4.7 Article

Novel variants at KCTD10, MVK, and MMAB genes interact with dietary carbohydrates to modulate HDL-cholesterol concentrations in the Genetics of Lipid Lowering Drugs and Diet Network Study

Journal

AMERICAN JOURNAL OF CLINICAL NUTRITION
Volume 90, Issue 3, Pages 686-694

Publisher

OXFORD UNIV PRESS
DOI: 10.3945/ajcn.2009.27738

Keywords

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Funding

  1. National Institutes of Health, Heart, Lung, and Blood Institute [U01 HL72524]
  2. Genetic and Environmental Determinants of Triglycerides [HL-54776, DK075030]
  3. US Department of Agriculture Research Service [53K06-5-10, 58-1950-9-001]
  4. Fulbright-Spanish Ministry of Education and Science [2007-1086]
  5. [T32 DK007651-19]

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Background: Several genome-wide association studies have identified novel loci (KCTD10, MVK, and MMAB) that are associated with HDL-cholesterol concentrations. Of the environmental factors that determine HDL cholesterol, high-carbohydrate diets have been shown to be associated with low concentrations. Objective: The objective was to evaluate the associations of 8 single nucleotide polymorphisms (SNPs) located within the KCTD10, MVK, and MMAB loci with lipids and their potential interactions with dietary carbohydrates. Design: KCTD10, MVK, and MMAB SNPs were genotyped in 920 subjects (441 men and 479 women) who participated in the Genetics of Lipid Lowering Drugs and Diet Network (GOLDN) Study. Biochemical measurements were made by using standard procedures. Dietary intakes were estimated by using a validated questionnaire. Results: For the SNPs KCTD10_i5642G -> C and MVK_S52NG -> A, homozygotes for the major alleles (G) had lower HDL-cholesterol concentrations than did carriers of the minor alleles (P = 0.005 and P = 0.019, respectively). For the SNP 12inter_108466061A -> G, homozygotes for the minor allele (G) had higher total cholesterol and LDL-cholesterol concentrations than did AG subjects (P = 0.030 and P = 0.034, respectively). Conversely, homozygotes for the major allele (G) at MMAB_3U3527G -> C had higher LDL-cholesterol concentrations than did carriers of the minor allele (P = 0.034). Significant gene-diet interactions for HDL cholesterol were found (P < 0.001-0.038), in which GG subjects at SNPs KCTD10_i5642G -> C and MMAB_3U3527G -> C and C allele carriers at SNP KCTD10_V206VT -> C had lower concentrations only if they consumed diets with a high carbohydrate content (P < 0.001 0.011). Conclusion: These findings suggest that the KCTD10 (V206VT -> C and i5642G -> C) and MMAB_3U3527G -> C variants may contribute to the variation in HDL-cholesterol concentrations, particularly in subjects with high carbohydrate intakes. Am J Clin Nutr 2009;90:686-94.

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