Brain metabolic maps in Mild Cognitive Impairment predict heterogeneity of progression to dementia

被引:95
作者
Cerami, Chiara [1 ,2 ,3 ]
Della Rosa, Pasquale Anthony [4 ]
Magnani, Giuseppe [5 ]
Santangelo, Roberto [5 ]
Marcone, Alessandra [3 ]
Cappa, Stefano F. [6 ]
Perani, Daniela [1 ,2 ,4 ,7 ]
机构
[1] Univ Vita Salute San Raffaele, Via Olgettina 60, I-20134 Milan, Italy
[2] Ist Sci San Raffaele, Div Neurosci, I-20132 Milan, Italy
[3] Hosp San Raffaele, Dept Clin Neurosci, Neurorehabil Unit, I-20132 Milan, Italy
[4] CNR, Ist Bioimmagini & Fisiol Mol, Segrate, Italy
[5] Hosp San Raffaele, Dept Neurol, I-20132 Milan, Italy
[6] Ist Univ Studi Super, Pavia, Italy
[7] Hosp San Raffaele, Nucl Med Unit, I-20132 Milan, Italy
关键词
Mild Cognitive Impairment; F-18]FDG; PET imaging; Dementia diagnosis; Alzheimer's disease; ALZHEIMERS ASSOCIATION WORKGROUPS; CEREBRAL GLUCOSE-METABOLISM; FDG-PET; DIAGNOSTIC GUIDELINES; NATIONAL INSTITUTE; CLINICAL PROGRESSION; DISEASE; CRITERIA; RECOMMENDATIONS; INVENTORY;
D O I
10.1016/j.nicl.2014.12.004
中图分类号
R445 [影像诊断学];
学科分类号
100207 ;
摘要
[F-18]FDG-PET imaging has been recognized as a crucial diagnostic marker in Mild Cognitive Impairment (MCI), supporting the presence or the exclusion of Alzheimer's Disease (AD) pathology. A clinical heterogeneity, however, underlies MCI definition. In this study, we aimed to evaluate the predictive role of single -subject voxelbased maps of [F-18]FDG distribution generated through statistical parametric mapping (SPM) in the progression to different dementia subtypes in a sample of 45 MCI. Their scans were compared to a large normal reference dataset developed and validated for comparison at single -subject level. Additionally, A beta 42 and Tau CSF values were available in 34 MCI subjects. Clinical follow-up (mean 28.5 +/- 7.8 months) assessed subsequent progression to AD or non -AD dementias. The SPM analysis showed: 1) normal brain metabolism in 14 MCI cases, none of them progressing to dementia; 2) the typical temporo-parietal pattern suggestive for prodromal AD in 15 cases 11 of them progressing to AD; 3) brain hypometabolism suggestive of frontotemporal lobar degeneration (FTLD) subtypes in 7 and dementia with Lewy bodies (DLB) in 2 subjects (all fulfilled HID or DLB clinical criteria at follow-up); and 4) 7 MCI cases showed a selective unilateral or bilateral temporo-medial hypometabolism without the typical AD pattern, and they all remained stable. In our sample, objective voxel-based analysis of [F-18]FDG-PET scans showed high predictive prognostic value, by identifying either normal brain metabolism or hypometabolic patterns suggestive of different underlying pathologies, as confirmed by progression at followup. These data support the potential usefulness of this SPM [F-18]FDG PET analysis in the early dementia diagnosis and for improving subject selection in clinical trials based on MCI definition. (C) 2014 Published by Elsevier Inc
引用
收藏
页码:187 / 194
页数:8
相关论文
共 73 条
[61]   Practical utility of amyloid and FDG-PET in an academic dementia center [J].
Sanchez-Juan, Pascual ;
Ghosh, Pia M. ;
Hagen, Jayne ;
Gesierich, Benno ;
Henry, Maya ;
Grinberg, Lea T. ;
O'Neil, James P. ;
Janabi, Mustafa ;
Huang, Eric J. ;
Trojanowski, John Q. ;
Vinters, Harry V. ;
Gorno-Tempini, Marilu ;
Seeley, William W. ;
Boxer, Adam L. ;
Rosen, Howard J. ;
Kramer, Joel H. ;
Miller, Bruce L. ;
Jagust, William J. ;
Rabinovici, Gil D. .
NEUROLOGY, 2014, 82 (03) :230-238
[62]   Neural correlates of Alzheimer's disease and mild cognitive impairment: A systematic and quantitative meta-analysis involving 1351 patients [J].
Schroeter, Matthias L. ;
Stein, Timo ;
Maslowski, Nina ;
Neumann, Jane .
NEUROIMAGE, 2009, 47 (04) :1196-1206
[63]   Rapid assessment of regional cerebral metabolic abnormalities in single subjects with quantitative and nonquantitative [18F]FDG PET:: A clinical validation of statistical parametric mapping [J].
Signorini, M ;
Paulesu, E ;
Friston, K ;
Perani, D ;
Colleluori, A ;
Lucignani, G ;
Grassi, F ;
Bettinardi, V ;
Frackowiak, RSJ ;
Fazio, F .
NEUROIMAGE, 1999, 9 (01) :63-80
[64]   Positron emission tomography scans obtained for the evaluation of cognitive dysfunction [J].
Silverman, Daniel H. S. ;
Mosconi, Lisa ;
Ercoli, Linda ;
Chen, Wei ;
Small, Gary W. .
SEMINARS IN NUCLEAR MEDICINE, 2008, 38 (04) :251-261
[65]   Using a white matter reference to remove the dependency of global signal on experimental conditions in SPELT analyses [J].
Spence, Jeffrey S. ;
Carmack, Patrick S. ;
Gunst, Richard F. ;
Schucany, William R. ;
Woodward, Wayne A. ;
Haley, Robert W. .
NEUROIMAGE, 2006, 32 (01) :49-53
[66]   Toward defining the preclinical stages of Alzheimer's disease: Recommendations from the National Institute on Aging-Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease [J].
Sperling, Reisa A. ;
Aisen, Paul S. ;
Beckett, Laurel A. ;
Bennett, David A. ;
Craft, Suzanne ;
Fagan, Anne M. ;
Iwatsubo, Takeshi ;
Jack, Clifford R., Jr. ;
Kaye, Jeffrey ;
Montine, Thomas J. ;
Park, Denise C. ;
Reiman, Eric M. ;
Rowe, Christopher C. ;
Siemers, Eric ;
Stern, Yaakov ;
Yaffe, Kristine ;
Carrillo, Maria C. ;
Thies, Bill ;
Morrison-Bogorad, Marcelle ;
Wagster, Molly V. ;
Phelps, Creighton H. .
ALZHEIMERS & DEMENTIA, 2011, 7 (03) :280-292
[67]   Cerebrospinal Fluid β-Amyloid 42 and Tau Proteins as Biomarkers of Alzheimer-Type Pathologic Changes in the Brain [J].
Tapiola, Tero ;
Alafuzoff, Irina ;
Herukka, Sanna-Kaisa ;
Parkkinen, Laura ;
Hartikainen, Paivi ;
Soininen, Hilkka ;
Pirttila, Tuula .
ARCHIVES OF NEUROLOGY, 2009, 66 (03) :382-389
[68]   Typical Cerebral Metabolic Patterns in Neurodegenerative Brain Diseases [J].
Teune, Laura K. ;
Bartels, Anna L. ;
de Jong, Bauke M. ;
Willemsen, Antoon T. M. ;
Eshuis, Silvia A. ;
de Vries, Jeroen J. ;
van Oostrom, Joost C. H. ;
Leenders, Klaus L. .
MOVEMENT DISORDERS, 2010, 25 (14) :2395-2404
[69]   Voxel-based classification of FDG PET in dementia using inter-scanner normalization [J].
Thiele, Frank ;
Young, Stewart ;
Buchert, Ralph ;
Wenzel, Fabian .
NEUROIMAGE, 2013, 77 :62-69
[70]   Mild cognitive impairment: Disparity of incidence and prevalence estimates [J].
Ward, Alex ;
Arrighi, H. Michael ;
Michels, Shannon ;
Cedarbaum, Jesse M. .
ALZHEIMERS & DEMENTIA, 2012, 8 (01) :14-21