255562
Subset
IM
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