Ontology highlight
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.
SUBMITTER: Stanziano M
PROVIDER: S-EPMC10963301 | biostudies-literature | 2024 Mar
REPOSITORIES: biostudies-literature
Stanziano Mario M Fedeli Davide D Manera Umberto U Ferraro Stefania S Medina Carrion Jean P JP Palermo Sara S Sciortino Paola P Cogoni Maurizio M Agosta Federica F Basaia Silvia S Filippi Massimo M Grisoli Marina M Valentini Maria C MC De Mattei Filippo F Canosa Antonio A Calvo Andrea A Bruzzone Maria G MG Chiò Adriano A Nigri Anna A Moglia Cristina C
Annals of clinical and translational neurology 20240117 3
<h4>Objective</h4>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.<h4>Methods</h4>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 ...[more]