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在生命早期体重增加可预测一级亲属患 1 型糖尿病儿童发生胰岛自身免疫的风险。

Weight gain in early life predicts risk of islet autoimmunity in children with a first-degree relative with type 1 diabetes.

机构信息

Department of Diabetes and Endocrinology, Women's and Children's Hospital and Discipline of Paediatrics, University of Adelaide, Adelaide, Australia.

出版信息

Diabetes Care. 2009 Jan;32(1):94-9. doi: 10.2337/dc08-0821. Epub 2008 Oct 3.

Abstract

OBJECTIVE

In a prospective birth cohort study, we followed infants who had a first-degree relative with type 1 diabetes to investigate the relationship between early growth and infant feeding and the risk of islet autoimmunity.

RESEARCH DESIGN AND METHODS

Infants with a first-degree relative with type 1 diabetes were identified during their mother's pregnancy. Dietary intake was recorded prospectively to determine duration of breast-feeding and age at introduction of cow's milk protein, cereals, meat, fruit, and vegetables. At 6-month reviews, length (or height) and weight, antibodies to insulin, GAD65, the tyrosine phosphatase-like insulinoma antigen, and tissue transglutaminase were measured. Islet autoimmunity was defined as persistent elevation of one or more islet antibodies at consecutive 6-month intervals, including the most recent measure, and was the primary outcome measure.

RESULTS

Follow-up of 548 subjects for 5.7 +/- 3.2 years identified 46 children with islet autoimmunity. Weight z score and BMI z score were continuous predictors of risk of islet autoimmunity (adjusted hazard ratios 1.43 [95% CI 1.10-1.84], P = 0.007, and 1.29 [1.01-1.67], P = 0.04, respectively). The risk of islet autoimmunity was greater in subjects with weight z score >0 than in those with weight z score < or =0 over time (2.61 [1.26-5.44], P = 0.01). Weight z score and BMI z score at 2 years and change in weight z score between birth and 2 years, but not dietary intake, also predicted risk of islet autoimmunity.

CONCLUSIONS

Weight gain in early life predicts risk of islet autoimmunity in children with a first-degree relative with type 1 diabetes.

摘要

目的

在一项前瞻性出生队列研究中,我们对一级亲属患有 1 型糖尿病的婴儿进行了随访,以研究早期生长和婴儿喂养与胰岛自身免疫风险之间的关系。

研究设计和方法

在母亲怀孕期间确定一级亲属患有 1 型糖尿病的婴儿。前瞻性记录饮食摄入量,以确定母乳喂养的持续时间以及引入牛奶蛋白、谷物、肉类、水果和蔬菜的年龄。在 6 个月的复查中,测量长度(或身高)和体重、胰岛素、GAD65、酪氨酸磷酸酶样胰岛素瘤抗原和组织转谷氨酰胺酶的抗体。胰岛自身免疫定义为在连续 6 个月的间隔内(包括最近一次测量)持续升高一种或多种胰岛抗体,是主要的结局测量指标。

结果

对 548 名受试者进行了 5.7 +/- 3.2 年的随访,发现 46 名儿童患有胰岛自身免疫。体重 z 评分和 BMI z 评分是胰岛自身免疫风险的连续预测指标(调整后的危险比分别为 1.43 [95% CI 1.10-1.84],P = 0.007 和 1.29 [1.01-1.67],P = 0.04)。体重 z 评分>0 的受试者比体重 z 评分<或=0 的受试者随时间推移发生胰岛自身免疫的风险更大(2.61 [1.26-5.44],P = 0.01)。2 岁时的体重 z 评分和 BMI z 评分以及出生到 2 岁之间体重 z 评分的变化,而不是饮食摄入,也预测了胰岛自身免疫的风险。

结论

婴儿期的体重增加预测了一级亲属患有 1 型糖尿病的儿童发生胰岛自身免疫的风险。

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