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Regional impairments of cortical folding in premature infants
OBJECTIVE: This study was undertaken to evaluate the influence of preterm birth and other factors on cerebral cortical maturation. METHODS: We have evaluated the effects of preterm birth on cortical folding by applying cortical cartography methods to a cohort of 52 preterm infants (<31 weeks gest...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BlackWell Publishing Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4324979/ https://www.ncbi.nlm.nih.gov/pubmed/25425403 http://dx.doi.org/10.1002/ana.24313 |
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author | Engelhardt, Erin Inder, Terrie E Alexopoulos, Dimitrios Dierker, Donna L Hill, Jason Van Essen, David Neil, Jeffrey J |
author_facet | Engelhardt, Erin Inder, Terrie E Alexopoulos, Dimitrios Dierker, Donna L Hill, Jason Van Essen, David Neil, Jeffrey J |
author_sort | Engelhardt, Erin |
collection | PubMed |
description | OBJECTIVE: This study was undertaken to evaluate the influence of preterm birth and other factors on cerebral cortical maturation. METHODS: We have evaluated the effects of preterm birth on cortical folding by applying cortical cartography methods to a cohort of 52 preterm infants (<31 weeks gestation, mild or no injury on conventional magnetic resonance imaging) and 12 term-born control infants. All infants were evaluated at term-equivalent postmenstrual age. RESULTS: Preterm infants had lower values for the global measures of gyrification index (GI; 2.06 ± 0.07 vs 1.80 ± 0.12, p < 0.001; control vs preterm) and cortical surface area (CSA; 316 ± 24 cm(2) vs 257 ± 40 cm(2), p < 0.001). Regional analysis of sulcal depth and cortical shape showed the greatest impact of preterm birth on the insula, superior temporal sulcus, and ventral portions of the pre- and postcentral sulci in both hemispheres. Although CSA and GI are related, CSA was more sensitive to antenatal and postnatal factors than GI. Both measures were lower in preterm infants of lower birth weight standard deviation scores and smaller occipitofrontal circumference at time of scan, whereas CSA alone was lower in association with smaller occipitofrontal circumference at birth. CSA was also lower in infants with higher critical illness in the first 24 hours of life, exposure to postnatal steroids, and prolonged endotracheal intubation. INTERPRETATION: Preterm birth disrupts cortical development in a regionally specific fashion with abnormalities evident by term-equivalent postmenstrual age. This disruption is influenced by both antenatal growth and postnatal course. |
format | Online Article Text |
id | pubmed-4324979 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BlackWell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-43249792015-04-08 Regional impairments of cortical folding in premature infants Engelhardt, Erin Inder, Terrie E Alexopoulos, Dimitrios Dierker, Donna L Hill, Jason Van Essen, David Neil, Jeffrey J Ann Neurol Research Articles OBJECTIVE: This study was undertaken to evaluate the influence of preterm birth and other factors on cerebral cortical maturation. METHODS: We have evaluated the effects of preterm birth on cortical folding by applying cortical cartography methods to a cohort of 52 preterm infants (<31 weeks gestation, mild or no injury on conventional magnetic resonance imaging) and 12 term-born control infants. All infants were evaluated at term-equivalent postmenstrual age. RESULTS: Preterm infants had lower values for the global measures of gyrification index (GI; 2.06 ± 0.07 vs 1.80 ± 0.12, p < 0.001; control vs preterm) and cortical surface area (CSA; 316 ± 24 cm(2) vs 257 ± 40 cm(2), p < 0.001). Regional analysis of sulcal depth and cortical shape showed the greatest impact of preterm birth on the insula, superior temporal sulcus, and ventral portions of the pre- and postcentral sulci in both hemispheres. Although CSA and GI are related, CSA was more sensitive to antenatal and postnatal factors than GI. Both measures were lower in preterm infants of lower birth weight standard deviation scores and smaller occipitofrontal circumference at time of scan, whereas CSA alone was lower in association with smaller occipitofrontal circumference at birth. CSA was also lower in infants with higher critical illness in the first 24 hours of life, exposure to postnatal steroids, and prolonged endotracheal intubation. INTERPRETATION: Preterm birth disrupts cortical development in a regionally specific fashion with abnormalities evident by term-equivalent postmenstrual age. This disruption is influenced by both antenatal growth and postnatal course. BlackWell Publishing Ltd 2015-01 2014-12-13 /pmc/articles/PMC4324979/ /pubmed/25425403 http://dx.doi.org/10.1002/ana.24313 Text en © 2014 The Authors Annals of Neurology published by Wiley Periodicals, Inc. on behalf of American Neurological Association http://creativecommons.org/licenses/by-nc/4.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Research Articles Engelhardt, Erin Inder, Terrie E Alexopoulos, Dimitrios Dierker, Donna L Hill, Jason Van Essen, David Neil, Jeffrey J Regional impairments of cortical folding in premature infants |
title | Regional impairments of cortical folding in premature infants |
title_full | Regional impairments of cortical folding in premature infants |
title_fullStr | Regional impairments of cortical folding in premature infants |
title_full_unstemmed | Regional impairments of cortical folding in premature infants |
title_short | Regional impairments of cortical folding in premature infants |
title_sort | regional impairments of cortical folding in premature infants |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4324979/ https://www.ncbi.nlm.nih.gov/pubmed/25425403 http://dx.doi.org/10.1002/ana.24313 |
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