Diaschisis Profiles in the Cerebellar Response to Hemodynamic Stimuli: Insights From Dynamic Measurement of Cerebrovascular Reactivity to Identify Occult and Transient Maxima

被引:2
作者
Dogra, Siddhant [2 ]
Wang, Xiuyuan [3 ]
Gee, James Michael [2 ]
Gupta, Alejandro [2 ]
Veraart, Jelle [2 ]
Ishida, Koto [4 ]
Qiu, Deqiang [5 ]
Dehkharghani, Seena [1 ,2 ,4 ]
机构
[1] NYU, Langone Med Ctr, Dept Radiol, 660 First Ave, New York, NY 10016 USA
[2] New York Univ Langone Hlth, Dept Radiol, New York, NY USA
[3] Weill Cornell Med Coll, Dept Radiol, New York, NY USA
[4] New York Univ Langone Hlth, Dept Neurol, New York, NY USA
[5] Emory Univ, Dept Radiol & Imaging Sci, Atlanta, GA USA
关键词
cerebrovascular reactivity; crossed cerebellar diaschisis; acetazolamide; CVR; CCD; BOLD MRI; STENO-OCCLUSIVE DISEASE; ACETAZOLAMIDE;
D O I
10.1002/jmri.28648
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Background: Crossed cerebellar diaschisis (CCD) refers to depressions in perfusion and metabolism within the cerebellar hemisphere contralateral to supratentorial disease. Prior investigation into CCD in cerebrovascular reactivity (CVR) has been limited to terminal CVR estimations (CVRend). We recently have demonstrated the presence of unsustained CVR maxima (CVRmax) using dynamic CVR analysis, offering a fully dynamic characterization of CVR to hemodynamic stimuli. Purpose: To investigate CCD in CVRmax from dynamic blood oxygen level-dependent (BOLD) MRI, by comparison with conventional CVRend estimation. Study Type: Retrospective. Population: A total of 23 patients (median age: 51 years, 10 females) with unilateral chronic steno-occlusive cerebrovascular disease, without prior knowledge of CCD status. Field Strength/Sequence: A 3-T, T1-weighted magnetization-prepared rapid gradient-echo (MPRAGE) and acetazolamide-augmented BOLD imaging performed with a gradient-echo echo-planar imaging (EPI) sequence. Assessment: A custom denoising pipeline was used to generate BOLD-CVR time signals. CVRend was established using the last minute of the BOLD response relative to the first-minute baseline. Following classification of healthy versus diseased cerebral hemispheres, CVRmax and CVRend were calculated for bilateral cerebral and cerebellar hemispheres. Three independent observers evaluated all data for the presence of CCD. Statistical Tests: Pearson correlations for comparing CVR across hemispheres, two-proportion Z-tests for comparing CCD prevalence, and Wilcoxon signed-rank tests for comparing median CVR. The level of statistical significance was set at P <= 0.05. Results: CCD-related changes were observed on both CVRend and CVRmax maps, with all CCD+ cases identifiable by inspection of either map. Diseased cerebral and contralateral cerebellar hemispheric CVR correlations in CCD+ patients were stronger when using CVRend (r = 0.728) as compared to CVRmax (r = 0.676). CVR correlations between healthy cerebral hemispheres and contralateral cerebellar hemispheres were stronger for CVRmax (r = 0.739) than for CVRend (r = 0.705). Data Conclusion: CCD-related alterations could be observed in CVR examinations. Conventional CVRend may underestimate CVR and could exaggerate CCD.
引用
收藏
页码:1462 / 1469
页数:8
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