Faculty of Sport and Health Sciences, University of Jyväskylä, Jyväskylä, Finland.
Institute of Biomedicine, University of Eastern Finland, Kuopio Campus, Finland.
J Alzheimers Dis. 2018;64(2):587-595. doi: 10.3233/JAD-180216.
We investigated the associations of genetic risk score (GRS) for Alzheimer's disease and apolipoprotein E (APOE) ɛ variant with cardiometabolic risk factors during 2-year follow-up in children and whether body fat percentage (BF%) modify these associations. A population-based sample of 469 children (246 boys, 223 girls) at baseline and 398 children (201 boys, 197 girls) at 2-year follow-up participated in the study. Genotyping was performed using the Illumina Custom Infinium CardioMetabo BeadChip and the Illumina Infinium HumanCoreExome BeadChip. The GRS was calculated using information on nine independent gene variants available in our genomic data. We assessed BF%, waist circumference, insulin, glucose, triglycerides, high-density lipoprotein (HDL) and low-density lipoprotein (LDL) cholesterol, and systolic and diastolic blood pressure. We computed a cardiometabolic risk score and Homeostatic Model Assessment for Insulin Resistance (HOMA-IR). In boys, the GRS was not associated with cardiometabolic risk factors. In girls, GRS was directly associated with LDL cholesterol (β= 0.133, 95% CI = 0.002 to 0.262) at baseline and with a higher cardiometabolic risk score (β= 0.154, 95% CI = 0.015 to 0.294), glucose (β= 0.143, 95% CI = 0.003 to 0.284), and HOMA-IR (β= 0.141, 95% CI = 0.004 to 0.278) at 2-year follow-up. GRS was directly associated with a cardiometabolic risk score at baseline and 2-year follow-up among girls in the highest third of BF% at baseline, but not in other girls (p < 0.05 for interaction). Children with the APOEɛ3/3 genotype had higher LDL cholesterol at and 2-year follow-up than those with the APOEɛ2/3 genotype. In conclusion, GRS was associated with increased cardiometabolic risk in girls and especially those with higher BF%.
我们研究了阿尔茨海默病的遗传风险评分(GRS)和载脂蛋白 E(APOE)ɛ 变体与儿童 2 年随访期间的心血管代谢风险因素的关联,以及体脂肪百分比(BF%)是否会改变这些关联。本研究基于人群,共纳入了 469 名儿童(246 名男孩,223 名女孩)作为基线人群,其中 398 名儿童(201 名男孩,197 名女孩)完成了 2 年随访。使用 Illumina Custom Infinium CardioMetabo BeadChip 和 Illumina Infinium HumanCoreExome BeadChip 进行基因分型。使用我们基因组数据中可用的 9 个独立基因变异的信息计算 GRS。我们评估了 BF%、腰围、胰岛素、血糖、甘油三酯、高密度脂蛋白(HDL)和低密度脂蛋白(LDL)胆固醇以及收缩压和舒张压。我们计算了心血管代谢风险评分和稳态模型评估的胰岛素抵抗(HOMA-IR)。在男孩中,GRS 与心血管代谢风险因素无关。在女孩中,GRS 与 LDL 胆固醇(β=0.133,95%CI=0.002-0.262)呈直接相关,与较高的心血管代谢风险评分(β=0.154,95%CI=0.015-0.294)、血糖(β=0.143,95%CI=0.003-0.284)和 HOMA-IR(β=0.141,95%CI=0.004-0.278)呈直接相关。在基线时 BF%最高的三分之一女孩中,GRS 与基线和 2 年随访时的心血管代谢风险评分呈直接相关,但在其他女孩中没有(交互作用 p<0.05)。APOEɛ3/3 基因型的儿童在基线和 2 年随访时的 LDL 胆固醇水平高于 APOEɛ2/3 基因型的儿童。结论:GRS 与女孩中心血管代谢风险的增加相关,尤其是那些 BF%较高的女孩。