Atypical cortical asymmetries in toddlers with congenital heart disease before surgery

IF 4.5 3区 医学 Q2 NEUROSCIENCES
Brain Research Bulletin Pub Date : 2026-10-15 Epub Date: 2026-09-21 DOI:10.1016/j.brainresbull.2026.112130
Huijun Li, Xueying Du, Longxian Cheng, Feng Yang, Siyu Ma, Fan lu, Meijiao Zhu, Huiling Wang, Ming Yang, Xuming Mo
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引用次数: 0

Abstract

Background

Patients with congenital heart disease (CHD) may exhibit atypical structural asymmetry in the brain, while the altered structural lateralization and its relationship with cognitive function have not been fully revealed.

Methods

We performed a cross-sectional structural imaging study of 109 toddlers of CHD, including 80 with mild CHD, 29 with moderate-severe CHD in our hospital and 56 normal controls (NC). Surface-based image analysis was used to compute lateralization index (LI) for cortical surface area (CSA), cortical thickness (CT), and cortical volume (CV) in CHD groups and NC group across 34 bilateral regions. Group comparisons were conducted using generalized linear models, and partial correlation analyses were performed to examine associations between LIs, clinical variables, and developmental quotients (DQs) assessed by the Gesell Developmental Scale.

Results

Compared to the NC group, both the mild and moderate-severe CHD groups showed overlapping altered lateralization regions in the caudal anterior cingulate gyrus, pars opercularis, superior temporal gyrus, cuneus cortex, medial orbitofrontal gyrus, parahippocampal gyrus, and posterior cingulate cortex (p_FDR < 0.05). Moreover, the LI of CT in the pars opercularis was negatively associated with personal-social skills DQ in the CHD group (r = -0.327, p<0.001 uncorrected; p_FDR = 0.021).

Conclusions

Mild and moderate-severe CHD groups showed comparable alterations in cerebral asymmetries, predominantly involving perisylvian and default-mode network regions. Notably, the association between the LI of CT in the pars opercularis and personal-social skills DQ highlights a potential structural correlate of neurodevelopmental risk in CHD.
先天性心脏病患儿术前非典型皮质不对称
背景:先天性心脏病(CHD)患者可能表现出非典型的大脑结构不对称,而结构侧化的改变及其与认知功能的关系尚未完全揭示。方法:对109例冠心病患儿进行横切面结构成像研究,其中本院轻度冠心病患儿80例,中重度冠心病患儿29例,正常人56例。采用基于表面的图像分析方法计算冠心病组和NC组34个双侧区域皮质表面积(CSA)、皮质厚度(CT)和皮质体积(CV)的侧化指数(LI)。采用广义线性模型进行组间比较,并进行偏相关分析以检验LIs、临床变量和格塞尔发育量表评定的发育商(DQs)之间的关系。结果:与NC组相比,轻、中重度冠心病组扣带前回尾部、包部、颞上回、楔叶皮质、眶额内侧回、海马旁回、扣带后皮质侧化区出现重叠改变(p_FDR < 0.05)。此外,冠心病组小包部CT LI与个人社交技能DQ呈负相关(r = -0.327, p<0.001,未经校正;p_FDR = 0.021)。结论:轻度和中重度冠心病组在大脑不对称方面表现出类似的改变,主要涉及外围和默认模式网络区域。值得注意的是,脑膜部CT的LI与个人社交技能DQ之间的关联突出了冠心病神经发育风险的潜在结构相关性。
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来源期刊
Brain Research Bulletin
Brain Research Bulletin 医学-神经科学
CiteScore
6.90
自引率
2.60%
发文量
253
审稿时长
67 days
期刊介绍: The Brain Research Bulletin (BRB) aims to publish novel work that advances our knowledge of molecular and cellular mechanisms that underlie neural network properties associated with behavior, cognition and other brain functions during neurodevelopment and in the adult. Although clinical research is out of the Journal''s scope, the BRB also aims to publish translation research that provides insight into biological mechanisms and processes associated with neurodegeneration mechanisms, neurological diseases and neuropsychiatric disorders. The Journal is especially interested in research using novel methodologies, such as optogenetics, multielectrode array recordings and life imaging in wild-type and genetically-modified animal models, with the goal to advance our understanding of how neurons, glia and networks function in vivo.
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