Division of Human Nutrition, Wageningen University Research Center, Wageningen, Netherlands.
Am J Clin Nutr. 2010 Jul;92(1):258-65. doi: 10.3945/ajcn.2009.29130. Epub 2010 May 19.
The delta-5 and delta-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.
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.
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.
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 (> or =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 (> or =5.26% of total energy, P = 0.004) but not in the group with a low intake (P for interaction = 0.02).
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.
δ-5 和 δ-6 去饱和酶由 FADS1 和 FADS2 基因编码,是多不饱和脂肪酸(PUFA)生物合成的限速酶。最近的全基因组关联研究表明,FADS 基因簇区域的单核苷酸多态性与血浆或红细胞膜磷脂中的 PUFA 浓度以及胆固醇浓度有关。
我们研究了 FADS 基因簇区域的遗传变异是否与 n-3(ω-3)和 n-6(ω-6)PUFA 的膳食摄入量相互作用,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。
在 Doetinchem 队列研究的第二次调查中,对 3575 名受试者进行了 n-3 和 n-6 PUFAs 的膳食摄入量、血浆总胆固醇和高密度脂蛋白胆固醇浓度以及 FADS 基因簇区域中的 rs174546、rs482548 和 rs174570 的检测。
在 n-3 PUFAs 摄入量高(>或=0.51%总能量)的组中,rs174546 基因型与总胆固醇和非高密度脂蛋白胆固醇浓度之间存在显著关联(P=0.006 和 0.047),但在低摄入量组中则无关联(交互作用 P 值分别为 0.32 和 0.51)。C 等位基因与高总胆固醇和非高密度脂蛋白胆固醇浓度相关。此外,在 n-6 PUFAs 摄入量高(>或=5.26%总能量)的组中,C 等位基因与高高密度脂蛋白胆固醇浓度显著相关(P=0.004),但在低摄入量组中则无关联(交互作用 P 值为 0.02)。
FADS1 基因的遗传变异可能与 PUFA 膳食摄入量相互作用,影响血浆胆固醇浓度,这需要在其他研究中进一步研究。