Arterial spin labeling perfusion predicts longitudinal decline in semantic variant primary progressive aphasia

被引:25
作者
Olm, Christopher A. [1 ]
Kandel, Benjamin M. [2 ]
Avants, Brian B. [2 ]
Detre, John A. [3 ,4 ]
Gee, James C. [2 ]
Grossman, Murray [1 ]
McMillan, Corey T. [1 ]
机构
[1] Univ Penn, Dept Neurol, Perelman Sch Med, Penn Frontotemporal Degenerat Ctr, 3 West Gates, Philadelphia, PA 19104 USA
[2] Penn Image Comp & Sci Lab, Dept Radiol, Philadelphia, PA 19104 USA
[3] Univ Penn, Dept Neurol, Philadelphia, PA 19104 USA
[4] Univ Penn, Dept Radiol, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
Frontotemporal degeneration; Semantic variant primary progressive aphasia; Arterial spin labeling; MRI; Functional neuroimaging; BLOOD-FLOW MRI; FRONTOTEMPORAL DEMENTIA; ALZHEIMERS-DISEASE; CORTICOBASAL DEGENERATION; IMAGE REGISTRATION; CEREBRAL PERFUSION; BRAIN; PATTERNS; HYPOPERFUSION; COMPREHENSION;
D O I
10.1007/s00415-016-8221-1
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The objective of the study was to evaluate the prognostic value of regional cerebral blood flow (CBF) measured by arterial spin labeled (ASL) perfusion MRI in patients with semantic variant primary progressive aphasia (svPPA). We acquired pseudo-continuous ASL (pCASL) MRI and whole-brain T1-weighted structural MRI in svPPA patients (N = 13) with cerebrospinal fluid biomarkers consistent with frontotemporal lobar degeneration pathology. Follow-up T1-weighted MRI was available in a subset of patients (N = 8). We performed whole-brain comparisons of partial volume-corrected CBF and cortical thickness between svPPA and controls, and compared baseline and follow-up cortical thickness in regions of significant hypoperfusion and hyperperfusion. Patients with svPPA showed partial volume-corrected hypoperfusion relative to controls in left temporal lobe and insula. svPPA patients also had typical cortical thinning in anterior temporal, insula, and inferior frontal regions at baseline. Volume-corrected hypoperfusion was seen in areas of significant cortical thinning such as the left temporal lobe and insula. Additional regions of hypoperfusion corresponded to areas without cortical thinning. We also observed regions of hyperperfusion, some associated with cortical thinning and others without cortical thinning, including right superior temporal, inferior parietal, and orbitofrontal cortices. Regions of hypoperfusion and hyperperfusion near cortical thinning at baseline had significant longitudinal thinning between baseline and follow-up scans, but perfusion changes in distant areas did not show progressive thinning. Our findings suggest ASL MRI may be sensitive to functional changes not readily apparent in structural MRI, and specific changes in perfusion may be prognostic markers of disease progression in a manner consistent with cell-to-cell spreading pathology.
引用
收藏
页码:1927 / 1938
页数:12
相关论文
共 43 条
[1]   Arterial Spin Labeling Blood Flow MRI: Its Role in the Early Characterization of Alzheimer's Disease [J].
Alsop, David C. ;
Dai, Weiying ;
Grossman, Murray ;
Detre, John A. .
JOURNAL OF ALZHEIMERS DISEASE, 2010, 20 (03) :871-880
[2]   Interhemispheric compensation: A hypothesis of TMS-induced effects on language-related areas [J].
Andoh, Jamila ;
Martinot, Jean-Luc .
EUROPEAN PSYCHIATRY, 2008, 23 (04) :281-288
[3]   Symmetric diffeomorphic image registration with cross-correlation: Evaluating automated labeling of elderly and neurodegenerative brain [J].
Avants, B. B. ;
Epstein, C. L. ;
Grossman, M. ;
Gee, J. C. .
MEDICAL IMAGE ANALYSIS, 2008, 12 (01) :26-41
[4]  
Avants B.B., 2012, Proceedings of Perfusion MRI: Standardization, Beyond CBF and Everyday Clinical Applications, International Society for Magnetic Resonance in Medicine Scientific Workshop, Amsterdam, P21
[5]   A reproducible evaluation of ANTs similarity metric performance in brain image registration [J].
Avants, Brian B. ;
Tustison, Nicholas J. ;
Song, Gang ;
Cook, Philip A. ;
Klein, Arno ;
Gee, James C. .
NEUROIMAGE, 2011, 54 (03) :2033-2044
[6]  
Baron J C, 1981, Trans Am Neurol Assoc, V105, P459
[7]   Dissociable brain mechanisms for processing social exclusion and rule violation [J].
Bolling, Danielle Z. ;
Pitskel, Naomi B. ;
Deen, Ben ;
Crowley, Michael J. ;
McPartland, James C. ;
Mayes, Linda C. ;
Pelphrey, Kevin A. .
NEUROIMAGE, 2011, 54 (03) :2462-2471
[8]   Cortical Hubs Revealed by Intrinsic Functional Connectivity: Mapping, Assessment of Stability, and Relation to Alzheimer's Disease [J].
Buckner, Randy L. ;
Sepulcre, Jorge ;
Talukdar, Tanveer ;
Krienen, Fenna M. ;
Liu, Hesheng ;
Hedden, Trey ;
Andrews-Hanna, Jessica R. ;
Sperling, Reisa A. ;
Johnson, Keith A. .
JOURNAL OF NEUROSCIENCE, 2009, 29 (06) :1860-1873
[9]  
Corouge I, 2012, MICCAI 2012 WORKSH N, P32
[10]   The hubs of the human connectome are generally implicated in the anatomy of brain disorders [J].
Crossley, Nicolas A. ;
Mechelli, Andrea ;
Scott, Jessica ;
Carletti, Francesco ;
Fox, Peter T. ;
McGuire, Philip ;
Bullmore, Edward T. .
BRAIN, 2014, 137 :2382-2395