Literature DB >> 16469979

Effect of a low-fat diet on fatty acid composition in red cells, plasma phospholipids, and cholesterol esters: investigation of a biomarker of total fat intake.

Irena B King1, Rozenn N Lemaitre, Mark Kestin.   

Abstract

BACKGROUND: The utility of fatty acids (FAs) as biomarkers of total fat intake is unknown.
OBJECTIVE: We compared FA changes in red cells (RCs), plasma phospholipids (PLs), and cholesterol esters (CEs) in response to a low-fat diet (LFD) and a moderate-fat diet (MFD) and assessed whether individual or combination of FAs predict LFD.
DESIGN: Postmenopausal women (n = 66) were randomly assigned to receive an LFD (17% of energy from fat) or an MFD (34% of energy from fat) for 6 wk. All foods were provided. FAs in diets and blood were determined by gas-liquid chromatography. FA changes between baseline and end of study were compared across diets by using t tests. FA predictors of an LFD were selected by logistic regression.
RESULTS: Many FAs in RCs, PLs, and CEs responded differently to the 2 diets. Changes from baseline with an LFD for palmitic acid (16:0) (3-11% increase), behenic (22:0) and lignoceric (24:0) acids (3-20% decrease, in RCs and PLs only), cis-monounsaturated FA (MUFA) (25-35% increase), linoleic acid (18:2n-6) (11-13% decrease), trans octadecanoic acids (trans 18:1) (7-20% decrease), and n-6 highly unsaturated FA (HUFA) (2-8% increase) were significantly different from changes with an MFD. Individually, 18:2n-6 and trans 18:1 were strong predictors of an LFD [receiver operating characteristic (ROC) curves: 0.92-0.80). A logistic regression model with trans 18:1, 18:2n-6, and vaccenic acid (18:1n-7) predicted an LFD with high specificity and sensitivity (ROC curves: 0.99).
CONCLUSIONS: Saturated FA, cisMUFA, n-6 HUFA, and exogenous FAs greatly differed in their response to the LFD and MFD. Parallel responses were observed in RCs, PLs, and CEs. A model with a combination of FAs almost perfectly differentiated the consumption of 34% fat from that of 17% fat.

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Year:  2006        PMID: 16469979     DOI: 10.1093/ajcn/83.2.227

Source DB:  PubMed          Journal:  Am J Clin Nutr        ISSN: 0002-9165            Impact factor:   7.045


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