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Centiloid recommendations for clinical context-of-use from the AMYPAD consortium
Lyduine E Collij1,2,3, Ariane Bollack4,5, Renaud La Joie6
1Department of Radiology & Nuclear Medicine, Amsterdam UMC, Vrije Universiteit, Amsterdam, The Netherlands.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|November 20, 2024
Summary
The Centiloid (CL) scale accurately measures amyloid-beta (Aβ) pathology in Alzheimer's disease (AD). CL values below 10 exclude Aβ, while above 30 indicate pathology, aiding diagnosis and treatment.
Area of Science:
- Neurology
- Nuclear Medicine
- Biomarker Research
Background:
- Alzheimer's disease (AD) diagnosis relies on detecting amyloid-beta (Aβ) pathology.
- Accurate Aβ quantification is crucial for clinical trials and patient management.
- The Centiloid (CL) scale offers a standardized, tracer-independent method for amyloid-PET quantification.
Purpose of the Study:
- To integrate existing literature and consortium data to establish clinical recommendations for the Centiloid (CL) scale.
- To define the clinical context-of-use for CL scale in Alzheimer's disease (AD) diagnosis and management.
- To highlight the utility of CL quantification in assessing Aβ pathology and guiding therapeutic decisions.
Main Methods:
- Review and integration of existing literature on Centiloid (CL) scale performance.
- Analysis of recent data from the AMYPAD consortium.
- Comparison of CL quantification with histopathology, visual reads, and cerebrospinal fluid biomarkers.
Main Results:
- Centiloid (CL) quantification robustly reflects the amount of Aβ pathology.
- CL values < 10 reliably exclude Aβ negativity, and CL values > 30 indicate Aβ positivity.
- Intermediate CL values (10-30) suggest an increased risk of disease progression.
Conclusions:
- Centiloid (CL) quantification is a valuable adjunct to visual assessment of amyloid-PET scans.
- CL quantification aids in determining eligibility for anti-amyloid therapies by assessing amyloid clearance.
- CL scale supports clinical trial design, treatment management, and identification of early Aβ pathology.

