Department of Clinical Science and Education, Division of Pediatrics, Karolinska Institutet, Stockholm, Sweden.
Sachsska Children's and Youth Hospital, Stockholm, Sweden.
Eur Psychiatry. 2024 Jan 22;67(1):e11. doi: 10.1192/j.eurpsy.2024.4.
There are few data on long-term neurological or cognitive outcomes in the offspring of mothers with type 1 diabetes (T1D). The aims of this study were to examine if maternal T1D increases the risk of intellectual disability (ID) in the offspring, estimate the amount of mediation through preterm birth, and examine if the association was modified by maternal glycated hemoglobin (HbA1c).
Population-based cohort study using population-based data from several national registries in Sweden.
All offspring born alive in Sweden between the years 1998 and 2015.
The risk of ID was estimated through hazard ratios with 95% confidence intervals (HR, 95% CI) from Cox proportional hazard models, adjusting for potential confounding. Risks were also assessed in mediation analyses and in subgroups of term/preterm births, in relation to maternal HbA1c and by severity of ID.
In total, 1,406,441 offspring were included. In this cohort, 7,794 (0.57%) offspring were born to mothers with T1D. The risk of ID was increased in offspring of mothers with T1D (HR; 1.77, 1.43-2.20), of which 47% (95% CI: 34-100) was mediated through preterm birth. The HRs were not modified by HbA1c.
T1D in pregnancy is associated with moderately increased risks of ID in the offspring. The risk is largely mediated by preterm birth, in particular for moderate/severe cases of ID. There was no support for risk-modification by maternal HbA1c.
关于患有 1 型糖尿病(T1D)的母亲所生子女的长期神经或认知结果数据较少。本研究旨在探讨母体 T1D 是否会增加子女智障(ID)的风险,估计通过早产的中介量,并检查这种关联是否因母体糖化血红蛋白(HbA1c)而改变。
使用瑞典多个国家登记处的基于人群的数据进行基于人群的队列研究。
1998 年至 2015 年期间在瑞典出生的所有活产子女。
通过 Cox 比例风险模型估计 ID 风险的风险比(HR)和 95%置信区间(HR,95%CI),并进行了潜在混杂因素的调整。还通过中介分析和与母体 HbA1c 以及 ID 严重程度有关的足月/早产亚组评估了风险。
共纳入 1406441 名子女。在该队列中,有 7794 名(0.57%)子女的母亲患有 T1D。患有 T1D 的母亲所生子女的 ID 风险增加(HR,1.77,1.43-2.20),其中 47%(95%CI:34-100)是通过早产介导的。HR 不受 HbA1c 的影响。
妊娠期间的 T1D 与子女 ID 风险的中度增加相关。风险主要通过早产来介导,尤其是中度/重度 ID 的病例。没有证据表明母体 HbA1c 可以改变风险。