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Multisite study of the relationships between antemortem [ 11 C]PIB-PET Centiloid values and postmortem measures of Alzheimer's disease neuropathology.

Authors :
La Joie R
Ayakta N
Seeley WW
Borys E
Boxer AL
DeCarli C
Doré V
Grinberg LT
Huang E
Hwang JH
Ikonomovic MD
Jack C Jr
Jagust WJ
Jin LW
Klunk WE
Kofler J
Lesman-Segev OH
Lockhart SN
Lowe VJ
Masters CL
Mathis CA
McLean CL
Miller BL
Mungas D
O'Neil JP
Olichney JM
Parisi JE
Petersen RC
Rosen HJ
Rowe CC
Spina S
Vemuri P
Villemagne VL
Murray ME
Rabinovici GD
Source :
Alzheimer's & dementia : the journal of the Alzheimer's Association [Alzheimers Dement] 2019 Feb; Vol. 15 (2), pp. 205-216. Date of Electronic Publication: 2018 Oct 19.
Publication Year :
2019

Abstract

Introduction: We sought to establish the relationships between standard postmortem measures of AD neuropathology and antemortem [ <superscript>11</superscript> C]PIB-positron emission tomography ([ <superscript>11</superscript> C]PIB-PET) analyzed with the Centiloid (CL) method, a standardized scale for Aβ-PET quantification.<br />Methods: Four centers contributed 179 participants encompassing a broad range of clinical diagnoses, PET data, and autopsy findings.<br />Results: CL values increased with each CERAD neuritic plaque score increment (median -3 CL for no plaques and 92 CL for frequent plaques) and nonlinearly with Thal Aβ phases (increases were detected starting at phase 2) with overlap between scores/phases. PET-pathology associations were comparable across sites and unchanged when restricting the analyses to the 56 patients who died within 2 years of PET. A threshold of 12.2 CL detected CERAD moderate-to-frequent neuritic plaques (area under the curve = 0.910, sensitivity = 89.2%, specificity = 86.4%), whereas 24.4 CL identified intermediate-to-high AD neuropathological changes (area under the curve = 0.894, sensitivity = 84.1%, specificity = 87.9%).<br />Discussion: Our study demonstrated the robustness of a multisite Centiloid [ <superscript>11</superscript> C]PIB-PET study and established a range of pathology-based CL thresholds.<br /> (Copyright © 2018 the Alzheimer's Association. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1552-5279
Volume :
15
Issue :
2
Database :
MEDLINE
Journal :
Alzheimer's & dementia : the journal of the Alzheimer's Association
Publication Type :
Academic Journal
Accession number :
30347188
Full Text :
https://doi.org/10.1016/j.jalz.2018.09.001