Beyerlein Andreas, Liu Xiang, Uusitalo Ulla M, Harsunen Minna, Norris Jill M, Foterek Kristina, Virtanen Suvi M, Rewers Marian J, She Jin-Xiong, Simell Olli, Lernmark Åke, Hagopian William, Akolkar Beena, Ziegler Anette-G, Krischer Jeffrey P, Hummel Sandra
Institute of Diabetes Research, Helmholtz Zentrum München, Munich, Germany;
Department of Pediatrics, Pediatrics Epidemiology Center, Morsani College of Medicine, University of South Florida, Tampa, FL;
Am J Clin Nutr. 2015 Aug;102(2):345-52. doi: 10.3945/ajcn.115.108159. Epub 2015 Jul 8.
Deficient soluble fiber intake has been suggested to dysregulate the immune response either directly or through alterations of the microbial composition in the gut.
We hypothesized that a high intake of dietary soluble fiber in early childhood decreases the risk of type 1 diabetes (T1D)-associated islet autoimmunity.
We analyzed 17,620 food records collected between age 9 and 48 mo from 3358 children from the United States and Germany prospectively followed in the TEDDY (The Environmental Determinants of Diabetes in the Young) study. HRs for the development of any/multiple islet autoantibodies (242 and 151 events, respectively) and T1D (71 events) by soluble fiber intake were calculated in Cox regression models and adjusted for potential confounders.
There were no statistically significantly protective associations observed between a high intake of soluble fiber and islet autoimmunity or T1D. For example, the adjusted HRs (95% CIs) for high intake (highest compared with lowest quintile) at age 12 mo were 0.90 (0.55, 1.45) for any islet autoantibody, 1.20 (0.69, 2.11) for multiple islet autoantibodies, and 1.24 (0.57, 2.70) for T1D. In analyzing soluble fiber intake as a time-varying covariate, there were also no short-term associations between soluble fiber intake and islet autoimmunity development, with adjusted HRs of 0.85 (0.51, 1.42) for high intake and development of any islet autoantibody, for example.
These results indicate that the intake level of dietary soluble fiber is not associated with islet autoimmunity or T1D in early life.
有人提出,可溶性纤维摄入不足会直接或通过改变肠道微生物组成来失调免疫反应。
我们假设幼儿期高膳食纤维摄入量可降低1型糖尿病(T1D)相关胰岛自身免疫的风险。
我们分析了来自美国和德国的3358名儿童在9至48个月期间收集的17620份食物记录,这些儿童在TEDDY(青少年糖尿病环境决定因素)研究中接受前瞻性随访。在Cox回归模型中计算可溶性纤维摄入量与任何/多种胰岛自身抗体(分别为242和151例事件)和T1D(71例事件)发生的风险比(HR),并对潜在混杂因素进行调整。
未观察到高可溶性纤维摄入量与胰岛自身免疫或T1D之间存在统计学上显著的保护关联。例如,12个月龄时高摄入量(最高五分位数与最低五分位数相比)的调整后HR(95%CI),任何胰岛自身抗体为0.90(0.55,1.45),多种胰岛自身抗体为1.20(0.69,2.11),T1D为1.24(0.57,2.70)。在将可溶性纤维摄入量作为随时间变化的协变量进行分析时,可溶性纤维摄入量与胰岛自身免疫发展之间也没有短期关联,例如,高摄入量与任何胰岛自身抗体发展的调整后HR为0.85(0.51,1.42)。
这些结果表明,饮食中可溶性纤维的摄入水平与生命早期的胰岛自身免疫或T1D无关。