In Utero MRI Identifies Impaired Second Trimester Subplate Growth in Fetuses with Congenital Heart Disease

Author:

Wu Yao1,Lu Yuan-Chiao1,Kapse Kushal1,Jacobs Marni2,Andescavage Nickie3,Donofrio Mary T4,Lopez Catherine1,Quistorff Jessica Lynn1,Vezina Gilbert5,Krishnan Anita4,du Plessis Adré J6,Limperopoulos Catherine15

Affiliation:

1. Developing Brain Institute, Children’s National Hospital, Washington, DC 20010, USA

2. School of Health Sciences, University of California San Diego, La Jolla, CA 92093, USA

3. Division of Neonatology, Children’s National Hospital, Washington, DC 20010, USA

4. Division of Cardiology, Children’s National Hospital, Washington, DC 20010, USA

5. Department of Diagnostic Imaging and Radiology, Children’s National Hospital, Washington, DC 20010, USA

6. Prenatal Pediatrics Institute, Children’s National Hospital, Washington, DC 20010, USA

Abstract

Abstract   The subplate is a transient brain structure which plays a key role in the maturation of the cerebral cortex. Altered brain growth and cortical development have been suggested in fetuses with complex congenital heart disease (CHD) in the third trimester. However, at an earlier gestation, the putative role of the subplate in altered brain development in CHD fetuses is poorly understood. This study aims to examine subplate growth (i.e., volume and thickness) and its relationship to cortical sulcal development in CHD fetuses compared with healthy fetuses by using 3D reconstructed fetal magnetic resonance imaging. We studied 260 fetuses, including 100 CHD fetuses (22.3–32 gestational weeks) and 160 healthy fetuses (19.6–31.9 gestational weeks). Compared with healthy fetuses, CHD fetuses had 1) decreased global and regional subplate volumes and 2) decreased subplate thickness in the right hemisphere overall, in frontal and temporal lobes, and insula. Compared with fetuses with two-ventricle CHD, those with single-ventricle CHD had reduced subplate volume and thickness in right occipital and temporal lobes. Finally, impaired subplate growth was associated with disturbances in cortical sulcal development in CHD fetuses. These findings suggested a potential mechanistic pathway and early biomarker for the third-trimester failure of brain development in fetuses with complex CHD. Significance Statement Our findings provide an early biomarker for brain maturational failure in fetuses with congenital heart disease, which may guide the development of future prenatal interventions aimed at reducing neurological compromise of prenatal origin in this high-risk population.

Funder

Thrasher Research Fund

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Cognitive Neuroscience

Reference58 articles.

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