Precuneal gliomas promote behaviorally relevant remodeling of the functional connectome.

awake surgery executive function functional connectivity low-grade glioma neuroplasticity oncology precuneus

Journal

Journal of neurosurgery
ISSN: 1933-0693
Titre abrégé: J Neurosurg
Pays: United States
ID NLM: 0253357

Informations de publication

Date de publication:
28 Oct 2022
Historique:
received: 25 07 2022
accepted: 08 09 2022
entrez: 29 10 2022
pubmed: 30 10 2022
medline: 30 10 2022
Statut: aheadofprint

Résumé

The precuneus hosts one of the most complex patterns of functional connectivity in the human brain. However, due to the extreme rarity of neurological lesions specifically targeting this structure, it remains unknown how focal damage to the precuneus may impact resting-state functional connectivity (rsFC) at the brainwide level. The aim of this study was to investigate glioma-induced rsFC modulations and to identify patterns of rsFC remodeling that accounted for the maintenance of cognitive performance after awake-guided surgical excision. In a unique series of patients with IDH1-mutated low-grade gliomas (LGGs) infiltrating the precuneus who were treated at a single neurosurgical center (Montpellier University Medical Center, 2014-2021), the authors gauged the dynamic modulations induced by tumors on rsFC in comparison with healthy participants. All patients received a preoperative resting-state functional MRI and underwent operation guided by awake cognitive mapping. Connectome multivariate pattern analysis (MVPA), seed-network analysis, and graph theoretical analysis were conducted and correlated to executive neurocognitive scores (i.e., phonological and semantic fluencies, Trail-Making Test [TMT] parts A and B) obtained 3 months after surgery. Seventeen patients with focal precuneal infiltration were selected (mean age 38.1 ± 11.2 years) and matched to 17 healthy participants (mean age 40.5 ± 10.4 years) for rsFC analyses. All patients underwent awake cognitive mapping, allowing total resection (n = 3) or subtotal resection (n = 14), with a mean extent of resection of 90.6% ± 7.3%. Using MVPA (cluster threshold: p-false discovery rate corrected < 0.05, voxel threshold: p-uncorrected < 0.001), remote hotspots with significant rsFC changes were identified, including both insulas, the anterior cingulate cortex, superior sensorimotor cortices, and both frontal eye fields. Further seed-network analyses captured 2 patterns of between-network redistribution especially involving hyperconnectivity between the salience, visual, and dorsal attentional networks. Finally, the global efficiency of the salience-visual-dorsal attentional networks was strongly and positively correlated to 3-month postsurgical scores (n = 15) for phonological fluency (r15 = 0.74, p = 0.0027); TMT-A (r15 = 0.65, p = 0.012); TMT-B (r15 = 0.70, p = 0.005); and TMT-B-A (r15 = 0.62, p = 0.018). In patients with LGGs infiltrating the precuneus, remote and distributed functional connectivity modulations in the preoperative setting are associated with better maintenance of cognitive performance after surgery. These findings provide a new vision of the mechanistic principles underlying neural plasticity and cognitive compensation in patients with LGGs.

Identifiants

pubmed: 36308476
doi: 10.3171/2022.9.JNS221723
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-11

Auteurs

Sam Ng (S)

Departments of1Neurosurgery and.
2Team "Neuroplasticity, Stem Cells and Low-grade Gliomas," Institute of Functional Genomics of Montpellier, University of Montpellier, CNRS, INSERM, Montpellier.

Jeremy Deverdun (J)

3I2FH, Institut d'Imagerie Fonctionnelle Humaine, Gui de Chauliac Hospital, Montpellier University Medical Center, Montpellier, France.
4Neuroradiology, Gui de Chauliac Hospital, Montpellier University Medical Center, Montpellier.

Anne-Laure Lemaitre (AL)

Departments of1Neurosurgery and.
2Team "Neuroplasticity, Stem Cells and Low-grade Gliomas," Institute of Functional Genomics of Montpellier, University of Montpellier, CNRS, INSERM, Montpellier.

Davide Giampiccolo (D)

5Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, University College London.
6Victor Horsley Department of Neurosurgery, National Hospital for Neurology and Neurosurgery, Queen Square, London; and.
7Department of Neurosurgery, Institute of Neurosciences, Cleveland Clinic London, United Kingdom.

Emmanuelle Le Bars (EL)

3I2FH, Institut d'Imagerie Fonctionnelle Humaine, Gui de Chauliac Hospital, Montpellier University Medical Center, Montpellier, France.
4Neuroradiology, Gui de Chauliac Hospital, Montpellier University Medical Center, Montpellier.

Sylvie Moritz-Gasser (S)

Departments of1Neurosurgery and.
2Team "Neuroplasticity, Stem Cells and Low-grade Gliomas," Institute of Functional Genomics of Montpellier, University of Montpellier, CNRS, INSERM, Montpellier.

Nicolas Menjot de Champfleur (N)

3I2FH, Institut d'Imagerie Fonctionnelle Humaine, Gui de Chauliac Hospital, Montpellier University Medical Center, Montpellier, France.
4Neuroradiology, Gui de Chauliac Hospital, Montpellier University Medical Center, Montpellier.

Hugues Duffau (H)

Departments of1Neurosurgery and.
2Team "Neuroplasticity, Stem Cells and Low-grade Gliomas," Institute of Functional Genomics of Montpellier, University of Montpellier, CNRS, INSERM, Montpellier.

Guillaume Herbet (G)

Departments of1Neurosurgery and.
2Team "Neuroplasticity, Stem Cells and Low-grade Gliomas," Institute of Functional Genomics of Montpellier, University of Montpellier, CNRS, INSERM, Montpellier.

Classifications MeSH