Liu Alexander, Munemo Lionel T, Martins Nuno, Kouranos Vasileios, Wells Athol U, Sharma Rakesh K, Wechalekar Kshama
Royal Brompton Hospital, London, United Kingdom.
Royal Brompton Hospital, London, United Kingdom
J Nucl Med Technol. 2025 Jun 4;53(2):123-129. doi: 10.2967/jnmt.124.268142.
F-FDG PET with CT is an important advanced imaging modality used to assess patients with suspected or known cardiac sarcoidosis (CS). F-FDG PET is indicated for CS work-up in patients with extra-CS and abnormal screening results for cardiac involvement, patients under 60 y old presenting with unexplained high-grade atrioventricular heart block, and patients with suspected CS and idiopathic ventricular arrhythmias. In patients with established CS, serial F-FDG PET can be used to assess response to immunosuppressive therapy and long-term surveillance for reactivation of myocardial inflammation in patients with low-grade or quiescent disease. Patient preparation before F-FDG PET scanning is key in ensuring adequate suppression of physiologic myocardial F-FDG uptake, to maximize the power of the test to detect pathology. Inadequate dietary preparation can cause diffuse or focal-on-diffuse F-FDG uptake in the absence of active inflammation. It is important to assess resting myocardial perfusion, typically with Rb cardiac PET. Several different patterns of abnormalities have been reported in patients with CS, including normal myocardial perfusion with focal or patchy F-FDG uptake suggesting myocardial inflammation without scarring; the presence of a myocardial perfusion defect with abnormal F-FDG uptake suggesting myocardial scarring with inflammation; and the presence of a myocardial perfusion defect without F-FDG uptake indicating myocardial scarring without inflammation. Prognostically, the presence of myocardial perfusion defects and abnormal F-FDG uptake has been shown to be an independent predictor of death or ventricular arrythmias. A high myocardial SUV in the left and right ventricles has been shown to be an independent predictor of adverse clinical outcomes. Although the diagnostic performance of F-FDG PET has been studied, the reference standard for CS tended to rely on clinical criteria, which may be less sensitive than F-FDG PET at detecting CS. Therefore, the diagnosis of CS should rely on a multidisciplinary team approach involving multimodality advanced imaging, including echocardiography, cardiovascular MR, and F-FDG PET.
氟代脱氧葡萄糖正电子发射断层显像(F-FDG PET)联合计算机断层扫描(CT)是用于评估疑似或已知心脏结节病(CS)患者的重要先进成像方式。F-FDG PET适用于心脏外结节病且心脏受累筛查结果异常的患者、60岁以下出现不明原因高度房室传导阻滞的患者以及疑似CS和特发性室性心律失常的患者进行CS检查。对于已确诊CS的患者,系列F-FDG PET可用于评估免疫抑制治疗的反应以及对病情较轻或静止期患者心肌炎症再激活的长期监测。F-FDG PET扫描前的患者准备是确保充分抑制生理性心肌F-FDG摄取的关键,以最大限度地提高检测病变的检查效能。饮食准备不足可在无活动性炎症的情况下导致弥漫性或局灶性加弥漫性F-FDG摄取。评估静息心肌灌注很重要,通常采用铷心脏PET。CS患者已报告有几种不同的异常模式,包括心肌灌注正常但有局灶性或斑片状F-FDG摄取,提示心肌炎症而无瘢痕形成;存在心肌灌注缺损且F-FDG摄取异常,提示心肌瘢痕形成伴有炎症;以及存在心肌灌注缺损但无F-FDG摄取,提示心肌瘢痕形成而无炎症。在预后方面,心肌灌注缺损和F-FDG摄取异常已被证明是死亡或室性心律失常的独立预测因素。左心室和右心室心肌标准化摄取值(SUV)高已被证明是不良临床结局的独立预测因素。尽管已对F-FDG PET的诊断性能进行了研究,但CS的参考标准往往依赖于临床标准,这在检测CS方面可能不如F-FDG PET敏感。因此,CS的诊断应依靠多学科团队方法,包括多模态先进成像,如超声心动图、心血管磁共振成像和F-FDG PET。