Functional Magnetic Resonance Imaging of Inhibitory Control Reveals Decreased Blood Oxygen Level Dependent Effect in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy.

CADASIL MRI, functional cerebral small vessel disease hemodynamic proactive inhibition reactive inhibition thalamus

Journal

Stroke
ISSN: 1524-4628
Titre abrégé: Stroke
Pays: United States
ID NLM: 0235266

Informations de publication

Date de publication:
Jan 2019
Historique:
medline: 26 12 2018
pubmed: 26 12 2018
entrez: 25 12 2018
Statut: ppublish

Résumé

Background and Purpose- Small-vessel damage in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is associated with impaired vascular constriction and dilation. We used a functional magnetic resonance imaging task with an event-related design of stimulus to explore the anticipated abnormally decreased blood oxygen level dependent effect in CADASIL. Methods- Twenty-one CADASIL patients and 16 healthy controls performed a Go/No-go task exploring reactive and proactive phases of inhibition control in a 3-T magnet. Results- Error number and reaction times were not different between patients and controls. Analysis of the reactive inhibition (No-go/baseline contrast) did not show clusters of lower or higher blood oxygen level dependent effect in patients or controls. Analysis of the proactive inhibition (alertness contrast) in CADASIL patients revealed a lower blood oxygen level dependent effect in the alerting network (anterior cingulate cortex and insula, thalamus), lower brain stem and left cerebellar hemisphere (crus I) that is involved in executive functions. Conclusions- In CADASIL patients, an event-related Go/No-go task reveals a lower blood oxygen level dependent effect in the alerting network and areas involved in executive functions possibly reflecting the altered hemodynamic response secondary to small-vessel changes. Our observation extends the role of MR in demonstrating one of the fundamental pathophysiological changes of CADASIL.

Identifiants

pubmed: 30580728
doi: 10.1161/STROKEAHA.118.022923
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

69-75

Auteurs

Gioele Gavazzi (G)

From the IRCCS SDN, Naples, Italy (G.G.).

Stefano Orsolini (S)

Department of Electrical, Electronic, and Information Engineering 'Guglielmo Marconi', University of Bologna, Cesena, Italy (S.O., S.D.).

Emilia Salvadori (E)

NEUROFARBA Department, Neuroscience Section (E.S., I.D., V.R.), University of Florence, Italy.

Andrea Bianchi (A)

Neuroradiology Unit (A.B.), Azienda Ospedaliero Universitaria Careggi, Florence, Italy.

Arianna Rossi (A)

Department of Neuroscience, Psychology, Drug Research, Child Health (A.R., M.P.V.), University of Florence, Italy.

Ida Donnini (I)

NEUROFARBA Department, Neuroscience Section (E.S., I.D., V.R.), University of Florence, Italy.

Valentina Rinnoci (V)

NEUROFARBA Department, Neuroscience Section (E.S., I.D., V.R.), University of Florence, Italy.

Francesca Pescini (F)

Stroke Unit (F.P.), Azienda Ospedaliero Universitaria Careggi, Florence, Italy.

Stefano Diciotti (S)

Department of Electrical, Electronic, and Information Engineering 'Guglielmo Marconi', University of Bologna, Cesena, Italy (S.O., S.D.).

Maria Pia Viggiano (MP)

Department of Neuroscience, Psychology, Drug Research, Child Health (A.R., M.P.V.), University of Florence, Italy.

Mario Mascalchi (M)

'Mario Serio' Department of Experimental and Clinical Biomedical Sciences (M.M.), University of Florence, Italy.

Leonardo Pantoni (L)

'Luigi Sacco' Department of Biomedical and Clinical Sciences, University of Milan, Italy (L.P.).

Classifications MeSH