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首页> 外文期刊>Metabolism: Clinical and Experimental >Homeostasis model assessment of insulin resistance*body mass index interactions at ages 9 to 10 years predict metabolic syndrome risk factor aggregate score at ages 18 to 19 years: a 10-year prospective study of black and white girls.
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Homeostasis model assessment of insulin resistance*body mass index interactions at ages 9 to 10 years predict metabolic syndrome risk factor aggregate score at ages 18 to 19 years: a 10-year prospective study of black and white girls.

机译:9至10岁时胰岛素抵抗*体重指数相互作用的稳态模型评估可预测18至19岁时的代谢综合征危险因素总评分:一项为期10年的黑人和白人女孩前瞻性研究。

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If homeostasis model assessment of insulin resistance (HOMA-IR) interactions with obesity (body mass index [BMI]) at ages 9 to 10 years predict aggregate metabolic syndrome risk factors at ages 18 to 19 years, this would identify novel avenues for primary prevention of metabolic syndrome. Our hypothesis was that HOMA-IR*BMI interactions at ages 9 to 10 years would predict aggregate metabolic syndrome risk factor z scores at ages 18 to 19 years in prospective studies of a biracial population of girls. Two centers in the National Heart, Lung, and Blood Institute Growth and Health Study measured serum insulin and glucose at ages 9 to 10 years and 5 metabolic syndrome risk factors at ages 18 to 19 years (triglyceride, high-density lipoprotein cholesterol, systolic/diastolic blood pressure, waist circumference, and glucose). Studies in Cincinnati, OH, included girls from public and parochial schools in the inner city, within-city residential neighborhoods, and suburban areas; and those in Washington, DC, included girls from a health maintenance organization. Girls (194 white, 281 black) were studied first at ages 9 to 10 years, then at ages 18 to 19 years. We assessed HOMA-IR*BMI interactions at ages 9 to 10 years with race-specific z scores for 5 metabolic syndrome risk factors at ages 18 to 19 years. The lowest summed z score (mean +/- SD) was observed for subjects in the lowest tertiles for both HOMA-IR and BMI (-1.15 +/- 2.05), and the highest z score (2.58 +/- 3.11) was for subjects in the highest tertiles for both HOMA-IR and BMI (P < .0001). For the top BMI tertile, there was a progressive increase in z score (increasing risk of metabolic syndrome) as HOMA-IR increased. Interaction of BMI with HOMA-IR at ages 9 to 10 years predicts aggregate metabolic risk score at ages 18 to 19 years, with progressive risk increments within the top BMI tertile as HOMA-IR increases, opening avenues for intervention to reduce both BMI and HOMA-IR at ages 9 to 10 years as a primary approach to prevention of metabolic syndrome at ages 18 to 19 years.
机译:如果在9至10岁时对胰岛素抵抗(HOMA-IR)与肥胖相互作用的体内稳态模型评估(体重指数[BMI])预测在18至19岁时发生了综合性代谢综合征危险因素,那么这将为一级预防找到新的途径代谢综合症。我们的假设是,在一项针对混血儿女孩的前瞻性研究中,9至10岁之间的HOMA-IR * BMI相互作用可预测18至19岁之间的综合代谢综合征危险因素z得分。美国国家心脏,肺和血液研究所生长与健康研究的两个中心在9至10岁时测量了血清胰岛素和葡萄糖,在18至19岁时测量了5种代谢综合征危险因素(甘油三酸酯,高密度脂蛋白胆固醇,收缩压/舒张压,腰围和葡萄糖)。俄亥俄州辛辛那提市的研究对象包括来自内城区,城市居民区和郊区的公立和公立学校的女孩;华盛顿特区的妇女包括来自健康维护组织的女孩。首先对女孩(194名白人,281名黑人)进行了9至10岁,然后是18至19岁的研究。我们评估了9至10岁年龄段的HOMA-IR * BMI相互作用,以及针对18至19岁年龄段的5种代谢综合征危险因素的种族特异性z评分。在HOMA-IR和BMI最低的三分位数中,受试者的z得分总和最低(平均值+/- SD),对于z得分最低的z得分(2.58 +/- 3.11)最高。 HOMA-IR和BMI的最高三分位数的受试者(P <.0001)。对于最高的BMI三分位数,随着HOMA-IR的增加,z评分逐渐升高(代谢综合征的风险增加)。 BMI与HOMA-IR在9至10岁之间的相互作用预测了18至19岁之间的总代谢风险评分,随着HOMA-IR的增加,最高BMI范围内的风险逐步增加,为降低BMI和HOMA的干预措施开辟了道路-9至10岁的IR是预防18至19岁的代谢综合征的主要方法。

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