Maternal psychological distress during the COVID-19 pandemic and structural changes of the human fetal brain.

Brain imaging Epidemiology Paediatric research Stress and resilience

Journal

Communications medicine
ISSN: 2730-664X
Titre abrégé: Commun Med (Lond)
Pays: England
ID NLM: 9918250414506676

Informations de publication

Date de publication:
2022
Historique:
received: 07 09 2021
accepted: 11 04 2022
entrez: 1 6 2022
pubmed: 2 6 2022
medline: 2 6 2022
Statut: epublish

Résumé

Elevated maternal psychological distress during pregnancy is linked to adverse outcomes in offspring. The potential effects of intensified levels of maternal distress during the COVID-19 pandemic on the developing fetal brain are currently unknown. We prospectively enrolled 202 pregnant women: 65 without known COVID-19 exposures during the pandemic who underwent 92 fetal MRI scans, and 137 pre-pandemic controls who had 182 MRI scans. Multi-plane, multi-phase single shot fast spin echo T2-weighted images were acquired on a GE 1.5 T MRI Scanner. Volumes of six brain tissue types were calculated. Cortical folding measures, including brain surface area, local gyrification index, and sulcal depth were determined. At each MRI scan, maternal distress was assessed using validated stress, anxiety, and depression scales. Generalized estimating equations were utilized to compare maternal distress measures, brain volume and cortical folding differences between pandemic and pre-pandemic cohorts. Stress and depression scores are significantly higher in the pandemic cohort, compared to the pre-pandemic cohort. Fetal white matter, hippocampal, and cerebellar volumes are decreased in the pandemic cohort. Cortical surface area and local gyrification index are also decreased in all four lobes, while sulcal depth is lower in the frontal, parietal, and occipital lobes in the pandemic cohort, indicating delayed brain gyrification. We report impaired fetal brain growth and delayed cerebral cortical gyrification in COVID-19 pandemic era pregnancies, in the setting of heightened maternal psychological distress. The potential long-term neurodevelopmental consequences of altered fetal brain development in COVID-era pregnancies merit further study.

Sections du résumé

Background UNASSIGNED
Elevated maternal psychological distress during pregnancy is linked to adverse outcomes in offspring. The potential effects of intensified levels of maternal distress during the COVID-19 pandemic on the developing fetal brain are currently unknown.
Methods UNASSIGNED
We prospectively enrolled 202 pregnant women: 65 without known COVID-19 exposures during the pandemic who underwent 92 fetal MRI scans, and 137 pre-pandemic controls who had 182 MRI scans. Multi-plane, multi-phase single shot fast spin echo T2-weighted images were acquired on a GE 1.5 T MRI Scanner. Volumes of six brain tissue types were calculated. Cortical folding measures, including brain surface area, local gyrification index, and sulcal depth were determined. At each MRI scan, maternal distress was assessed using validated stress, anxiety, and depression scales. Generalized estimating equations were utilized to compare maternal distress measures, brain volume and cortical folding differences between pandemic and pre-pandemic cohorts.
Results UNASSIGNED
Stress and depression scores are significantly higher in the pandemic cohort, compared to the pre-pandemic cohort. Fetal white matter, hippocampal, and cerebellar volumes are decreased in the pandemic cohort. Cortical surface area and local gyrification index are also decreased in all four lobes, while sulcal depth is lower in the frontal, parietal, and occipital lobes in the pandemic cohort, indicating delayed brain gyrification.
Conclusions UNASSIGNED
We report impaired fetal brain growth and delayed cerebral cortical gyrification in COVID-19 pandemic era pregnancies, in the setting of heightened maternal psychological distress. The potential long-term neurodevelopmental consequences of altered fetal brain development in COVID-era pregnancies merit further study.

Identifiants

pubmed: 35647608
doi: 10.1038/s43856-022-00111-w
pii: 111
pmc: PMC9135751
doi:

Types de publication

Journal Article

Langues

eng

Pagination

47

Subventions

Organisme : NHLBI NIH HHS
ID : R01 HL116585
Pays : United States

Informations de copyright

© The Author(s) 2022.

Déclaration de conflit d'intérêts

Competing interestsThe authors declare no competing interests.

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Auteurs

Yuan-Chiao Lu (YC)

Developing Brain Institute, Children's National Hospital, Washington, DC USA.

Nickie Andescavage (N)

Developing Brain Institute, Children's National Hospital, Washington, DC USA.
Department of Pediatrics, School of Medicine and Health Sciences, the George Washington University, Washington, DC USA.

Yao Wu (Y)

Developing Brain Institute, Children's National Hospital, Washington, DC USA.

Kushal Kapse (K)

Developing Brain Institute, Children's National Hospital, Washington, DC USA.

Nicole R Andersen (NR)

Developing Brain Institute, Children's National Hospital, Washington, DC USA.

Jessica Quistorff (J)

Developing Brain Institute, Children's National Hospital, Washington, DC USA.

Haleema Saeed (H)

MedStar Washington Hospital Center, Washington, DC USA.

Catherine Lopez (C)

Developing Brain Institute, Children's National Hospital, Washington, DC USA.

Diedtra Henderson (D)

Developing Brain Institute, Children's National Hospital, Washington, DC USA.

Scott D Barnett (SD)

Developing Brain Institute, Children's National Hospital, Washington, DC USA.

Gilbert Vezina (G)

Developing Brain Institute, Children's National Hospital, Washington, DC USA.

David Wessel (D)

Critical Care Medicine, Children's National Hospital, Washington, DC USA.

Adre du Plessis (A)

Prenatal Pediatrics Institute, Children's National Hospital, Washington, DC USA.

Catherine Limperopoulos (C)

Developing Brain Institute, Children's National Hospital, Washington, DC USA.
Department of Pediatrics, School of Medicine and Health Sciences, the George Washington University, Washington, DC USA.

Classifications MeSH