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首页> 外文期刊>The American Journal of Clinical Nutrition: Official Journal of the American Society for Clinical Nutrition >Dietary n-3 and n-6 polyunsaturated fatty acid intake interacts with FADS1 genetic variation to affect total and HDL-cholesterol concentrations in the Doetinchem Cohort Study
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Dietary n-3 and n-6 polyunsaturated fatty acid intake interacts with FADS1 genetic variation to affect total and HDL-cholesterol concentrations in the Doetinchem Cohort Study

机译:在Doetinchem队列研究中,饮食中的n-3和n-6多不饱和脂肪酸摄入与FADS1遗传变异相互作用,影响总胆固醇和HDL胆固醇浓度

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Background: The δ-5 and δ-6 desaturases, encoded by the FADS1 and FADS2 genes, are rate-limiting enzymes in polyunsaturated fatty acid (PUFA) biosynthesis. Single nucleotide polymorphisms in the FADS gene cluster region have been associated with both PUFA concentrations in plasma or erythrocyte membrane phospholipids and cholesterol concentrations in recent genome-wide association studies. Objective: We examined whether genetic variations in the FADS gene cluster region interact with dietary intakes of n-3 (omega-3) and n-6 (omega-6) PUFAs to affect plasma total, HDL-, and non-HDL-cholesterol concentrations. Design: Dietary intakes of n-3 and n-6 PUFAs, plasma concentrations of total and HDL cholesterol, and rs174546, rs482548, and rs174570 in the FADS gene cluster region were measured in 3575 subjects in the second survey of the Doetinchem Cohort Study. Results: Significant associations between rs174546 genotypes and total and non-HDL-cholesterol concentrations were observed in the group with a high intake of n-3 PUFAs (≥0.51% of total energy; P = 0.006 and 0.047, respectively) but not in the low-intake group (P for interaction = 0.32 and 0.51, respectively). The C allele was associated with high total and non-HDL-cholesterol concentrations. Furthermore, the C allele was significantly associated with high HDL-cholesterol concentrations in the group with a high intake of n-6 PUFAs (≥5.26% of total energy, P = 0.004) but not in the group with a low intake (P for interaction = 0.02). Conclusion: Genetic variation in the FADS1 gene potentially interacts with dietary PUFA intakes to affect plasma cholesterol concentrations, which should be investigated further in other studies.
机译:背景:由FADS1和FADS2基因编码的δ-5和δ-6去饱和酶是多不饱和脂肪酸(PUFA)生物合成中的限速酶。在最近的全基因组关联研究中,FADS基因簇区域中的单核苷酸多态性与血浆或红细胞膜磷脂中的PUFA浓度和胆固醇浓度相关。目的:我们检查了FADS基因簇区域的遗传变异是否与饮食中n-3(omega-3)和n-6(omega-6)PUFA的摄入量相互作用,从而影响血浆总胆固醇,高密度脂蛋白胆固醇和非高密度脂蛋白胆固醇浓度。设计:在Doetinchem队列研究的第二次调查中,对3575名受试者的FADS基因簇区域中的n-3和n-6 PUFA的饮食摄入量,总胆固醇和HDL胆固醇的血浆浓度以及rs174546,rs482548和rs174570进行了测量。结果:在摄入高n-3 PUFA(总能量≥0.51%;分别为P = 0.006和0.047)的组中,观察到rs174546基因型与总和非HDL-胆固醇浓度之间存在显着关联。低摄入量组(相互作用的P分别为0.32和0.51)。 C等位基因与高总和非HDL胆固醇浓度有关。此外,C等位基因与高摄入n-6 PUFA的组(≥总能量的5.26%,P = 0.004)与高HDL-胆固醇浓度显着相关,而在低摄入量的组(P代表P等于0.004)互动= 0.02)。结论:FADS1基因的遗传变异可能与饮食中摄取的PUFA相互作用,从而影响血浆胆固醇浓度,这应在其他研究中进一步研究。

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