Early-Emerging Sulcal Patterns Are Atypical in Fetuses with Congenital Heart Disease. (1st October 2018)

• Record Type: Journal Article
• Authors: Ortinau, Cynthia M; Rollins, Caitlin K; Gholipour, Ali; Yun, Hyuk Jin; Marshall, Mackenzie; Gagoski, Borjan; Afacan, Onur; Friedman, Kevin; Tworetzky, Wayne; Warfield, Simon K; Newburger, Jane W; Inder, Terrie E; Grant, P Ellen; Im, Kiho
• Is Part Of: Cerebral cortex. Volume 29:Number 8(2019)
• Page Start: 3605
• Page End: 3616
• Publication Date: 2018-10-01
• Subjects: brain -- congenital heart disease -- fetus -- magnetic resonance imaging -- sulcal pattern; Cerebral cortex -- Periodicals; Brain -- Periodicals; 612.825
• DOI: 10.1093/cercor/bhy235
• Languages: English
• ISSNs: 1047-3211

Abstract

Abstract: Fetuses with congenital heart disease (CHD) have third trimester alterations in cortical development on brain magnetic resonance imaging (MRI). However, the intersulcal relationships contributing to global sulcal pattern remain unknown. This study applied a novel method for examining the geometric and topological relationships between sulci to fetal brain MRIs from 21–30 gestational weeks in CHD fetuses ( n = 19) and typically developing (TD) fetuses ( n = 17). Sulcal pattern similarity index ( SI ) to template fetal brain MRIs was determined for the position, area, and depth for corresponding sulcal basins and intersulcal relationships for each subject. CHD fetuses demonstrated altered global sulcal patterns in the left hemisphere compared with TD fetuses (TD [ SI, mean ± SD]: 0.822 ± 0.023, CHD: 0.795 ± 0.030, P = 0.002). These differences were present in the earliest emerging sulci and were driven by differences in the position of corresponding sulcal basins (TD: 0.897 ± 0.024, CHD: 0.878 ± 0.019, P = 0.006) and intersulcal relationships (TD: 0.876 ± 0.031, CHD: 0.857 ± 0.018, P = 0.033). No differences in cortical gyrification index, mean curvature, or surface area were present. These data suggest our methods may be more sensitive than traditional measures for evaluating cortical developmental alterations early in gestation.