Fat oxidation before and after a high fat load in the obese insulin-resistant state

被引:60
作者
Blaak, EE
Hul, G
Verdich, C
Stich, V
Martinez, A
Petersen, M
Feskens, EFM
Patel, K
Oppert, JM
Barbe, P
Toubro, S
Anderson, I
Saris, WHM
机构
[1] Maastricht Univ, Nutr & Toxicol Res Ctr NUTRIM, Dept Human Biol, Maastricht, Netherlands
[2] Natl Inst Publ Hlth & Environm, Dept Hlth & Nutr, NL-3720 BA Bilthoven, Netherlands
[3] Univ Copenhagen Hosp, Danish Epidemiol Sci Ctr, DK-2100 Copenhagen, Denmark
[4] Charles Univ, Fac Med 3, Ctr Prevent Med, Dept Sports Med, Prague, Czech Republic
[5] Univ Navarra, Dept Physiol & Nutr, E-31080 Pamplona, Spain
[6] Royal Vet & Agr Univ, Inst Human Nutr, Copenhagen, Denmark
[7] Univ Nottingham, Sch Med, Queens Med Ctr, Sch Biomed Sci, Nottingham, England
[8] Hop Hotel Dieu, Dept Nutr, Paris, France
[9] Louis Bugnard Inst, French Inst Hlth & Med Res, U586, Obes Res Unit, Toulouse, France
[10] Univ Toulouse 3, Toulouse Univ Hosp, Clin Invest Ctr, F-31062 Toulouse, France
[11] Huddinge Univ Hosp, Karolinska Inst, Dept Med, Stockholm, Sweden
关键词
D O I
10.1210/jc.2005-1598
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Obesity may be associated with a lowered use of fat as a fuel, which may contribute to the enlarged adipose tissue stores. Aim: The aim of the present study was to study fatty acid use in the fasting state and in response to a high fat load in a large cohort of obese subjects ( n = 701) and a lean reference group ( n = 113). Methods: Subjects from eight European centers underwent a test meal challenge containing 95 en% fat [ energy content 50% of estimated resting energy expenditure (EE)]. Fasting and postprandial fat oxidation and circulating metabolites and hormones were determined over a 3-h period. Results: Postprandial fat oxidation ( as percent of postprandial EE, adjusted for fat mass, age, gender, center, and energy content of the meal) decreased with increasing body mass index (BMI) category ( P < 0.01), an effect present only in those obese subjects with a relatively low fasting fat oxidation ( below median, interaction BMI category x fasting fat oxidation, P < 0.001). Fasting fat oxidation increased with increasing BMI category ( P < 0.001), which was normalized after adjustment for fat-free mass and fat mass. Furthermore, insulin resistance was positively associated with postprandial fat oxidation ( P < 0.05) and negatively associated with fasting fat oxidation ( expressed as percent of EE), independent of body composition. Conclusions: The present data indicate an impaired capacity to regulate fat oxidation in the obese insulin-resistant state, which is hypothesized to play a role in the etiology of both obesity and insulin resistance.
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页码:1462 / 1469
页数:8
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