Semi-physiological model of postprandial triglyceride response in lean, obese and very obese individuals after a high-fat meal

被引:3
|
作者
Leohr, Jennifer [1 ]
Heathman, Michael [1 ]
Kjellsson, Maria C. [2 ]
机构
[1] Eli Lilly & Co, Lilly Corp Ctr, Indianapolis, IN 46285 USA
[2] Uppsala Univ, Pharmacometr Res Grp, Dept Pharmaceut Biosci, Uppsala, Sweden
来源
DIABETES OBESITY & METABOLISM | 2018年 / 20卷 / 03期
关键词
body composition; clinical trial; pharmacodynamics; triglycerides; VLDL; postprandial; CARDIOVASCULAR-DISEASE; NONMEM; MEN;
D O I
10.1111/dom.13138
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
AimsTo quantify the postprandial triglyceride (TG) response of chylomicrons and very-low-density lipoprotein-V6 (VLDL-V6) after a high-fat meal in lean, obese and very obese healthy individuals, using a mechanistic population lipokinetic modelling approach. MethodsHealthy individuals from three body mass index population categories: lean (18.5-24.9kg/m(2)), obese (30-33kg/m(2)), and very obese (34-40kg/m(2)) were enrolled in a clinical study to assess the TG response after a high-fat meal, containing 60% fat. Non-linear mixed-effect modelling was used to analyse the TG concentrations of chylomicrons and large VLDL-V6 particles. ResultsThe TGs in chylomicrons and VLDL-V6 particles had a prominent postprandial peak and represented the majority of the postprandial response; only the VLDL-V6 showed a difference across the populations. A turn-over model successfully described the TG concentration-time profiles of both chylomicrons and large VLDL-V6 particles after the high-fat meal. This model consisted of four compartments: two transit compartments for the lag between meal consumption and appearance of TGs in the blood, and one compartment each for the chylomicrons and large VLDL-V6 particles. The rate constants for the production of chylomicrons and elimination of large VLDL-V6 particles, along with the conversion rate of chylomicrons to large VLDL-V6 particles were well defined. ConclusionsThis is the first lipokinetic model to describe the absorption of TGs from dietary fats into the blood stream and compares the dynamics of TGs in chylomicrons and large VLDL-V6 particles among lean, obese and very obese people. Such a model can be used to identify where pharmacological therapies act, thereby improving the determination of efficacy, and identifying complementary mechanisms for combinational drug therapies.
引用
收藏
页码:660 / 666
页数:7
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