Abstract

Little is known about the associations of FADS1 genetic variants with circulating levels of PUFA and lipids in Asian populations who have a different dietary pattern and dyslipidemia prevalence compared with Western populations. In a population-based sample of 3,210 unrelated Han Chinese living in Beijing and Shanghai, we examined a FADS1 genetic variant, rs174550, in relation to blood PUFA and lipid levels. C-allele of rs174550 was significantly associated with levels of erythrocyte PUFAs in upstream and downstream pathways of delta-5 desaturase (D5D) (P ≤ 0.003). Moreover, rs174550 C-allele was associated with a lower HDL cholesterol level (P = 0.02) in total population and a higher triglyceride level (P = 0.0002) in Beijing residents. Interestingly, erythrocyte levels of 18:2n-6 and 18:3n-3 modified the effect of rs174550 on HDL cholesterol level: stronger associations between rs174550 C-allele and lower HDL cholesterol levels were exhibited when erythrocyte 18:2n-6 or 18:3n-3 level was low (P for interaction = 0.02 and 0.03, respectively). These data suggested that FADS1 genetic variant was associated with circulating PUFA and lipid levels and that its effect on HDL cholesterol might depend on PUFA status in the Han Chinese population.

Highlights

  • Little is known about the associations of fatty acid desaturase 1 (FADS1) genetic variants with circulating levels of PUFA and lipids in Asian populations who have a different dietary pattern and dyslipidemia prevalence compared with Western populations

  • Analysis of pairwise linkage disequilibrium (LD) among the single nucleotide polymorphism (SNP) within the FADS1 gene showed that LD is perfect (r2 >0.9) in the HapMap Chinese Han in Beijing (CHB) sample and in the genome-wide association studies (GWAS) data of our population

  • The association between FADS1 rs174550 and plasma high-density lipoprotein (HDL) cholesterol was modified by erythrocyte 18:2n-6 and 18:3n-3 status, with low 18:2n-6 or 18:3n-3 level

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Summary

Introduction

Little is known about the associations of FADS1 genetic variants with circulating levels of PUFA and lipids in Asian populations who have a different dietary pattern and dyslipidemia prevalence compared with Western populations. Erythrocyte levels of 18:2n-6 and 18:3n-3 modified the effect of rs174550 on HDL cholesterol level: stronger associations between rs174550 C-allele and lower HDL cholesterol levels were exhibited when erythrocyte 18:2n-6 or 18:3n-3 level was low (P for interaction = 0.02 and 0.03, respectively) These data suggested that FADS1 genetic variant was associated with circulating PUFA and lipid levels and that its effect on HDL cholesterol might depend on PUFA status in the Han Chinese population.—Zhu, J., Q. Findings from three studies conducted among peoples with European ancestry suggested that dietary PUFA intake may modify the associations between FADS1 genetic variant and blood lipids [27,28,29] One of these studies found that rs174547 was associated with lower LDL cholesterol only if dietary long-chain n-3 PUFA was low [29]. It is of interest to examine whether such an interaction may exist in the Chinese population

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