Crossed Cerebellar Diaschisis in Patients With Symptomatic Unilateral Anterior Circulation Stroke Is Associated With Hemodynamic Impairment in the Ipsilateral MCA Territory.

BOLD-fMRI MCA territory cerebrovascular reactivity crossed cerebellar diaschisis hemodynamic perfusion-weighted MRI

Journal

Journal of magnetic resonance imaging : JMRI
ISSN: 1522-2586
Titre abrégé: J Magn Reson Imaging
Pays: United States
ID NLM: 9105850

Informations de publication

Date de publication:
04 2021
Historique:
revised: 06 10 2020
received: 27 08 2020
accepted: 09 10 2020
pubmed: 30 10 2020
medline: 15 5 2021
entrez: 29 10 2020
Statut: ppublish

Résumé

In patients with steno-occlusive disease, recent findings suggest that hemodynamic alterations may also be associated with crossed cerebellar diaschisis (CCD) rather than a functional disruption alone. To use a quantitative multiparametric hemodynamic MRI to gain a better understanding of hemodynamic changes related to CCD in patients with unilateral anterior circulation stroke. Prospective cohort study. Twenty-four patients (25 datasets) with symptomatic unilateral anterior circulation stroke. 3T/two sequences: single-shot (echo-planar imaging) EPI sequence and T The presence of CCD was inferred from the cerebellar asymmetry index (CAI) of the blood oxygenation-level dependent cerebrovascular reactivity (BOLD-CVR) exam, which was calculated from the mean BOLD-CVR and standard deviation of the CAI of the healthy control group. For all perfusion-weighted (PW)-MRI parameters, the cerebellar and middle cerebral artery (MCA) territory asymmetry indices were calculated. Independent Student's t-test to compare the variables from the CCD positive(+) and CCD negative(-) groups and analysis of covariance (ANCOVA) to statistically control the effect of covariates (infarct volume and time since ischemia onset). CCD was present in 33% of patients. In the MCA territory of the affected hemisphere, BOLD-CVR was significantly more impaired in the CCD(+) group as compared to the CCD(-) group (mean BOLD-CVR ± SD [%BOLD signal/ΔmmHgCO Our findings show that, in patients with symptomatic unilateral anterior circulation stroke, CCD is associated with hemodynamic impairment in the ipsilateral MCA territory, which further supports the concept of a vascular component of CCD. 3 TECHNICAL EFFICACY STAGE: 3.

Sections du résumé

BACKGROUND
In patients with steno-occlusive disease, recent findings suggest that hemodynamic alterations may also be associated with crossed cerebellar diaschisis (CCD) rather than a functional disruption alone.
PURPOSE
To use a quantitative multiparametric hemodynamic MRI to gain a better understanding of hemodynamic changes related to CCD in patients with unilateral anterior circulation stroke.
STUDY TYPE
Prospective cohort study.
POPULATION
Twenty-four patients (25 datasets) with symptomatic unilateral anterior circulation stroke.
FIELD STRENGTH/SEQUENCE
3T/two sequences: single-shot (echo-planar imaging) EPI sequence and T
ASSESSMENT
The presence of CCD was inferred from the cerebellar asymmetry index (CAI) of the blood oxygenation-level dependent cerebrovascular reactivity (BOLD-CVR) exam, which was calculated from the mean BOLD-CVR and standard deviation of the CAI of the healthy control group. For all perfusion-weighted (PW)-MRI parameters, the cerebellar and middle cerebral artery (MCA) territory asymmetry indices were calculated.
STATISTICAL TESTS
Independent Student's t-test to compare the variables from the CCD positive(+) and CCD negative(-) groups and analysis of covariance (ANCOVA) to statistically control the effect of covariates (infarct volume and time since ischemia onset).
RESULTS
CCD was present in 33% of patients. In the MCA territory of the affected hemisphere, BOLD-CVR was significantly more impaired in the CCD(+) group as compared to the CCD(-) group (mean BOLD-CVR ± SD [%BOLD signal/ΔmmHgCO
DATA CONCLUSION
Our findings show that, in patients with symptomatic unilateral anterior circulation stroke, CCD is associated with hemodynamic impairment in the ipsilateral MCA territory, which further supports the concept of a vascular component of CCD.
LEVEL OF EVIDENCE
3 TECHNICAL EFFICACY STAGE: 3.

Identifiants

pubmed: 33118301
doi: 10.1002/jmri.27410
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1190-1197

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2020 International Society for Magnetic Resonance in Medicine.

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Auteurs

Martina Sebök (M)

Department of Neurosurgery, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Clinical Neuroscience Center, University Hospital Zurich, Zurich, Switzerland.

Christiaan Hendrik Bas van Niftrik (CHB)

Department of Neurosurgery, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Clinical Neuroscience Center, University Hospital Zurich, Zurich, Switzerland.

Marco Piccirelli (M)

Clinical Neuroscience Center, University Hospital Zurich, Zurich, Switzerland.
Department of Neuroradiology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.

Giovanni Muscas (G)

Department of Neurosurgery, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Clinical Neuroscience Center, University Hospital Zurich, Zurich, Switzerland.

Athina Pangalu (A)

Clinical Neuroscience Center, University Hospital Zurich, Zurich, Switzerland.
Department of Neuroradiology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.

Susanne Wegener (S)

Clinical Neuroscience Center, University Hospital Zurich, Zurich, Switzerland.
Department of Neurology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.

Christoph Stippich (C)

Clinical Neuroscience Center, University Hospital Zurich, Zurich, Switzerland.
Department of Neuroradiology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.

Luca Regli (L)

Department of Neurosurgery, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Clinical Neuroscience Center, University Hospital Zurich, Zurich, Switzerland.

Jorn Fierstra (J)

Department of Neurosurgery, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Clinical Neuroscience Center, University Hospital Zurich, Zurich, Switzerland.

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