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A Comparison of the Diagnostic Sensitivity of MRI, CBF-SPECT, FDG-PET and Cerebrospinal Fluid Biomarkers for Detecting Alzheimer's Disease in a Memory Clinic
被引:38
作者:
Morinaga, Akiyoshi
[1
,2
]
Ono, Kenjiro
[1
]
Ikeda, Tokuhei
[1
]
Ikeda, Yoshihisa
[1
]
Shima, Keisuke
[1
]
Noguchi-Shinohara, Moeko
[1
,3
]
Samuraki, Miharu
[1
,4
]
Yanase, Daisuke
[1
]
Yoshita, Mitsuhiro
[1
]
Iwasa, Kazuo
[1
]
Mastunari, Ichiro
[5
]
Yamada, Masahito
[1
]
机构:
[1] Kanazawa Univ, Grad Sch Med Sci, Dept Neurol & Neurobiol Aging, Kanazawa, Ishikawa 9208640, Japan
[2] Natl Hosp Org Iou Hosp, Dept Neurol, Kanazawa, Ishikawa, Japan
[3] Ishikawa Prefectural Cent Hosp, Dept Neurol, Kanazawa, Ishikawa, Japan
[4] Keiju Med Ctr, Dept Neurol, Nanao, Japan
[5] Med & Pharmacol Res Ctr Fdn, Hakui, Japan
关键词:
Alzheimer's disease;
MRI;
CBF-SPECT;
FDG-PET;
CSF biomarkers;
Amyloid beta-protein 1-42;
Total tau;
Phosphorylated tau;
MILD COGNITIVE IMPAIRMENT;
CSF BIOMARKERS;
TAU-PROTEIN;
DEMENTIA;
ATROPHY;
IMAGES;
HIPPOCAMPAL;
PERFORMANCE;
PIB;
D O I:
10.1159/000320265
中图分类号:
R592 [老年病学];
C [社会科学总论];
学科分类号:
03 ;
0303 ;
100203 ;
摘要:
Background/Aim: Magnetic resonance imaging (MRI), cerebral blood flow single photon emission computed tomography (CBF-SPECT), fluorodeoxyglucose-positron emission tomography (FDG-PET) and cerebrospinal fluid (CSF) biomarkers are used for the diagnosis of Alzheimer's disease (AD). We aimed to reveal the relative sensitivity of these tools in a memory clinic setting. Methods: In 207 patients with probable AD in our memory clinic, medial temporal lobe atrophy on MRI, hypoperfusion/hypometabolism of the parietotemporal lobe and posterior cingulate gyrus in ethylcysteinate dimer-CBF-SPECT/FDG-PET, and abnormalities of CSF amyloid beta-protein 1-42, total tau and phosphorylated tau were evaluated as findings characteristic of AD. Results: The AD findings were observed in 77.4% of all AD patients with MRI, 81.6% with CBF-SPECT, 93.1% with FDG-PET and 94.0% with CSF biomarkers. At the stage of Clinical Dementia Rating (CDR) 0.5, CSF biomarkers were the most sensitive (90.0%); at the stage of CDR 1, FDG-PET (96.7%) and CSF biomarkers (95.5%) were highly sensitive. At the stage of CDR 2, all tools showed high positive percentages. Conclusion: The diagnosis of AD was most often supported by CSF biomarkers and FDG-PET at the early stage of dementia (CDR 1) and by CSF biomarkers at the earlier stage (CDR 0.5). Copyright (C) 2010 S. Karger AG, Basel
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页码:285 / 292
页数:8
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