Impact of shortening time on diagnosis of 18F-florbetaben PET.

IF 3.1 3区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Phuong T H Trinh, Doo-Young Kim, Kang-Ho Choi, Jahae Kim
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引用次数: 0

Abstract

Background: 18F-Florbetaben amyloid positron emission tomography (PET) scan is crucial for diagnosing Alzheimer's disease, typically involving a 20 min acquisition. However, maintaining such prolonged scans can be challenging in some cases. This study explores the diagnostic impact and feasibility of reducing scan durations by comparing quantitative measures between shortened and standard scans. Additionally, we identified the optimal Centiloid threshold to distinguish between positive and negative amyloid results.

Results: We analyzed 307 PET scans from our memory clinic, each followed up for a minimum of two years. The scans, conducted 90 to 110 min after approximately 300 MBq of 18F-Florbetaben injection, were categorized into four sets of 5 min durations: 5, 10, 15, and 20 min. Nuclear medicine physicians validated and rated each scan as either amyloid-positive or negative. For quantitative assessments, we employed the standardized uptake value ratio (SUVR) and Centiloid scales, comparing total SUVR and Centiloid values across five subregions (global, frontal, posterior cingulate-precuneus, lateral temporal, and parietal) using Bland-Altman analysis. Receiver operator characteristic (ROC) curves were utilized to develop optimal Centiloid thresholds. Comparing the images at 5, 10, 15, and 20 min images, SUVR and Centiloid values gradually increased with prolonged scan times. The mean SUVR difference between 5 and 20 min was 0.03 for the amyloid-positive and 0.01 for the amyloid-negative groups; Centiloid differences were 4.60 and 2.38, respectively. Additionally, no significant variation was observed in total SUVR and Centiloid values among the durations across all subregions in positive and negative groups (all p > 0.1). ROC analysis indicated that a Centiloid threshold of 21.86 at 5 min provided optimal agreement with visual assessments (AUC = 0.985, sensitivity = 0.950, specificity = 0.972), especially using the global area.

Conclusions: This study demonstrated that 5 min image scans with an optimal threshold of CL = 21.86 exhibited minimal bias in SUVR and Centiloid values compared to longer scans (10, 15, and 20 min). Our findings suggest that shorter scan times are a viable and effective option for brain amyloid PET imaging in clinical settings.

缩短时间对 18F - 氟贝特宾 PET 诊断的影响。
背景:18F-氟贝特宾淀粉样蛋白正电子发射断层扫描(PET)是诊断阿尔茨海默病的关键,通常需要 20 分钟的采集时间。然而,在某些情况下,维持如此长时间的扫描具有挑战性。本研究通过比较缩短扫描时间和标准扫描时间的定量指标,探讨了缩短扫描时间对诊断的影响和可行性。此外,我们还确定了区分淀粉样蛋白阳性和阴性结果的最佳Centiloid阈值:我们分析了来自记忆诊所的 307 次 PET 扫描,每次扫描至少随访两年。扫描在注射约 300 MBq 18F-Florbetaben 后 90 至 110 分钟进行,扫描持续时间分为四组,每组 5 分钟:5、10、15 和 20 分钟。核医学医生对每次扫描进行验证,并将其评定为淀粉样蛋白阳性或阴性。在定量评估方面,我们采用了标准化摄取值比(SUVR)和Centiloid量表,并使用Bland-Altman分析法比较了五个亚区域(总体、额叶、后扣带回-楔形、颞外侧和顶叶)的总SUVR和Centiloid值。利用接收操作者特征曲线(ROC)来制定最佳的Centiloid阈值。比较 5、10、15 和 20 分钟的图像,SUVR 和 Centiloid 值随着扫描时间的延长而逐渐增加。淀粉样蛋白阳性组和淀粉样蛋白阴性组 5 至 20 分钟的平均 SUVR 差值分别为 0.03 和 0.01;Centiloid 差值分别为 4.60 和 2.38。此外,在阳性组和阴性组的所有亚区域中,总 SUVR 和 Centiloid 值在不同持续时间内无明显差异(均 p > 0.1)。ROC分析表明,5分钟时21.86的Centiloid阈值与目测评估具有最佳一致性(AUC = 0.985,灵敏度 = 0.950,特异性 = 0.972),尤其是使用全球区域:本研究表明,与较长的扫描时间(10、15 和 20 分钟)相比,5 分钟图像扫描的最佳阈值为 CL = 21.86,其 SUVR 和 Centiloid 值的偏差最小。我们的研究结果表明,在临床环境中,较短的扫描时间是脑淀粉样蛋白 PET 成像可行且有效的选择。
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来源期刊
EJNMMI Research
EJNMMI Research RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING&nb-
CiteScore
5.90
自引率
3.10%
发文量
72
审稿时长
13 weeks
期刊介绍: EJNMMI Research publishes new basic, translational and clinical research in the field of nuclear medicine and molecular imaging. Regular features include original research articles, rapid communication of preliminary data on innovative research, interesting case reports, editorials, and letters to the editor. Educational articles on basic sciences, fundamental aspects and controversy related to pre-clinical and clinical research or ethical aspects of research are also welcome. Timely reviews provide updates on current applications, issues in imaging research and translational aspects of nuclear medicine and molecular imaging technologies. The main emphasis is placed on the development of targeted imaging with radiopharmaceuticals within the broader context of molecular probes to enhance understanding and characterisation of the complex biological processes underlying disease and to develop, test and guide new treatment modalities, including radionuclide therapy.
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