Avid Radiopharmaceuticals, Inc., Philadelphia, PA 19104, USA.
J Nucl Med. 2012 Mar;53(3):378-84. doi: 10.2967/jnumed.111.090340. Epub 2012 Feb 13.
The objectives of this study were to examine the effective dose range and the test-retest reliability of florbetapir F 18 using, first, visual assessment by independent raters masked to clinical information and, second, semiautomated quantitative measures of cortical target area to cerebellum standardized uptake value ratios (SUVr) as primary outcome measures. Visual ratings of PET image quality and tracer retention or β-amyloid (Aβ) binding expressed as SUVrs were compared after intravenous administration of either 111 MBq (3 mCi) or 370 MBq (10 mCi) of florbetapir F 18 in patients with Alzheimer's disease (AD) (n = 9) and younger healthy controls (YHCs) (n = 11). In a separate set of subjects (AD, n = 10; YHCs, n = 10), test-retest reliability was evaluated by comparing intrasubject visual read ratings and SUVrs for 2 PET images acquired within 4 wk of each other.
There were no meaningful differences between the 111-MBq (3-mCi) and 370-MBq (10-mCi) dose in the visual rating or SUVr. The difference in the visual quality across 111 and 370 MBq showed a trend toward lower image quality, but no statistical significance was achieved (t test; t(1) = -1.617, P = 0.12) in this relatively small sample of subjects. At both dose levels, visual ratings of amyloid burden identified 100% of AD subjects as Aβ-positive and 100% of YHCs as Aβ-negative. Mean intrasubject test-retest variability for cortical average SUVrs with the cerebellum as a reference over the 50- to 70-min period was 2.4% ± 1.41% for AD subjects and 1.5% ± 0.84% for controls. The overall SUVr test-retest correlation coefficient was 0.99. The overall κ-statistic for test-retest agreement for Aβ classification of the masked reads was 0.89 (95% confidence interval, 0.69-1.0).
Florbetapir F 18 appears to have a wide effective dose range and a high test-retest reliability for both quantitative (SUVr) values and visual assessment of the ligand. These imaging performance properties provide important technical information on the use of florbetapir F 18 and PET to detect cerebral amyloid aggregates.
本研究的目的是使用独立的、对临床信息进行盲法评估的阅片者,首先通过视觉评估,其次通过皮质靶区与小脑标准化摄取值比值(SUVr)的半自动定量测量,来检测氟代脱氧葡萄糖 F 18 的有效剂量范围和测试-重测信度。对静脉注射氟代脱氧葡萄糖 F 18(111MBq[3mCi]或 370MBq[10mCi])后,阿尔茨海默病(AD)患者(n=9)和年轻健康对照者(YHCs)(n=11)的 PET 图像质量和示踪剂保留或β-淀粉样蛋白(Aβ)结合的视觉评分以及 SUVr 进行了比较。在另一组受试者(AD,n=10;YHCs,n=10)中,通过比较在 4 周内采集的 2 次 PET 图像的受试者内视觉读片评分和 SUVr,评估了测试-重测信度。
在视觉评分或 SUVr 方面,111-MBq(3mCi)和 370-MBq(10mCi)剂量之间没有显著差异。在较小的受试者样本中,两种剂量水平的视觉质量差异均显示出图像质量较低的趋势,但未达到统计学意义(t 检验;t(1)=-1.617,P=0.12)。在这两种剂量水平下,基于皮质的平均 SUVr 与小脑作为参考,对 50 至 70 分钟期间的皮质平均 SUVr 进行的视觉评分可准确识别 100%的 AD 患者为 Aβ阳性,100%的 YHCs 为 Aβ阴性。AD 患者皮质平均 SUVr 的个体内测试-重测变异性为 2.4%±1.41%,对照组为 1.5%±0.84%。总体 SUVr 测试-重测相关系数为 0.99。基于对阅片者进行盲法分析的 Aβ分类的总体κ统计量为 0.89(95%置信区间,0.69-1.0)。
氟代脱氧葡萄糖 F 18 似乎具有广泛的有效剂量范围和高测试-重测信度,无论是定量(SUVr)值还是配体的视觉评估。这些成像性能特性为使用氟代脱氧葡萄糖 F 18 和 PET 检测脑内淀粉样蛋白聚集物提供了重要的技术信息。