Department of Epidemiology and Public Health, University College Cork, Cork, Ireland The Irish Centre for Fetal and Neonatal Translational Research, Department of Obstetrics and Gynaecology, University College Cork, Cork, Ireland
The Irish Centre for Fetal and Neonatal Translational Research, Department of Obstetrics and Gynaecology, University College Cork, Cork, Ireland.
Diabetes Care. 2015 Dec;38(12):2308-15. doi: 10.2337/dc15-0897. Epub 2015 Oct 30.
We investigated the effects of gestational age, birth weight, small for gestational age (SGA), and large for gestational age (LGA) on risk of childhood type 1 diabetes.
We conducted a population-based cohort study of all singleton live births in Sweden between 1973 and 2009 and a sibling control study. Perinatal data were extracted from the Swedish Medical Birth Register. Children with type 1 diabetes diagnosis were identified from the Swedish National Patient Register. Log-linear Poisson regression and conditional logistic regression were used for data analysis.
The study cohort consisted of 3,624,675 singleton live births (42,411,054 person-years). There were 13,944 type 1 diabetes cases during the study period. The sibling control study consisted of 11,403 children with type 1 diabetes and 17,920 siblings. Gestational age between 33 and 36 weeks (relative risk [RR] 1.18 [95% CI 1.09, 1.28) and 37 and 38 weeks (RR 1.12 [95% CI 1.07, 1.17]) was associated with type 1 diabetes in the cohort study and remained significant in the sibling control study. SGA (RR 0.83 [95% CI 0.75, 0.93]) and LGA (RR 1.14 [95% CI 1.04, 1.24]) were associated with type 1 diabetes in the cohort study. The SGA association remained unchanged in the sibling study, while the LGA association disappeared. Very low birth weight was associated with a reduced risk of type 1 diabetes.
The findings suggest a small association between gestational age and type 1 diabetes that is not likely due to familial confounding factors. Gestational age and type 1 diabetes may be related to insulin resistance due to early life growth restriction or altered gut microbiota in preterm babies.
研究胎龄、出生体重、小于胎龄儿(SGA)和大于胎龄儿(LGA)对儿童 1 型糖尿病风险的影响。
我们进行了一项基于人群的队列研究,纳入了 1973 年至 2009 年期间瑞典所有单胎活产儿,并进行了一项同胞对照研究。围产期数据从瑞典医学出生登记处提取。通过瑞典国家患者登记处确定患有 1 型糖尿病的儿童。使用对数线性泊松回归和条件逻辑回归进行数据分析。
研究队列包括 3624675 名单胎活产儿(42411054 人年)。在研究期间,有 13944 例 1 型糖尿病病例。同胞对照研究包括 11403 例 1 型糖尿病儿童和 17920 名同胞。队列研究中,33 至 36 周(相对风险 [RR] 1.18 [95% CI 1.09, 1.28)和 37 至 38 周(RR 1.12 [95% CI 1.07, 1.17))与糖尿病相关,在同胞对照研究中仍具有统计学意义。SGA(RR 0.83 [95% CI 0.75, 0.93)和 LGA(RR 1.14 [95% CI 1.04, 1.24))与糖尿病相关。SGA 关联在同胞研究中保持不变,而 LGA 关联消失。极低出生体重与 1 型糖尿病风险降低相关。
研究结果表明,胎龄与 1 型糖尿病之间存在小的关联,这不太可能是由于家族性混杂因素造成的。胎龄和 1 型糖尿病可能与胰岛素抵抗有关,这是由于早产婴儿的早期生长受限或肠道微生物群改变。