Advances in Brain and Child Health Development Research Laboratory, Research Institute of the McGill University Health Centre, Montreal, Quebec, Canada.
Department of Pediatrics, Division of Cardiology, Montreal Children's Hospital, McGill University Health Centre, Montreal, Quebec, Canada.
Hum Brain Mapp. 2019 Aug 15;40(12):3548-3560. doi: 10.1002/hbm.24615. Epub 2019 May 9.
There is a high prevalence of neurodevelopmental impairments in individuals living with congenital heart disease (CHD) and the neural correlates of these impairments are not yet fully understood. Recent studies have shown that hippocampal volume and shape differences may provide unique biomarkers for neurodevelopmental disorders. The hippocampus is vulnerable to early life injury, especially in populations at risk for hypoxemia or hemodynamic instability such as in neonates with CHD. We compared hippocampal gray and white matter volume and morphometry between youth born with CHD (n = 50) aged 16-24 years and healthy peers (n = 48). We also explored whether hippocampal gray and white matter volume and morphometry are associated with executive function and self-regulation deficits. To do so, participants underwent 3T brain magnetic resonance imaging and completed the self-reported Behavior Rating Inventory of Executive Function-Adult version. We found that youth with CHD had smaller hippocampal volumes (all statistics corrected for false discovery rate; q < 0.05) as compared to controls. We also observed significant smaller surface area bilaterally and inward displacement on the left hippocampus predominantly on the ventral side (q < 0.10) in the CHD group that were not present in the controls. Left CA1 and CA2/3 were negatively associated with working memory (p < .05). Here, we report, for the first-time, hippocampal morphometric alterations in youth born with CHD when compared to healthy peers, as well as, structure-function relationships between hippocampal volumes and executive function. These differences may reflect long lasting alterations in brain development specific to individual with CHD.
患有先天性心脏病 (CHD) 的个体中神经发育障碍的患病率很高,但这些障碍的神经相关性尚不完全清楚。最近的研究表明,海马体体积和形状的差异可能为神经发育障碍提供独特的生物标志物。海马体易受早期损伤的影响,尤其是在易发生低氧血症或血流动力学不稳定的人群中,如患有 CHD 的新生儿。我们比较了患有 CHD(n=50)的青少年(16-24 岁)和健康同龄人(n=48)的海马体灰质和白质体积及形态。我们还探讨了海马体灰质和白质体积及形态是否与执行功能和自我调节缺陷有关。为此,参与者接受了 3T 脑磁共振成像检查,并完成了自我报告的行为评定量表-成人版。我们发现,与对照组相比,患有 CHD 的青少年的海马体体积较小(所有统计学数据均经假发现率校正;q<0.05)。我们还观察到 CHD 组双侧海马体表面积明显较小,左侧海马体向内移位,主要在腹侧(q<0.10),而对照组则没有。左侧 CA1 和 CA2/3 与工作记忆呈负相关(p<0.05)。在这里,我们首次报告了与健康同龄人相比,患有 CHD 的青少年的海马体形态改变,以及海马体体积与执行功能之间的结构-功能关系。这些差异可能反映了特定于 CHD 个体的大脑发育的长期改变。