Vol. 2, No. 3, 2009
Issue release date: October 2009
Free Access
J Nutrigenet Nutrigenomics 2009;2:140–148
(DOI:10.1159/000235562)
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Polyunsaturated Fatty Acids and Cardiovascular Disease: Implications for Nutrigenetics

Allayee H.a, b · Roth N.a · Hodis H.N.a, c
aDepartment of Preventive Medicine, bInstitute for Genetic Medicine and cAtherosclerosis Research Unit, Keck School of Medicine, University of Southern California, Los Angeles, Calif., USA
email Corresponding Author


 goto top of outline Key Words

  • Cardiovascular disease
  • Genes
  • Fatty acids
  • 5-Lipoxygenase
  • Leukotriene

 goto top of outline Abstract

Cardiovascular disease (CVD) arises as a result of genetic predisposition in the context of a disease-promoting environment. While several risk factors have been identified for CVD, such as elevated serum lipid levels and hypertension, most of the genes identified thus far do not appear to involve such ‘conventional’ risk factors. Moreover, the interactions between genes and environment, such as a diet high in certain fats, adds another level of complexity to CVD and renders identification of the underlying genetic factors even more difficult. Polyunsaturated fatty acids (PUFAs), such as the ω–6 and ω–3 fatty acids, which have multiple roles in membrane structure, lipid metabolism, blood clotting, blood pressure, and, in particular, inflammation, have been linked to the reduction in CVD. Linoleic (ω–6) and α-linolenic acid (ω–3) are essential fatty acids that can be converted into long-chain PUFAs, such as arachidonic acid (AA) and eicosapentaenoic acid (EPA)/docosahexaenoic acid (DHA), respectively. These long-chain PUFAs are metabolized by enzymatically catalyzed systems via cyclooxygenases and lipoxygenases. The 5-lipoxygenase (5-LO)/leukotriene (LT) biosynthesis pathway has been biochemically and genetically associated with CVD traits in mice and humans, particularly in the context of dietary AA and EPA/DHA. In this review, we summarize the biochemical metabolism of ω–3 and ω–6 PUFAs, evaluate the evidence for genetic and nutrigenetic contributions of 5-LO pathway genes to CVD, and discuss the potential of future studies that could identify other gene-dietary interactions between PUFAs and CVD traits.

Copyright © 2009 S. Karger AG, Basel


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 goto top of outline Author Contacts

Hooman Allayee, PhD
Department of Preventive Medicine, USC Keck School of Medicine
2250 Alcazar Street, CSC 206
Los Angeles, CA 90033 (USA)
Tel. +1 323 442 1736, Fax +1 332 442 2764, E-Mail hallayee@usc.edu


 goto top of outline Article Information

Published online: September 23, 2009
Number of Print Pages : 9
Number of Figures : 3, Number of Tables : 2, Number of References : 69


 goto top of outline Publication Details

Journal of Nutrigenetics and Nutrigenomics

Vol. 2, No. 3, Year 2009 (Cover Date: October 2009)

Journal Editor: Pérusse L. (Quebec, Que.)
ISSN: 1661-6499 (Print), eISSN: 1661-6758 (Online)

For additional information: http://www.karger.com/JNN


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