Institute of Diabetes Research, Helmholtz Zentrum München and Forschergruppe Diabetes der Technischen Universität München, Munich, Germany.
JAMA Pediatr. 2013 Sep;167(9):800-7. doi: 10.1001/jamapediatrics.2013.158.
There is evidence for a role of infections within the pathogenesis of islet autoimmunity and type 1 diabetes mellitus (T1D), but previous studies did not allow assessment of potential critical time windows in this context.
To examine whether early, short-term, or cumulative exposures to episodes of infection and fever during the first 3 years of life were associated with the initiation of persistent islet autoimmunity in children at increased T1D risk.
Prospective cohort study with daily infection records and regular assessment of islet autoimmunity.
Diabetes Research Institute, Munich, Germany.
A total of 148 children at high T1D risk with documentation of 1245 infectious events in 90,750 person-days during their first 3 years of life.
Hazard ratios (HRs) for seroconversion to persistent islet autoantibodies were assessed in Cox regression models with numbers of respiratory, gastrointestinal, and other infections, adjusting for sex, delivery mode, intervention group, season of birth, and antibiotic use.
An increased HR of islet autoantibody seroconversion was associated with respiratory infections during the first 6 months of life (HR = 2.27; 95% CI, 1.32-3.91) and ages 6.0 to 11.9 months (HR = 1.32; 95% CI, 1.08-1.61). During the second year of life, no meaningful effects were detected for any infectious category. A higher number of respiratory infections in the 6 months prior to islet autoantibody seroconversion was also associated with an increased HR (HR = 1.42; 95% CI, 1.12-1.80).
Respiratory infections in early childhood are a potential risk factor for the development of T1D.
有证据表明感染在胰岛自身免疫和 1 型糖尿病(T1D)的发病机制中起作用,但以前的研究无法评估这种情况下潜在的关键时间窗。
研究儿童生命的前 3 年内早期、短期或累积暴露于感染和发热事件是否与增加的 T1D 风险儿童持续性胰岛自身免疫的发生有关。
前瞻性队列研究,每天记录感染情况,定期评估胰岛自身免疫。
德国慕尼黑糖尿病研究所。
共有 148 名高 T1D 风险儿童,在生命的前 3 年内有 1245 次感染事件,共 90750 人天。
使用 Cox 回归模型评估 Cox 回归模型中与持续性胰岛自身抗体血清转化率相关的危害比(HR),共纳入呼吸道感染、胃肠道感染和其他感染数量,调整性别、分娩方式、干预组、出生季节和抗生素使用情况。
与生命的前 6 个月(HR=2.27;95%CI,1.32-3.91)和 6.0 至 11.9 个月(HR=1.32;95%CI,1.08-1.61)的呼吸道感染相比,胰岛自身抗体血清转化率升高与呼吸道感染相关。在生命的第二年,任何感染类别都没有发现有意义的影响。在胰岛自身抗体血清转化率之前的 6 个月内,呼吸道感染次数增加也与 HR 升高相关(HR=1.42;95%CI,1.12-1.80)。
儿童早期的呼吸道感染是 T1D 发展的一个潜在危险因素。