Key result
Youth CHD is associated with lower white matter myelination compared to healthy controls.
Why the study?
Brain injury and dysmaturation in fetuses and neonates with CHD is hypothesized to cause persistent myelination deficits, but myelin content had not been quantified and compared in vivo.
Does a history of congenital heart disease result in persistent myelination deficits in youth compared to healthy controls?
Cross-Sectional (n=89)
Does a history of congenital heart disease result in persistent myelination deficits in youth compared to healthy controls?
Youth born with congenital heart disease exhibit widespread myelination deficits on brain MRI compared to healthy controls, suggesting long-lasting consequences of early-life brain dysmaturation.
Persistent myelination deficits may underlie neurodevelopmental impairments in CHD survivors; leaves open biomarker utility pending prospective validation.
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 T1 and T2 (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.
No takes yet. Share an insight, caveat, or question.
Easson et al. (2022) conducted a cross-sectional in Congenital heart disease (n=89). Congenital heart disease vs. Healthy age- and sex-matched controls was evaluated on Average myelin water fraction (MWF) for 33 white matter tracts and White Matter Myelination Index. Youth born with congenital heart disease had lower tract-average myelin water fraction and White Matter Myelination Index compared to healthy controls.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: