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. Author manuscript; available in PMC: 2018 Dec 3.
Published in final edited form as: Gastroenterology. 2013 Dec 4;146(3):726–735. doi: 10.1053/j.gastro.2013.11.049

Table 2.

Kinetic measures of metabolism

LowLF (n=11) HighLF (n=13) P-value
Energy Expenditure and Substrate Oxidation a
Energy expenditure (kcal/kg BW/day) 14.4 ± 2.9 15.5 ± 2.4 .32
Glucose oxidation (mg/kg BW/min) 1.07 ± 0.35 0.96 ± 0.36 .48
Fat oxidation (mg/kg BW/min) 0.55 ± 0.18 0.68 ± 0.19 .10
Insulin Sensitivity Measures b
SI (10−4 * min−1 per μU/mL) 3.1 ± 1.4 2.2 ± 1.4 .14
AIRg (μU/mL * min) 568 ± 407 489 ± 304 .60
Disposition index (unitless) 1431 ± 668 962 ± 637 .09
Plasma FFA Kinetics c
Total RaFFA μmol/kg FM/min) 9.98 ± 2.80 12.73 ± 6.30 .20
 Adipose RaFFA μmol/kg FM/min) 9.57 ± 2.65 12.28 ± 6.17 .19
 RaSpillover μmol/kg FM/min) 0.37 ± 0.29 0.43 ± 0.23 .53
Mean FFA residence time (min) d 6.54 ± 1.66 6.75 ± 2.97 .84
T½ life (min) 4.5 ± 1.2 4.7 ± 2.1 .84
VLDL-TG Concentrations and Kinetics e
VLDL-TG concentration (mmol/L) 0.39 ± 0.22 0.60 ± 0.29 .07
Total Production Rate (ìmol/min) 8.6 ± 3.0 11.0 ± 4.5 .16
 TG Production from Adipose (ìmol/min) 4.34 ± 1.82 4.06 ± 2.57 .77
 TG Production from Evening Meal (ìmol/min) 0.46 ± 0.24 0.56 ± 0.25 .39
 TG Production from Lipogenesis (ìmol/min) 0.78 ± 0.42 2.57 ± 1.53 .001
 Fractional Catabolic Rate (% / hr) 28.0 ± 11.1 24.8 ± 7.6 .44
T½ life (h) 2.9 ± 1.2 3.1 ± 1.3 .65
Clearance Rate (mL/min) 27.0 ± 12.2 20.1 ± 6.3 .11

Data are mean ± SD. Abbreviations: SI, insulin sensitivity index; AIRg, acute insulin response to glucose, RaFFA, rate of appearance of FFA.

a

Fasting energy expenditure and substrate oxidation were determined at 0800.

b

Data are calculated from the frequently-sampled insulin-modified IVGTT using MINMOD software.

c

Plasma FFA kinetics were determined by the average values taken at the end of the study sampling period (1030, 1145).

d

Mean residence time is the average time a FFA molecule spends in the volume of distribution.

e

n=11/group; two subjects in the high liver fat (LF) group were excluded from this analysis because they had VLDL-TG concentrations that were more than 2 SD greater than the mean of all other subjects.