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

被引:19
作者
Andersen, Mette Korre [1 ]
Jorsboe, Emil [2 ]
Sandholt, Camilla Helene [1 ]
Grarup, Niels [1 ]
Jorgensen, Marit Eika [3 ]
Frgeman, Nils Joakim [4 ]
Bjerregaard, Peter [5 ,6 ]
Pedersen, Oluf [1 ]
Moltke, Ida [2 ]
Hansen, Torben [1 ,7 ]
Albrechtsen, Anders [2 ]
机构
[1] Univ Copenhagen, Fac Hlth & Med Sci, Sect Metab Genet, Novo Nordisk Fdn,Ctr Basic Metab Res, Copenhagen, Denmark
[2] Univ Copenhagen, Dept Biol, Bioinformat Ctr, Copenhagen, Denmark
[3] Steno Diabet Ctr, Gentofte, Denmark
[4] Univ Southern Denmark, Dept Biochem & Mol Biol, Villum Ctr Bioanalyt Sci, Odense, Denmark
[5] Univ Southern Denmark, Natl Inst Publ Hlth, Copenhagen, Denmark
[6] Univ Greenland, Greenland Ctr Hlth Res, Nuuk, Greenland
[7] Univ Southern Denmark, Fac Hlth Sci, Odense, Denmark
基金
英国医学研究理事会;
关键词
GENOME-WIDE ASSOCIATION; MIDDLE-AGED ADULTS; INSULIN-RESISTANCE; ATHEROSCLEROSIS RISK; AGING RESEARCH; PLASMA; HEART; SERUM; CLUSTER; DIETARY;
D O I
10.1371/journal.pgen.1006119
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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.
引用
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页数:19
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