Department of Radiology.
Department of Neurology.
Nucl Med Commun. 2024 Dec 1;45(12):1047-1054. doi: 10.1097/MNM.0000000000001902. Epub 2024 Sep 13.
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 11 C- and 18 F-PET scans.
Cognitively unimpaired (CU) younger adults ( N = 30; 39.5 ± 6.0 years), CU older adults ( N = 30; 68.6 ± 5.9 years), and adults with AD ( N = 22; 67.0 ± 8.5 years) underwent brain MRI, 11 C-Pittsburgh compound-B (PiB)-PET, and 18 F-flutemetamol-PET. Amyloid-β deposition was assessed visually by two nuclear medicine specialists on 11 C-PiB-PET and 18 F-flutemetamol-PET, and quantitatively by PET centiloids.
Seventy-two 11 C-PiB-PET and 18 F-flutemetamol-PET visual reads were concordant. However, 1 18 F-flutemetamol-PET and 9 11 C-PiB-PET were discordant with quantitative values. In four additional cases, while 11 C-PiB-PET and 18 F-flutemetamol-PET visual reads were concordant, they were discordant with quantitative values. Disagreements in CU younger adults were only with 11 C-PiB-PET visual reads. The remaining disagreements were with CU older adults.
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 11 C-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 18 F-flutemetamol, whereas 11 C-PiB can detect true regional positivity. Understanding these differences will improve patient care and treatment evaluation in clinic and clinical trials.
用于阿尔茨海默病(AD)诊断和治疗评估的淀粉样蛋白-β PET 视觉评估,在使用不同的 PET 配体时需要谨慎。由于灰质(GM)和白质(WM)配体结合随年龄而变化,因此本研究旨在探讨 11 C-和 18 F-PET 扫描的视觉读数之间的一致性。
认知正常的年轻成年人(CU 年轻组;N=30;39.5±6.0 岁)、认知正常的老年成年人(CU 老年组;N=30;68.6±5.9 岁)和 AD 成年人(N=22;67.0±8.5 岁)接受脑 MRI、11 C-匹兹堡化合物-B(PiB)-PET 和 18 F-氟噻吨美托胺-PET。由两名核医学专家对 11 C-PiB-PET 和 18 F-氟噻吨美托胺-PET 进行视觉评估,并通过 PET 百分位数进行定量评估。
72 次 11 C-PiB-PET 和 18 F-氟噻吨美托胺-PET 视觉读数一致。然而,1 次 18 F-氟噻吨美托胺-PET 和 9 次 11 C-PiB-PET 视觉读数与定量值不一致。在另外 4 例中,虽然 11 C-PiB-PET 和 18 F-氟噻吨美托胺-PET 视觉读数一致,但与定量值不一致。在 CU 年轻成年人中,只有 11 C-PiB-PET 视觉读数不一致。其余的不一致发生在 CU 老年成年人中。
年龄、GM/WM 结合、淀粉样蛋白-β负荷和疾病严重程度可能会影响 PET 配体的视觉评估。随着年龄的增长,WM 结合的增加会导致 11 C-PiB-PET 中 GM 和 WM 之间的对比度降低,尤其是在 CU 年轻成年人中,从而导致假阳性。在 CU 老年成年人中,WM 信号的增加可能会更多地渗透到皮质区域,掩盖皮质摄取的细微变化,特别是在使用 18 F-氟噻吨美托胺时,而 11 C-PiB 可以检测到真正的区域性阳性。了解这些差异将提高临床和临床试验中患者的护理和治疗评估。