Several studies have shown that, in spite of the fact that motor symptoms manifest late in the course of Alzheimer's disease (AD), neuropathological progression in the motor cortex parallels that in other brain areas generally considered more specific targets of the neurodegenerative process. It has been suggested that motor cortex excitability is enhanced in AD from the early stages, and that this is related to disease's severity and progression. To investigate the neurophysiological hallmarks of motor cortex functionality in early AD we combined transcranial magnetic stimulation (TMS) with electroencephalography (EEG). We demonstrated that in mild AD the sensorimotor system is hyperexcitable, despite the lack of clinically evident motor manifestations. This phenomenon causes a stronger response to stimulation in a specific time window, possibly due to locally acting reinforcing circuits, while network activity and connectivity is reduced. These changes could be interpreted as a compensatory mechanism allowing for the preservation of sensorimotor programming and execution over a long period of time, regardless of the disease's progression.

Sensorimotor cortex excitability and connectivity in Alzheimer's disease. A TMS-EEG Co-registration study / Ferreri, Florinda; Vecchio, Fabrizio; Vollero, Luca; Guerra, Andrea; Petrichella, Sara; Ponzo, David; Määtta, Sara; Mervaala, Esa; Könönen, Mervi; Ursini, Francesca; Pasqualetti, Patrizio; Iannello, Giulio; Rossini, Paolo Maria; Di Lazzaro, Vincenzo. - In: HUMAN BRAIN MAPPING. - ISSN 1065-9471. - 37:6(2016), pp. 2083-2096. [10.1002/hbm.23158]

Sensorimotor cortex excitability and connectivity in Alzheimer's disease. A TMS-EEG Co-registration study

GUERRA, Andrea;PASQUALETTI, PATRIZIO;
2016

Abstract

Several studies have shown that, in spite of the fact that motor symptoms manifest late in the course of Alzheimer's disease (AD), neuropathological progression in the motor cortex parallels that in other brain areas generally considered more specific targets of the neurodegenerative process. It has been suggested that motor cortex excitability is enhanced in AD from the early stages, and that this is related to disease's severity and progression. To investigate the neurophysiological hallmarks of motor cortex functionality in early AD we combined transcranial magnetic stimulation (TMS) with electroencephalography (EEG). We demonstrated that in mild AD the sensorimotor system is hyperexcitable, despite the lack of clinically evident motor manifestations. This phenomenon causes a stronger response to stimulation in a specific time window, possibly due to locally acting reinforcing circuits, while network activity and connectivity is reduced. These changes could be interpreted as a compensatory mechanism allowing for the preservation of sensorimotor programming and execution over a long period of time, regardless of the disease's progression.
2016
alzheimer's disease; eeg; navigated transcranial magnetic stimulation; sensorimotor cortex connectivity; sensorimotor cortex excitability; anatomy; radiological and ultrasound technology; radiology, nuclear medicine and imaging; neurology; neurology (clinical)
01 Pubblicazione su rivista::01a Articolo in rivista
Sensorimotor cortex excitability and connectivity in Alzheimer's disease. A TMS-EEG Co-registration study / Ferreri, Florinda; Vecchio, Fabrizio; Vollero, Luca; Guerra, Andrea; Petrichella, Sara; Ponzo, David; Määtta, Sara; Mervaala, Esa; Könönen, Mervi; Ursini, Francesca; Pasqualetti, Patrizio; Iannello, Giulio; Rossini, Paolo Maria; Di Lazzaro, Vincenzo. - In: HUMAN BRAIN MAPPING. - ISSN 1065-9471. - 37:6(2016), pp. 2083-2096. [10.1002/hbm.23158]
File allegati a questo prodotto
File Dimensione Formato  
Ferreri_Sensorimotor_2016.pdf

solo gestori archivio

Tipologia: Versione editoriale (versione pubblicata con il layout dell'editore)
Licenza: Tutti i diritti riservati (All rights reserved)
Dimensione 597.32 kB
Formato Adobe PDF
597.32 kB Adobe PDF   Contatta l'autore

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/969267
Citazioni
  • ???jsp.display-item.citation.pmc??? 28
  • Scopus 83
  • ???jsp.display-item.citation.isi??? 68
social impact