BACKGROUND: The nitrogen isotope ratio (expressed as delta(15)N) of red blood cells (RBCs) is highly correlated with the RBC long-chain omega-3 (n-3) fatty acids eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) in Yup'ik Eskimos. Because delta(15)N can also be measured in hair samples, it could provide a noninvasive, retrospective biomarker for EPA and DHA intakes. OBJECTIVES: We investigated the agreement between delta(15)N in hair and RBCs and then evaluated the relations between hair delta(15)N and RBC EPA and DHA. We also assessed the agreement in carbon isotope ratios (delta(13)C) between hair and RBCs, because delta(13)C has been proposed as a dietary biomarker in other populations. DESIGN: We assessed relations between hair and RBC delta(15)N and delta(13)C in a community-based sample of 144 Yup'ik Eskimos and examined the correlations between delta(15)N and RBC EPA and DHA in a subset of these participants (n = 44). RESULTS: We showed a 1:1 relation with good agreement between hair and RBC delta(15)N (r = 0.91) and delta(13)C (r = 0.87). Hair isotope ratios were greater than RBC ratios by 1.5 per thousand for delta(15)N and by 2.3 per thousand for delta(13)C. There were strong correlations between hair delta(15)N and RBC EPA and DHA (r = 0.83 and 0.84, respectively). CONCLUSIONS: These results support the use of hair delta(15)N values as a biomarker of EPA and DHA intakes. Because hair collection is noninvasive and the samples require no special processing, studies of EPA and DHA intakes in large populations could use biomarkers rather than self-reports to assess these fatty acids.
BACKGROUND: The nitrogen isotope ratio (expressed as delta(15)N) of red blood cells (RBCs) is highly correlated with the RBC long-chain omega-3 (n-3) fatty acidseicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) in Yup'ik Eskimos. Because delta(15)N can also be measured in hair samples, it could provide a noninvasive, retrospective biomarker for EPA and DHA intakes. OBJECTIVES: We investigated the agreement between delta(15)N in hair and RBCs and then evaluated the relations between hair delta(15)N and RBC EPA and DHA. We also assessed the agreement in carbon isotope ratios (delta(13)C) between hair and RBCs, because delta(13)C has been proposed as a dietary biomarker in other populations. DESIGN: We assessed relations between hair and RBC delta(15)N and delta(13)C in a community-based sample of 144 Yup'ik Eskimos and examined the correlations between delta(15)N and RBC EPA and DHA in a subset of these participants (n = 44). RESULTS: We showed a 1:1 relation with good agreement between hair and RBC delta(15)N (r = 0.91) and delta(13)C (r = 0.87). Hair isotope ratios were greater than RBC ratios by 1.5 per thousand for delta(15)N and by 2.3 per thousand for delta(13)C. There were strong correlations between hair delta(15)N and RBC EPA and DHA (r = 0.83 and 0.84, respectively). CONCLUSIONS: These results support the use of hair delta(15)N values as a biomarker of EPA and DHA intakes. Because hair collection is noninvasive and the samples require no special processing, studies of EPA and DHA intakes in large populations could use biomarkers rather than self-reports to assess these fatty acids.
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