Data di Pubblicazione:
2024
Abstract:
Objective: The resting-state functional connectome has not been extensively investigated in amyotrophic lateral sclerosis (ALS) spectrum disease, in particular in relationship with patients' genetic status. Methods: Here we studied the network-to-network connectivity of 19 ALS patients carrying the C9orf72 hexanucleotide repeat expansion (C9orf72+), 19 ALS patients not affected by C9orf72 mutation (C9orf72-), and 19 ALS-mimic patients (ALSm) well-matched for demographic and clinical variables. Results: When compared with ALSm, we observed greater connectivity of the default mode and frontoparietal networks with the visual network for C9orf72+ patients (P = 0.001). Moreover, the whole-connectome showed greater node degree (P < 0.001), while sensorimotor cortices resulted isolated in C9orf72+. Interpretation: Our results suggest a crucial involvement of extra-motor functions in ALS spectrum disease. In particular, alterations of the visual cortex may have a pathogenic role in C9orf72-related ALS. The prominent feature of these patients would be increased visual system connectivity with the networks responsible of the functional balance between internal and external attention.
Tipologia CRIS:
03A-Articolo su Rivista
Elenco autori:
Stanziano, Mario; Fedeli, Davide; Manera, Umberto; Ferraro, Stefania; Medina Carrion, Jean P; Palermo, Sara; Sciortino, Paola; Cogoni, Maurizio; Agosta, Federica; Basaia, Silvia; Filippi, Massimo; Grisoli, Marina; Valentini, Maria C; De Mattei, Filippo; Canosa, Antonio; Calvo, Andrea; Bruzzone, Maria G; Chiò, Adriano; Nigri, Anna; Moglia, Cristina
Link alla scheda completa:
Pubblicato in: