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婴儿期饮食干预与后期胰岛细胞自身免疫的相关征象。

Dietary intervention in infancy and later signs of beta-cell autoimmunity.

机构信息

Hospital for Children and Adolescents, University of Helsinki and Helsinki University Central Hospital, Helsinki, Finland.

出版信息

N Engl J Med. 2010 Nov 11;363(20):1900-8. doi: 10.1056/NEJMoa1004809.

Abstract

BACKGROUND

Early exposure to complex dietary proteins may increase the risk of beta-cell autoimmunity and type 1 diabetes in children with genetic susceptibility. We tested the hypothesis that supplementing breast milk with highly hydrolyzed milk formula would decrease the cumulative incidence of diabetes-associated autoantibodies in such children.

METHODS

In this double-blind, randomized trial, we assigned 230 infants with HLA-conferred susceptibility to type 1 diabetes and at least one family member with type 1 diabetes to receive either a casein hydrolysate formula or a conventional, cow's-milk-based formula (control) whenever breast milk was not available during the first 6 to 8 months of life. Autoantibodies to insulin, glutamic acid decarboxylase (GAD), the insulinoma-associated 2 molecule (IA-2), and zinc transporter 8 were analyzed with the use of radiobinding assays, and islet-cell antibodies were analyzed with the use of immunofluorescence, during a median observation period of 10 years (mean, 7.5). The children were monitored for incident type 1 diabetes until they were 10 years of age.

RESULTS

The unadjusted hazard ratio for positivity for one or more autoantibodies in the casein hydrolysate group, as compared with the control group, was 0.54 (95% confidence interval [CI], 0.29 to 0.95), and the hazard ratio adjusted for an observed difference in the duration of exposure to the study formula was 0.51 (95% CI, 0.28 to 0.91). The unadjusted hazard ratio for positivity for two or more autoantibodies was 0.52 (95% CI, 0.21 to 1.17), and the adjusted hazard ratio was 0.47 (95% CI, 0.19 to 1.07). The rate of reported adverse events was similar in the two groups.

CONCLUSIONS

Dietary intervention during infancy appears to have a long-lasting effect on markers of beta-cell autoimmunity--markers that may reflect an autoimmune process leading to type 1 diabetes. (ClinicalTrials.gov number, NCT00570102.).

摘要

背景

早期接触复杂的膳食蛋白质可能会增加具有遗传易感性的儿童发生胰岛自身免疫和 1 型糖尿病的风险。我们检验了这样一个假设,即给母乳喂养的婴儿补充高度水解的配方奶会降低这些儿童发生与糖尿病相关的自身抗体的累积发生率。

方法

在这项双盲、随机试验中,我们将 230 名具有 HLA 易感性的婴儿(即至少有一位一级亲属患有 1 型糖尿病)分为两组,一组接受牛乳配方奶(对照组),另一组接受牛乳蛋白水解配方奶(实验组)。当婴儿在生命的前 6 至 8 个月无法母乳喂养时,两组均可以使用这些配方奶。在中位观察期为 10 年(平均 7.5 年)的时间里,我们使用放射配体结合测定法分析了胰岛素、谷氨酸脱羧酶(GAD)、胰岛瘤相关 2 分子(IA-2)和锌转运蛋白 8 的自身抗体,并用免疫荧光法分析了胰岛细胞抗体。我们对儿童进行了 10 年的随访,以监测其是否发生 1 型糖尿病。

结果

在未校正的情况下,与对照组相比,实验组发生一种或多种自身抗体阳性的风险比为 0.54(95%置信区间[CI],0.29 至 0.95),在校正了研究配方的暴露时间观察差异后,风险比为 0.51(95%CI,0.28 至 0.91)。在未校正的情况下,发生两种或更多种自身抗体阳性的风险比为 0.52(95%CI,0.21 至 1.17),校正后的风险比为 0.47(95%CI,0.19 至 1.07)。两组报告的不良事件发生率相似。

结论

婴儿期的饮食干预似乎对胰岛自身免疫的标志物有持久的影响——这些标志物可能反映了导致 1 型糖尿病的自身免疫过程。(临床试验注册编号:NCT00570102.)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9eeb/4242902/42090101bf0f/nihms638150f1.jpg

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