1. Palmitoleic acid is elevated in fatty liver disease and reflects hepatic lipogenesis.
- Author
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Lee JJ, Lambert JE, Hovhannisyan Y, Ramos-Roman MA, Trombold JR, Wagner DA, and Parks EJ
- Subjects
- Adiposity, Adult, Algorithms, Biomarkers blood, Biomarkers metabolism, Body Mass Index, Cross-Sectional Studies, Deuterium Oxide metabolism, Diet, Fat-Restricted, Fatty Acids, Monounsaturated metabolism, Fatty Acids, Nonesterified blood, Female, Humans, Insulin Resistance, Lipoproteins, VLDL metabolism, Liver enzymology, Male, Non-alcoholic Fatty Liver Disease diet therapy, Non-alcoholic Fatty Liver Disease etiology, Non-alcoholic Fatty Liver Disease metabolism, Overweight physiopathology, Palmitic Acid blood, Palmitic Acid metabolism, Stearoyl-CoA Desaturase metabolism, Triglycerides metabolism, Fatty Acids, Monounsaturated blood, Lipogenesis, Lipoproteins, VLDL blood, Liver metabolism, Non-alcoholic Fatty Liver Disease blood, Triglycerides blood, Up-Regulation
- Abstract
Background: Biochemical evidence has linked the coordinate control of fatty acid (FA) synthesis with the activity of stearoyl-CoA desaturase-1 (SCD1). The ratio of 16:1n-7 to 16:0 [SCD1₁₆] in plasma triacylglycerol FA has been used as an index to reflect liver SCD1₁₆ activity and has been proposed as a biomarker of FA synthesis, although this use has not been validated by comparison with isotopically measured de novo lipogenesis (DNL(Meas))., Objective: We investigated plasma lipid 16:1n-7 and FA indexes of elongation and desaturation in relation to lipogenesis., Design: In this cross-sectional investigation of metabolism, 24 overweight adults, who were likely to have elevated DNL, consumed D2O for 10 d and had liver fat (LF) measured by magnetic resonance spectroscopy. Very-low-density lipoprotein (VLDL)-triacylglycerols and plasma free FA [nonesterified fatty acids (NEFAs)] were analyzed by using gas chromatography for the FA composition (molar percentage) and gas chromatography-mass spectrometry and gas chromatography-combustion isotope ratio mass spectrometry for deuterium enrichment., Results: In all subjects, VLDL-triacylglycerol 16:1n-7 was significantly (P < 0.01) related to DNL(Meas) (r = 0.56), liver fat (r = 0.53), and adipose insulin resistance (r = 0.56); similar positive relations were shown with the SCD1₁₆ index, and the pattern in NEFAs echoed that of VLDL-triacylglycerols. Compared with subjects with low LF (3.1 ± 2.7%; n = 11), subjects with high LF (18.4 ± 3.6%; n = 13) exhibited a 45% higher VLDL-triacylglycerol 16:1n-7 molar percentage (P < 0.01), 16% of subjects had lower 18:2n-6 (P = 0.01), and 27% of subjects had higher DNL as assessed by using a published DNL index (ratio of 16:0 to 18:2n-6; P = 0.03), which was isotopically confirmed by DNL(Meas) (increased 2.5-fold; P < 0.01). Compared with 16:0 in the diet, the low amount of dietary 16:1n-7 in VLDL-triacylglycerols corresponded to a stronger signal of elevated DNL., Conclusion: The current data provide support for the use of the VLDL-triacylglycerol 16:1n-7 molar percentage as a biomarker for elevated liver fat when isotope use is not feasible; however, larger-scale confirmatory studies are needed., (© 2015 American Society for Nutrition.)
- Published
- 2015
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