Abstract | OBJECTIVE: RESEARCH METHODS AND PROCEDURES: Hepatic secretion of VLDL was measured using an intravenous infusion of 1-[(13)C]- leucine in 51 men with a wide range of body mass index (25.1 to 42.2 kg/m(2)). Isotopic enrichment of VLDL- apoB was measured using gas chromatography-mass spectrometry and a multicompartmental model used to estimate VLDL- apoB metabolic parameters. IPATM, RPATM, and SAATM (kilograms) were quantified between T11 and S1 using magnetic resonance imaging; TATM (kilograms) was determined using bioelectrical impedance. Insulin resistance was estimated by homeostasis model assessment (HOMA) score. RESULTS: In stepwise regression, IPATM was the best predictor of hepatic secretion of VLDL- apoB (r = 0.390, p < 0.005) and TATM was the best predictor of VLDL- apoB fractional catabolic rate (r = 0.282, p < 0.05). IPATM remained significantly associated with VLDL- apoB secretion after adjusting for TATM or HOMA score (r = 0.360, p < 0.01 and r = 0.310, p < 0.05, respectively). This association was also independent of age, dietary intake, and body mass index. None of the fat compartments were significantly associated with the fractional catabolic rate of VLDL- apoB after adjusting for HOMA score. DISCUSSION: In overweight/obese men, the quantity of both IPATM and TATM determine the kinetics of VLDL- apoB. The effect of IPATM on VLDL- apoB secretion is independent of both total fat mass and the degree of insulin resistance.
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Authors | Gerald F Watts, Dick C Chan, P Hugh R Barrett, Andrei V Susekov, Jianmin Hua, Swithin Song |
Journal | Obesity research
(Obes Res)
Vol. 11
Issue 1
Pg. 152-9
(Jan 2003)
ISSN: 1071-7323 [Print] United States |
PMID | 12529498
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Apolipoprotein B-100
- Apolipoproteins B
- Blood Glucose
- Carbon Isotopes
- Fatty Acids, Nonesterified
- Lipoproteins, VLDL
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Topics |
- Adipose Tissue
- Adult
- Apolipoprotein B-100
- Apolipoproteins B
(blood, metabolism)
- Blood Glucose
(analysis)
- Body Composition
- Carbon Isotopes
- Diabetes Mellitus
(physiopathology)
- Diet
- Electric Impedance
- Fatty Acids, Nonesterified
(blood)
- Gas Chromatography-Mass Spectrometry
- Glucose Intolerance
(physiopathology)
- Homeostasis
- Humans
- Insulin Resistance
- Kinetics
- Lipoproteins, VLDL
(metabolism)
- Liver
(metabolism)
- Magnetic Resonance Imaging
- Male
- Middle Aged
- Obesity
(physiopathology)
- Regression Analysis
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