Children’s Nutrition Research Center Staff Publications

Language

English

Publication Date

7-28-2021

Journal

Communications Biology

DOI

10.1038/s42003-021-02431-4

PMID

34321601

PMCID

PMC8319323

PubMedCentral® Posted Date

7-28-2021

PubMedCentral® Full Text Version

Post-print

Abstract

Long chain polyunsaturated fatty acids (LC-PUFAs) have critical signaling roles that regulate dyslipidemia and inflammation. Genetic variation in the FADS gene cluster accounts for a large portion of interindividual differences in circulating and tissue levels of LC-PUFAs, with the genotypes most strongly predictive of low LC-PUFA levels at strikingly higher frequencies in Amerind ancestry populations. In this study, we examined relationships between genetic ancestry and FADS variation in 1102 Hispanic American participants from the Multi-Ethnic Study of Atherosclerosis. We demonstrate strong negative associations between Amerind genetic ancestry and LC-PUFA levels. The FADS rs174537 single nucleotide polymorphism (SNP) accounted for much of the AI ancestry effect on LC-PUFAs, especially for low levels of n-3 LC-PUFAs. Rs174537 was also strongly associated with several metabolic, inflammatory and anthropomorphic traits including circulating triglycerides (TGs) and E-selectin in MESA Hispanics. Our study demonstrates that Amerind ancestry provides a useful and readily available tool to identify individuals most likely to have FADS-related n-3 LC-PUFA deficiencies and associated cardiovascular risk.

Keywords

Fatty Acid Desaturases, Fatty Acids, Omega-3, Genetic Variation, Heredity, Hispanic or Latino, Humans, Indians, North American, Longitudinal Studies, Multigene Family, United States, Risk factors, Genetic association study, Heritable quantitative trait

Published Open-Access

yes

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