Maternal type 1 diabetes, preterm birth, and risk of intellectual disability in the offspring: A nation-wide study in Sweden

被引:0
|
作者
Persson, Martina [1 ,2 ]
Tedroff, Kristina [3 ,4 ]
Yin, Weiyao [5 ]
Franko, Mikael Andersson [1 ,5 ]
Sandin, Sven [5 ,6 ,7 ]
机构
[1] Karolinska Inst, Dept Clin Sci & Educ, Div Pediat, Stockholm, Sweden
[2] Sachsska Childrens & Youth Hosp, Stockholm, Sweden
[3] Karolinska Inst, Dept Womens & Childrens Hlth, Neuropediat Unit, Stockholm, Sweden
[4] Karolinska Univ Hosp, Stockholm, Sweden
[5] Karolinska Inst, Dept Med Epidemiol & Biostat, Stockholm, Sweden
[6] Icahn Sch Med Mt Sinai, Dept Psychiat, New York, NY 10029 USA
[7] Seaver Autism Ctr Res & Treatment Mt Sinai, New York, NY 10029 USA
基金
欧盟地平线“2020”; 芬兰科学院; 瑞典研究理事会;
关键词
Type; 1; diabetes; Intellectual disability; Population-based; Preterm birth; neurdevelopment; PREGNANCY; DURATION; ASPHYXIA; OBESITY; MOTHERS; ADULTS; IMPACT; WOMEN;
D O I
10.1192/j.eurpsy.2024.4
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective 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).Design Population-based cohort study using population-based data from several national registries in Sweden.Setting and participants All offspring born alive in Sweden between the years 1998 and 2015.Main outcome measure 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.Results 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.Conclusion 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.
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页数:7
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