Arterial spin labeling brain MRI study to evaluate the impact of deafness on cerebral perfusion in 79 children before cochlear implantation.


Journal

NeuroImage. Clinical
ISSN: 2213-1582
Titre abrégé: Neuroimage Clin
Pays: Netherlands
ID NLM: 101597070

Informations de publication

Date de publication:
2021
Historique:
received: 01 04 2020
revised: 06 11 2020
accepted: 16 11 2020
pubmed: 29 12 2020
medline: 29 6 2021
entrez: 28 12 2020
Statut: ppublish

Résumé

Age at implantation is considered to be a major factor, influencing outcomes after pediatric cochlear implantation. In the absence of acoustic input, it has been proposed that cross-modal reorganization can be detrimental for adaptation to the new electrical input provided by a cochlear implant. Here, through a retrospective study, we aimed to investigate differences in cerebral blood flow (CBF) at rest prior to implantation in children with congenital deafness compared to normally hearing children. In addition, we looked at the putative link between pre-operative rest-CBF and the oral intelligibility scores at 12 months post-implantation. Finally, we observed the evolution of perfusion with age, within brain areas showing abnormal rest-CBF associated to deafness, in deaf children and in normally hearing children. In children older than 5 years old, results showed a significant bilateral hypoperfusion in temporal regions in deaf children, particularly in Heschl's gyrus, and a significant hyperperfusion of occipital regions. Furthermore, in children older than 5 years old, whole brain voxel-by-voxel correlation analysis between pre-operative rest-CBF and oral intelligibility scores at 12 months post-implantation, showed significant negative correlation localized in the occipital regions: children who performed worse in the speech perception test one year after implantation were those presenting higher preoperative CBF values in these occipital regions. Finally, when comparing mean relative perfusion (extracted from the temporal regions found abnormal on whole-brain voxel-based analysis) across ages in patients and controls, we observed that the temporal perfusion evolution was significantly different in deaf children than in normally hearing children. Indeed, while temporal perfusion increased with age in normally hearing children, it remained stable in deaf children. We showed a critical period around 4 years old, where in the context of auditory deprivation, there is a lack of synaptic activity in auditory regions. These results support the benefits of early cochlear implantation to maximize the effectiveness of auditory rehabilitation and to avoid cross-modal reorganization.

Identifiants

pubmed: 33369563
pii: S2213-1582(20)30347-8
doi: 10.1016/j.nicl.2020.102510
pmc: PMC7777537
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

102510

Informations de copyright

Copyright © 2020. Published by Elsevier Inc.

Auteurs

Arnaud Coez (A)

Service de radiologie pédiatrique, Hôpital Necker Enfants Malades, Assistance Publique Hôpitaux de Paris, APHP, Université de Paris, INSERM U1163, Institut Imagine, Paris, France; Service d'oto-rhino-laryngologie pédiatrique, Centre de Réference des Surdités Génétiques, Hôpital Necker Enfants Malades, AP-HP, Université de Paris, Paris, France; Laboratoire de correction auditive, Bizaguet, Paris, France; Institut de l'Audition, Paris, France. Electronic address: acoez@noos.fr.

Ludovic Fillon (L)

Service de radiologie pédiatrique, Hôpital Necker Enfants Malades, Assistance Publique Hôpitaux de Paris, APHP, Université de Paris, INSERM U1163, Institut Imagine, Paris, France.

Ana Saitovitch (A)

Service de radiologie pédiatrique, Hôpital Necker Enfants Malades, Assistance Publique Hôpitaux de Paris, APHP, Université de Paris, INSERM U1163, Institut Imagine, Paris, France.

Caroline Rutten (C)

Service de radiologie pédiatrique, Hôpital Necker Enfants Malades, Assistance Publique Hôpitaux de Paris, APHP, Université de Paris, INSERM U1163, Institut Imagine, Paris, France.

Sandrine Marlin (S)

Service de Génétique Médicale, Centre de Référence des Surdités Génétiques, Hôpital Necker Enfants Malades, AP-HP, Université de Paris, Paris, France.

Jennifer Boisgontier (J)

Service de radiologie pédiatrique, Hôpital Necker Enfants Malades, Assistance Publique Hôpitaux de Paris, APHP, Université de Paris, INSERM U1163, Institut Imagine, Paris, France.

Alice Vinçon-Leite (A)

Service de radiologie pédiatrique, Hôpital Necker Enfants Malades, Assistance Publique Hôpitaux de Paris, APHP, Université de Paris, INSERM U1163, Institut Imagine, Paris, France.

Hervé Lemaitre (H)

Service de radiologie pédiatrique, Hôpital Necker Enfants Malades, Assistance Publique Hôpitaux de Paris, APHP, Université de Paris, INSERM U1163, Institut Imagine, Paris, France.

David Grévent (D)

Service de radiologie pédiatrique, Hôpital Necker Enfants Malades, Assistance Publique Hôpitaux de Paris, APHP, Université de Paris, INSERM U1163, Institut Imagine, Paris, France.

Charles-Joris Roux (CJ)

Service de radiologie pédiatrique, Hôpital Necker Enfants Malades, Assistance Publique Hôpitaux de Paris, APHP, Université de Paris, INSERM U1163, Institut Imagine, Paris, France.

Volodia Dangouloff-Ros (V)

Service de radiologie pédiatrique, Hôpital Necker Enfants Malades, Assistance Publique Hôpitaux de Paris, APHP, Université de Paris, INSERM U1163, Institut Imagine, Paris, France.

Raphaël Levy (R)

Service de radiologie pédiatrique, Hôpital Necker Enfants Malades, Assistance Publique Hôpitaux de Paris, APHP, Université de Paris, INSERM U1163, Institut Imagine, Paris, France.

Eric Bizaguet (E)

Service d'oto-rhino-laryngologie pédiatrique, Centre de Réference des Surdités Génétiques, Hôpital Necker Enfants Malades, AP-HP, Université de Paris, Paris, France; Laboratoire de correction auditive, Bizaguet, Paris, France.

Isabelle Rouillon (I)

Service d'oto-rhino-laryngologie pédiatrique, Centre de Réference des Surdités Génétiques, Hôpital Necker Enfants Malades, AP-HP, Université de Paris, Paris, France.

Eréa Noël Garabédian (EN)

Service d'oto-rhino-laryngologie pédiatrique, Centre de Réference des Surdités Génétiques, Hôpital Necker Enfants Malades, AP-HP, Université de Paris, Paris, France.

Françoise Denoyelle (F)

Service d'oto-rhino-laryngologie pédiatrique, Centre de Réference des Surdités Génétiques, Hôpital Necker Enfants Malades, AP-HP, Université de Paris, Paris, France; Institut de l'Audition, Paris, France.

Monica Zilbovicius (M)

Service de radiologie pédiatrique, Hôpital Necker Enfants Malades, Assistance Publique Hôpitaux de Paris, APHP, Université de Paris, INSERM U1163, Institut Imagine, Paris, France; INSERM ERL "Developmental Trajectories & Psychiatry", Université Paris Saclay, Ecole Normale Supérieure Paris-Saclay, Université de Paris, CNRS, Centre Borelli, France.

Natalie Loundon (N)

Service d'oto-rhino-laryngologie pédiatrique, Centre de Réference des Surdités Génétiques, Hôpital Necker Enfants Malades, AP-HP, Université de Paris, Paris, France; Institut de l'Audition, Paris, France.

Nathalie Boddaert (N)

Service de radiologie pédiatrique, Hôpital Necker Enfants Malades, Assistance Publique Hôpitaux de Paris, APHP, Université de Paris, INSERM U1163, Institut Imagine, Paris, France; INSERM ERL "Developmental Trajectories & Psychiatry", Université Paris Saclay, Ecole Normale Supérieure Paris-Saclay, Université de Paris, CNRS, Centre Borelli, France.

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