Ingram School of Nursing, McGill University, Montreal, Quebec, Canada.
Centre de Recherche du CHU Sainte-Justine, Montreal, Quebec, Canada.
J Clin Endocrinol Metab. 2018 Dec 1;103(12):4524-4532. doi: 10.1210/jc.2018-00525.
We examined pathways linking birth weight, weight gain from 0 to 2 years, and adiposity during childhood with insulin sensitivity in early adolescence.
Data were from a longitudinal cohort of 630 Quebec white children with a parental history of obesity (Quebec Adipose and Lifestyle Investigation in Youth study). In a subsample of children born at term (n = 395), weight-for-length z score (zWFL) from 0 to 2 years were computed. At 8 to 10 years, the percentage of body fat was assessed using dual energy X-ray absorptiometry. At 10 to 12 years, the Matsuda insulin sensitivity index (ISI) and the homeostasis model assessment for insulin resistance were determined. A linear regression-based approach for mediation analysis was used to estimate the distinct pathways linking zWFL at 0 to 2 years to insulin sensitivity.
Every additional unit in zWFL at birth was associated with a 10% (95% CI, 5.26% to 14.85%) increase in the Matsuda ISI in early adolescence, independently of the weight at 0 to 2 years and in childhood. An indirect effect of zWFL at birth on the Matsuda ISI was also observed but in the opposite direction (-4.44; 95% CI, -7.91 to -1.05). This relation was mediated by childhood adiposity but not by weight gain from 0 to 2 years. The indirect effect of weight gain from 0 to 2 years, via childhood adiposity, also led to lower insulin sensitivity (-4.83%, 95% CI, -7.34 to -2.53). The findings were similar for the homeostasis model assessment for insulin resistance or when restricted to children with appropriate-for-gestational-age birth weights.
A greater birth weight-for-length resulted in improved insulin sensitivity in early adolescence. However, in the presence of excess childhood adiposity, both a greater birth weight and a faster rate of weight gain from 0 to 2 years resulted in lower insulin sensitivity.
我们研究了出生体重、0 至 2 岁体重增长和儿童时期肥胖与青春期早期胰岛素敏感性之间的关联途径。
数据来自魁北克白种人有肥胖家族史的纵向队列(魁北克青少年脂肪和生活方式研究)的 630 名儿童。在足月出生的儿童亚组(n=395)中,计算了 0 至 2 岁的体重-身长 z 评分(zWFL)。在 8 至 10 岁时,使用双能 X 射线吸收法评估体脂百分比。在 10 至 12 岁时,测定了 Matsuda 胰岛素敏感性指数(ISI)和稳态模型评估的胰岛素抵抗。使用基于线性回归的中介分析方法来估计将 0 至 2 岁的 zWFL 与胰岛素敏感性联系起来的不同途径。
出生时 zWFL 每增加一个单位,与青春期早期 Matsuda ISI 增加 10%(95%CI,5.26%至 14.85%)相关,与 0 至 2 岁时的体重无关,并且在儿童时期也无关。出生时 zWFL 对 Matsuda ISI 的间接影响也存在,但方向相反(-4.44;95%CI,-7.91 至-1.05)。这种关系是通过儿童时期肥胖来介导的,但不是通过 0 至 2 岁的体重增长来介导的。0 至 2 岁体重增长通过儿童时期肥胖导致的间接效应也导致胰岛素敏感性降低(-4.83%,95%CI,-7.34 至-2.53)。当限制为出生体重符合胎龄的儿童时,这些发现对于稳态模型评估的胰岛素抵抗或对于胰岛素抵抗也是相似的。
较大的出生体重-身长比导致青春期早期胰岛素敏感性提高。然而,在存在过多儿童肥胖的情况下,较大的出生体重和 0 至 2 岁体重增长速度较快都会导致胰岛素敏感性降低。