Literature DB >> 10926955

Cerebral hemodynamics in CADASIL before and after acetazolamide challenge assessed with MRI bolus tracking.

H Chabriat1, S Pappata, L Ostergaard, C A Clark, M Pachot-Clouard, K Vahedi, A Jobert, D Le Bihan, M G Bousser.   

Abstract

BACKGROUND: White matter lesions in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) are underlaid by severe ultrastructural changes of the arteriolar wall. Although chronic ischemia is presumed to cause the tissue lesions, the pattern of perfusion abnormalities and hemodynamic reserve in CADASIL, particularly within the white matter, remains unknown.
METHODS: We used the MRI bolus tracking method in 15 symptomatic patients with CADASIL (5 with dementia) and 10 age-matched control subjects before and 20 minutes after the intravenous injection of acetazolamide (ACZ, 17 mg/kg). Cerebral blood flow (CBF), blood volume (CBV), and mean transit time (MTT) were calculated both in the cortex and in the white matter according to the singular value decomposition technique. Perfusion parameters were obtained in regions of hyperintensities and within the normal-appearing white matter as observed on T2-weighted images. Analysis was performed with both absolute and relative (region/whole brain) values.
RESULTS: A significant reduction in absolute and relative CBF and CBV was found within areas of T2 hyperintensities in white matter in the absence of significant variations of MTT. This reduction was more severe in demented than in nondemented patients. No significant change in absolute CBF and CBV values was observed in the cortex of patients with CADASIL. A decrease in relative CBF and CBV values was detected in the occipital cortex. After ACZ administration, CBF and CBV increased significantly in both the cortex and white matter of affected subjects, but the increase in absolute CBF was lower within areas of increased signal on T2-weighted images in patients than in the white matter of control subjects.
CONCLUSIONS: In CADASIL, both basal perfusion and hemodynamic reserve are decreased in areas of T2 hyperintensities in the white matter. This hypoperfusion appears to be related to the clinical severity. The significant effect of ACZ on CBF and CBV suggests that cerebral perfusion might be increased using pharmacological vasodilation in CADASIL.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 10926955     DOI: 10.1161/01.str.31.8.1904

Source DB:  PubMed          Journal:  Stroke        ISSN: 0039-2499            Impact factor:   7.914


  39 in total

Review 1.  Genetic animal models of cerebral vasculopathies.

Authors:  Jeong Hyun Lee; Brian J Bacskai; Cenk Ayata
Journal:  Prog Mol Biol Transl Sci       Date:  2012       Impact factor: 3.622

Review 2.  Migraine and small vessel diseases.

Authors:  E Agostoni; A Rigamonti
Journal:  Neurol Sci       Date:  2012-05       Impact factor: 3.307

Review 3.  CADASIL: experimental insights from animal models.

Authors:  Cenk Ayata
Journal:  Stroke       Date:  2010-10       Impact factor: 7.914

4.  Shorter telomeres in patients with cerebral autosomal dominant arteriopathy and leukoencephalopathy (CADASIL).

Authors:  Michele Ragno; Luigi Pianese; Michele Pinelli; Serena Silvestri; Gabriella Cacchiò; Fabio Di Marzio; Maria Scarcella; Francesco Coretti; Fabiana Altamura; Antonella Monticelli; Imma Castaldo
Journal:  Neurogenetics       Date:  2011-09-01       Impact factor: 2.660

Review 5.  CADASIL: Treatment and Management Options.

Authors:  Anna Bersano; Gloria Bedini; Joshua Oskam; Caterina Mariotti; Franco Taroni; Silvia Baratta; Eugenio Agostino Parati
Journal:  Curr Treat Options Neurol       Date:  2017-09       Impact factor: 3.598

6.  CADASIL mutant NOTCH3(R90C) decreases the viability of HS683 oligodendrocytes via apoptosis.

Authors:  Mibo Tang; Changhe Shi; Bo Song; Jing Yang; Ting Yang; Chengyuan Mao; Yusheng Li; Xinjing Liu; Shuyu Zhang; Hui Wang; Haiyang Luo; Yuming Xu
Journal:  Mol Biol Rep       Date:  2017-06-10       Impact factor: 2.316

7.  Cerebrovascular reactivity and dynamic autoregulation in nondemented patients with CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy).

Authors:  Sumeet Singhal; Hugh S Markus
Journal:  J Neurol       Date:  2005-02       Impact factor: 4.849

8.  Assessment of brain perfusion with MRI: methodology and application to acute stroke.

Authors:  C B Grandin
Journal:  Neuroradiology       Date:  2003-10-14       Impact factor: 2.804

9.  Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a genetic cause of cerebral small vessel disease.

Authors:  Jay Chol Choi
Journal:  J Clin Neurol       Date:  2010-03-26       Impact factor: 3.077

10.  Neuropathological correlates of temporal pole white matter hyperintensities in CADASIL.

Authors:  Yumi Yamamoto; Masafumi Ihara; Carina Tham; Roger W C Low; Janet Y Slade; Tim Moss; Arthur E Oakley; Tuomo Polvikoski; Raj N Kalaria
Journal:  Stroke       Date:  2009-04-09       Impact factor: 7.914

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.