Aberrant gyrification contributes to the link between gestational age and adult IQ after premature birth.


Journal

Brain : a journal of neurology
ISSN: 1460-2156
Titre abrégé: Brain
Pays: England
ID NLM: 0372537

Informations de publication

Date de publication:
01 05 2019
Historique:
received: 08 10 2018
revised: 23 01 2019
accepted: 30 01 2019
entrez: 30 4 2019
pubmed: 30 4 2019
medline: 4 3 2020
Statut: ppublish

Résumé

Gyrification is a hallmark of human brain development, starting in the second half of gestation in primary cortices, followed by unimodal and then transmodal associative cortices. Alterations in gyrification have been noted in premature-born newborns and children, suggesting abnormal cortical folding to be a permanent feature of prematurity. Furthermore, both gyrification and prematurity are tightly linked with cognitive performance, indicating a link between prematurity, gyrification, and cognitive performance. To investigate this triangular relation, we tested the following two hypotheses: (i) gyrification is aberrant in premature-born adults; and (ii) aberrant gyrification contributes to the impact of prematurity on adult cognitive performance. One hundred and one very premature-born adults (i.e. adults born before 32 weeks of gestation, and/or with birth weight <1500 g) and 111 mature-born adults were assessed by structural MRI and cognitive testing at 27 years of age. Gyrification was measured by local cortical absolute mean curvature (AMC), evaluated through structural MRI. Cognitive performance was assessed by the Wechsler Adult Intelligence Scale, full-scale IQ test. Two-sample t-tests, regression and mediation analyses were used to assess AMC group differences and the relation between AMC, birth-related variables, and full-scale IQ. Three key findings were identified. First, local AMC was widely increased in fronto-temporo-parietal primary and associative cortices of very premature-born adults. Increase of AMC was inversely associated with gestational age and birth weight and positively associated with medical complications at birth, respectively. Second, increased AMC of temporal associative cortices specifically contributed to the association between prematurity and reduced adult IQ (two-path mediation), indicating that aberrant gyrification of temporal associative cortices is critical for impaired cognitive performance after premature birth. Finally, further investigation of the relationship of gyrification between the early folding postcentral cortices and associative temporal cortices, folding later during neurodevelopment, revealed that the effect of gyrification abnormalities in associative temporal cortices on adult IQ is influenced itself by gyrification abnormalities occurring in the early folding postcentral cortices (three-path mediation). These results indicate that gyrification development across cortical areas in the brain conveys prematurity effects on adult IQ. Overall, these results provide evidence that premature birth leads to permanently aberrant gyrification patterns suggesting an altered neurodevelopmental trajectory. Statistical mediation modelling suggests that both aberrant gyrification itself as well as its propagation across the cortex express aspects of impaired neurodevelopment after premature birth and lead to reduced cognitive performance in adulthood. Thus, markers of gyrification appear as potential candidates for prognosis and treatment of prematurity effects.

Identifiants

pubmed: 31032850
pii: 5445411
doi: 10.1093/brain/awz071
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1255-1269

Informations de copyright

© The Author(s) (2019). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

Auteurs

Dennis M Hedderich (DM)

TUM-NIC Neuroimaging Center, Technische Universität München, Munich, Germany.
Department of Neuroradiology, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.

Josef G Bäuml (JG)

TUM-NIC Neuroimaging Center, Technische Universität München, Munich, Germany.
Department of Neuroradiology, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.

Maria T Berndt (MT)

TUM-NIC Neuroimaging Center, Technische Universität München, Munich, Germany.
Department of Neuroradiology, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.

Aurore Menegaux (A)

TUM-NIC Neuroimaging Center, Technische Universität München, Munich, Germany.
Department of Neuroradiology, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Graduate School of Systemic Neurosciences GSN, Ludwig-Maximilians-University Munich, Munich, Germany.

Lukas Scheef (L)

Functional Neuroimaging Group, Department of Radiology, University Hospital Bonn, Bonn, Germany.

Marcel Daamen (M)

Functional Neuroimaging Group, Department of Radiology, University Hospital Bonn, Bonn, Germany.
Department of Neonatology, University Hospital Bonn, Bonn, Germany.

Claus Zimmer (C)

Department of Neuroradiology, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.

Peter Bartmann (P)

Department of Neonatology, University Hospital Bonn, Bonn, Germany.

Henning Boecker (H)

Functional Neuroimaging Group, Department of Radiology, University Hospital Bonn, Bonn, Germany.

Dieter Wolke (D)

Department of Psychology, University of Warwick, Coventry, UK.
Warwick Medical School, University of Warwick, Coventry, UK.

Christian Gaser (C)

Department of Psychiatry and Neurology, University Hospital Jena, Jena, Germany.

Christian Sorg (C)

TUM-NIC Neuroimaging Center, Technische Universität München, Munich, Germany.
Department of Neuroradiology, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Department of Psychiatry, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.

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