TY - JOUR
T1 - Genetic Variants in the FADS Gene
T2 - Implications for Dietary Recommendations for Fatty Acid Intake
AU - Mathias, Rasika A.
AU - Pani, Vrindarani
AU - Chilton, Floyd H.
N1 - Funding Information:
This work was supported by a grant from the National Institutes of Health, P50 AT002782.
PY - 2014/6
Y1 - 2014/6
N2 - Unequivocally, genetic variants within the fatty acid desaturase (FADS) cluster are determinants of long chain polyunsaturated fatty acid (LC-PUFA) levels in circulation, cells, and tissues. A recent series of papers have addressed these associations in the context of ancestry; evidence clearly supports that the associations are robust to ethnicity. However, ~80 % of African Americans carry two copies of the alleles associated with increased levels of arachidonic acid compared with only ~45 % of European Americans, raising important questions of whether gene-PUFA interactions induced by a modern western diet are differentially driving the risk of diseases of inflammation in diverse populations, and are these interactions leading to health disparities. We highlight an important aspect thus far missing in the debate regarding dietary recommendations; we contend that current evidence from genetics strongly suggest that an individual's, or at the very least the population from which an individual is sampled, genetic architecture must be factored into dietary recommendations currently in place.
AB - Unequivocally, genetic variants within the fatty acid desaturase (FADS) cluster are determinants of long chain polyunsaturated fatty acid (LC-PUFA) levels in circulation, cells, and tissues. A recent series of papers have addressed these associations in the context of ancestry; evidence clearly supports that the associations are robust to ethnicity. However, ~80 % of African Americans carry two copies of the alleles associated with increased levels of arachidonic acid compared with only ~45 % of European Americans, raising important questions of whether gene-PUFA interactions induced by a modern western diet are differentially driving the risk of diseases of inflammation in diverse populations, and are these interactions leading to health disparities. We highlight an important aspect thus far missing in the debate regarding dietary recommendations; we contend that current evidence from genetics strongly suggest that an individual's, or at the very least the population from which an individual is sampled, genetic architecture must be factored into dietary recommendations currently in place.
KW - Arachidonic acid
KW - Cardiovascular disease
KW - Eicosanoids
KW - Fatty acid desaturase
KW - Genetic variants
KW - Inflammation
KW - Nutrition
KW - Polyunsaturated fatty acids
KW - Single nucleotide polymorphisms
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U2 - 10.1007/s13668-014-0079-1
DO - 10.1007/s13668-014-0079-1
M3 - Review article
AN - SCOPUS:84979907627
SN - 2161-3311
VL - 3
SP - 139
EP - 148
JO - Current Nutrition Reports
JF - Current Nutrition Reports
IS - 2
ER -