Insulin sensitivity determines the effectiveness of dietary macronutrient composition on weight loss in obese women

被引:93
作者
Cornier, MA
Donahoo, WT
Pereira, R
Gurevich, I
Westergren, R
Enerback, S
Eckel, PJ
Goalstone, ML
Hill, JO
Eckel, RH
Draznin, B
机构
[1] Vet Adm Med Ctr, Res Serv, Denver, CO 80220 USA
[2] Univ Colorado, Hlth Sci Ctr, Dept Med, Boulder, CO 80309 USA
[3] Univ Colorado, Hlth Sci Ctr, Dept Pediat, Boulder, CO 80309 USA
[4] Univ Colorado, Hlth Sci Ctr, Adult Gen Clin Res Ctr, Boulder, CO 80309 USA
[5] Univ Colorado, Hlth Sci Ctr, Ctr Human Nutr, Boulder, CO 80309 USA
[6] Gothenburg Univ, Dept Med Biochem, Gothenburg, Sweden
来源
OBESITY RESEARCH | 2005年 / 13卷 / 04期
关键词
CHO; fat; insulin resistance;
D O I
10.1038/oby.2005.79
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To determine whether macronutrient composition of a hypocaloric diet can enhance its effectiveness and whether insulin sensitivity (Si) affects the response to hypocaloric diets. Research Methods and Procedures: Obese nondiabetic insulin-sensitive (fasting insulin < 10 mu U/mL; n = 12) and obese nondiabetic insulin-resistant (fasting insulin > 15 mu U/mL; n = 9) women (23 to 53 years old) were randomized to either a high carbohydrate (CHO) (HQ/low fat (LF) (60% CHO, 20% fat) or low CHO (LC)/high fat (HF) (40% CHO, 40% fat) hypocaloric diet. Primary outcome measures after a 16-week dietary intervention were: changes in body weight (BW), Si, resting metabolic rate, and fasting lipids. Results: Insulin-sensitive women on the HC/LF diet lost 13.5 +/- 1.2% (p < 0.001) of their initial BW, whereas those on the LC/HF diet lost 6.8 +/- 1.2% (p < 0.001; p < 0.002 between the groups). In contrast, among the insulin-resistant women, those on the LC/HF diet lost 13.4 +/- 1.3% (p < 0.001) of their initial BW as compared with 8.5 +/- 1.4% (p < 0.001) lost by those on the HC/LF diet (p < 0.04 between two groups). These differences could not be explained by changes in resting metabolic rate, activity, or intake. Overall, changes in Si were associated with the degree of weight loss (r = -0.57, p < 0.05). Discussion: The state of Si determines the effectiveness of macronutrient composition of hypocaloric diets in obese women. For maximal benefit, the macronutrient composition of a hypocaloric diet may need to be adjusted to correspond to the state of Si.
引用
收藏
页码:703 / 709
页数:7
相关论文
共 33 条
[1]  
ALFORD BB, 1990, J AM DIET ASSOC, V90, P534
[2]  
[Anonymous], 1998, Clinical guidelines on the identification, evaluation, and treatment of overweight and obesity in adults: The evidence report
[3]   A RANDOMIZED CONTROLLED TRIAL OF LOW CARBOHYDRATE AND LOW FAT HIGH-FIBER DIETS FOR WEIGHT-LOSS [J].
BARON, JA ;
SCHORI, A ;
CROW, B ;
CARTER, R ;
MANN, JI .
AMERICAN JOURNAL OF PUBLIC HEALTH, 1986, 76 (11) :1293-1296
[4]   ASSESSMENT OF INSULIN SENSITIVITY INVIVO - A CRITICAL-REVIEW [J].
BERGMAN, RN ;
HOPE, ID ;
YANG, YJ ;
WATANABE, RM ;
MEADOR, MA ;
YOUN, JH ;
ADER, M .
DIABETES-METABOLISM REVIEWS, 1989, 5 (05) :411-429
[5]   A randomized trial comparing a very low carbohydrate diet and a calorie-restricted low fat diet on body weight and cardiovascular risk factors in healthy women [J].
Brehm, BJ ;
Seeley, RJ ;
Daniels, SR ;
D'Alessio, DA .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2003, 88 (04) :1617-1623
[6]   INTERRELATIONSHIPS BETWEEN BODY-WEIGHT, BODY-FAT DISTRIBUTION AND INSULIN IN OBESE WOMEN BEFORE AND AFTER HYPOCALORIC FEEDING AND WEIGHT-LOSS [J].
CASIMIRRI, F ;
PASQUALI, R ;
CESARI, MP ;
MELCHIONDA, N ;
BARBARA, L .
ANNALS OF NUTRITION AND METABOLISM, 1989, 33 (02) :79-87
[7]   FOXC2 is a winged helix gene that counteracts obesity, hypertriglyceridemia, and diet-induced insulin resistance [J].
Cederberg, A ;
Gronning, LM ;
Ahrén, B ;
Taskén, K ;
Carlsson, P ;
Enerbäck, S .
CELL, 2001, 106 (05) :563-573
[8]  
DEFRONZO RA, 1979, AM J PHYSIOL, V237, P214
[9]   How to measure insulin sensitivity [J].
Ferrannini, E ;
Mari, A .
JOURNAL OF HYPERTENSION, 1998, 16 (07) :895-906
[10]   Insulin resistance and hypersecretion in obesity [J].
Ferrannini, E ;
Natali, A ;
Bell, P ;
CavalloPerin, P ;
Lalic, N ;
Mingrone, G .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (05) :1166-1173