Defining a Centiloid scale threshold predicting long-term progression to dementia in patients attending the memory clinic: an [18F] flutemetamol amyloid PET study
Language English Country Germany Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
Grant support
SPD28094292
Fonds De La Recherche Scientifique - FNRS
PubMed
32601802
PubMed Central
PMC7835306
DOI
10.1007/s00259-020-04942-4
PII: 10.1007/s00259-020-04942-4
Knihovny.cz E-resources
- Keywords
- AD dementia, Amyloid PET, Centiloids, Diagnostic accuracy, Mild cognitive impairment,
- MeSH
- Alzheimer Disease * MeSH
- Amyloid beta-Peptides metabolism MeSH
- Aniline Compounds MeSH
- Benzothiazoles MeSH
- Dementia * diagnostic imaging MeSH
- Cognitive Dysfunction * diagnostic imaging MeSH
- Middle Aged MeSH
- Humans MeSH
- Brain metabolism MeSH
- Positron-Emission Tomography MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Amyloid beta-Peptides MeSH
- Aniline Compounds MeSH
- Benzothiazoles MeSH
- flutemetamol MeSH Browser
PURPOSE: To evaluate cerebral amyloid-β(Aβ) pathology in older adults with cognitive complaints, visual assessment of PET images is approved as the routine method for image interpretation. In research studies however, Aβ-PET semi-quantitative measures are associated with greater risk of progression to dementia; but until recently, these measures lacked standardization. Therefore, the Centiloid scale, providing standardized Aβ-PET semi-quantitation, was recently validated. We aimed to determine the predictive values of visual assessments and Centiloids in non-demented patients, using long-term progression to dementia as our standard of truth. METHODS: One hundred sixty non-demented participants (age, 54-86) were enrolled in a monocentric [18F] flutemetamol Aβ-PET study. Flutemetamol images were interpreted visually following the manufacturers recommendations. SUVr values were converted to the Centiloid scale using the GAAIN guidelines. Ninety-eight persons were followed until dementia diagnosis or were clinically stable for a median of 6 years (min = 4.0; max = 8.0). Twenty-five patients with short follow-up (median = 2.0 years; min = 0.8; max = 3.9) and 37 patients with no follow-up were excluded. We computed ROC curves predicting subsequent dementia using baseline PET data and calculated negative (NPV) and positive (PPV) predictive values. RESULTS: In the 98 participants with long follow-up, Centiloid = 26 provided the highest overall predictive value = 87% (NPV = 85%, PPV = 88%). Visual assessment corresponded to Centiloid = 40, which predicted dementia with an overall predictive value = 86% (NPV = 81%, PPV = 92%). Inclusion of the 25 patients who only had a 2-year follow-up decreased the PPV = 67% (NPV = 88%), reflecting the many positive cases that did not progress to dementia after short follow-ups. CONCLUSION: A Centiloid threshold = 26 optimally predicts progression to dementia 6 years after PET. Visual assessment provides similar predictive value, with higher specificity and lower sensitivity. TRIAL REGISTRATION: Eudra-CT number: 2011-001756-12.
Department of Psychology Wayne State University Detroit MI USA
Genetics Department Saint Luc University Hospital Brussels Belgium
Institute of Experimental and Clinical Research Université Catholique de Louvain Brussels Belgium
Institute of Neuroscience Université Catholique de Louvain Brussels Belgium
Neurology Department Saint Luc University Hospital Av Hippocrate 10 1200 Brussels Belgium
Nuclear Medicine Department Saint Luc University Hospital Brussels Belgium
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