Jensen Heidi A R, Harsløf Laurine B S, Nielsen Maria S, Christensen Line B, Ritz Christian, Michaelsen Kim F, Vogel Ulla, Lauritzen Lotte
From the Department of Nutrition, Exercise and Sports, Faculty of Science, University of Copenhagen, Copenhagen, Denmark (HARJ, LBSH, MSN, LBC, CR, KFM, and LL), and the National Research Centre for the Working Environment, Copenhagen, Denmark (UV).
Am J Clin Nutr. 2014 Sep;100(3):826-32. doi: 10.3945/ajcn.114.087882. Epub 2014 Jul 30.
Docosahexaenoic acid (DHA), supplied by the diet or endogenous biosynthesis from α-linolenic acid, accretes during the perinatal brain growth spurt. Results regarding a potential programming effect on cognitive function and behavior in humans are inconclusive.
Here we aimed to investigate whether behavioral outcomes in childhood were associated with FADS tag-single-nucleotide polymorphisms (SNPs) previously found to have opposing effects on infant erythrocyte DHA.
At 36 mo, we assessed psychomotor development with the third edition of the Ages & Stages Questionnaire (n = 256) and physical activity by accelerometry (n = 231) in children from the SKOT [Småbørns Kost Og Trivsel (Diet and Thriving in Young Children)] cohort. Blood samples were taken to determine erythrocyte DHA (n = 200), FADS tag-SNPs (n = 255), and PPARG-Pro12Ala (n = 255). All outcomes were analyzed in models, including all 3 SNPs, SNP-sex interactions, erythrocyte DHA at 36 mo, and covariates.
As previously shown, the minor allele carriers of the FADS SNP rs1535 had increased erythrocyte DHA at 9 mo, whereas DHA decreased in minor allele carriers of rs174448 and rs174575 (effect size around 0.5 percentage points per allele). No overall effects were observed for any of the FADS SNPs on the outcomes reported here, but FADS SNP-sex interactions were found for a number of DHA-increasing FADS alleles on both communication and problem solving (P = 0.005 and 0.013). DHA-increasing FADS alleles resulted in reduced scores in girls and improved abilities in boys, with an effect size of ∼1 score-point/allele. No associations were found between current erythrocyte DHA and any of the behavioral outcomes. The P value for the triple interaction between DHA-increasing FADS alleles, PPARG, and sex for communication was 0.051, and subsequent analyses showed the FADS-sex interaction only in PPARG minor allele carriers (n = 70). Furthermore, FADS-PPARG interactions were seen for problem solving in boys and for fine motor skills in girls.
FADS SNPs seem to have a sex-specific, possibly peroxisome proliferator-activated receptor-mediated effect on behavior in children, indicating a programming effect of early DHA exposure.
饮食中摄入的二十二碳六烯酸(DHA)或由α-亚麻酸内源性生物合成的DHA,在围产期脑发育快速期会不断积累。关于其对人类认知功能和行为的潜在编程效应的研究结果尚无定论。
我们旨在研究儿童期行为结果是否与脂肪酸去饱和酶(FADS)标签单核苷酸多态性(SNP)相关,此前发现这些多态性对婴儿红细胞DHA有相反影响。
在36个月时,我们通过《年龄与发育阶段问卷》第三版评估了来自SKOT [Småbørns Kost Og Trivsel(幼儿饮食与健康)]队列中儿童的心理运动发育情况(n = 256),并通过加速度计评估了身体活动情况(n = 231)。采集血样以测定红细胞DHA(n = 200)、FADS标签SNP(n = 255)和PPARG - Pro12Ala(n = 255)。所有结果在模型中进行分析,模型包括所有3个SNP、SNP与性别的相互作用、36个月时的红细胞DHA以及协变量。
如先前所示,FADS SNP rs1535的次要等位基因携带者在9个月时红细胞DHA增加,而rs174448和rs174575的次要等位基因携带者的DHA减少(每个等位基因的效应大小约为0.5个百分点)。对于此处报告的结果,未观察到任何FADS SNP的总体效应,但在沟通和解决问题方面,发现一些增加DHA的FADS等位基因存在FADS SNP与性别的相互作用(P = 0.005和0.013)。增加DHA的FADS等位基因导致女孩得分降低,男孩能力提高,效应大小约为1分/等位基因。未发现当前红细胞DHA与任何行为结果之间存在关联。增加DHA的FADS等位基因、PPARG和性别之间在沟通方面的三重相互作用的P值为0.051,随后分析表明仅在PPARG次要等位基因携带者(n = 70)中存在FADS与性别的相互作用。此外,在男孩解决问题和女孩精细运动技能方面发现了FADS - PPARG相互作用。
FADS SNP似乎对儿童行为有性别特异性的、可能由过氧化物酶体增殖物激活受体介导的影响,表明早期DHA暴露具有编程效应。