Novel Imaging and Genetic Risk Markers in Takotsubo Syndrome

被引:15
作者
Arcari, Luca [1 ]
Limite, Luca Rosario [2 ]
Adduci, Carmen [3 ]
Sclafani, Matteo [3 ]
Tini, Giacomo [3 ]
Palano, Francesca [3 ]
Cosentino, Pietro [3 ]
Cristiano, Ernesto [3 ]
Cacciotti, Luca [1 ]
Russo, Domitilla [3 ]
Rubattu, Speranza [3 ,4 ]
Volpe, Massimo [3 ]
Autore, Camillo [3 ]
Musumeci, Maria Beatrice [3 ]
Francia, Pietro [3 ]
机构
[1] Mother Giuseppina Vannini Hosp, Cardiol Unit, Rome, Italy
[2] IRCCS San Raffaele Sci Inst, Dept Cardiac Electrophysiol & Arrhythmol, Milan, Italy
[3] Sapienza Univ Rome, Fac Med & Psychol, Cardiol Clin & Mol Med Dept, Rome, Italy
[4] IRCCS Neuromed, Pozzilli, Italy
关键词
takotsubo; cardiac magnetic resonance imaging; T1; mapping; T2; speckle tracking echocardiography; particle imaging velocimetry; genetic; prognosis; CARDIAC MAGNETIC-RESONANCE; TAKO-TSUBO CARDIOMYOPATHY; ADRENERGIC-RECEPTOR POLYMORPHISMS; CLINICAL-FEATURES; NATURAL-HISTORY; MYOCARDIAL-INFARCTION; CORONARY-ARTERIES; SYNDROME WELCOME; RECOVERY; DYSFUNCTION;
D O I
10.3389/fcvm.2021.703418
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Takotsubo syndrome (TTS) is an increasingly recognized condition burdened by significant acute and long-term adverse events. The availability of novel techniques expanded the knowledge on TTS and allowed a more accurate risk-stratification, potentially guiding clinical management. The present review aims to summarize the recent advances in TTS prognostic evaluation with a specific focus on novel imaging and genetic markers. Parametric deformation analysis by speckle-tracking echocardiography, as well as tissue characterization by cardiac magnetic resonance imaging T1 and T2 mapping techniques, currently appear the most clinically valuable applications. Notwithstanding, computed tomography and nuclear imaging studies provided limited but promising data. A genetic predisposition to TTS has been hypothesized, though available evidence is still not sufficient. Although a genetic predisposition appears likely, further studies are needed to fully characterize the genetic background of TTS, in order to identify genetic markers that could assist in predicting disease recurrences and help in familial screening.</p>
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页数:11
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