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本文引用的文献

1
Clinical and Prognostic Implications of Right Ventricular Uptake on Bone Scintigraphy in Transthyretin Amyloid Cardiomyopathy.转甲状腺素蛋白淀粉样心肌病中右心室摄取骨闪烁显像的临床和预后意义。
Circulation. 2024 Apr 9;149(15):1157-1168. doi: 10.1161/CIRCULATIONAHA.123.066524. Epub 2024 Feb 8.
2
Impact of vutrisiran on exploratory cardiac parameters in hereditary transthyretin-mediated amyloidosis with polyneuropathy.转甲状腺素蛋白介导的遗传性神经病淀粉样变患者中 vutrisiran 对探索性心脏参数的影响。
Eur J Heart Fail. 2024 Feb;26(2):397-410. doi: 10.1002/ejhf.3138. Epub 2024 Feb 6.
3
Efficacy and Safety of Acoramidis in Transthyretin Amyloid Cardiomyopathy.阿伐曲泊帕在转甲状腺素蛋白淀粉样心肌病中的疗效和安全性。
N Engl J Med. 2024 Jan 11;390(2):132-142. doi: 10.1056/NEJMoa2305434.
4
Quantification of right ventricular amyloid burden with 18F-florbetapir positron emission tomography/computed tomography and its association with right ventricular dysfunction and outcomes in light-chain amyloidosis.用 18F-氟苯丙氨酸正电子发射断层扫描/计算机断层扫描定量检测右心室淀粉样变负荷及其与轻链淀粉样变性患者右心功能障碍和结局的关系。
Eur Heart J Cardiovasc Imaging. 2024 Apr 30;25(5):687-697. doi: 10.1093/ehjci/jead350.
5
Effect of Eplontersen on Cardiac Structure and Function in Patients With Hereditary Transthyretin Amyloidosis.依洛硫酸酯酶治疗遗传性转甲状腺素蛋白淀粉样变性心肌病患者的心脏结构和功能的影响。
J Card Fail. 2024 Aug;30(8):973-980. doi: 10.1016/j.cardfail.2023.11.016. Epub 2023 Dec 7.
6
Eplontersen for Hereditary Transthyretin Amyloidosis With Polyneuropathy.依洛硫酸酯酶纳治疗遗传性转甲状腺素蛋白淀粉样变性多发性神经病。
JAMA. 2023 Oct 17;330(15):1448-1458. doi: 10.1001/jama.2023.18688.
7
Right ventricular to pulmonary artery coupling and outcome in patients with cardiac amyloidosis.心脏淀粉样变性患者的右心室与肺动脉耦合及预后
Eur Heart J Cardiovasc Imaging. 2023 Sep 26;24(10):1405-1414. doi: 10.1093/ehjci/jead145.
8
Phase 1 Trial of Antibody NI006 for Depletion of Cardiac Transthyretin Amyloid.抗心肌转甲状腺素蛋白抗体 NI006 用于清除心脏淀粉样变性的 1 期临床试验。
N Engl J Med. 2023 Jul 20;389(3):239-250. doi: 10.1056/NEJMoa2303765. Epub 2023 May 20.
9
Monitoring tafamidis treatment with quantitative SPECT/CT in transthyretin amyloid cardiomyopathy.用定量 SPECT/CT 监测转甲状腺素蛋白淀粉样心肌病中的塔法米迪治疗。
Eur Heart J Cardiovasc Imaging. 2023 Jul 24;24(8):1019-1030. doi: 10.1093/ehjci/jead030.
10
Reduction in CMR Derived Extracellular Volume With Patisiran Indicates Cardiac Amyloid Regression.用帕替沙那治疗可降低 CMR 衍生细胞外体积，表明心脏淀粉样变得到了逆转。
JACC Cardiovasc Imaging. 2021 Jan;14(1):189-199. doi: 10.1016/j.jcmg.2020.07.043. Epub 2020 Oct 28.

Right Ventricular Bone-Avid Tracer Uptake: A Novel Risk Marker in Transthyretin Amyloid Cardiomyopathy.

作者信息

Dorbala Sharmila

机构信息

Division of Nuclear Medicine and Molecular Imaging, Department of Radiology, Cardiac Amyloidosis Program, Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA.

出版信息

Circulation. 2024 Apr 9;149(15):1169-1171. doi: 10.1161/CIRCULATIONAHA.124.067985. Epub 2024 Apr 8.

DOI:10.1161/CIRCULATIONAHA.124.067985
PMID:38588337
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11216712/
Abstract
摘要