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预测儿童时期成人 BMI 特定代谢风险。

Predicting adult body mass index-specific metabolic risk from childhood.

机构信息

Pennington Biomedical Research Center, Baton Rouge, Louisiana 70808, USA.

出版信息

Metab Syndr Relat Disord. 2010 Apr;8(2):165-72. doi: 10.1089/met.2009.0063.

Abstract

BACKGROUND

Metabolic risk varies within adult body mass index (BMI) categories; however, the development of BMI-specific metabolic risk from childhood is unknown.

METHODS

The sample included 895 adults (20-38 years of age; 43% male, 34% black) from the Bogalusa Heart Study (1995-2002), who had been measured as children (5-18 years of age) in 1981-1982. Adult metabolic risk was assessed using two definitions: Cardiometabolic risk factor clustering (RFC) included two or more abnormal risk factors [blood pressure, high-density lipoprotein cholesterol (HDL-C), triglycerides, and fasting glucose] and insulin resistance (IR), comprising the top quartile of the homeostasis model of insulin resistance (HOMA-IR) distribution. Logistic regression, within BMI categories, was used to predict adult metabolic risk from childhood mean arterial pressure (MAP), HDL-C, low-density lipoprotein cholesterol (LDL-C), glucose, and triglycerides. Covariates included childhood age, race, sex, adult BMI, and length of follow-up.

RESULTS

The prevalence of the adult abnormal metabolic risk profile varied by definitions of metabolic risk (normal weight, 5%-9%; overweight, 15%-23%; and obese, 40%-53%). The adult abnormal profile was associated with higher childhood LDL-C [IR, odds ratio (OR), 1.95; 95% confidence interval (CI), 1.06-3.58) and insulin (IR, OR, 1.69; CI, 1.10-2.58) in normal-weight adults; lower childhood HDL-C in overweight adults (RFC, OR, 0.61; CI, 0.40-0.94); and higher childhood MAP (RFC, OR, 1.75; CI, 1.24-2.47) and glucose (IR, OR,1.38; CI, 1.06-1.81) in obese adults.

CONCLUSIONS

Some childhood metabolic risk factors are moderately associated with adult BMI-specific metabolic risk profiles. The ability to identify children with high future adult cardiovascular risk may initiate early treatment options.

摘要

背景

代谢风险在成年人体重指数(BMI)类别内存在差异;然而,从儿童期到成年期 BMI 特异性代谢风险的发展情况尚不清楚。

方法

该样本包括来自博加卢萨心脏研究(1995-2002 年)的 895 名成年人(20-38 岁;43%为男性,34%为黑人),他们在 1981-1982 年儿童时期(5-18 岁)进行了测量。采用两种定义评估成人代谢风险:代谢风险因子聚集(RFC)包括两个或更多异常风险因素[血压、高密度脂蛋白胆固醇(HDL-C)、甘油三酯和空腹血糖]和胰岛素抵抗(IR),包含胰岛素抵抗稳态模型(HOMA-IR)分布的四分位上限。在 BMI 类别内,使用逻辑回归预测儿童时期平均动脉压(MAP)、HDL-C、低密度脂蛋白胆固醇(LDL-C)、血糖和甘油三酯与成年期代谢风险的关系。协变量包括儿童期年龄、种族、性别、成年 BMI 和随访时间。

结果

根据代谢风险的定义(正常体重、超重和肥胖),成年人异常代谢风险谱的患病率不同(正常体重者为 5%-9%,超重者为 15%-23%,肥胖者为 40%-53%)。在正常体重的成年人中,成年期异常谱与较高的儿童 LDL-C[IR,比值比(OR)1.95;95%置信区间(CI)1.06-3.58]和胰岛素(IR,OR 1.69;CI 1.10-2.58)有关;在超重的成年人中,与较低的儿童 HDL-C(RFC,OR 0.61;CI 0.40-0.94)有关;在肥胖的成年人中,与较高的儿童 MAP(RFC,OR 1.75;CI 1.24-2.47)和葡萄糖(IR,OR 1.38;CI 1.06-1.81)有关。

结论

一些儿童期代谢风险因素与成年 BMI 特异性代谢风险谱中度相关。识别具有高未来成人心血管风险的儿童可能会启动早期治疗方案。

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