Lorenzini Massimiliano, Elliott Perry M
University College London Institute for Cardiovascular Science & Barts Heart Centre, St Bartholomew's Hospital, London, UK.
Cardiology, Department of Experimental, Diagnostic & Specialty Medicine, Alma Mater Studiorum University of Bologna, Bologna, Italy.
Future Cardiol. 2019 Mar;15(2):53-61. doi: 10.2217/fca-2018-0078. Epub 2019 Feb 15.
Transthyretin (TTR) related cardiomyopathy is an underdiagnosed cause of heart failure but is increasingly recognized in various settings - from patients admitted with heart failure to symptomatic aortic stenosis - and is rapidly becoming the most frequent form of systemic amyloidosis. Following the recent publication of the landmark ATTR-ACT trial that showed tafamidis to be the first treatment to improve survival in patients with TTR-related cardiac amyloidosis and heart failure, we reviewed the drug's rationale, characteristics and evidence supporting its use in TTR amyloidosis.
转甲状腺素蛋白(TTR)相关心肌病是心力衰竭的一个诊断不足的病因,但在各种情况下越来越受到认可——从因心力衰竭入院的患者到有症状的主动脉瓣狭窄患者——并且正迅速成为系统性淀粉样变性最常见的形式。继具有里程碑意义的ATTR-ACT试验最近发表,该试验表明tafamidis是首个可改善TTR相关心脏淀粉样变性和心力衰竭患者生存率的治疗方法之后,我们回顾了该药物的理论依据、特性以及支持其用于TTR淀粉样变性的证据。