TY - JOUR
T1 - Functional correlates of t-Tau, p-Tau and Aβ1-42 amyloid cerebrospinal fluid levels in Alzheimer's disease
T2 - A 18F-FDG PET/CT study
AU - Chiaravalloti, Agostino
AU - Martorana, Alessandro
AU - Koch, Giacomo
AU - Toniolo, Sofia
AU - Di Biagio, Daniele
AU - Di Pietro, Barbara
AU - Schillaci, Orazio
PY - 2015/4/14
Y1 - 2015/4/14
N2 - Aim: The aim of the study was to investigate the relationships between cerebrospinal fluid (CSF) levels of t-Tau, p-Tau and amyloid-β (Aβ1-42) amyloid peptide and fluorine-18 fluorodeoxyglucose (18F-FDG) brain distribution in a group of patients with Alzheimer's disease. Materials and methods: The study included 81 newly diagnosed Alzheimer's disease patients according to the NINCDS-ADRDA criteria. The mean (± SD) age of the patients was 70 (± 6) years; 44 were male and 37 were female. All patients underwent a CSF assay and MRI before 18F-FDG PET scanning. The relationships were evaluated by means of statistical parametric mapping (SPM8). Results: Increased t-Tau CSF levels were related to reduced glucose consumption in a wide portion of the right frontal lobe [Brodmann area (BA 47)] and limbic lobe bilaterally (BA 31,32), whereas no areas of increased 18F-FDG uptake related to t-Tau levels were detected. Elevated p-Tau concentrations in CSF were related to increased glucose consumption in both the right and the left limbic lobe and in the left frontal lobe (BA 32 and 8). We did not find any specific cortical area of reduced glucose consumption being related to low levels of Aβ1-42 in CSF, whereas a spawn of 18F-FDG uptake was detectable in BA 18,19 and in the right cerebellum. Conclusion: The results of our study suggest that reduced Aβ1-42 concentrations in CSF are related to a wide cortical dysfunction, whereas t-Tau and p-Tau are related to more selective cortical metabolic patterns that mainly involve the cingulate cortex.
AB - Aim: The aim of the study was to investigate the relationships between cerebrospinal fluid (CSF) levels of t-Tau, p-Tau and amyloid-β (Aβ1-42) amyloid peptide and fluorine-18 fluorodeoxyglucose (18F-FDG) brain distribution in a group of patients with Alzheimer's disease. Materials and methods: The study included 81 newly diagnosed Alzheimer's disease patients according to the NINCDS-ADRDA criteria. The mean (± SD) age of the patients was 70 (± 6) years; 44 were male and 37 were female. All patients underwent a CSF assay and MRI before 18F-FDG PET scanning. The relationships were evaluated by means of statistical parametric mapping (SPM8). Results: Increased t-Tau CSF levels were related to reduced glucose consumption in a wide portion of the right frontal lobe [Brodmann area (BA 47)] and limbic lobe bilaterally (BA 31,32), whereas no areas of increased 18F-FDG uptake related to t-Tau levels were detected. Elevated p-Tau concentrations in CSF were related to increased glucose consumption in both the right and the left limbic lobe and in the left frontal lobe (BA 32 and 8). We did not find any specific cortical area of reduced glucose consumption being related to low levels of Aβ1-42 in CSF, whereas a spawn of 18F-FDG uptake was detectable in BA 18,19 and in the right cerebellum. Conclusion: The results of our study suggest that reduced Aβ1-42 concentrations in CSF are related to a wide cortical dysfunction, whereas t-Tau and p-Tau are related to more selective cortical metabolic patterns that mainly involve the cingulate cortex.
KW - Alzheimer
KW - Amyloid
KW - Cerebrospinal fluid biomarkers
KW - Fluorine-18 fluorodeoxyglucose
KW - PET
KW - Tau
UR - http://www.scopus.com/inward/record.url?scp=84927571653&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84927571653&partnerID=8YFLogxK
U2 - 10.1097/MNM.0000000000000272
DO - 10.1097/MNM.0000000000000272
M3 - Article
C2 - 25646706
AN - SCOPUS:84927571653
SN - 0143-3636
VL - 36
SP - 461
EP - 468
JO - Nuclear Medicine Communications
JF - Nuclear Medicine Communications
IS - 5
ER -