Dumitriu Dani, Baldwin Elena, Coenen Roozie J J, Hammond Luke A, Peterka Darcy S, Heilbrun Lynne, Frye Richard E, Palmer Raymond, Norrman Hjalmar Nobel, Fridell Anna, Remnelius Karl Lundin, Isaksson Johan, Austin Christine, Curtin Paul, Bölte Sven, Arora Manish
Departments of Neuroscience and Pediatrics, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Environmental Medicine and Public Health, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
iScience. 2023 Feb 21;26(3):106247. doi: 10.1016/j.isci.2023.106247. eCollection 2023 Mar 17.
Atypical regulation of inflammation has been proposed in the etiology of autism spectrum disorder (ASD); however, measuring the temporal profile of fetal inflammation associated with future ASD diagnosis has not been possible. Here, we present a method to generate approximately daily profiles of prenatal and early childhood inflammation as measured by developmentally archived C-reactive protein (CRP) in incremental layers of deciduous tooth dentin. In our discovery population, a group of Swedish twins, we found heightened inflammation in the third trimester in children with future ASD diagnosis relative to controls (n = 66; 14 ASD cases; critical window: -90 to -50 days before birth). In our replication study, in the US, we observed a similar increase in CRP in ASD cases during the third trimester (n = 47; 23 ASD cases; -128 to -21 days before birth). Our results indicate that the third trimester is a critical period of atypical fetal inflammatory regulation in ASD.
非典型炎症调节已被认为与自闭症谱系障碍(ASD)的病因有关;然而,测量与未来ASD诊断相关的胎儿炎症的时间变化情况此前一直无法实现。在此,我们提出一种方法,可通过乳牙牙本质增量层中发育存档的C反应蛋白(CRP)来生成大约每日的产前和幼儿期炎症变化情况。在我们的发现队列(一组瑞典双胞胎)中,我们发现,相对于对照组,未来被诊断为ASD的儿童在孕晚期炎症水平升高(n = 66;14例ASD病例;关键窗口期:出生前-90至-50天)。在我们在美国进行的重复研究中,我们观察到ASD病例在孕晚期CRP也有类似升高(n = 47;23例ASD病例;出生前-128至-21天)。我们的结果表明,孕晚期是ASD中胎儿炎症非典型调节的关键时期。