Intra-individual variability of long-chain fatty acids (C12-C24) in plasma and red blood cells.

T Yuzyuk, B Lozier, E L Schwarz, K Viau, E Kish-Trier, I De Biase

Journal: Prostaglandins, leukotrienes, and essential fatty acids 2019;135():30-38

PMID: 30103929

Abstract

Long-chain fatty acids (LCFA) play key roles in mammalian cells as sources of energy, structural components and signaling molecules. Given their importance in numerous physiological processes, the roles of LCFAs in health and disease have been extensively investigated. In the majority of studies, correlations are established using a single measurement in plasma or red blood cells (RBCs). Although a few studies have reported on reproducibility of individual fatty acid measurements, the comprehensive analysis of intra-individual LCFA variability has not been performed. Therefore, our goal was to determine intra-individual variability for the 22 most abundant LCFAs in both plasma and RBC samples collected from healthy individuals on a regular diet after overnight fasting. The measurements of LCFAs in RBCs were consistent throughout the course of study reflecting long-term nutritional status. In contrast, the results in plasma showed considerable LCFA intra-individual variability, even between fatty acids of the same type. Plasma intra-individual variability for omega-3 alpha-linolenic and eicosapentaenoic acids in some participants were >40% whereas the variability of docosahexaenoic acid was consistently <12.8%. Omega-6 linoleic and arachidonic acids also showed low variability in plasma. The results suggest that some LCFAs have less variability and would be more reliable as biomarkers. Reliability of biomarkers can have a profound impact on the research outcomes. Intra-individual variability of LCFAs should be taken into consideration in designing, conducting and interpreting results of clinical studies.

Copyright © 2018. Published by Elsevier Ltd.

Address: Department of Pathology, University of Utah, Salt Lake City, UT, USA; ARUP Laboratories, Salt Lake City, UT, USA; ARUP Institute of Clinical & Experimental Pathology, Salt Lake City, UT, USA. Electronic address: [email protected].; ARUP Institute of Clinical & Experimental Pathology, Salt Lake City, UT, USA.; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA, USA.; ARUP Institute of Clinical & Experimental Pathology, Salt Lake City, UT, USA; Navigen, Salt Lake City, UT, USA (present affiliation).; Department of Pathology, University of Utah, Salt Lake City, UT, USA; ARUP Laboratories, Salt Lake City, UT, USA; ARUP Institute of Clinical & Experimental Pathology, Salt Lake City, UT, USA.

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