Doctoral Program in Nutrition and Health Sciences, Laney Graduate School, Emory University, Atlanta, GA, United States.
Center for Nutrition and Health Research, National Institute of Public Health, Cuernavaca, Mexico.
J Nutr. 2024 May;154(5):1540-1548. doi: 10.1016/j.tjnut.2024.03.004. Epub 2024 Mar 6.
Single-nucleotide polymorphisms (SNPs) in fatty acid desaturase (FADS) genes may modify dietary fatty acid requirements and influence cardiometabolic health (CMH).
We evaluated the role of selected variants in maternal and offspring FADS genes on offspring CMH at the age of 11 y and assessed interactions of genotype with diet quality and prenatal docosahexaenoic acid (DHA) supplementation.
We used data from offspring (n = 203) born to females who participated in a randomized controlled trial of DHA supplementation (400 mg/d) from midgestation to delivery. We generated a metabolic syndrome (MetS) score from body mass index, high-density lipoprotein cholesterol, triglycerides, systolic blood pressure, and fasting glucose and identified 6 distinct haplotypes from 5 offspring FADS SNPs. Dietary n-6 (ω-6):n-3 fatty acid ratios were derived from 24-h recall data (n = 141). We used generalized linear models to test associations of offspring diet and FADS haplotypes with MetS score and interactions of maternal and offspring FADS SNP rs174602 with prenatal treatment group and dietary n-6:n-3 ratio on MetS score.
Associations between FADS haplotypes and MetS score were null. Offspring SNP rs174602 did not modify the association of prenatal DHA supplementation with MetS score. Among children with TT or TC genotype for SNP rs174602 (n = 88), those in the highest n-6:n-3 ratio tertile (>8.61) had higher MetS score relative to the lowest tertile [<6.67) (Δ= 0.36; 95% confidence interval (CI): 0.03, 0.69]. Among children with CC genotype (n = 53), those in the highest n-6:n-3 ratio tertile had a lower MetS score relative to the lowest tertile (Δ= -0.23; 95% CI: -0.61, 0.16).
There was evidence of an interaction of offspring FADS SNP rs174602 with current dietary polyunsaturated fatty acid intake, but not with prenatal DHA supplementation, on MetS score. Further studies may help to determine the utility of targeted supplementation strategies and dietary recommendations based on genetic profile.
脂肪酸去饱和酶(FADS)基因中的单核苷酸多态性(SNP)可能改变膳食脂肪酸的需求,并影响心脏代谢健康(CMH)。
我们评估了母体和后代 FADS 基因中选定变异对 11 岁后代 CMH 的作用,并评估了基因型与饮食质量和产前二十二碳六烯酸(DHA)补充之间的相互作用。
我们使用了来自参加随机对照试验的女性所生后代的数据(n=203),这些女性在妊娠中期至分娩期间接受了 DHA 补充(400mg/d)。我们从体重指数、高密度脂蛋白胆固醇、甘油三酯、收缩压和空腹血糖中生成了代谢综合征(MetS)评分,并从 5 个后代 FADS SNP 中生成了 6 个不同的单倍型。膳食 n-6(ω-6):n-3 脂肪酸比值来自 24 小时回顾性数据(n=141)。我们使用广义线性模型来检验后代饮食和 FADS 单倍型与 MetS 评分的关联,以及母体和后代 FADS SNP rs174602 与产前治疗组和膳食 n-6:n-3 比值对 MetS 评分的交互作用。
FADS 单倍型与 MetS 评分之间无关联。后代 SNP rs174602 不能改变产前 DHA 补充与 MetS 评分之间的关联。在 SNP rs174602 的 TT 或 TC 基因型的儿童中(n=88),与最低 tertile([6.67)相比,处于最高 n-6:n-3 比值 tertile(>8.61)的儿童的 MetS 评分更高(Δ=0.36;95%置信区间(CI):0.03,0.69)。在 CC 基因型的儿童中(n=53),与最低 tertile 相比,处于最高 n-6:n-3 比值 tertile 的儿童的 MetS 评分更低(Δ=-0.23;95%CI:-0.61,0.16)。
有证据表明,后代 FADS SNP rs174602 与当前饮食多不饱和脂肪酸摄入之间存在相互作用,但与产前 DHA 补充之间不存在相互作用,对 MetS 评分有影响。进一步的研究可能有助于确定基于遗传特征的靶向补充策略和饮食建议的效用。