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KMID : 1148920210550020071
Nuclear Medicine and Molecular Imaging
2021 Volume.55 No. 2 p.71 ~ p.78
A 4-Year Follow-Up of Subjects with Visually Equivocal Amyloid Positron Emission Tomography Findings from the Alzheimer¡¯s Disease Neuroimaging Initiative Cohort
Oh Min-Young

Seo Min-Jung
Oh Sun-Young
Kim Hee-Young
Choi Byung-Wook
Oh Jung-Su S.
Kim Jae-Seung
Abstract
Background: To date, the clinical significance of visually equivocal amyloid positron emission tomography (PET) has not been well established.

Objective: We studied the clinical significance of equivocal amyloid PET images from the Alzheimer¡¯s Disease Neuroimaging Initiative (ADNI).

Methods: Subjects with F-18 florbetapir PET scans at baseline who were followed up for 4 years were selected. Clinical characteristics, imaging biomarkers, cognitive function, and rate of conversion to AD were compared in subjects with visually equivocal findings.

Results: Of 249 subjects who completed the follow-up, 153 (61.4%), 20 (8.0%), and 129 (30.5%) were F-18 florbetapir-negative, -equivocal, and -positive, respectively. The mean standardized uptake value ratios (SUVR) of F-18 florbetapir PET were 0.75 ¡¾ 0.04, 0.85 ¡¾ 0.10, and 1.00 ¡¾ 0.09 for each group (p <0.001 between groups), and 15.0%, 70.0%, and 98.7% of patients were quantitatively above the positive threshold. The change in the SUVR of F-18 florbetapir PET was higher in the equivocal (6.09 ¡¾ 3.61%, p <0.001) and positive (3.13 ¡¾ 4.38%, p <0.001) groups than the negative group (0.88 ¡¾ 4.28%). Among the subjects with normal or subjective memory impairment and mild cognitive impairment, 5.3% with negative amyloid PET and 37.5% with positive amyloid PET converted to AD over the 4-year period. None of the equivocal amyloid PET subjects converted to AD during this period.

Conclusion: Approximately 8% of subjects from the ADNI cohort showed visually equivocal amyloid PET scans with intermediate load and rapid accumulation of amyloid, but did not convert to AD during the 4-year follow-up.
KEYWORD
Amyloid, Positron-emission tomography, Alzheimer disease, Cognitive dysfunction
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