Metformin reduces weight, centripetal obesity, insulin, leptin, and low-density lipoprotein cholesterol in nondiabetic, morbidly obese subjects with body mass index greater than 30

被引:145
作者
Glueck, CJ
Fontaine, RN
Wang, P
Subbiah, MTR
Weber, K
Illig, E
Streicher, P
Sieve-Smith, L
Tracy, TM
Lang, JE
McCullough, P
机构
[1] Jewish Hosp Cincinnati, Ctr Cholesterol, Cincinnati, OH 45229 USA
[2] Mol Diagnost Labs, Cincinnati, OH USA
来源
METABOLISM-CLINICAL AND EXPERIMENTAL | 2001年 / 50卷 / 07期
关键词
D O I
10.1053/meta.2001.24192
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We studied 31 nondiabetic. habitually (greater than or equal to5 years) morbidly obese subjects (mean +/- SD body mass index [BMI] 43 +/- 8.7, median 43). Our specific aim was to determine whether metformin (2.55 g/d for 28 weeks) would ameliorate morbid obesity and reduce centripetal obesity; lipid and lipoprotein cholesterol, insulin, and leptin levels; and plasminogen activator inhibitor activity (PAI-Fx), risk factors for coronary heart disease (CHD). The patients were instructed to continue their prestudy dietary and exercise regimens without change. After 2 baseline visits 1 week apart, the 27 women and 4 men began receiving metformin, 2.55 g/d, which was continued for 28 weeks with follow-up visits at study weeks 5, 13, 21, and 29. Daily food intake was recorded by patients for 7 days before visits then reviewed with a dietitian. Kilocalories per day and per week were calculated. At each visit, fasting blood was obtained for measurement of lipid profile, insulin, leptin, and PAI-Fx. The mean +/- SD kilocalories consumed per day, 1,951 +/- 661 at entry, fell by week 29 to 1,719 +/- 493 (P = .014) but did not differ at weeks 5, 13, and 21 from that at week 29 (P > .2). Weight fell from 258 +/- 62 pounds at entry to 245 +/- 54 pounds at week 29 (P = .0001). Girth was reduced from 51.8 coproduct 6.2 to 49.2 +/- 4.5 inches (P = .0001). Waist circumference fell from 44.0 +/- 6.4 inches to 41.3 +/- 5.9 (P = .0001). The waist/hip ratio fell from 0.85 +/- 0.09 to 0.84 +/- 0.09 (P = .04). Fasting serum insulin, 28 coproduct 15 muU/mL at entry, fell to 21 +/- 11 muU/mL at week 29 (P = .0001), and leptin fell from 79 +/- 33 ng/mL to 55 +/- 27 ng/mL (P = .0001). On metformin, there were linear trends in decrements in weight, girth, waist circumference, waist/hip ratio, insulin, and leptin throughout the study period (P < .007). Low-density lipoprotein (LDL) cholesterol, 126 +/- 34 mg/dL at study entry, fell to 112 +/- 43 mg/dL at week 29 (P = .001), with a linear trend toward decreasing levels throughout (P = .036). By stepwise linear regression, the higher the entry weight, the larger the reduction in weight on metformin therapy (partial R-2 = 31%, P = .001). The greater the reduction in kilocalories consumed per day, the greater the decrease in weight on meformin therapy (partial W = 15%, P = .011). The higher the waist/hip ratio at entry, the greater its reduction on metformin therapy (partial R-2 = 11%. P = .004). The higher the entry serum leptin, the greater its reduction on metformin therapy (partial R-2 = 29%, P = .002). The geater the reduction in insulin on metformin, the greater the reduction in leptin (partial R-2 = 8%, P = .03), The higher the entry PAI-Fx, the greater the reduction in PAI-Fx on metformin (partial R-2 = 43%, P = .0001). Metformin safely and effectively reduces CHD risk factors (weight, fasting insulin, leptin, LDL cholesterol, centripetal obesity) in morbidly obese, nondiabetic subjects with BMI > 30, probably by virtue of its insulin-sensitizing action. Copyright (C) 2001 by W.B. Saunders Company.
引用
收藏
页码:856 / 861
页数:6
相关论文
共 37 条
[31]   Effect of intensive blood-glucose control with metformin on complications in overweight patients with type 2 diabetes (UKPDS 34) [J].
Turner, RC ;
Holman, RR ;
Stratton, IM ;
Cull, CA ;
Matthews, DR ;
Manley, SE ;
Frighi, V ;
Wright, D ;
Neil, A ;
Kohner, E ;
McElroy, H ;
Fox, C ;
Hadden, D .
LANCET, 1998, 352 (9131) :854-865
[32]   Leptin responses to weight loss in postmenopausal women: Relationship to sex-hormone binding globulin and visceral obesity [J].
van Rossum, EFC ;
Nicklas, BJ ;
Dennis, KE ;
Berman, DM ;
Goldberg, AP .
OBESITY RESEARCH, 2000, 8 (01) :29-35
[33]   Metformin therapy is associated with a decrease in plasma plasminogen activator inhibitor-1, lipoprotein(a), and immunoreactive insulin levels in patients with the polycystic ovary syndrome [J].
Velazquez, EM ;
Mendoza, SG ;
Wang, P ;
Glueck, CJ .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1997, 46 (04) :454-457
[34]   Weight change and duration of overweight and obesity in the incidence of type 2 diabetes [J].
Wannamethee, SG ;
Shaper, AG .
DIABETES CARE, 1999, 22 (08) :1266-1272
[35]   United kingdom prospective diabetes study 24: A 6-year, randomized, controlled trial comparing sulfonylurea, insulin, and metformin therapy in patients with newly diagnosed type 2 diabetes that could not be controlled with diet therapy [J].
Wright, A ;
Cull, C ;
Holman, R ;
Turner, R ;
Murchison, L ;
Wright, AD ;
Oakley, N ;
Kohner, E ;
Hayes, R ;
Scarpello, J ;
Hadden, D ;
Spathis, AG ;
Yudkin, J ;
Greenwood, R ;
Borthwick, L ;
Day, J ;
Newton, R ;
Fox, C ;
Paisey, R ;
Roland, J ;
Humphriss, D ;
Peacock, I ;
Boulton, A ;
Dornan, T ;
Burden, F ;
Tooke, J .
ANNALS OF INTERNAL MEDICINE, 1998, 128 (03) :165-175
[36]   RISK-FACTORS FOR CORONARY-ARTERY DISEASE IN HEALTHY-PERSONS WITH HYPERINSULINEMIA AND NORMAL GLUCOSE-TOLERANCE [J].
ZAVARONI, I ;
BONORA, E ;
PAGLIARA, M ;
DALLAGLIO, E ;
LUCHETTI, L ;
BUONANNO, G ;
BONATI, PA ;
BERGONZANI, M ;
GNUDI, L ;
PASSERI, M ;
REAVEN, G .
NEW ENGLAND JOURNAL OF MEDICINE, 1989, 320 (11) :702-706
[37]   Etiology of the Metabolic Syndrome: Potential role of insulin resistance, leptin resistance, and other players [J].
Zimmet, P ;
Boyko, EJ ;
Collier, GR ;
De Courten, M .
THE METABOLIC SYNDROME X: CONVERGENCE OF INSULIN RESISTANCE, GLUCOSE INTOLERANCE, HYPERTENSION, OBESITY, AND DYSLIPIDEMIAS-SEARCHING FOR THE UNDERLYING DEFECTS, 1999, 892 :25-44