Department of Nuclear Medicine and Molecular Imaging, University Medical Centre Groningen and Amyloidosis Centre of Expertise, Groningen, The Netherlands.
Department of Cardiology, University Medical Centre Groningen and Amyloidosis Centre of Expertise, Groningen, The Netherlands.
Eur J Nucl Med Mol Imaging. 2024 Feb;51(3):681-690. doi: 10.1007/s00259-023-06459-y. Epub 2023 Oct 16.
There is a need for early quantitative markers of potential treatment response in patients with hereditary transthyretin (ATTRv) amyloidosis to guide therapy. This study aims to evaluate changes in cardiac tracer uptake on bone scintigraphy in ATTRv amyloidosis patients on different treatments.
In this retrospective cohort study, outcomes of 20 patients treated with the transthyretin (TTR) gene silencer patisiran were compared to 12 patients treated with a TTR-stabilizer. Changes in NYHA class, cardiac biomarkers in serum, wall thickness, and diastolic parameters on echocardiography and NYHA class during treatment were evaluated.
Median heart/whole-body (H/WB) ratio on bone scintigraphy decreased from 4.84 [4.00 to 5.31] to 4.16 [3.66 to 4.81] (p < .001) in patients treated with patisiran for 29 [15-34] months. No changes in the other follow-up parameters were observed. In patients treated with a TTR-stabilizer for 24 [20 to 30] months, H/WB ratio increased from 4.46 [3.24 to 5.13] to 4.96 [ 3.39 to 5.80] (p = .010), and troponin T increased from 19.5 [9.3 to 34.0] ng/L to 20.0 [11.8 to 47.8] ng/L (p = .025). All other parameters did not change during treatment with a TTR-stabilizer.
A change in cardiac tracer uptake on bone scintigraphy may be an early marker of treatment-specific response or disease progression in ATTRv amyloidosis patients.
遗传性转甲状腺素蛋白(ATTRv)淀粉样变性患者需要早期的潜在治疗反应的定量标志物来指导治疗。本研究旨在评估不同治疗方法对ATTRv 淀粉样变性患者骨扫描中心脏示踪剂摄取的影响。
在这项回顾性队列研究中,比较了 20 名接受转甲状腺素(TTR)基因沉默剂 patisiran 治疗的患者和 12 名接受 TTR 稳定剂治疗的患者的结果。评估了治疗期间 NYHA 心功能分级、血清中心脏标志物、壁厚度和舒张参数的变化以及 NYHA 心功能分级的变化。
接受 patisiran 治疗 29 [15-34] 个月的患者,骨扫描中心脏/全身(H/WB)比值中位数从 4.84 [4.00 至 5.31] 降至 4.16 [3.66 至 4.81](p<0.001)。其他随访参数没有变化。接受 TTR 稳定剂治疗 24 [20-30] 个月的患者,H/WB 比值从 4.46 [3.24 至 5.13] 增加到 4.96 [3.39 至 5.80](p=0.010),肌钙蛋白 T 从 19.5 [9.3 至 34.0] ng/L 增加到 20.0 [11.8 至 47.8] ng/L(p=0.025)。在接受 TTR 稳定剂治疗期间,所有其他参数均无变化。
骨扫描中心脏示踪剂摄取的变化可能是 ATTRv 淀粉样变性患者治疗特异性反应或疾病进展的早期标志物。