Within amygdala: Basolateral parts are selectively impaired in premature-born adults

While it is known that whole amygdala volume is lastingly reduced after premature birth, it is unknown whether different amygdala nuclei are distinctively affected by prematurity. This question is motivated by two points: First, the observation that developmental trajectories of superficial, centrom...

Full description

Bibliographic Details
Main Authors: Benita Schmitz-Koep, Juliana Zimmermann, Aurore Menegaux, Rachel Nuttall, Josef G. Bäuml, Sebastian C. Schneider, Marcel Daamen, Henning Boecker, Claus Zimmer, Dieter Wolke, Peter Bartmann, Dennis M. Hedderich, Christian Sorg
Format: Article
Language:English
Published: Elsevier 2021-01-01
Series:NeuroImage: Clinical
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2213158221002242
id doaj-d430db7057d94061aed31d500e865e82
record_format Article
collection DOAJ
language English
format Article
sources DOAJ
author Benita Schmitz-Koep
Juliana Zimmermann
Aurore Menegaux
Rachel Nuttall
Josef G. Bäuml
Sebastian C. Schneider
Marcel Daamen
Henning Boecker
Claus Zimmer
Dieter Wolke
Peter Bartmann
Dennis M. Hedderich
Christian Sorg
spellingShingle Benita Schmitz-Koep
Juliana Zimmermann
Aurore Menegaux
Rachel Nuttall
Josef G. Bäuml
Sebastian C. Schneider
Marcel Daamen
Henning Boecker
Claus Zimmer
Dieter Wolke
Peter Bartmann
Dennis M. Hedderich
Christian Sorg
Within amygdala: Basolateral parts are selectively impaired in premature-born adults
NeuroImage: Clinical
Premature birth
Human
Brain development
Amygdala nuclei
Basolateral amygdala
Structural magnetic resonance imaging
author_facet Benita Schmitz-Koep
Juliana Zimmermann
Aurore Menegaux
Rachel Nuttall
Josef G. Bäuml
Sebastian C. Schneider
Marcel Daamen
Henning Boecker
Claus Zimmer
Dieter Wolke
Peter Bartmann
Dennis M. Hedderich
Christian Sorg
author_sort Benita Schmitz-Koep
title Within amygdala: Basolateral parts are selectively impaired in premature-born adults
title_short Within amygdala: Basolateral parts are selectively impaired in premature-born adults
title_full Within amygdala: Basolateral parts are selectively impaired in premature-born adults
title_fullStr Within amygdala: Basolateral parts are selectively impaired in premature-born adults
title_full_unstemmed Within amygdala: Basolateral parts are selectively impaired in premature-born adults
title_sort within amygdala: basolateral parts are selectively impaired in premature-born adults
publisher Elsevier
series NeuroImage: Clinical
issn 2213-1582
publishDate 2021-01-01
description While it is known that whole amygdala volume is lastingly reduced after premature birth, it is unknown whether different amygdala nuclei are distinctively affected by prematurity. This question is motivated by two points: First, the observation that developmental trajectories of superficial, centromedial and basolateral amygdala nuclei are different. And second, the expectation that these different developmental pathways are distinctively affected by prematurity. Furthermore, we stated the question whether alterations in amygdala nuclei are associated with increased adults’ anxiety traits after premature birth.We investigated 101 very premature-born adults (<32 weeks of gestation and/or birth weight below 1500 g) and 108 full-term controls of a prospectively and longitudinally collected cohort at 26 years of age using automated amygdala nuclei segmentation based on structural MRI.We found selectively reduced volumes of bilateral accessory basal nuclei (pertaining to the basolateral amygdala of claustral developmental trajectory) adjusted for whole amygdala volume. Volumes of bilateral accessory basal nuclei were positively associated with gestational age and negatively associated with duration of ventilation. Furthermore, structural covariance within the basolateral amygdala was increased in premature-born adults. We did not find an association between reduced volumes of basolateral amygdala and increased social anxiety in the prematurity group.These results demonstrate specifically altered basolateral amygdala structure in premature-born adults. Data suggest that prematurity has distinct effects on amygdala nuclei.
topic Premature birth
Human
Brain development
Amygdala nuclei
Basolateral amygdala
Structural magnetic resonance imaging
url http://www.sciencedirect.com/science/article/pii/S2213158221002242
work_keys_str_mv AT benitaschmitzkoep withinamygdalabasolateralpartsareselectivelyimpairedinprematurebornadults
AT julianazimmermann withinamygdalabasolateralpartsareselectivelyimpairedinprematurebornadults
AT auroremenegaux withinamygdalabasolateralpartsareselectivelyimpairedinprematurebornadults
AT rachelnuttall withinamygdalabasolateralpartsareselectivelyimpairedinprematurebornadults
AT josefgbauml withinamygdalabasolateralpartsareselectivelyimpairedinprematurebornadults
AT sebastiancschneider withinamygdalabasolateralpartsareselectivelyimpairedinprematurebornadults
AT marceldaamen withinamygdalabasolateralpartsareselectivelyimpairedinprematurebornadults
AT henningboecker withinamygdalabasolateralpartsareselectivelyimpairedinprematurebornadults
AT clauszimmer withinamygdalabasolateralpartsareselectivelyimpairedinprematurebornadults
AT dieterwolke withinamygdalabasolateralpartsareselectivelyimpairedinprematurebornadults
AT peterbartmann withinamygdalabasolateralpartsareselectivelyimpairedinprematurebornadults
AT dennismhedderich withinamygdalabasolateralpartsareselectivelyimpairedinprematurebornadults
AT christiansorg withinamygdalabasolateralpartsareselectivelyimpairedinprematurebornadults
_version_ 1721187671214129152
spelling doaj-d430db7057d94061aed31d500e865e822021-08-28T04:45:36ZengElsevierNeuroImage: Clinical2213-15822021-01-0131102780Within amygdala: Basolateral parts are selectively impaired in premature-born adultsBenita Schmitz-Koep0Juliana Zimmermann1Aurore Menegaux2Rachel Nuttall3Josef G. Bäuml4Sebastian C. Schneider5Marcel Daamen6Henning Boecker7Claus Zimmer8Dieter Wolke9Peter Bartmann10Dennis M. Hedderich11Christian Sorg12Department of Diagnostic and Interventional Neuroradiology, School of Medicine, Technical University of Munich, Ismaninger Str. 22, Munich 81675, Germany; TUM-NIC Neuroimaging Center, School of Medicine, Technical University of Munich, Ismaninger Str. 22, Munich 81675, Germany; Corresponding author at: Department of Diagnostic and Interventional Neuroradiology, School of Medicine, Technical University of Munich, Ismaninger Str. 22, Munich 81675, Germany.Department of Diagnostic and Interventional Neuroradiology, School of Medicine, Technical University of Munich, Ismaninger Str. 22, Munich 81675, Germany; TUM-NIC Neuroimaging Center, School of Medicine, Technical University of Munich, Ismaninger Str. 22, Munich 81675, GermanyDepartment of Diagnostic and Interventional Neuroradiology, School of Medicine, Technical University of Munich, Ismaninger Str. 22, Munich 81675, Germany; TUM-NIC Neuroimaging Center, School of Medicine, Technical University of Munich, Ismaninger Str. 22, Munich 81675, GermanyDepartment of Diagnostic and Interventional Neuroradiology, School of Medicine, Technical University of Munich, Ismaninger Str. 22, Munich 81675, Germany; TUM-NIC Neuroimaging Center, School of Medicine, Technical University of Munich, Ismaninger Str. 22, Munich 81675, GermanyDepartment of Diagnostic and Interventional Neuroradiology, School of Medicine, Technical University of Munich, Ismaninger Str. 22, Munich 81675, Germany; TUM-NIC Neuroimaging Center, School of Medicine, Technical University of Munich, Ismaninger Str. 22, Munich 81675, GermanyDepartment of Diagnostic and Interventional Neuroradiology, School of Medicine, Technical University of Munich, Ismaninger Str. 22, Munich 81675, Germany; TUM-NIC Neuroimaging Center, School of Medicine, Technical University of Munich, Ismaninger Str. 22, Munich 81675, GermanyFunctional Neuroimaging Group, Department of Diagnostic and Interventional Radiology, University Hospital Bonn, Venusberg-Campus 1, Bonn, Germany; Department of Neonatology, University Hospital Bonn, Venusberg-Campus 1, Bonn, GermanyFunctional Neuroimaging Group, Department of Diagnostic and Interventional Radiology, University Hospital Bonn, Venusberg-Campus 1, Bonn, GermanyDepartment of Diagnostic and Interventional Neuroradiology, School of Medicine, Technical University of Munich, Ismaninger Str. 22, Munich 81675, Germany; TUM-NIC Neuroimaging Center, School of Medicine, Technical University of Munich, Ismaninger Str. 22, Munich 81675, GermanyDepartment of Psychology, University of Warwick, University Road, Coventry CV4 7AL, United Kingdom; Warwick Medical School, University of Warwick, University Road, Coventry CV4 7AL, United KingdomDepartment of Neonatology, University Hospital Bonn, Venusberg-Campus 1, Bonn, GermanyDepartment of Diagnostic and Interventional Neuroradiology, School of Medicine, Technical University of Munich, Ismaninger Str. 22, Munich 81675, Germany; TUM-NIC Neuroimaging Center, School of Medicine, Technical University of Munich, Ismaninger Str. 22, Munich 81675, GermanyDepartment of Diagnostic and Interventional Neuroradiology, School of Medicine, Technical University of Munich, Ismaninger Str. 22, Munich 81675, Germany; TUM-NIC Neuroimaging Center, School of Medicine, Technical University of Munich, Ismaninger Str. 22, Munich 81675, Germany; Department of Psychiatry, School of Medicine, Technical University of Munich, Ismaninger Str. 22, Munich 81675, GermanyWhile it is known that whole amygdala volume is lastingly reduced after premature birth, it is unknown whether different amygdala nuclei are distinctively affected by prematurity. This question is motivated by two points: First, the observation that developmental trajectories of superficial, centromedial and basolateral amygdala nuclei are different. And second, the expectation that these different developmental pathways are distinctively affected by prematurity. Furthermore, we stated the question whether alterations in amygdala nuclei are associated with increased adults’ anxiety traits after premature birth.We investigated 101 very premature-born adults (<32 weeks of gestation and/or birth weight below 1500 g) and 108 full-term controls of a prospectively and longitudinally collected cohort at 26 years of age using automated amygdala nuclei segmentation based on structural MRI.We found selectively reduced volumes of bilateral accessory basal nuclei (pertaining to the basolateral amygdala of claustral developmental trajectory) adjusted for whole amygdala volume. Volumes of bilateral accessory basal nuclei were positively associated with gestational age and negatively associated with duration of ventilation. Furthermore, structural covariance within the basolateral amygdala was increased in premature-born adults. We did not find an association between reduced volumes of basolateral amygdala and increased social anxiety in the prematurity group.These results demonstrate specifically altered basolateral amygdala structure in premature-born adults. Data suggest that prematurity has distinct effects on amygdala nuclei.http://www.sciencedirect.com/science/article/pii/S2213158221002242Premature birthHumanBrain developmentAmygdala nucleiBasolateral amygdalaStructural magnetic resonance imaging