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Neuroimaging assessment of pediatric cerebral changes associated with SARS-CoV-2 infection during pregnancy
BACKGROUND: SARS-CoV-2 infection and perinatal neurologic outcomes are still not fully understood. However, there is recent evidence of white matter disease and impaired neurodevelopment in newborns following maternal SARS-CoV-2 infection. These appear to occur as a consequence of both direct viral...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10244818/ https://www.ncbi.nlm.nih.gov/pubmed/37292371 http://dx.doi.org/10.3389/fped.2023.1194114 |
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author | Alves de Araujo Junior, David Motta, Felipe Fernandes, Geraldo Magela Castro, Maria Eduarda Canellas De Sasaki, Lizandra Moura Paravidine Luna, Licia Pacheco Rodrigues, Thalys Sampaio Kurizky, Patricia Shu Soares, Alexandre Anderson De Sousa Munhoz Nobrega, Otavio de Toledo Espindola, Laila Salmen Zaconeta, Alberto Moreno Gomes, Ciro Martins Martins-Filho, Olindo Assis de Albuquerque, Cleandro Pires da Mota, Licia Maria Henrique |
author_facet | Alves de Araujo Junior, David Motta, Felipe Fernandes, Geraldo Magela Castro, Maria Eduarda Canellas De Sasaki, Lizandra Moura Paravidine Luna, Licia Pacheco Rodrigues, Thalys Sampaio Kurizky, Patricia Shu Soares, Alexandre Anderson De Sousa Munhoz Nobrega, Otavio de Toledo Espindola, Laila Salmen Zaconeta, Alberto Moreno Gomes, Ciro Martins Martins-Filho, Olindo Assis de Albuquerque, Cleandro Pires da Mota, Licia Maria Henrique |
author_sort | Alves de Araujo Junior, David |
collection | PubMed |
description | BACKGROUND: SARS-CoV-2 infection and perinatal neurologic outcomes are still not fully understood. However, there is recent evidence of white matter disease and impaired neurodevelopment in newborns following maternal SARS-CoV-2 infection. These appear to occur as a consequence of both direct viral effects and a systemic inflammatory response, with glial cell/myelin involvement and regional hypoxia/microvascular dysfunction. We sought to characterize the consequences of maternal and fetal inflammatory states in the central nervous system of newborns following maternal SARS-CoV-2 infection. METHODS: We conducted a longitudinal prospective cohort study from June 2020 to December 2021, with follow-up of newborns born to mothers exposed or not exposed to SARS-CoV-2 infection during pregnancy. Brain analysis included data from cranial ultrasound scans (CUS) with grayscale, Doppler studies (color and spectral), and ultrasound-based brain elastography (shear-wave mode) in specific regions of interest (ROIs): deep white matter, superficial white matter, corpus callosum, basal ganglia, and cortical gray matter. Brain elastography was used to estimate brain parenchymal stiffness, which is an indirect quantifier of cerebral myelin tissue content. RESULTS: A total of 219 single-pregnancy children were enrolled, including 201 born to mothers exposed to SARS-CoV-2 infection and 18 from unexposed controls. A neuroimaging evaluation was performed at 6 months of adjusted chronological age and revealed 18 grayscale and 21 Doppler abnormalities. Predominant findings were hyperechogenicity of deep brain white matter and basal ganglia (caudate nuclei/thalamus) and a reduction in the resistance and pulsatility indices of intracranial arterial flow. The anterior brain circulation (middle cerebral and pericallosal arteries) displayed a wider range of flow variation than the posterior circulation (basilar artery). Shear-wave US elastography analysis showed a reduction in stiffness values in the SARS-CoV-2 exposed group in all analyzed regions of interest, especially in the deep white matter elasticity coefficients (3.98 ± 0.62) compared to the control group (7.76 ± 0.77); p-value < 0.001. CONCLUSION: This study further characterizes pediatric structural encephalic changes associated with SARS-CoV-2 infection during pregnancy. The maternal infection has been shown to be related to cerebral deep white matter predominant involvement, with regional hyperechogenicity and reduction of elasticity coefficients, suggesting zonal impairment of myelin content. Morphologic findings may be subtle, and functional studies such as Doppler and elastography may be valuable tools to more accurately identify infants at risk of neurologic damage. |
format | Online Article Text |
id | pubmed-10244818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102448182023-06-08 Neuroimaging assessment of pediatric cerebral changes associated with SARS-CoV-2 infection during pregnancy Alves de Araujo Junior, David Motta, Felipe Fernandes, Geraldo Magela Castro, Maria Eduarda Canellas De Sasaki, Lizandra Moura Paravidine Luna, Licia Pacheco Rodrigues, Thalys Sampaio Kurizky, Patricia Shu Soares, Alexandre Anderson De Sousa Munhoz Nobrega, Otavio de Toledo Espindola, Laila Salmen Zaconeta, Alberto Moreno Gomes, Ciro Martins Martins-Filho, Olindo Assis de Albuquerque, Cleandro Pires da Mota, Licia Maria Henrique Front Pediatr Pediatrics BACKGROUND: SARS-CoV-2 infection and perinatal neurologic outcomes are still not fully understood. However, there is recent evidence of white matter disease and impaired neurodevelopment in newborns following maternal SARS-CoV-2 infection. These appear to occur as a consequence of both direct viral effects and a systemic inflammatory response, with glial cell/myelin involvement and regional hypoxia/microvascular dysfunction. We sought to characterize the consequences of maternal and fetal inflammatory states in the central nervous system of newborns following maternal SARS-CoV-2 infection. METHODS: We conducted a longitudinal prospective cohort study from June 2020 to December 2021, with follow-up of newborns born to mothers exposed or not exposed to SARS-CoV-2 infection during pregnancy. Brain analysis included data from cranial ultrasound scans (CUS) with grayscale, Doppler studies (color and spectral), and ultrasound-based brain elastography (shear-wave mode) in specific regions of interest (ROIs): deep white matter, superficial white matter, corpus callosum, basal ganglia, and cortical gray matter. Brain elastography was used to estimate brain parenchymal stiffness, which is an indirect quantifier of cerebral myelin tissue content. RESULTS: A total of 219 single-pregnancy children were enrolled, including 201 born to mothers exposed to SARS-CoV-2 infection and 18 from unexposed controls. A neuroimaging evaluation was performed at 6 months of adjusted chronological age and revealed 18 grayscale and 21 Doppler abnormalities. Predominant findings were hyperechogenicity of deep brain white matter and basal ganglia (caudate nuclei/thalamus) and a reduction in the resistance and pulsatility indices of intracranial arterial flow. The anterior brain circulation (middle cerebral and pericallosal arteries) displayed a wider range of flow variation than the posterior circulation (basilar artery). Shear-wave US elastography analysis showed a reduction in stiffness values in the SARS-CoV-2 exposed group in all analyzed regions of interest, especially in the deep white matter elasticity coefficients (3.98 ± 0.62) compared to the control group (7.76 ± 0.77); p-value < 0.001. CONCLUSION: This study further characterizes pediatric structural encephalic changes associated with SARS-CoV-2 infection during pregnancy. The maternal infection has been shown to be related to cerebral deep white matter predominant involvement, with regional hyperechogenicity and reduction of elasticity coefficients, suggesting zonal impairment of myelin content. Morphologic findings may be subtle, and functional studies such as Doppler and elastography may be valuable tools to more accurately identify infants at risk of neurologic damage. Frontiers Media S.A. 2023-05-24 /pmc/articles/PMC10244818/ /pubmed/37292371 http://dx.doi.org/10.3389/fped.2023.1194114 Text en © 2023 Alves de Araujo Junior, Motta, Fernandes, Castro, Sasaki, Luna, Rodrigues, Kurizky, Soares, Nobrega, Espindola, Zaconeta, Gomes, Martins-Filho, Albuquerque and Mota. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/) . The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pediatrics Alves de Araujo Junior, David Motta, Felipe Fernandes, Geraldo Magela Castro, Maria Eduarda Canellas De Sasaki, Lizandra Moura Paravidine Luna, Licia Pacheco Rodrigues, Thalys Sampaio Kurizky, Patricia Shu Soares, Alexandre Anderson De Sousa Munhoz Nobrega, Otavio de Toledo Espindola, Laila Salmen Zaconeta, Alberto Moreno Gomes, Ciro Martins Martins-Filho, Olindo Assis de Albuquerque, Cleandro Pires da Mota, Licia Maria Henrique Neuroimaging assessment of pediatric cerebral changes associated with SARS-CoV-2 infection during pregnancy |
title | Neuroimaging assessment of pediatric cerebral changes associated with SARS-CoV-2 infection during pregnancy |
title_full | Neuroimaging assessment of pediatric cerebral changes associated with SARS-CoV-2 infection during pregnancy |
title_fullStr | Neuroimaging assessment of pediatric cerebral changes associated with SARS-CoV-2 infection during pregnancy |
title_full_unstemmed | Neuroimaging assessment of pediatric cerebral changes associated with SARS-CoV-2 infection during pregnancy |
title_short | Neuroimaging assessment of pediatric cerebral changes associated with SARS-CoV-2 infection during pregnancy |
title_sort | neuroimaging assessment of pediatric cerebral changes associated with sars-cov-2 infection during pregnancy |
topic | Pediatrics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10244818/ https://www.ncbi.nlm.nih.gov/pubmed/37292371 http://dx.doi.org/10.3389/fped.2023.1194114 |
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