Source:http://linkedlifedata.com/resource/pubmed/id/21209257
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2011-2-21
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pubmed:abstractText |
APOA5 is one of the strongest regulators of plasma TG concentrations; nevertheless, its mechanisms of action are poorly characterized. Genetic variability at the APOA5 locus has also been associated with increased cardiovascular disease risk; however, this predisposition could be attenuated in the context of a prudent diet as traditionally consumed in the Mediterranean countries. We have investigated the interaction between a single nucleotide polymorphism (SNP) at the APOA5 gene (-1131T > C) and dietary fat that may modulate TG-rich lipoprotein concentrations and anthropometric measures in overweight and obese participants. We recruited 1465 participants from a Spanish population (20-65 y old; BMI 25-40 kg/m(2)) attending outpatient obesity clinics. Consistent with previous reports, we found an association between the APOA5-1131T > C SNP and TG-rich lipoprotein concentrations that were higher in carriers of the minor allele than in noncarriers (P < 0.001). Moreover, we found a significant genotype-dietary fat interaction for obesity traits. Participants homozygous for the -1131T major allele had a positive association between fat intake and obesity, whereas in those carrying the APOA5-1131C minor allele, higher fat intakes were not associated with higher BMI. Likewise, we found genotype-dietary fat interactions for TG-rich lipoproteins (P < 0.001). In conclusion, we have replicated previous gene-diet interactions between APOA5 -1131T > C SNP and fat intake for obesity traits and detected a novel interaction for TG-rich lipoprotein concentrations. Our data support the hypothesis that the minor C-allele may protect those consuming a high-fat diet from obesity and elevated concentrations of TG-rich lipoproteins.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/APOA5 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Apolipoproteins A,
http://linkedlifedata.com/resource/pubmed/chemical/Dietary Fats,
http://linkedlifedata.com/resource/pubmed/chemical/Lipoproteins,
http://linkedlifedata.com/resource/pubmed/chemical/Lipoproteins, VLDL,
http://linkedlifedata.com/resource/pubmed/chemical/Triglycerides,
http://linkedlifedata.com/resource/pubmed/chemical/lipoprotein triglyceride
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
1541-6100
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
141
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
380-5
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pubmed:meshHeading |
pubmed-meshheading:21209257-Adult,
pubmed-meshheading:21209257-Aged,
pubmed-meshheading:21209257-Apolipoproteins A,
pubmed-meshheading:21209257-Body Mass Index,
pubmed-meshheading:21209257-Cardiovascular Diseases,
pubmed-meshheading:21209257-Dietary Fats,
pubmed-meshheading:21209257-Female,
pubmed-meshheading:21209257-Genetic Association Studies,
pubmed-meshheading:21209257-Humans,
pubmed-meshheading:21209257-Hypertriglyceridemia,
pubmed-meshheading:21209257-Lipoproteins,
pubmed-meshheading:21209257-Lipoproteins, VLDL,
pubmed-meshheading:21209257-Male,
pubmed-meshheading:21209257-Mediterranean Region,
pubmed-meshheading:21209257-Middle Aged,
pubmed-meshheading:21209257-Obesity,
pubmed-meshheading:21209257-Overweight,
pubmed-meshheading:21209257-Polymorphism, Single Nucleotide,
pubmed-meshheading:21209257-Promoter Regions, Genetic,
pubmed-meshheading:21209257-Risk Factors,
pubmed-meshheading:21209257-Spain,
pubmed-meshheading:21209257-Triglycerides,
pubmed-meshheading:21209257-Young Adult
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pubmed:year |
2011
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pubmed:articleTitle |
APOA5 gene variation interacts with dietary fat intake to modulate obesity and circulating triglycerides in a Mediterranean population.
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pubmed:affiliation |
Department of Physiology, University of Murcia, Campus de Espinardo, s/n. 30100, Murcia, Spain.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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