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Prospectrive Flutemetamol Positron Emission Tomography and Histopathollogy in Normal Pressure Hydrocephalus
被引:16
|作者:
Rinne, Juha O.
[1
,2
]
Frantzen, Janek
[3
]
Leinonen, Ville
[4
,5
]
Lonnrot, Kimmo
[6
]
Laakso, Aki
[7
]
Virtanen, Kirsi A.
[1
,2
]
Solin, Olof
[1
,2
]
Kotkansalo, Anna
[3
]
Koivisto, Anne
[5
,8
]
Sajanti, Juha
[6
]
Karppinen, Atte
[7
]
Lehto, Hanna
[7
]
Rummukainen, Jaana
[9
]
Buckley, Chris
[11
]
Smith, Adrian
[12
]
Jones, Paul A.
[12
]
Sherwin, Paul
[14
]
Farrar, Gill
[13
]
McLain, Richard
[15
]
Kailajarvi, Marita
[10
]
Grachev, Igor D.
[14
]
机构:
[1] Univ Turku, Turku PET Ctr, FI-20520 Turku, Finland
[2] Turku Univ Hosp, FIN-20520 Turku, Finland
[3] Turku Univ Hosp, Dept Neurosurg, FIN-20520 Turku, Finland
[4] Kuopio Univ Hosp, Dept Neurosurg, SF-70210 Kuopio, Finland
[5] Univ Eastern Finland, Inst Clin Med, Kuopio, Finland
[6] Seinajoki Cent Hosp, Seinajoki, Finland
[7] Univ Helsinki, Cent Hosp, Dept Neurosurg, Helsinki, Finland
[8] Kuopio Univ Hosp, Dept Neurol, SF-70210 Kuopio, Finland
[9] Kuopio Univ Hosp, Dept Pathol, SF-70210 Kuopio, Finland
[10] GE Healthcare, Clin Dev Med Diagnost, Turku, Finland
[11] GE Healthcare, Imaging Technol, Amersham, England
[12] GE Healthcare, Discovery Biol, Amersham, England
[13] GE Healthcare, Program & Project Management Med Diagnost, Amersham, England
[14] GE Healthcare, Clin Dev Med Diagnost, Princeton, NJ USA
[15] PFP Stat Consulting LLC, Livonia, MI USA
关键词:
Flutennetamol;
Positron emission tomography;
Histopathology;
Amyloid-beta;
Normal pressure hydrocephalus;
Cortical brain biopsy;
Ventriculoperitoneal shunting;
MILD COGNITIVE IMPAIRMENT;
CORTICAL BRAIN BIOPSY;
PITTSBURGH-COMPOUND-B;
ALZHEIMERS-DISEASE;
SHUNT RESPONSE;
PIB;
PET;
F-18-FLUTEMETAMOL;
DEPOSITION;
PATHOLOGY;
D O I:
10.1159/000355256
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Backgound/Objective: To determine the level of association between uptake of the amyloid positron emission tomography (PET) imaging agent [F-18]flutemetamol and the level of amyloid-P measured by immunohistochemical and histochemical staining in a frontal cortical region biopsy site. Methods: Seventeen patients with probable normal pressure hydrocephalus (NPH) underwent prospective [F-18]flutennetannol PET and subsequent frontal cortical brain biopsy during ventriculoperitoneal shunting. Tissue amyloid-beta was evaluated using the monoclonal antibody 4G8, thioflavin S and Bielschowsky silver stain. Results: Four of the 17 patients (23.5%) had amyloid-beta pathology based on the overall pathology read and also showed increased [F-18]flutemetamol uptake. [F-18]Flutemetamol standardized uptake values from the biopsy site were significantly associated with biopsy specimen amyloid-beta levels (Pearson's r = 0.67; p = 0.006). There was also good correlation between the biopsy specimen amyloid-beta level and uptake of [F-18]flutemetamol in the region contralateral to the biopsy site (r = 0.67; p = 0.006), as well as with composite cortical [F-18]flutemetamol uptake (r = 0.65; p = 0.008). The blinded visual read showed a high level of agreement between all readers (K = 0.88). Two of 3 readers were in full agreement on all images; 1 reader disagreed on 1 of the 17 NPH cases. Blinded visual assessments of PET images by 1 reader were associated with 100% sensitivity to the overall pathology read, and assessments by the 2 others were associated with 75% sensitivity (overall sensitivity by majority read was 75%); specificity of all readers was 100%. Conclusions: [F-18]Flutemetamol detects brain amyloid-beta in vivo and shows promise as a valuable tool to study and possibly facilitate diagnosis of Alzheimer's disease both in patients with suspected NPH and among the wider population. (C) 2013 S. Karger AG, Basel
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页码:237 / 245
页数:9
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