Enhanced diagnostic and prognostic assessment of cardiac amyloidosis using combined 11C-PiB PET/CT and 99mTc-DPD scintigraphy

IF 7.6 1区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING European Journal of Nuclear Medicine and Molecular Imaging Pub Date : 2025-02-28 DOI:10.1007/s00259-025-07157-7
Zhihui Hong, Clemens P. Spielvogel, Song Xue, Raffaella Calabretta, Zewen Jiang, Josef Yu, Kilian Kluge, David Haberl, Christian Nitsche, Stefan Grünert, Marcus Hacker, Xiang Li
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Abstract

Background

Cardiac amyloidosis (CA) is a severe condition characterized by amyloid fibril deposition in the myocardium, leading to restrictive cardiomyopathy and heart failure. Differentiating between amyloidosis subtypes is crucial due to distinct treatment strategies. The individual conventional diagnostic methods lack the accuracy needed for effective subtype identification. This study aimed to evaluate the efficacy of combining 11C-PiB PET/CT and 99mTc-DPD scintigraphy in detecting CA and distinguishing between its main subtypes, light chain (AL) and transthyretin (ATTR) amyloidosis while assessing the association of imaging findings with patient prognosis.

Methods

We retrospectively evaluated the diagnostic efficacy of combining 11C-PiB PET/CT and 99mTc-DPD scintigraphy in a cohort of 50 patients with clinical suspicion of CA. Semi-quantitative imaging markers were extracted from the images. Diagnostic performance was calculated against biopsy results or genetic testing. Both machine learning models and a rationale-based model were developed to detect CA and classify subtypes. Survival prediction over five years was assessed using a random survival forest model. Prognostic value was assessed using Kaplan-Meier estimators and Cox proportional hazards models.

Results

The combined imaging approach significantly improved diagnostic accuracy, with 11C-PiB PET and 99mTc-DPD scintigraphy showing complementary strengths in detecting AL and ATTR, respectively. The machine learning model achieved an AUC of 0.94 (95% CI 0.93–0.95) for CA subtype differentiation, while the rationale-based model demonstrated strong diagnostic ability with AUCs of 0.95 (95% CI 0.88-1.00) for ATTR and 0.88 (95% CI 0.770–0.961) for AL. Survival prediction models identified key prognostic markers, with significant stratification of overall mortality based on predicted survival (p value = 0.006; adj HR 2.43 [95% CI 1.03–5.71]).

Conclusion

The integration of 11C-PiB PET/CT and 99mTc-DPD scintigraphy, supported by both machine learning and rationale-based models, enhances the diagnostic accuracy and prognostic assessment of cardiac amyloidosis, with significant implications for clinical practice.

Graphical abstracts

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11C-PiB PET/CT和99mTc-DPD联合显像增强心脏淀粉样变性的诊断和预后评估
背景:心脏淀粉样变性(CA)是一种严重的疾病,其特征是淀粉样纤维沉积在心肌中,导致限制性心肌病和心力衰竭。由于不同的治疗策略,区分淀粉样变亚型至关重要。单个常规诊断方法缺乏有效亚型识别所需的准确性。本研究旨在评价11C-PiB PET/CT联合99mTc-DPD显像检测CA及区分其主要亚型轻链(AL)和转甲状腺素(ATTR)淀粉样变的疗效,同时评估影像学表现与患者预后的关系。方法回顾性评价11C-PiB PET/CT联合99mTc-DPD对50例临床怀疑CA的患者的诊断效果,提取半定量影像学标志物。诊断性能是根据活检结果或基因检测来计算的。开发了机器学习模型和基于原理的模型来检测CA并对亚型进行分类。使用随机生存森林模型评估五年以上的生存预测。使用Kaplan-Meier估计器和Cox比例风险模型评估预后价值。结果联合显像方法显著提高了诊断准确性,11C-PiB PET和99mTc-DPD显像分别在检测AL和ATTR方面具有互补优势。机器学习模型对CA亚型分化的AUC为0.94 (95% CI 0.93-0.95),而基于原理的模型显示出较强的诊断能力,对ATTR的AUC为0.95 (95% CI 0.88-1.00),对AL的AUC为0.88 (95% CI 0.70 - 0.961)。生存预测模型确定了关键的预后标记,基于预测生存的总死亡率有显著分层(p值= 0.006;[95% CI 1.03-5.71])。结论11C-PiB PET/CT和99mTc-DPD显像的整合,在机器学习和基于理性的模型的支持下,提高了心脏淀粉样变性的诊断准确性和预后评估,对临床实践具有重要意义。图形抽象
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来源期刊
CiteScore
15.60
自引率
9.90%
发文量
392
审稿时长
3 months
期刊介绍: The European Journal of Nuclear Medicine and Molecular Imaging serves as a platform for the exchange of clinical and scientific information within nuclear medicine and related professions. It welcomes international submissions from professionals involved in the functional, metabolic, and molecular investigation of diseases. The journal's coverage spans physics, dosimetry, radiation biology, radiochemistry, and pharmacy, providing high-quality peer review by experts in the field. Known for highly cited and downloaded articles, it ensures global visibility for research work and is part of the EJNMMI journal family.
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