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CADASIL affects multiple aspects of cerebral small vessel function on 7T-MRI

Publication year 2023
Published in Annals of Neurology
Authors Hilde van den Brink, Anna Kopczak, Tine Arts, Laurien Onkenhout, Jeroen C. W. Siero, Jaco J M Zwanenburg, Sandra Hein, Mathias Hübner, Benno Gesierich, Marco Duering, Michael S Stringer, Jeroen Hendrikse, Joanna M Wardlaw, Anne Joutel, Martin Dichgans, Geert Jan Biessels

OBJECTIVE: Cerebral small vessel diseases (cSVDs) are a major cause of stroke and dementia. We used cutting-edge 7T-MRI techniques in patients with CADASIL, to establish which aspects of cerebral small vessel function are affected by this monogenic form of cSVD.

METHODS: We recruited 23 CADASIL patients (age 51.1±10.1 years, 52% women) and 13 age- and sex-matched controls (46.1±12.6, 46% women). Small vessel function measures included: basal ganglia and centrum semiovale perforating artery blood flow velocity and pulsatility, vascular reactivity to a visual stimulus in the occipital cortex and reactivity to hypercapnia in the cortex, subcortical grey matter, white matter and white matter hyperintensities.

RESULTS: Compared with controls, CADASIL patients showed lower blood flow velocity and higher pulsatility index within perforating arteries of the centrum semiovale (mean difference -0.09 cm/s, p=0.03 and 0.20,p=0.009) and basal ganglia (mean difference -0.98 cm/s, p=0.003 and 0.17, p=0.06). Small vessel reactivity to a short visual stimulus was decreased (BOLD mean difference -0.21%,p=0.04) in patients, while reactivity to hypercapnia was preserved in the cortex, subcortical grey matter and normal appearing white matter. Among patients, reactivity to hypercapnia was decreased in white matter hyperintensities compared to normal appearing white matter (BOLD mean difference -0.29%, p=0.02).

INTERPRETATION: Multiple aspects of cerebral small vessel function on 7T-MRI were abnormal in CADASIL patients, indicative of increased arteriolar stiffness and regional abnormalities in reactivity, locally also in relation to white matter injury. These observations provide novel markers of cSVD for mechanistic and intervention studies. This article is protected by copyright. All rights reserved.

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