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Biostatistical Estimation of Tau Threshold Hallmarks (BETTH) Algorithm for Human Tau PET Imaging Studies.
Gogola, Alexandra; Lopresti, Brian J; Tudorascu, Dana; Snitz, Beth; Minhas, Davneet; Doré, Vincent; Ikonomovic, Milos D; Shaaban, C Elizabeth; Matan, Cristy; Bourgeat, Pierrick; Mason, N Scott; Aizenstein, Howard; Mathis, Chester A; Klunk, William E; Rowe, Christopher C; Lopez, Oscar L; Cohen, Ann D; Villemagne, Victor L.
Affiliation
  • Gogola A; Department of Radiology, University of Pittsburgh, Pittsburgh, Pennsylvania; alexandra-gogola@pitt.edu.
  • Lopresti BJ; Department of Radiology, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Tudorascu D; Department of Psychiatry, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Snitz B; Department of Neurology, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Minhas D; Department of Radiology, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Doré V; Department of Molecular Imaging and Therapy, Austin Health, Melbourne, Victoria, Australia.
  • Ikonomovic MD; Health and Biosecurity, Commonwealth Scientific and Industrial Research Organisation, Melbourne, Victoria, Australia.
  • Shaaban CE; Department of Neurology, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Matan C; Geriatric Research Education and Clinical Center, Veterans Affairs Pittsburgh Healthcare System, Pittsburgh, Pennsylvania; and.
  • Bourgeat P; Department of Epidemiology, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Mason NS; Department of Radiology, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Aizenstein H; Health and Biosecurity, Commonwealth Scientific and Industrial Research Organisation, Melbourne, Victoria, Australia.
  • Mathis CA; Department of Radiology, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Klunk WE; Department of Psychiatry, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Rowe CC; Department of Radiology, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Lopez OL; Department of Psychiatry, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Cohen AD; Department of Molecular Imaging and Therapy, Austin Health, Melbourne, Victoria, Australia.
  • Villemagne VL; Department of Neurology, University of Pittsburgh, Pittsburgh, Pennsylvania.
J Nucl Med ; 64(11): 1798-1805, 2023 11.
Article de En | MEDLINE | ID: mdl-37709531
ABSTRACT
A methodology for determining tau PET thresholds is needed to confidently detect early tau deposition. We compared multiple threshold-determining methods in participants who underwent either 18F-flortaucipir or 18F-MK-6240 PET scans.

Methods:

18F-flortaucipir (n = 798) and 18F-MK-6240 (n = 216) scans were processed and sampled to obtain regional SUV ratios. Subsamples of the cohorts were based on participant diagnosis, age, amyloid-ß status (positive or negative), and neurodegeneration status (positive or negative), creating older-adult (age ≥ 55 y) cognitively unimpaired (amyloid-ß-negative, neurodegeneration-negative) and cognitively impaired (mild cognitive impairment/Alzheimer disease, amyloid-ß-positive, neurodegeneration-positive) groups, and then were further subsampled via matching to reduce significant differences in diagnostic prevalence, age, and Mini-Mental State Examination score. We used the biostatistical estimation of tau threshold hallmarks (BETTH) algorithm to determine sensitivity and specificity in 6 composite regions.

Results:

Parametric double receiver operating characteristic analysis yielded the greatest joint sensitivity in 5 of the 6 regions, whereas hierarchic clustering, gaussian mixture modeling, and k-means clustering all yielded perfect joint specificity (2.00) in all regions.

Conclusion:

When 18F-flortaucipir and 18F-MK-6240 are used, Alzheimer disease-related tau status is best assessed using 2 thresholds, a sensitivity one based on parametric double receiver operating characteristic analysis and a specificity one based on gaussian mixture modeling, delimiting an uncertainty zone indicating participants who may require further evaluation.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Maladie d'Alzheimer / Dysfonctionnement cognitif Type d'étude: Prognostic_studies Limites: Humans / Middle aged Langue: En Journal: J Nucl Med Année: 2023 Type de document: Article

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Maladie d'Alzheimer / Dysfonctionnement cognitif Type d'étude: Prognostic_studies Limites: Humans / Middle aged Langue: En Journal: J Nucl Med Année: 2023 Type de document: Article