Department of Nutrition, Exercise and Sports, University of Copenhagen, Copenhagen, Denmark.
Clinical Epidemiology, Steno Diabetes Center Copenhagen, Gentofte, Denmark.
Am J Clin Nutr. 2019 Nov 1;110(5):1175-1185. doi: 10.1093/ajcn/nqz170.
Both impaired and accelerated postnatal growth have been associated with adult risks of obesity and cardiometabolic diseases, like type 2 diabetes and cardiovascular disease. However, the timing of the onset of cardiometabolic changes and the specific growth trajectories linking early growth with later disease risks are not well understood.
The aim of this study was to identify distinct trajectories of BMI growth from 0 to 5 y and examine their associations with body composition and markers of cardiometabolic risk at age 5 y.
In a prospective birth cohort study of 453 healthy and term Ethiopian children with BMIs assessed a median of 9 times during follow-up, we identified subgroups of distinct BMI trajectories in early childhood using latent class trajectory modeling. Associations of the identified growth trajectories with cardiometabolic markers and body composition at 5 y were analyzed using multiple linear regression analyses in 4 adjustment models for each outcome.
We identified 4 heterogeneous BMI growth trajectories: stable low BMI (19.2%), normal BMI (48.8%), rapid catch-up to high BMI (17.9%), and slow catch-up to high BMI (14.1%). Compared with the normal BMI trajectory, children in the rapid catch-up to high BMI trajectory had higher triglycerides (TGs) (range of β-coefficients in Models 1-4: 19-21%), C-peptides (23-25%), fat masses (0.48-0.60 kg), and fat-free masses (0.50-0.77 kg) across the 4 adjustment models. Children in the stable low BMI trajectory had lower LDL cholesterol concentrations (0.14-0.17 mmol/L), HDL cholesterol concentrations (0.05-0.09 mmol/L), fat masses (0.60-0.64 kg), and fat-free masses (0.35-0.49 kg), but higher TGs (11-13%).
The development of obesity and cardiometabolic risks may be established already in early childhood; thus, our data provide a further basis for timely interventions targeted at young children from low-income countries with unfavorable growth patterns. The birth cohort was registered at ISRCTN as ISRCTN46718296.
受损和加速的产后生长都与肥胖和心血管疾病的成年风险有关,如 2 型糖尿病和心血管疾病。然而,心血管代谢变化的起始时间以及将早期生长与后期疾病风险联系起来的特定生长轨迹尚不清楚。
本研究旨在确定 0 至 5 岁时 BMI 生长的不同轨迹,并研究其与 5 岁时身体成分和心血管代谢风险标志物的关系。
在一项前瞻性出生队列研究中,对 453 名健康且足月的埃塞俄比亚儿童进行了研究,他们在随访期间平均接受了 9 次 BMI 评估。使用潜在类别轨迹建模方法,在早期儿童中确定了不同 BMI 轨迹的亚组。使用多元线性回归分析,在每个结局的 4 个调整模型中,分析了确定的生长轨迹与 5 岁时心血管代谢标志物和身体成分的关系。
我们发现了 4 种不同的 BMI 生长轨迹:稳定的低 BMI(19.2%)、正常 BMI(48.8%)、快速追赶至高 BMI(17.9%)和缓慢追赶至高 BMI(14.1%)。与正常 BMI 轨迹相比,快速追赶至高 BMI 轨迹的儿童在 4 个调整模型中的甘油三酯(TGs)(β系数范围为 19-21%)、C 肽(23-25%)、脂肪量(0.48-0.60kg)和去脂体重(0.50-0.77kg)均较高。稳定的低 BMI 轨迹的儿童 LDL 胆固醇浓度(0.14-0.17mmol/L)、HDL 胆固醇浓度(0.05-0.09mmol/L)、脂肪量(0.60-0.64kg)和去脂体重(0.35-0.49kg)较低,但 TGs(11-13%)较高。
肥胖和心血管代谢风险的发展可能早在儿童早期就已经确立;因此,我们的数据为来自低收入国家的具有不利生长模式的幼儿提供了及时干预的进一步依据。该队列研究在 ISRCTN 注册为 ISRCTN46718296。