Office of Public Health Studies, University of Hawai'i at Mānoa, Honolulu, Hawai'i.
Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, ON, Canada.
Int J Epidemiol. 2017 Oct 1;46(5):1512-1522. doi: 10.1093/ije/dyx081.
Recent studies have implicated the FTO gene in child and adult obesity. A longer duration of exclusive breastfeeding (EXBF) has been shown to reduce body mass index (BMI) and the risk of being overweight in the general population and among FTO gene carriers. However, it remains unclear whether the preventive effect of EXBF could be explained by its impact on early life growth development, e.g. ages at adiposity peak (AP) and adiposity rebound (AR) and BMI velocities in the first years of life, which are major determinants of overweight and obesity later in life.
We studied 5590 children from the British Avon Longitudinal Study of Parents and Children (ALSPAC) cohort and modelled their longitudinal BMI profiles with mixed effects models from birth to 16 years of age, as well as their ages at AP, AR and BMI velocities in relation to the FTO gene variant and EXBF.
A longer duration of EXBF (i.e. at least 5 months) has substantial impact on BMI growth trajectories among children carrying the FTO adverse variant by modulating the age at AP, age at AR and BMI velocities. EXBF acts antagonistically to the FTO rs9939609 risk allele and by the age of 15, the predicted reduction in BMI after 5 months of EXBF is 0.56 kg/m2 [95% confidence interval (CI) 0.11-1.01; P = 0.003] and 1.14 kg/m2 (95% CI 0.67-1.62; P < 0.0001) in boys and girls, respectively.
EXBF influences early life growth development and thus plays a critical role in preventing the risks of overweight and obesity even when those are exacerbated by genetic factors.
最近的研究表明 FTO 基因与儿童和成人肥胖有关。研究表明,较长时间的纯母乳喂养(EXBF)可降低普通人群和 FTO 基因携带者的体重指数(BMI)和超重风险。然而,EXBF 的预防作用是否可以通过其对生命早期生长发育的影响来解释,例如肥胖峰值(AP)和肥胖反弹(AR)的年龄以及生命头几年的 BMI 速度,这些都是超重和肥胖的主要决定因素在以后的生活中。
我们研究了来自英国阿冯纵向研究父母和孩子(ALSPAC)队列的 5590 名儿童,并使用混合效应模型从出生到 16 岁对他们的纵向 BMI 曲线进行建模,以及他们的 AP、AR 和 BMI 速度年龄与 FTO 基因变异和 EXBF 有关。
较长时间的 EXBF(即至少 5 个月)通过调节 AP、AR 和 BMI 速度的年龄对携带 FTO 不利变异的儿童的 BMI 生长轨迹有显著影响。EXBF 与 FTO rs9939609 风险等位基因拮抗,在 15 岁时,5 个月 EXBF 后 BMI 的预测降低量为 0.56kg/m2[95%置信区间(CI)0.11-1.01;P=0.003]和 1.14kg/m2(95%CI 0.67-1.62;P<0.0001),分别在男孩和女孩中。
EXBF 影响生命早期的生长发育,因此即使在遗传因素加剧超重和肥胖风险的情况下,它也在预防超重和肥胖风险方面发挥着关键作用。