Children with Congenital Heart Diseases Exhibit Altered Deep Gray Matter Structures

Nils D Forkert1,2,3,4, Sarah J MacEachern5,6,7, Allison K Duh8

  • 1Department of Radiology, Cumming School of Medicine, University of Calgary, 3330 Hospital Drive NW, T2N 4N1, Calgary, AB, Canada. nils.forkert@ucalgary.ca.

PubMed

Insights

Children with congenital heart disease (CHD) show brain structure differences despite normal MRI scans. These findings in subcortical gray matter may explain neurological deficits and impact neurodevelopment.

Area of Science:

  • Neuroimaging
  • Pediatric Cardiology
  • Developmental Neuroscience

Background:

  • Congenital heart diseases (CHDs) increase the risk of neurologic deficits in children.
  • These deficits can occur even with normal-appearing brain MRI scans.
  • Subcortical gray matter structures are crucial for neurodevelopment.

Purpose of the Study:

  • To compare quantitative macro- and microstructural brain properties in pediatric CHD patients with normal MRIs to healthy controls.
  • To investigate subcortical gray matter differences in children with coarctation of the aorta (COA) and hypoplastic left heart syndrome (HLHS).

Main Methods:

  • Retrospective review of 24 pediatric CHD patients (17 COA, 7 HLHS) with normal brain MRI.
  • Atlas-based analysis of subcortical gray matter volume and apparent diffusion coefficient (ADC).
  • Multivariate statistical comparison with 100 typically developing children.

Main Results:

  • Pediatric CHD patients showed significant differences in subcortical brain structure volume and ADC compared to controls (p < 0.001).
  • Reduced brain volumes were observed in most investigated subcortical regions.
  • Elevated thalamic ADC values were found in children with CHD.

Conclusions:

  • Children with CHD exhibit widespread macro- and microstructural brain differences, even with normal-appearing MRIs.
  • These subcortical structural alterations may negatively impact neurodevelopment.
  • Findings suggest potential for neurological deficits in CHD patients during childhood and beyond.
Abstract