Publication:
Longitudinal validity of PET-based staging of regional amyloid deposition.

dc.contributor.authorJelistratova, Irina
dc.contributor.authorTeipel, Stefan J
dc.contributor.authorGrothe, Michel J
dc.date.accessioned2023-02-09T09:36:43Z
dc.date.available2023-02-09T09:36:43Z
dc.date.issued2020-07-10
dc.description.abstractPositron emission tomography (PET)-based staging of regional amyloid deposition has recently emerged as a promising tool for sensitive detection and stratification of pathology progression in Alzheimer's Disease (AD). Here we present an updated methodological framework for PET-based amyloid staging using region-specific amyloid-positivity thresholds and assess its longitudinal validity using serial PET acquisitions. We defined region-specific thresholds of amyloid-positivity based on Florbetapir-PET data of 13 young healthy individuals (age ≤ 45y), applied these thresholds to Florbetapir-PET data of 179 cognitively normal older individuals to estimate a regional amyloid staging model, and tested this model in a larger sample of patients with mild cognitive impairment (N = 403) and AD dementia (N = 85). 2-year follow-up Florbetapir-PET scans from a subset of this sample (N = 436) were used to assess the longitudinal validity of the cross-sectional model based on individual stage transitions and data-driven longitudinal trajectory modeling. Results show a remarkable congruence between cross-sectionally estimated and longitudinally modeled trajectories of amyloid accumulation, beginning in anterior temporal areas, followed by frontal and medial parietal areas, the remaining associative neocortex, and finally primary sensory-motor areas and subcortical regions. Over 98% of individual amyloid deposition profiles and longitudinal stage transitions adhered to this staging scheme of regional pathology progression, which was further supported by corresponding changes in cerebrospinal fluid biomarkers. In conclusion, we provide a methodological refinement and longitudinal validation of PET-based staging of regional amyloid accumulation, which may help improving early detection and in-vivo stratification of pathologic disease progression in AD.
dc.identifier.doi10.1002/hbm.25121
dc.identifier.essn1097-0193
dc.identifier.pmcPMC7502828
dc.identifier.pmid32648624
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7502828/pdf
dc.identifier.unpaywallURLhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/hbm.25121
dc.identifier.urihttp://hdl.handle.net/10668/15915
dc.issue.number15
dc.journal.titleHuman brain mapping
dc.journal.titleabbreviationHum Brain Mapp
dc.language.isoen
dc.organizationInstituto de Biomedicina de Sevilla-IBIS
dc.organizationHospital Universitario Virgen del Rocío
dc.page.number4219-4231
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectAlzheimer's disease
dc.subjectamyloid-PET
dc.subjectin-vivo amyloid staging
dc.subjectlongitudinal progression
dc.subject.meshAged
dc.subject.meshAged, 80 and over
dc.subject.meshAlzheimer Disease
dc.subject.meshAmyloid beta-Peptides
dc.subject.meshAniline Compounds
dc.subject.meshBiomarkers
dc.subject.meshCerebral Cortex
dc.subject.meshCognitive Dysfunction
dc.subject.meshCross-Sectional Studies
dc.subject.meshDisease Progression
dc.subject.meshEthylene Glycols
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshLongitudinal Studies
dc.subject.meshMale
dc.subject.meshMiddle Aged
dc.subject.meshNeuroimaging
dc.subject.meshPositron-Emission Tomography
dc.subject.meshReproducibility of Results
dc.titleLongitudinal validity of PET-based staging of regional amyloid deposition.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number41
dspace.entity.typePublication

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