Key result
Takotsubo syndrome was associated with higher septal native T1 (1116 vs 970 msec, P<0.001), T2, and extracellular volume fraction compared with controls, indicating increased myocardial water content.
Why the study?
Myocardial oedema is common in takotsubo syndrome and may alter myocardial morphology and function, but its relationships with mechanical and electrical abnormalities remained to be described.
Does myocardial oedema assessed by CMR correlate with mechanical and electrocardiographic changes in takotsubo syndrome?
Case-Control (n=55)
Does myocardial oedema assessed by CMR correlate with mechanical and electrocardiographic changes in takotsubo syndrome?
Absolute Event Rate: 1116% vs 970%
p-value: p=<0.001
In acute takotsubo syndrome, CMR T1 and T2 mapping reveals increased myocardial oedema that correlates with mechanical dysfunction and electrocardiographic changes.
May link edema to dysfunction in Takotsubo; leaves open diagnostic or prognostic utility pending prospective validation.
AIMS: myocardial oedema is largely represented in takotsubo syndrome (TTS) and may contribute to alter the myocardium morphology and function. The aim of the study is to describe relationships between oedema, mechanical, and electrical abnormalities in TTS. METHODS AND RESULTS: the study included n = 32 hospitalized TTS patients and n = 23 controls. Cardiac magnetic resonance (CMR) with tissue mapping and feature tracking was performed with concomitant 12-lead electrocardiogram (ECG) recording. Mean age of TTS was 72 ± 12 years old, 94% women. Compared with controls, patients had higher left ventricular (LV) mass, worse systolic function, higher septal native T1 (1116 ± 73 msec vs. 970 ± 23 msec, P < 0.001), T2 (56 ± 5 msec vs. 46 ± 2 msec, P < 0.001), and extracellular volume (ECV) fraction (32 ± 5% vs. 24 ± 1%, P < 0.001). TTS patients had higher apicobasal gradient of T2 values (12 ± 6 msec vs. 2 ± 6 msec, P < 0.001); basal LV wall displayed higher native T1, T2, and ECV (all P < 0.002) but similar circumferential strain against controls (-23 ± 3% vs. -24 ± 4%, P = 0.351). In the TTS cohort, septal T2 values showed significant correlations with native T1 (r = 0.609, P < 0.001), ECV (r = 0.689, P < 0.001), left ventricular ejection fraction (r = -0.459, P = 0.008) and aVR voltage (r = -0.478, P = 0.009). Negative T-wave voltage and QTc length correlated with apicobasal T2 mapping gradient (r = 0.499, P = 0.007 and r = 0.372, P = 0.047, respectively) but not with other tissue mapping measurements. CONCLUSIONS: CMR T1 and T2 mapping demonstrated increased myocardial water content conditioning interstitial expansion in acute TTS, detected even outside areas of abnormal wall motion. Oedema burden and distribution associated with mechanical and electrocardiographic changes, making it a potential prognostic marker and therapeutic target in TTS.
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Arcari et al. (2023) conducted a case-control in Takotsubo syndrome (n=55). Takotsubo syndrome vs. Controls was evaluated on Septal native T1 (p=<0.001). Takotsubo syndrome was associated with higher septal native T1 (1116 vs 970 msec, P<0.001), T2, and extracellular volume fraction compared with controls, indicating increased myocardial water content.
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