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Anatomical and functional abnormalities on MRI in kabuki syndrome

Authors :
Ana Saitovitch
Jennifer Boisgontier
Elza Rechtman
Ludovic Fillon
David Grevent
Odile Boute
Elise Schaefer
Elodie Sanchez
Damien Sanlaville
Natacha Lehman
Laurence Faivre
David Geneviève
Vincent Gatinois
Nathalie Boddaert
Jean Marc Tacchella
Kim-Hanh Le Quang Sang
Marlène Rio
M. Zilbovicius
Hervé Lemaitre
Stanislas Lyonnet
Guilaine Boursier
Geneviève Baujat
Neuroimagerie en psychiatrie (U1000)
Université Paris-Sud - Paris 11 (UP11)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut National de la Santé et de la Recherche Médicale (INSERM)
CHU Necker - Enfants Malades [AP-HP]
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)
Imagine - Institut des maladies génétiques (IHU) (Imagine - U1163)
Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Paris (UP)
Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier)
Cellules Souches, Plasticité Cellulaire, Médecine Régénératrice et Immunothérapies (IRMB)
Université de Montpellier (UM)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier)
Hôpital Jeanne de Flandre [Lille]
Centre de génétique - Centre de référence des maladies rares, anomalies du développement et syndromes malformatifs (CHU de Dijon)
Centre Hospitalier Universitaire de Dijon - Hôpital François Mitterrand (CHU Dijon)
Service de génétique médicale
CHU Strasbourg-Hôpital de Hautepierre [Strasbourg]
Centre de recherche en neurosciences de Lyon (CRNL)
Université Claude Bernard Lyon 1 (UCBL)
Université de Lyon-Université de Lyon-Université Jean Monnet [Saint-Étienne] (UJM)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
Hospices Civils de Lyon (HCL)
Part of this work was supported by the French Ministry of Health(ProgrammeHospitalierdeRechercheCliniquenationalAOM07-090),Fondation Maladies Rares, and the French Kabuki Associationhttp://www.syndromekabuki.fr/.WethanktheFrenchKabukiAssociationfortheirhelpinthisstudy.
Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris Cité (UPCité)
Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM)
Centre de recherche en neurosciences de Lyon - Lyon Neuroscience Research Center (CRNL)
Université de Lyon-Université de Lyon-Université Jean Monnet - Saint-Étienne (UJM)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
Michel-Avella, Amandine
Source :
Neuroimage-Clinical, Neuroimage-Clinical, Elsevier, 2019, 21, pp.101610. ⟨10.1016/j.nicl.2018.11.020⟩, NeuroImage: Clinical, Vol 21, Iss, Pp-(2019), NeuroImage : Clinical, Neuroimage-Clinical, 2019, 21, pp.101610. ⟨10.1016/j.nicl.2018.11.020⟩
Publication Year :
2019
Publisher :
HAL CCSD, 2019.

Abstract

Kabuki syndrome (KS) is a rare congenital disorder (1/32000 births) characterized by distinctive facial features, intellectual disability, short stature, and dermatoglyphic and skeletal abnormalities. In the last decade, mutations in KMT2D and KDM6A were identified as a major cause of kabuki syndrome. Although genetic abnormalities have been highlighted in KS, brain abnormalities have been little explored. Here, we have investigated brain abnormalities in 6 patients with KS (4 males; Mage = 10.96 years, SD = 2.97 years) with KMT2D mutation in comparison with 26 healthy controls (17 males; Mage = 10.31 years, SD = 2.96 years). We have used MRI to explore anatomical and functional brain abnormalities in patients with KS. Anatomical abnormalities in grey matter volume were assessed by cortical and subcortical analyses. Functional abnormalities were assessed by comparing rest cerebral blood flow measured with arterial spin labeling-MRI. When compared to healthy controls, KS patients had anatomical alterations characterized by grey matter decrease localized in the bilateral precentral gyrus and middle frontal gyrus. In addition, KS patients also presented functional alterations characterized by cerebral blood flow decrease in the left precentral gyrus and middle frontal gyrus. Moreover, subcortical analyses revealed significantly decreased grey matter volume in the bilateral hippocampus and dentate gyrus in patients with KS. Our results strongly indicate anatomical and functional brain abnormalities in KS. They suggest a possible neural basis of the cognitive symptoms observed in KS, such as fine motor impairment, and indicate the need to further explore the consequences of such brain abnormalities in this disorder. Finally, our results encourage further imaging-genetics studies investigating the link between genetics, anatomical and functional brain alterations in KS.<br />Highlights • Kabuki syndrome children show decreased grey matter in precentral and frontal areas • Decreased rest cerebral blood flow is also observed in the same regions • Hippocampus and dentate gyrus volumes are reduced • Brain abnormalities, so far understudied, could underpin clinical deficits

Details

Language :
English
ISSN :
22131582
Database :
OpenAIRE
Journal :
Neuroimage-Clinical, Neuroimage-Clinical, Elsevier, 2019, 21, pp.101610. ⟨10.1016/j.nicl.2018.11.020⟩, NeuroImage: Clinical, Vol 21, Iss, Pp-(2019), NeuroImage : Clinical, Neuroimage-Clinical, 2019, 21, pp.101610. ⟨10.1016/j.nicl.2018.11.020⟩
Accession number :
edsair.doi.dedup.....fb98025bcde8087c27465afe3e28b583
Full Text :
https://doi.org/10.1016/j.nicl.2018.11.020⟩