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Original Paper

Circulating Triglycerides and the Association of Triglycerides with Dietary Intake Are Altered by Alpha-2-Heremans-Schmid Glycoprotein Polymorphisms

Robinson K.N.a · Vazquez-Vidal I.b · Marques C.a · Andrade F.C.D.c · Aradillas-Garcia C.d · Teran-Garcia M.a, e · The UP AMIGOS Team

Author affiliations

aDivision of Nutritional Sciences, bDepartment of Food Science and Human Nutrition, and cDepartment of Kinesiology and Community Health, University of Illinois at Urbana-Champaign, Urbana, IL, USA; dCoordination for the Innovation and Application of Science and Technology, Autonomous University of San Luis Potosí, San Luis Potosí, Mexico; eDepartment of Human Development and Family Studies, Cooperative Extension, Family Resiliency Center, University of Illinois at Urbana-Champaign, Urbana, IL, USA

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J Nutrigenet Nutrigenomics 2017;10:75-83

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Article / Publication Details

First-Page Preview
Abstract of Original Paper

Received: October 17, 2016
Accepted: June 13, 2017
Published online: August 31, 2017
Issue release date: November 2017

Number of Print Pages: 9
Number of Figures: 2
Number of Tables: 5

ISSN: 1661-6499 (Print)
eISSN: 1661-6758 (Online)

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

Abstract

Background: Circulating fetuin-A (FetA) inhibits insulin receptor signaling and activates the toll-like receptor 4 proinflammatory cascade; thus, it may contribute to metabolic syndrome. Polymorphisms in alpha-2-Heremans-Schmid glycoprotein (AHSG), the gene which codes FetA, may influence metabolic syndrome progression in higher-risk ethnic groups. We aimed to identify whether individual variation in AHSG influences biomarkers of metabolic disease and obesity in young Mexican adults. Methods: The participants were Mexican college applicants (18-25 years, n = 641). Dietary intake, anthropometric data, and blood for the analysis of biomarkers and genetics were collected. Single nucleotide polymorphisms (SNPs) in AHSG (rs2518136 and rs4917) were genotyped. Results: Neither AHSG SNP was associated with body mass index (BMI) or waist circumference. rs4917 C allele carriers had lower triglycerides (TG) than T allele homozygotes (98.85 ± 2.3 vs. 112.2 ± 5.2 mg/dL, p = 0.0113). BMI was strongly associated with TG (p < 0.0001) regardless of genotype. The relationship between circulating TG and dietary intake of carbohydrates and saturated fat was significant in rs4917 CT allele heterozygotes only (p = 0.03 and p = 0.02, respectively). Conclusions: rs4917 T allele carriers had higher TG. This relationship was exaggerated in individuals with overweight and obesity. Dietary intake was significantly associated with TG in only those with heterozygosity at rs4917, suggesting that these individuals may be more susceptible to dietary interventions.

© 2017 S. Karger AG, Basel


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Article / Publication Details

First-Page Preview
Abstract of Original Paper

Received: October 17, 2016
Accepted: June 13, 2017
Published online: August 31, 2017
Issue release date: November 2017

Number of Print Pages: 9
Number of Figures: 2
Number of Tables: 5

ISSN: 1661-6499 (Print)
eISSN: 1661-6758 (Online)

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


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