Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Research Centre of Applied and Preventive Cardiovascular Medicine, University of Turku, Turku, Finland.
Int J Obes (Lond). 2019 Oct;43(10):2007-2016. doi: 10.1038/s41366-019-0414-0. Epub 2019 Jul 22.
Most obese children show cardiometabolic impairments, such as insulin resistance, dyslipidemia, and hypertension. Yet some obese children retain a normal cardiometabolic profile. The mechanisms underlying this variability remain largely unknown. We examined whether genetic loci associated with increased insulin sensitivity and relatively higher fat storage on the hip than on the waist in adults are associated with a normal cardiometabolic profile despite higher adiposity in children.
We constructed a genetic score using variants previously linked to increased insulin sensitivity and/or decreased waist-hip ratio adjusted for body mass index (BMI), and examined the associations of this genetic score with adiposity and cardiometabolic impairments in a meta-analysis of six cohorts, including 7391 European children aged 3-18 years.
The genetic score was significantly associated with increased degree of obesity (higher BMI-SDS beta = 0.009 SD/allele, SE = 0.003, P = 0.003; higher body fat mass beta = 0.009, SE = 0.004, P = 0.031), yet improved body fat distribution (lower WHR beta = -0.014 SD/allele, SE = 0.006, P = 0.016), and favorable concentrations of blood lipids (higher HDL cholesterol: beta = 0.010 SD/allele, SE = 0.003, P = 0.002; lower triglycerides: beta = -0.011 SD/allele, SE = 0.003, P = 0.001) adjusted for age, sex, and puberty. No differences were detected between prepubertal and pubertal/postpubertal children. The genetic score predicted a normal cardiometabolic profile, defined by the presence of normal glucose and lipid concentrations, among obese children (OR = 1.07 CI 95% 1.01-1.13, P = 0.012, n = 536).
Genetic predisposition to higher body fat yet lower cardiometabolic risk exerts its influence before puberty.
大多数肥胖儿童表现出代谢异常,如胰岛素抵抗、血脂异常和高血压。然而,一些肥胖儿童的代谢情况仍保持正常。导致这种差异的机制在很大程度上尚不清楚。我们研究了与成年人中胰岛素敏感性增加以及臀部脂肪相对高于腰部脂肪相关的遗传位点,是否与肥胖儿童的代谢情况正常有关,尽管这些儿童的体脂更高。
我们构建了一个遗传评分,该评分使用了先前与胰岛素敏感性增加和/或腰围身高比降低相关的变体,这些变体通过体重指数(BMI)进行了调整,然后我们在六项队列的荟萃分析中,检测了该遗传评分与肥胖和代谢异常之间的关联,这些队列共包含 7391 名年龄在 3-18 岁的欧洲儿童。
遗传评分与肥胖程度的增加显著相关(BMI-SDS 更高的β=0.009 SD/等位基因,SE=0.003,P=0.003;体脂肪量更高的β=0.009,SE=0.004,P=0.031),但改善了体脂分布(WHR 更低的β=-0.014 SD/等位基因,SE=0.006,P=0.016),以及血脂浓度的改善(更高的高密度脂蛋白胆固醇:β=0.010 SD/等位基因,SE=0.003,P=0.002;更低的甘油三酯:β=-0.011 SD/等位基因,SE=0.003,P=0.001),这些都通过年龄、性别和青春期进行了调整。在青春期前和青春期/青春期后儿童之间未发现差异。遗传评分预测了肥胖儿童中存在正常血糖和血脂浓度的正常代谢特征(OR=1.07,95%CI 1.01-1.13,P=0.012,n=536)。
在青春期前,身体脂肪更高但心血管代谢风险更低的遗传倾向发挥了作用。