Visual assessments of 11C-Pittsburgh compound-B PET vs. 18F-flutemetamol PET across the age spectrum

Author:

Zeydan Burcu12,Johnson Derek R.1,Schwarz Christopher G.1,Przybelski Scott A.3,Lesnick Timothy G.3,Senjem Matthew L.14,Kantarci Orhun H.2,Min Paul H.1,Kemp Bradley J.1,Jack Clifford R.1,Kantarci Kejal1,Lowe Val J.1

Affiliation:

1. Department of Radiology

2. Department of Neurology

3. Department of Quantitative Health Sciences

4. Department of Information Technology, Mayo Clinic, Rochester, Minnesota, USA

Abstract

Objective Visual assessments of amyloid-β PET, used for Alzheimer’s disease (AD) diagnosis and treatment evaluation, require a careful approach when different PET ligands are utilized. Because the gray matter (GM) and white matter (WM) ligand bindings vary with age, the objective was to investigate the agreement between visual reads of 11C- and 18F-PET scans. Methods Cognitively unimpaired (CU) younger adults (N =30; 39.5±6.0years), CU older adults (N =30; 68.6±5.9years), and adults with AD (N =22; 67.0±8.5years) underwent brain MRI, 11C-Pittsburgh compound-B (PiB)-PET, and 18F-flutemetamol-PET. Amyloid-β deposition was assessed visually by two nuclear medicine specialists on 11C-PiB-PET and 18F-flutemetamol-PET, and quantitatively by PET centiloids. Results Seventy-two 11C-PiB-PET and 18F-flutemetamol-PET visual reads were concordant. However, 1 18F-flutemetamol-PET and 9 11C-PiB-PET were discordant with quantitative values. In four additional cases, while 11C-PiB-PET and 18F-flutemetamol-PET visual reads were concordant, both were discordant with quantitative values. Disagreements in CU younger adults were only with 11C-PiB-PET visual reads. The remaining disagreements were with CU older adults. Conclusion Age, GM/WM binding, amyloid-β load, and disease severity may affect visual assessments of PET ligands. Increase in WM binding with age causes a loss of contrast between GM and WM on 11C-PiB-PET, particularly in CU younger adults, leading to false positivity. In CU older adults, increased WM signal may bleed more into cortical regions, hiding subtle cortical uptake, especially with 18F-flutemetamol, whereas 11C-PiB can detect true regional positivity. Understanding these differences will improve patient care and treatment evaluation in clinic and clinical trials.

Funder

National Institutes of Health

Publisher

Ovid Technologies (Wolters Kluwer Health)

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