Smiley Dia A, Einstein Andrew J, O'Gorman Kevin J, Santana Denisse, Teruya Sergio, Chan Nicholas, Nalbandian Ani, Poterucha Timothy J, Helmke Stephen T, Mintz Akiva, Goldner Kim, Sekulic Miroslav, Mirabal Alfonsina, Cuomo Margaret O, Guadalupe Samantha, De Los Santos Jeffeny, Paulino Mary E, Mateo Kimberly A, Rodriguez Carlos M, Jimenez Massiel, Wardhere Abdirahman, Bampatsias Dimitrios, Castillo Michelle, Peng Boyu, Maurer Mathew S
Seymour, Paul, and Gloria Milstein Division of Cardiology, Department of Medicine, Columbia University Irving Medical Center/NewYork-Presbyterian Hospital, New York, New York, USA.
Seymour, Paul, and Gloria Milstein Division of Cardiology, Department of Medicine, Columbia University Irving Medical Center/NewYork-Presbyterian Hospital, New York, New York, USA; Department of Radiology, Columbia University Irving Medical Center/NewYork-Presbyterian Hospital, New York, New York, USA.
JACC Cardiovasc Imaging. 2025 Jul;18(7):799-811. doi: 10.1016/j.jcmg.2025.01.018. Epub 2025 May 28.
Early detection of transthyretin cardiac amyloidosis (ATTR-CA) is vital, because currently available therapies are most effective early in the disease course. Although Perugini grade 2 or 3 uptake on scintigraphy using bone-avid tracers such as Tc-pyrophosphate is highly specific for ATTR-CA, absent monoclonal proteins, sensitivity is about 70%. Positron emission tomographic (PET)/computed tomographic (CT) imaging using the novel radiolabeled heparan sulfate proteoglycan-binding peptide I-evuzamitide has been shown to be useful for quantifying cardiac amyloid load in systemic amyloidosis.
The aim of this study was to quantify myocardial I-evuzamitide PET uptake and compare diagnostic performance with that of Tc-pyrophosphate in patients with ATTR-CA and carriers.
Twenty-five subjects underwent imaging using I-evuzamitide PET/CT imaging: 7 with wild-type ATTR-CA (all Columbia stage I) and 18 transthyretin amyloidosis (ATTR) variant-allele carriers with cardiomyopathy and/or neuropathy. Myocardial uptake was determined as left ventricular percentage of injected dose (mean activity concentration × volume/injected activity) and cardiac amyloid activity (mean specific uptake value × volume) within voxels with uptake above blood pool.
Eleven subjects with ATTR and Perugini grade 0 or 1 Tc-pyrophosphate cardiac scans had cardiac uptake of I-evuzamitide, suggesting that I-evuzamitide PET/CT imaging may detect ATTR amyloid deposits when Tc-pyrophosphate cardiac scintigraphy does not. I-evuzamitide showed myocardial uptake in all 5 subjects with variant ATTR with biopsy-proven disease and in 2 subjects with wild-type ATTR and negative (grade 0) results on Tc-pyrophosphate scans but extracardiac biopsies showing ATTR. Myocardial amyloid load was moderately to strongly correlated with disease stage and with echocardiographic and quality-of-life measures.
I-evuzamitide PET/CT imaging can identify myocardial amyloid in variant transthyretin allele carriers and wild-type subjects when Tc-pyrophosphate does not. (Evuzamitide in PET/CT to Measure Potential Therapeutic Response in ATTR; NCT05635045).
甲状腺转运蛋白心脏淀粉样变性(ATTR-CA)的早期检测至关重要,因为目前可用的治疗方法在疾病病程早期最为有效。尽管使用锝焦磷酸盐等亲骨示踪剂进行闪烁扫描时,佩鲁吉尼2级或3级摄取对ATTR-CA具有高度特异性,且无单克隆蛋白,但敏感性约为70%。使用新型放射性标记的硫酸乙酰肝素蛋白聚糖结合肽I-依武扎米肽进行正电子发射断层扫描(PET)/计算机断层扫描(CT)成像已被证明可用于量化系统性淀粉样变性中的心脏淀粉样蛋白负荷。
本研究的目的是量化心肌I-依武扎米肽PET摄取,并将ATTR-CA患者及其携带者的诊断性能与焦磷酸锝的诊断性能进行比较。
25名受试者接受了I-依武扎米肽PET/CT成像:7名野生型ATTR-CA患者(均为哥伦比亚I期)和18名患有心肌病和/或神经病变的甲状腺转运蛋白淀粉样变性(ATTR)变异等位基因携带者。心肌摄取量通过左心室注射剂量百分比(平均活性浓度×体积/注射活性)和血池摄取量以上体素内的心脏淀粉样蛋白活性(平均比摄取值×体积)来确定。
11名ATTR患者且佩鲁吉尼焦磷酸锝心脏扫描为0级或1级,其心肌摄取了I-依武扎米肽,这表明当焦磷酸锝心脏闪烁扫描未检测到时,I-依武扎米肽PET/CT成像可能检测到ATTR淀粉样蛋白沉积。I-依武扎米肽在所有5名经活检证实患有变异型ATTR的受试者以及2名野生型ATTR且焦磷酸锝扫描结果为阴性(0级)但心脏外活检显示ATTR的受试者中均显示出心肌摄取。心肌淀粉样蛋白负荷与疾病分期、超声心动图和生活质量指标呈中度至强相关。
当焦磷酸锝无法检测到时,I-依武扎米肽PET/CT成像可以识别变异型甲状腺转运蛋白等位基因携带者和野生型受试者中的心肌淀粉样蛋白。(PET/CT中的依武扎米肽用于测量ATTR中的潜在治疗反应;NCT05635045)