4.6 Article

Identification of Novel Genetic Determinants of Erythrocyte Membrane Fatty Acid Composition among Greenlanders

期刊

PLOS GENETICS
卷 12, 期 6, 页码 -

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PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pgen.1006119

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资金

  1. Novo Nordisk Foundation
  2. Danish Diabetes Academy by the Novo Nordisk Foundation
  3. Karen Elise Jensen's Foundation
  4. NunaFonden
  5. Medical Research Council of Denmark
  6. Medical Research Council of Greenland
  7. Commission for Scientific Research in Greenland
  8. Lundbeck Foundation [R215-2015-4174] Funding Source: researchfish
  9. NNF Center for Basic Metabolic Research [Grarup Group] Funding Source: researchfish
  10. Novo Nordisk Fonden [NNF16OC0019986, NNF15OC0017918] Funding Source: researchfish
  11. Villum Fonden [00007292] Funding Source: researchfish

向作者/读者索取更多资源

Fatty acids (FAs) are involved in cellular processes important for normal body function, and perturbation of FA balance has been linked to metabolic disturbances, including type 2 diabetes. An individual's level of FAs is affected by diet, lifestyle, and genetic variation. We aimed to improve the understanding of the mechanisms and pathways involved in regulation of FA tissue levels, by identifying genetic loci associated with inter-individual differences in erythrocyte membrane FA levels. We assessed the levels of 22 FAs in the phospholipid fraction of erythrocyte membranes from 2,626 Greenlanders in relation to single nucleotide polymorphisms genotyped on the MetaboChip or imputed. We identified six independent association signals. Novel loci were identified on chromosomes 5 and 11 showing strongest association with oleic acid (rs76430747 in ACSL6, beta (SE): -0.386% (0.034), p = 1.8x10(-28)) and docosahexaenoic acid (rs6035106 in DTD1, 0.137% (0.025), p = 6.4x10(-8)), respectively. For a missense variant (rs80356779) in CPT1A, we identified a number of novel FA associations, the strongest with 11-eicosenoic acid (0.473% (0.035), p = 2.6x10(-38)), and for variants in FADS2 (rs174570), LPCAT3 (rs2110073), and CERS4 (rs11881630) we replicated known FA associations. Moreover, we observed metabolic implications of the ACSL6 (rs76430747) and CPT1A (rs80356779) variants, which both were associated with altered HbA1c (0.051% (0.013), p = 5.6x10(-6) and -0.034% (0.016), p = 3.1x10(-4), respectively). The latter variant was also associated with reduced insulin resistance (HOMA-IR, -0.193 (0.050), p = 3.8x10(-6)), as well as measures of smaller body size, including weight (-2.676 kg (0.523), p = 2.4x10(-7)), lean mass (-1.200 kg (0.271), p = 1.7x10(-6)), height (-0.966 cm (0.230), p = 2.0x10(-5)), and BMI (-0.638 kg/m(2) (0.181), p = 2.8x10(-4)). In conclusion, we have identified novel genetic determinants of FA composition in phospholipids in erythrocyte membranes, and have shown examples of links between genetic variants associated with altered FA membrane levels and changes in metabolic traits.

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