Diet induced thermogenesis, fat oxidation and food intake following sequential meals: Influence of calcium and vitamin D

被引:44
作者
Ping-Delfos, Wendy Chan She [1 ]
Soares, Mario [1 ]
机构
[1] Curtin Univ Technol, Program Nutr, Sch Publ Hlth, Curtin Hlth Innovat Res Inst, Perth, WA 6845, Australia
关键词
Sequential; Dairy calcium; Vitamin D; Postprandial metabolism; Spontaneous food intake; BODY-WEIGHT; LEPTIN; ENERGY; DAIRY; METABOLISM; ADIPOSITY; RESPONSES; APPETITE; INSULIN; SATIETY;
D O I
10.1016/j.clnu.2010.11.006
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background & aims: The mechanisms linking dietary calcium and vitamin D to body weight regulation require confirmation. Methods: Eleven subjects, aged (mean +/- SEM) 54 +/- 1.2 y and BMI 31 +/- 2.4 kg/m(2), participated in a randomised within-subject, sequential meal protocol comparing a low calcium trial (LCT) to an iso-energetic high calcium trial (Ha). Diet induced thermogenesis (DIT), fat oxidation rates (FOR), serum leptin, subjective feelings of hunger/satiety were measured at fasting and hourly over 8 h. Spontaneous food intake at a buffet and over the following 30 h was recorded. Postprandial responses, calculated as change (Delta) from baseline for each meal, were analysed by paired t-tests and 2 x 2 repeated measures ANOVA. Results: HCT resulted in lesser suppression of Delta FOR (p = 0.02) and a significantly greater DIT (p = 0.01). Further, the buffet to dinner interval was prolonged (p = 0. 083) and reported 24 h energy intake following this trial was significantly reduced (p = 0.017). Delta leptin following HCT but not LCT was negatively related to 24 h fat intake (r = -0.81, p = 0.016). Conclusions: Higher calcium and vitamin D intake at a breakfast meal acutely increased postprandial FOR and DIT over two successive meals, and reduced spontaneous energy intake in the subsequent 24 h period. Australian New Zealand Clinical Trials Registry (ANZCTR) number: ACTRN12609000418279. (C) 2010 Elsevier Ltd and European Society for Clinical Nutrition and Metabolism. All rights reserved.
引用
收藏
页码:376 / 383
页数:8
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