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从出生到 23 岁的 BMI 轨迹与成年早期的心血管代谢风险有关。

BMI Trajectories from Birth to 23 Years by Cardiometabolic Risks in Young Adulthood.

机构信息

Department of Pediatrics, School of Medicine, University of California, San Diego, La Jolla, California, USA.

Department of Pediatrics, University of Michigan, Ann Arbor, Michigan, USA.

出版信息

Obesity (Silver Spring). 2020 Apr;28(4):813-821. doi: 10.1002/oby.22754. Epub 2020 Feb 28.

Abstract

OBJECTIVE

The aim of this study was to investigate whether the level, rate, and acceleration of BMI growth differ according to the presence or absence of adult cardiometabolic (CM) risks.

METHODS

BMI was measured in 1,000 Chileans at nine time points from birth to 23 years, and metabolic syndrome and its components were assessed at young adulthood. BMI growth was analyzed in the following three developmental periods: birth to 6 months, 6 months to 5 years, and 5 to 23 years.

RESULTS

Individuals with CM risks had a specific constellation of early-life growth (faster growth after infancy, lower BMI decline approaching age 5, absence of a definitive BMI nadir in early childhood, higher 5-year BMI) and distinct young adult growth (larger BMI increases from childhood to young adulthood and lower levels of expected growth deceleration approaching young adulthood). Those with CM risks also attained BMI ≥ 25 at significantly younger ages than those absent risks (metabolic syndrome: 12.3 years vs. 20.1 years; hyperglycemia: 13.1 years vs. 18.9 years; hypertension: 13.2 years vs. 19.4 years; hypertriglyceridemia: 14.3 years vs. 19.5 years; inflammation: 15.9 years vs. 20.6 years).

CONCLUSIONS

Larger and faster increases in BMI and a failure of BMI growth to decline or decelerate at specific developmental periods distinguished individuals who would and would not have adult CM risks.

摘要

目的

本研究旨在探讨体重指数(BMI)的增长水平、速率和加速度是否因是否存在成年心血管代谢(CM)风险而有所不同。

方法

在 9 个时间点从出生到 23 岁对 1000 名智利人进行 BMI 测量,并在成年早期评估代谢综合征及其组成部分。BMI 生长在以下三个发育阶段进行分析:出生至 6 个月、6 个月至 5 岁和 5 至 23 岁。

结果

具有 CM 风险的个体具有特定的早期生长模式(婴儿期后生长较快、接近 5 岁时 BMI 下降较低、幼儿期无明确 BMI 最低点、5 岁时 BMI 较高)和明显的成年早期生长(从儿童期到成年早期 BMI 增加较大,接近成年早期的预期生长减速程度较低)。具有 CM 风险的个体也比没有风险的个体更早达到 BMI≥25 的年龄(代谢综合征:12.3 岁比 20.1 岁;高血糖:13.1 岁比 18.9 岁;高血压:13.2 岁比 19.4 岁;高三酰甘油血症:14.3 岁比 19.5 岁;炎症:15.9 岁比 20.6 岁)。

结论

BMI 的更大和更快增长,以及 BMI 生长在特定发育阶段未能下降或减速,区分了那些将有和不会有成年 CM 风险的个体。

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