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Dietary conjugated linoleic acid (CLA) intake assessment and possible biomarkers of CLA intake in young women

Published online by Cambridge University Press:  02 January 2007

Dorothee Fremann*
Affiliation:
Lehrstuhl für Ernährungslehre, Department für Lebensmittel und Emährung, Technische Universität München–Weihenstephan, Alte Akademie 16, D-85350 Freising, Germany
Jakob Linseisen
Affiliation:
Lehrstuhl für Ernährungslehre, Department für Lebensmittel und Emährung, Technische Universität München–Weihenstephan, Alte Akademie 16, D-85350 Freising, Germany Deutsches Krebsforschungszentrum, Abteilung für Klinische Epidemiologie, Im Neuenheimer Feld 280, D-69120 Heidelberg, Germany
Günther Wolfram
Affiliation:
Lehrstuhl für Ernährungslehre, Department für Lebensmittel und Emährung, Technische Universität München–Weihenstephan, Alte Akademie 16, D-85350 Freising, Germany
*
*Corresponding author: Email: [email protected]
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Abstract

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Objective:

The habitual intake of the conjugated linoleic acid (CLA) isomer C18:2 c9t11 (rumenic acid, RA) was assessed and compared with plasma biomarkers.

Design:

The newly developed food-frequency questionnaire (FFQ) comprised 46 food items and was validated by means of a 7-day estimated record (7-d ER). Additionally, the dietary intake results of the FFQ, 7-d ER, the last day (1-d ER) and the last two days (2-d ER) before blood sampling of the 7-d ER were compared to the content of C18:2 c9t11 in plasma phospholipids (PL) and triglycerides (TG) as possible biomarkers.

Setting:

Metabolic unit of a university institute.

Subjects:

Fifty-seven students completed both dietary instruments. From all participants fasting blood samples were taken.

Results:

Mean daily intake of rumenic acid was 246 mg day−1 and 323 mg day−1 as measured by the FFQ and the 7-d-ER, respectively. The degree of correspondence between both assessment methods was acceptable; this is indicated by a total kappa value of κ = 0.31 (P < 0.01) and a Pearson correlation coefficient of r = 0.46 (P < 0.01). Rumenic acid content in plasma triglycerides was twice as high as found in phospholipids. The correlation between the intake results gained with the 7-d ER and the plasma PL contents of C18:2 c9t11 was statistically significant; this was also true for the C18:2 c9t11 values in plasma TG compared with the intake results of one or two days before blood sampling.

Conclusions:

Regarding RA intake, the FFQ data revealed an acceptable degree of correspondence with the 7-d ER data but failed to show significant correlations to the potential biomarkers. However, with respect to the results of the 7-d ER, the RA content in plasma PL and TG are possible biomarkers of short-term and medium-term intake, respectively.

Type
Research Article
Copyright
Copyright © CABI Publishing 2002

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