Divergent growth of the transient brain compartments in fetuses with nonsyndromic isolated clefts involving the primary and secondary palate

Author:

Masse Olivia1,Brumfield Olivia1,Ahmad Esha1,Velasco-Annis Clemente2,Zhang Jennings1,Rollins Caitlin K3,Connolly Susan24,Barnewolt Carol24,Shamshirsaz Alireza A4,Qaderi Shohra4,Javinani Ali4,Warfield Simon K2,Yang Edward2,Gholipour Ali2,Feldman Henry A15,Grant Patricia E12,Mulliken John B6,Pierotich Lana1,Estroff Judy24

Affiliation:

1. Division of Newborn Medicine, Boston Children’s Hospital and Harvard Medical School , Boston, MA 02115 , United States

2. Department of Radiology, Boston Children’s Hospital and Harvard Medical School , Boston, MA 02115 , United States

3. Department of Neurology Medicine, Boston Children’s Hospital and Harvard Medical School , Boston, MA 02115 , United States

4. Maternal Fetal Care Center, Boston Children’s Hospital , Boston, MA 02115 , United States

5. Institutional Centers for Clinical and Translational Research, Boston Children’s Hospital and Harvard Medical School , Boston, MA 02115 , United States

6. Department of Plastic and Oral Surgery, Boston Children’s Hospital and Harvard Medical School , Boston, MA 02115 , United States

Abstract

Abstract Cleft lip/palate is a common orofacial malformation that often leads to speech/language difficulties as well as developmental delays in affected children, despite surgical repair. Our understanding of brain development in these children is limited. This study aimed to analyze prenatal brain development in fetuses with cleft lip/palate and controls. We examined in utero MRIs of 30 controls and 42 cleft lip/palate fetal cases and measured regional brain volumes. Cleft lip/palate was categorized into groups A (cleft lip or alveolus) and B (any combination of clefts involving the primary and secondary palates). Using a repeated-measures regression model with relative brain hemisphere volumes (%), and after adjusting for multiple comparisons, we did not identify significant differences in regional brain growth between group A and controls. Group B clefts had significantly slower weekly cerebellar growth compared with controls. We also observed divergent brain growth in transient brain structures (cortical plate, subplate, ganglionic eminence) within group B clefts, depending on severity (unilateral or bilateral) and defect location (hemisphere ipsilateral or contralateral to the defect). Further research is needed to explore the association between regional fetal brain growth and cleft lip/palate severity, with the potential to inform early neurodevelopmental biomarkers and personalized diagnostics.

Funder

National Institutes of Health

Publisher

Oxford University Press (OUP)

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