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Functional magnetic resonance imaging responses in CADASIL.

Authors :
Cheema I
Switzer AR
McCreary CR
Hill MD
Frayne R
Goodyear BG
Smith EE
Source :
Journal of the neurological sciences [J Neurol Sci] 2017 Apr 15; Vol. 375, pp. 248-254. Date of Electronic Publication: 2017 Feb 03.
Publication Year :
2017

Abstract

Objectives: The magnitude of the blood oxygen dependent level (BOLD) functional MRI (fMRI) response to visual stimulation is reduced in the small vessel disease cerebral amyloid angiopathy (CAA), reflecting impaired vascular reactivity. We determined whether BOLD responses were reduced in another small vessel disease, cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).<br />Methods: BOLD fMRI data were collected using a visual stimulus (contrast-reversing checkerboard) and motor task (finger-tapping). The amplitude of BOLD responses in the visual cortex (visual stimulus) and motor cortex (motor task) were compared between 5 CADASIL, 18 CAA and 18 control subjects, controlling for age and hypertension.<br />Results: BOLD response varied by group for the visual stimulus (p<0.001) but not the motor task (p=0.47). After adjusting for age and hypertension, the estimated mean visual cortex BOLD amplitude response was 3.95% in CADASIL (95% confidence interval, CI 3.15-4.75%), 1.73% in CAA (95% CI 1.19-2.27%), and 2.88% (95% CI 2.39-3.37%) in controls. In CADASIL, the visual BOLD response was greater than in CAA (p<0.001) and controls (p=0.04).<br />Conclusions: We observed increased and unchanged BOLD amplitude responses in the visual and motor cortices of CADASIL patients, respectively. This suggests that cortical blood flow regulation by neuronal activity may be relatively preserved in CADASIL, in contrast to CAA where occipital vascular reactivity is impaired. Cortical vascular reactivity in CADASIL may be preserved because the disease-related injury is primarily subcortical, whereas increased activation may reflect compensatory mechanisms for subcortical injury.<br /> (Copyright © 2017 Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
1878-5883
Volume :
375
Database :
MEDLINE
Journal :
Journal of the neurological sciences
Publication Type :
Academic Journal
Accession number :
28320141
Full Text :
https://doi.org/10.1016/j.jns.2017.02.004