Literature DB >> 24845162

Congenital heart disease is associated with reduced cortical and hippocampal volume in patients with 22q11.2 deletion syndrome.

Daniel M Fountain1, Marie Schaer2, A Kadir Mutlu3, Maude Schneider4, Martin Debbané5, Stephan Eliez6.   

Abstract

OBJECTIVE: There is increasing evidence that congenital heart disease (CHD) affects brain structure, but little is known about the long-term trajectory of brain maturation and its impact on the cognitive development of patients with CHD. We proposed to address this question in a longitudinally-followed cohort of individuals with 22q11.2 deletion syndrome (22q11DS), the most common microdeletion syndrome in humans.
METHODS: A total of 80 participants were included in this longitudinal analysis. The volumes of thirty-four cortical regions and eight hippocampal regions were measured in each hemisphere with FreeSurfer software. This paper utilized linear mixed modelling to investigate cerebral morphometry and age-related maturational changes of all regions. The effect of CHD was assessed for intercept and slope significance.
RESULTS: We observed significant (p < .05/34) volumetric reductions in patients with CHD compared to patients without in fifteen out of the sixty-eight cortical sub-regions. Similarly, global hippocampal volumes and twelve of the hippocampal sub-regions were significantly smaller (p < .05/8). The results demonstrate significant absolute volumetric differences, but did not show any significant differences in the way the cortical or hippocampal regions developed over time. There was limited evidence of any effect of the presence of CHD on key cognitive measures.
CONCLUSIONS: We propose that cerebral hypoperfusion, due to the presence of CHD or its surgery, impairs early cortical and particularly hippocampal growth, potentially due to the damaging effects of stress, but not subsequent maturational processes in children and adolescents.
Copyright © 2014 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Brain morphometry; Cardiac defects; Neurodevelopmental disorders; Velo-cardio-facial syndrome; Volumetric MRI

Mesh:

Year:  2014        PMID: 24845162     DOI: 10.1016/j.cortex.2014.04.004

Source DB:  PubMed          Journal:  Cortex        ISSN: 0010-9452            Impact factor:   4.027


  8 in total

1.  Reduced cortical volume and thickness and their relationship to medical and operative features in post-Fontan children and adolescents.

Authors:  Christopher G Watson; Christian Stopp; David Wypij; Jane W Newburger; Michael J Rivkin
Journal:  Pediatr Res       Date:  2017-02-03       Impact factor: 3.756

2.  [A prenatal ultrasound study of cerebral sulci and gyrus development in fetuses with tetralogy of Fallot].

Authors:  Jia-Min He; Sheng-Li Li; Xi Chen; Hua-Xuan Wen; Ying Yuan; Dan-Dan Luo
Journal:  Nan Fang Yi Ke Da Xue Xue Bao       Date:  2017-06-20

3.  Positive psychotic symptoms are associated with divergent developmental trajectories of hippocampal volume during late adolescence in patients with 22q11DS.

Authors:  Valentina Mancini; Corrado Sandini; Maria C Padula; Daniela Zöller; Maude Schneider; Marie Schaer; Stephan Eliez
Journal:  Mol Psychiatry       Date:  2019-06-04       Impact factor: 15.992

Review 4.  Cross disorder comparisons of brain structure in schizophrenia, bipolar disorder, major depressive disorder, and 22q11.2 deletion syndrome: A review of ENIGMA findings.

Authors:  Eun-Jin Cheon; Carrie E Bearden; Daqiang Sun; Christopher R K Ching; Ole A Andreassen; Lianne Schmaal; Dick J Veltman; Sophia I Thomopoulos; Peter Kochunov; Neda Jahanshad; Paul M Thompson; Jessica A Turner; Theo G M van Erp
Journal:  Psychiatry Clin Neurosci       Date:  2022-02-26       Impact factor: 12.145

5.  Subcortical Signatures of Hemizygosity and Psychosis in 22q11.2 Deletion Syndrome: Finding Common Ground in Rare Genetic Variation.

Authors:  Daniel P Eisenberg; Michael D Gregory; Karen F Berman
Journal:  Am J Psychiatry       Date:  2020-07-01       Impact factor: 19.242

6.  An affected core drives network integration deficits of the structural connectome in 22q11.2 deletion syndrome.

Authors:  František Váša; Alessandra Griffa; Elisa Scariati; Marie Schaer; Sébastien Urben; Stephan Eliez; Patric Hagmann
Journal:  Neuroimage Clin       Date:  2015-11-26       Impact factor: 4.881

7.  Epilepsy and Other Neuropsychiatric Manifestations in Children and Adolescents with 22q11.2 Deletion Syndrome.

Authors:  Eun Hee Kim; Mi Sun Yum; Beom Hee Lee; Hyo Won Kim; Hyun Jeoung Lee; Gu Hwan Kim; Yun Jeong Lee; Han Wook Yoo; Tae Sung Ko
Journal:  J Clin Neurol       Date:  2016-01       Impact factor: 3.077

8.  Genetic mouse models of autism spectrum disorder present subtle heterogenous cardiac abnormalities.

Authors:  Stephania Assimopoulos; Christopher Hammill; Darren J Fernandes; Tara Leigh Spencer Noakes; Yu-Qing Zhou; Lauryl M J Nutter; Jacob Ellegood; Evdokia Anagnostou; John G Sled; Jason P Lerch
Journal:  Autism Res       Date:  2022-04-21       Impact factor: 4.633

  8 in total

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