Factors associated with diabetes onset during metformin versus placebo therapy in the Diabetes Prevention Program

被引:77
作者
Lachin, John M.
Christophi, Costas A.
Edelstein, Sharon L.
Ehrmann, David A.
Hamman, Richard F.
Kahn, Steven E.
Knowler, William C.
Nathan, David M.
机构
[1] George Washington Univ, Ctr Biostat, Diabet Prevent Program Coordinating Ctr, Rockville, MD 20852 USA
[2] Univ Chicago, Chicago, IL 60637 USA
[3] Univ Colorado, Sch Med, Denver, CO USA
[4] VA PUget Sound Hlth Care Syst, Dept Internal Med, Div Metab Endocrinol & Nutr, Seattle, WA USA
[5] Univ Washington, Seattle, WA 98195 USA
[6] NIDDKD, Phoenix, AZ 85016 USA
[7] Massachusetts Gen Hosp, Boston, MA 02114 USA
关键词
D O I
10.2337/db06-0918
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
In the Diabetes Prevention Program, treatment of subjects with impaired glucose tolerance with metformin > 3.2 years reduced the risk of developing type 2 diabetes by 30% compared with placebo. This study describes the mechanisms of this effect. In proportional hazards regression models with 2,155 subjects, changes in weight, the insulinogenic index (IGR), fasting insulin, and proinsulin were predictive of diabetes, though to different degrees within each group. The mean change in weight, fasting insulin, and proinsulin, but not IGR, differed between groups during the study. The 1.7-kg weight loss with metformin versus a 0.3-kg gain with placebo alone explained 64% of the beneficial metformin effect on diabetes risk. Adjustment for weight, fasting insulin, proinsulin, and other metabolic factors combined explained 81% of the beneficial metformin effect, but it remained nominally significant (P = 0.034). After the addition of changes in fasting glucose, 99% of the group effect was explained and is no longer significant. Treatment of high-risk subjects with metformin results in modest weight loss and favorable changes in insulin sensitivity and proinsulin, which contribute to a reduction in the risk of diabetes apart from the associated reductions in fasting glucose.
引用
收藏
页码:1153 / 1159
页数:7
相关论文
共 24 条
[1]
[Anonymous], BIOSTATISTICAL METHO
[2]
Bray GA, 1999, DIABETES CARE, V22, P623
[3]
COX DR, 1972, J R STAT SOC B, V34, P187
[4]
Metabolic effects of metformin on glucose and lactate metabolism in noninsulin-dependent diabetes mellitus [J].
Cusi, K ;
Consoli, A ;
DeFronzo, RA .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1996, 81 (11) :4059-4067
[5]
Pharmacologic therapy for type 2 diabetes mellitus [J].
DeFronzo, RA .
ANNALS OF INTERNAL MEDICINE, 1999, 131 (04) :281-303
[6]
Diggle P., 2002, Analysis of Longitudinal Data
[7]
Gavin JR, 1997, DIABETES CARE, V20, P1183
[8]
STRUCTURAL DOMAINS AND MOLECULAR LIFE-STYLES OF INSULIN AND ITS PRECURSORS IN THE PANCREATIC BETA-CELL [J].
HALBAN, PA .
DIABETOLOGIA, 1991, 34 (11) :767-778
[9]
Effect of weight loss with lifestyle intervention on risk of diabetes [J].
Hamman, Richard F. ;
Wing, Rena R. ;
Edelstein, Sharon L. ;
Lachin, John M. ;
Bray, George A. ;
Delahanty, Linda ;
Hoskin, Mary ;
Kriska, Andrea M. ;
Mayer-Davis, Elizabeth J. ;
Pi-Sunyer, Xavier ;
Regensteiner, Judith ;
Venditti, Beth ;
Wylie-Rosett, Judith .
DIABETES CARE, 2006, 29 (09) :2102-2107
[10]
Hanson RL, 2000, AM J EPIDEMIOL, V151, P190