Advances in Brain & Child Development (ABCD) Research Laboratory, Research Institute of the McGill University Health Centre, Montreal, Quebec, Canada.
Department of Neurology & Neurosurgery, Faculty of Medicine, McGill University, Montreal, Quebec, Canada.
Hum Brain Mapp. 2022 Aug 1;43(11):3545-3558. doi: 10.1002/hbm.25866. Epub 2022 Apr 12.
Brain injury and dysmaturation is common in fetuses and neonates with congenital heart disease (CHD) and is hypothesized to result in persistent myelination deficits. This study aimed to quantify and compare myelin content in vivo between youth born with CHD and healthy controls. Youth aged 16 to 24 years born with CHD and healthy age- and sex-matched controls underwent brain magnetic resonance imaging including multicomponent driven equilibrium single pulse observation of T and T (mcDESPOT). Average myelin water fraction (MWF) values for 33 white matter tracts, as well as a summary measure of average white matter MWF, the White Matter Myelination Index, were calculated and compared between groups. Tract-average MWF was lower throughout the corpus callosum and in many bilateral association tracts and left hemispheric projection tracts in youth with CHD (N = 44) as compared to controls (N = 45). The White Matter Myelination Index was also lower in the CHD group. As such, this study provides specific evidence of widespread myelination deficits in youth with CHD, likely representing a long-lasting consequence of early-life brain dysmaturation in this population. This deficient myelination may underlie the frequent neurodevelopmental impairments experienced by CHD survivors and could eventually serve as a biomarker of neuropsychological function.
脑损伤和发育不良在患有先天性心脏病 (CHD) 的胎儿和新生儿中很常见,据推测这会导致持续的髓鞘缺陷。本研究旨在定量比较 CHD 患儿和健康对照组之间体内的髓鞘含量。年龄在 16 至 24 岁之间的患有 CHD 的青少年和健康的年龄及性别匹配的对照组接受了脑部磁共振成像检查,包括多分量驱动平衡单脉冲观察 T1 和 T2(mcDESPOT)。计算并比较了 33 个白质束的平均髓鞘水分数 (MWF) 值以及平均白质 MWF 的综合指标,即白质髓鞘指数,以比较组间差异。与对照组(N=45)相比,CHD 组(N=44)的胼胝体和许多双侧联合束以及左侧半球投射束的束平均 MWF 均较低。CHD 组的白质髓鞘指数也较低。因此,本研究提供了 CHD 患儿广泛髓鞘缺陷的具体证据,这可能代表该人群在生命早期大脑发育不良的长期后果。这种髓鞘缺陷可能是 CHD 幸存者经常出现神经发育障碍的基础,并且最终可能成为神经心理功能的生物标志物。