• This record comes from PubMed

Defining a Centiloid scale threshold predicting long-term progression to dementia in patients attending the memory clinic: an [18F] flutemetamol amyloid PET study

. 2021 Jan ; 48 (1) : 302-310. [epub] 20200629

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

Links

PubMed 32601802
PubMed Central PMC7835306
DOI 10.1007/s00259-020-04942-4
PII: 10.1007/s00259-020-04942-4
Knihovny.cz E-resources

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.

See more in PubMed

Klunk WE, et al. Imaging brain amyloid in Alzheimer’s disease with Pittsburgh Compound-B. Ann Neurol. 2004;55(3):306–319. doi: 10.1002/ana.20009. PubMed DOI

Mintun MA, et al. [11C]PIB in a nondemented population: potential antecedent marker of Alzheimer disease. Neurology. 2006;67(3):446–452. doi: 10.1212/01.wnl.0000228230.26044.a4. PubMed DOI

Lim YY, et al. Abeta and cognitive change: examining the preclinical and prodromal stages of Alzheimer’s disease. Alzheimers Dement. 2014;10(6):743–751. doi: 10.1016/j.jalz.2013.11.005. PubMed DOI

Donohue MC, et al. Association between elevated brain amyloid and subsequent cognitive decline among cognitively normal persons. JAMA. 2017;317(22):2305–2316. doi: 10.1001/jama.2017.6669. PubMed DOI PMC

Wolk DA, et al. Use of flutemetamol F 18-labeled positron emission tomography and other biomarkers to assess risk of clinical progression in patients with amnestic mild cognitive impairment. JAMA Neurol. 2018;75(9):1114–1123. doi: 10.1001/jamaneurol.2018.0894. PubMed DOI PMC

Hanseeuw BJ, et al. PET staging of amyloidosis using striatum. Alzheimers Dement. 2018;14(10):1281–92. PubMed PMC

Ma Y, et al. Predictive accuracy of amyloid imaging for progression from mild cognitive impairment to Alzheimer disease with different lengths of follow-up: a systematic review. Medicine (Baltimore) 2014;93(27):e150. doi: 10.1097/MD.0000000000000150. PubMed DOI PMC

Harn NR, et al. Augmenting amyloid PET interpretations with quantitative information improves consistency of early amyloid detection. Clin Nucl Med. 2017;42(8):577–581. doi: 10.1097/RLU.0000000000001693. PubMed DOI PMC

Klunk WE, et al. The Centiloid Project: standardizing quantitative amyloid plaque estimation by PET. Alzheimers Dement. 2015;11(1):1–15. doi: 10.1016/j.jalz.2014.07.003. PubMed DOI PMC

Ivanoiu A, et al. Classification of non-demented patients attending a memory clinic using the new diagnostic criteria for Alzheimer’s disease with disease-related biomarkers. J Alzheimers Dis. 2015;43(3):835–847. doi: 10.3233/JAD-140651. PubMed DOI

Hanseeuw B, et al. Patients with amyloid-negative mild cognitive impairment have cortical hypometabolism but the hippocampus is preserved. J Alzheimers Dis. 2016;53(2):651–660. doi: 10.3233/JAD-160204. PubMed DOI

Lhommel R, et al. In vivo amyloid plaques quantification using F18-flutemetamol in 30 healthy elderly controls and 62 MCI patients: SUVr comparison between PMOD 3.2 and PNEURO 3.5 analysis. J Nucl Med. 2016;57(supplement 2):515.

Gerard T, et al. Is there an interest to perform regional Amyloid quantification in comparison to overall cortical index in MCI patients? J Nucl Med. 2016;57(supplement 2):513.

Lhommel R, et al. How to convert F18-Flutemetamol centiloid SUVr to Centiloid scale values ? A simple-method using PNEURO 3.9 software. Eur J Nucl Med Mol Imaging. 2019;46(Suppl 1):S1–S952. doi: 10.1007/s00259-019-04486-2. DOI

Lhommel R, et al. In vivo Amyloid Plaques quantification using F18- Flutemetamol PET/CT in 31 healthy controls and 130 MCI: SUVr methods’s comparison and transposition in the centiloid scale. Eur J Nucl Med Mol Imaging. 2019;46(Suppl 1):S1–S952. doi: 10.1007/s00259-019-04486-2. DOI

Battle MR, Pillay LC, Lowe VJ, et al. Centiloid scaling for quantification of brain amyloid with [(18)F]flutemetamol using multiple processing methods. EJNMMI Res. 2018;8(1):107. doi: 10.1186/s13550-018-0456-7. PubMed DOI PMC

Thurfjell L, et al. Automated quantification of 18F-flutemetamol PET activity for categorizing scans as negative or positive for brain amyloid: concordance with visual image reads. J Nucl Med. 2014;55(10):1623–1628. doi: 10.2967/jnumed.114.142109. PubMed DOI

La Joie R, et al. Multisite study of the relationships between antemortem [(11)C]PIB-PET Centiloid values and postmortem measures of Alzheimer’s disease neuropathology. Alzheimers Dement. 2019;15(2):205–216. doi: 10.1016/j.jalz.2018.09.001. PubMed DOI PMC

Frisoni GB, et al. Strategic roadmap for an early diagnosis of Alzheimer’s disease based on biomarkers. Lancet Neurol. 2017;16(8):661–676. doi: 10.1016/S1474-4422(17)30159-X. PubMed DOI

Chiotis K, et al. Clinical validity of increased cortical uptake of amyloid ligands on PET as a biomarker for Alzheimer’s disease in the context of a structured 5-phase development framework. Neurobiol Aging. 2017;52:214–227. doi: 10.1016/j.neurobiolaging.2016.07.012. PubMed DOI

Bullich S, et al. Optimized classification of (18)F-Florbetaben PET scans as positive and negative using an SUVR quantitative approach and comparison to visual assessment. Neuroimage Clin. 2017;15:325–332. doi: 10.1016/j.nicl.2017.04.025. PubMed DOI PMC

Schreiber S, et al. Comparison of visual and quantitative florbetapir F 18 positron emission tomography analysis in predicting mild cognitive impairment outcomes. JAMA Neurol. 2015;72(10):1183–1190. doi: 10.1001/jamaneurol.2015.1633. PubMed DOI

Villemagne VL, et al. Amyloid beta deposition, neurodegeneration, and cognitive decline in sporadic Alzheimer’s disease: a prospective cohort study. Lancet Neurol. 2013;12(4):357–367. doi: 10.1016/S1474-4422(13)70044-9. PubMed DOI

Hanseeuw BJ, et al. Association of amyloid and tau with cognition in preclinical Alzheimer disease: a longitudinal study. JAMA Neurol. 2019;76(8):915–24. PubMed PMC

Jack CR, Jr, et al. Defining imaging biomarker cut points for brain aging and Alzheimer’s disease. Alzheimers Dement. 2017;13(3):205–216. doi: 10.1016/j.jalz.2016.08.005. PubMed DOI PMC

Navitsky M, et al. Standardization of amyloid quantitation with florbetapir standardized uptake value ratios to the Centiloid scale. Alzheimers Dement. 2018;14(12):1565–1571. doi: 10.1016/j.jalz.2018.06.1353. PubMed DOI

Amadoru S, et al. Comparison of amyloid PET measured in Centiloid units with neuropathological findings in Alzheimer’s disease. Alzheimers Res Ther. 2020;12(1):22. doi: 10.1186/s13195-020-00587-5. PubMed DOI PMC

Salvado G, et al. Centiloid cut-off values for optimal agreement between PET and CSF core AD biomarkers. Alzheimers Res Ther. 2019;11(1):27. doi: 10.1186/s13195-019-0478-z. PubMed DOI PMC

Dore V, et al. Comparison of (18)F-florbetaben quantification results using the standard Centiloid, MR-based, and MR-less CapAIBL((R)) approaches: validation against histopathology. Alzheimers Dement. 2019;15(6):807–816. doi: 10.1016/j.jalz.2019.02.005. PubMed DOI

Yamane T, et al. Inter-rater variability of visual interpretation and comparison with quantitative evaluation of (11)C-PiB PET amyloid images of the Japanese Alzheimer’s Disease Neuroimaging Initiative (J-ADNI) multicenter study. Eur J Nucl Med Mol Imaging. 2017;44(5):850–857. doi: 10.1007/s00259-016-3591-2. PubMed DOI

Collij LE, et al. Assessing amyloid pathology in cognitively normal subjects using (18)F-flutemetamol PET: comparing visual reads and quantitative methods. J Nucl Med. 2019;60(4):541–547. doi: 10.2967/jnumed.118.211532. PubMed DOI PMC

Pontecorvo MJ, et al. Quantitation of PET signal as an adjunct to visual interpretation of florbetapir imaging. Eur J Nucl Med Mol Imaging. 2017;44(5):825–837. doi: 10.1007/s00259-016-3601-4. PubMed DOI

Fantoni E, et al. The spatial-temporal ordering of amyloid pathology and opportunities for PET imaging. J Nucl Med. 2020;61(2):166–171. doi: 10.2967/jnumed.119.235879. PubMed DOI

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...