Garza-Martínez Mayra J, Á Hernández-Mariano José, Hurtado-Salgado Erika M, Cupul-Uicab Lea A
School of Public Health of México, National Institute of Public Health, Cuernavaca, Morelos, Mexico.
School of Public Health of México, National Institute of Public Health, Cuernavaca, Morelos, Mexico; Research Department, Hospital Juárez of México, México City, Mexico.
J Psychiatr Res. 2025 Feb;182:100-115. doi: 10.1016/j.jpsychires.2025.01.003. Epub 2025 Jan 8.
Whether in utero exposure to pregestational (type 2 [T2D] and type 1 diabetes [T1D]) and gestational diabetes (GDM) are contributing factors in the rise of neurodevelopmental alterations such as autism is yet unclear. Therefore, we summarized the evidence from studies that assessed such association.
A systematic review with meta-analyses was performed following the Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) guidelines; eligible studies were identified in PubMed, Web of Science, and EBSCO up to April 3rd, 2023. We estimated pooled OR of autism from random effects meta-analyses for each type of maternal diabetes.
26 publications were selected (18 cohorts and 8 case-controls); 17 had data for the meta-analysis. We observed an increased risk of autism in the offspring exposed in utero to T2D (pooled OR = 1.48; 95%CI: 1.31, 1.68; n = 3,141,255), T1D (pooled OR = 1.73; 95%CI: 1.05, 2.87; n = 2,791,607), and GDM (pooled OR = 1.31; 95% CI: 1.16, 1.47; n = 3,259,557) compared to those unexposed. No evidence of heterogeneity (I = 0.0%) was observed for T2D, whereas for T1D the heterogeneity was substantial (I = 64.7%) and for GDM was moderate (I = 53.1%). The evidence was stronger for in utero exposure to GDM, followed by T2D and T1D.
Our results support the hypothesis that in utero exposure to maternal T2D or GDM moderately increased the offspring's risk of developing autism later in life. Prospectively conducted studies are still warranted to better estimate the size of the effect of maternal diabetes on autism risk.
子宫内暴露于孕前糖尿病(2型糖尿病[T2D]和1型糖尿病[T1D])以及妊娠期糖尿病(GDM)是否是自闭症等神经发育改变增加的促成因素尚不清楚。因此,我们总结了评估这种关联的研究证据。
按照系统评价和Meta分析的首选报告项目(PRISMA)指南进行了系统评价和Meta分析;截至2023年4月3日,在PubMed、科学网和EBSCO中检索符合条件的研究。我们通过随机效应Meta分析估计了每种类型的母亲糖尿病患儿患自闭症的合并比值比。
选择了26篇出版物(18个队列研究和8个病例对照研究);17篇有Meta分析的数据。我们观察到,与未暴露的后代相比,子宫内暴露于T2D(合并比值比=1.48;95%置信区间:1.31,1.68;n=3,141,255)、T1D(合并比值比=1.73;95%置信区间:1.05,2.87;n=2,791,607)和GDM(合并比值比=1.31;95%置信区间:1.16,1.47;n=3,259,557)的后代患自闭症的风险增加。T2D未观察到异质性证据(I=0.0%),而T1D的异质性较大(I=64.7%),GDM的异质性为中度(I=53.1%)。子宫内暴露于GDM的证据更强,其次是T2D和T1D。
我们的结果支持以下假设,即子宫内暴露于母亲的T2D或GDM会适度增加后代日后患自闭症的风险。仍有必要进行前瞻性研究,以更好地估计母亲糖尿病对自闭症风险的影响大小。