Gene-nutrient interactions with dietary fat modulate the association between genetic variation of the ACSL1 gene and metabolic syndrome.

C.M. Phillips, L. Goumidi, S. Bertrais, M.R. Field, L.A. Cupples, J.M. Ordovas, C. Defoort, J.A. Lovegrove, C.A. Drevon, M.J. Gibney, E.E. Blaak, B. Kiec Wilk, B. Karlstrom, J. Lopez Miranda, R. McManus, S. Hercberg, D. Lairon, R. Planells, H.M. Roche*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review


Abstract Long chain acyl CoA synthetase 1 (ACSL1) plays an important role in fatty acid metabolism and triacylglycerol (TAG) synthesis. Disturbance of these pathways may result in dyslipidemia and insulin resistance, hallmarks of the metabolic syndrome (MetS). Dietary fat is a key environmental factor which may interact with genetic determinants of lipid metabolism to affect MetS risk. We investigated the relationship between ACSL1 polymorphisms (rs4862417, rs6552828, rs13120078, rs9997745 and rs12503643) and MetS risk, and determined potential interactions with dietary fat in the LIPGENE-SU.VI.MAX study of MetS cases and matched controls (n = 1754). GG homozygotes for rs9997745 had increased MetS risk (OR 1.90 [CI 1.15, 3.13] P = 0.01), displayed elevated fasting glucose (P = 0.001) and insulin concentrations (P = 0.002) and increased insulin resistance (P = 0.03) relative to the A allele carriers. MetS risk was modulated by dietary fat, whereby the risk conferred by GG homozygosity was abolished among individuals consuming either a low-fat (< 35% energy) or a high polyunsaturated fat (PUFA) diet (> 5.5% energy). In conclusion ACSL1 rs9997745 influences MetS risk, most likely via disturbances in fatty acid metabolism, which was modulated by dietary fat consumption, particularly PUFA intake, suggesting novel gene-nutrient interactions.
Original languageEnglish
Pages (from-to)1793-1800
JournalJournal of Lipid Research
Issue number7
Publication statusPublished - 1 Jan 2010

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