Cerebral Hypoperfusion and Hypometabolism Detected by Arterial Spin Labeling MRI and FDG-PET in Early-Onset Alzheimer's Disease

被引:79
作者
Verclytte, Sebastien [1 ,2 ]
Lopes, Renaud [4 ]
Lenfant, Pierre [5 ]
Rollin, Adeline [6 ]
Semah, Franck [5 ]
Leclerc, Xavier [3 ,4 ]
Pasquier, Florence [6 ]
Delmaire, Christine [3 ,4 ]
机构
[1] Inst Catholique Lille, Groupement Hop, Fac Med & Matemet, Lille, France
[2] Hosp St Philibert, Dept Radiol, Lomme Les Lille, France
[3] CHU Lille, Dept Neuroradiol, F-59037 Lille, France
[4] Univ Lille Nord France, In Vivo Imaging Platform Predict Med & Therapeut, U1171, Lille, France
[5] CHU Lille, Neuroimaging Dept, F-59037 Lille, France
[6] CHU Lille, Memory Resources & Res Ctr, F-59037 Lille, France
关键词
Arterial spin labeling; Alzheimer's disease; early-onset Alzheimer's disease; positron emission tomography; dementia; MILD COGNITIVE IMPAIRMENT; BLOOD-FLOW; F-18-FDG PET; DEMENTIA; ATROPHY; DIAGNOSIS; PROGRESSION; IMAGES; CORTEX;
D O I
10.1111/jon.12264
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BACKGROUND AND PURPOSEEarly-onset Alzheimer's disease (EOAD) is frequently associated with atypical clinical presentations and its early detection remains a challenging issue. In this study, we used arterial spin labeling (ASL), a noninvasive perfusion MRI sequence, and [F-18]-FDG-PET to detect the perfusion and metabolic features in patients with EOAD. METHODSAll patients were investigated in the French reference center for young-onset dementia and were assessed by MRI, including a pseudo-continuous ASL (pCASL) sequence, and [F-18]-FDG-PET. Quantitative analyses and intermodality comparison with correlation analysis were made after data processing including correction of partial volume effects, cortical projection, and specific intensity normalization. RESULTSWe prospectively included 37 patients with EOAD with a mean age of 58.3 years. The areas of most severe hypoperfusion detected with ASL were located in the parietal lobes, the precuneus, the right posterior cingulate cortex, and the frontal lobes (P < .05). The areas of lowest glucose metabolism detected by [F-18]-FDG-PET were identified in the temporoparietal cortex and the precuneus (P < .05). Hypometabolic regions were more extensive than hypoperfused regions on ASL maps whereas ASL highlighted alterations in the frontal lobes without apparent hypometabolism on [F-18]-FDG-PET maps. CONCLUSIONSASL and [F-18]-FDG-PET detected pathological areas of similar distribution mainly located in the inferior parietal lobules and local zones in the temporal cortex in patients with EOAD. Our preliminary study showed that ASL and [F-18]-FDG-PET may have a complementary role in combination with structural MRI for the assessment of suspected EOAD.
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收藏
页码:207 / 212
页数:6
相关论文
共 49 条
[1]   Perfusion abnormalities in mild cognitive impairment and mild dementia in Alzheimer's disease measured by pulsed arterial spin labeling MRI [J].
Alexopoulos, Panagiotis ;
Sorg, Christian ;
Foerschler, Annette ;
Grimmer, Timo ;
Skokou, Maria ;
Wohlschlaeger, Afra ;
Perneczky, Robert ;
Zimmer, Claus ;
Kurz, Alexander ;
Preibisch, Christine .
EUROPEAN ARCHIVES OF PSYCHIATRY AND CLINICAL NEUROSCIENCE, 2012, 262 (01) :69-77
[2]   Recommended Implementation of Arterial Spin-Labeled Perfusion MRI for Clinical Applications: A Consensus of the ISMRM Perfusion Study Group and the European Consortium for ASL in Dementia [J].
Alsop, David C. ;
Detre, John A. ;
Golay, Xavier ;
Guenther, Matthias ;
Hendrikse, Jeroen ;
Hernandez-Garcia, Luis ;
Lu, Hanzhang ;
MacIntosh, Bradley J. ;
Parkes, Laura M. ;
Smits, Marion ;
van Osch, Matthias J. P. ;
Wang, Danny J. J. ;
Wong, Eric C. ;
Zaharchuk, Greg .
MAGNETIC RESONANCE IN MEDICINE, 2015, 73 (01) :102-116
[3]  
Alsop DC, 2000, ANN NEUROL, V47, P93, DOI 10.1002/1531-8249(200001)47:1<93::AID-ANA15>3.0.CO
[4]  
2-8
[5]   Clinical features and APOE genotype of pathologically proven early-onset Alzheimer disease [J].
Balasa, M. ;
Gelpi, E. ;
Antonell, A. ;
Rey, M. J. ;
Sanchez-Valle, R. ;
Molinuevo, J. L. ;
Llado, A. .
NEUROLOGY, 2011, 76 (20) :1720-1725
[6]   Cerebral Blood Flow Measured with 3D Pseudocontinuous Arterial Spin-labeling MR Imaging in Alzheimer Disease and Mild Cognitive Impairment: A Marker for Disease Severity [J].
Binnewijzend, Maja A. A. ;
Kuijer, Joost P. A. ;
Benedictus, Marije R. ;
van der Flier, Wiesje M. ;
Wink, Alle Meije ;
Wattjes, Mike P. ;
van Berckel, Bart N. M. ;
Scheltens, Philip ;
Barkhof, Frederik .
RADIOLOGY, 2013, 267 (01) :221-230
[7]   Effectiveness and Safety of 18F-FDG PET in the Evaluation of Dementia: A Review of the Recent Literature [J].
Bohnen, Nicolaas I. ;
Djang, David S. W. ;
Herholz, Karl ;
Anzai, Yoshimi ;
Minoshima, Satoshi .
JOURNAL OF NUCLEAR MEDICINE, 2012, 53 (01) :59-71
[8]   Biological parametric mapping: A statistical toolbox for multimodality brain image analysis [J].
Casanova, Ramon ;
Srikanth, Ryali ;
Baer, Aaron ;
Laurienti, Paul J. ;
Burdett, Jonathan H. ;
Hayasaka, Satoru ;
Flowers, Lynn ;
Wood, Frank ;
Maldjian, Joseph A. .
NEUROIMAGE, 2007, 34 (01) :137-143
[9]   Medial temporal atrophy in early and late-onset Alzheimer's disease [J].
Cavedo, Enrica ;
Pievani, Michela ;
Boccardi, Marina ;
Galluzzi, Samantha ;
Bocchetta, Martina ;
Bonetti, Matteo ;
Thompson, Paul M. ;
Frisoni, Giovanni B. .
NEUROBIOLOGY OF AGING, 2014, 35 (09) :2004-2012
[10]   Voxel-level comparison of arterial spin-labeled perfusion MRI and FDG-PET in Alzheimer disease [J].
Chen, Y. ;
Wolk, D. A. ;
Eddin, J. S. R. ;
Korczykowski, M. ;
Martinez, P. M. ;
Pvlusiek, E. S. ;
Newberg, A. B. ;
Julin, P. ;
Arnold, S. E. ;
Greenberg, J. H. ;
Detre, J. A. .
NEUROLOGY, 2011, 77 (22) :1977-1985