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肌纤维瘢痕形成作为磷酸化酶脑型同工酶基因 Arg14del 突变携带者的早期特征:心血管磁共振成像的表型见解。

Myocardial fibrosis as an early feature in phospholamban p.Arg14del mutation carriers: phenotypic insights from cardiovascular magnetic resonance imaging.

机构信息

Department of Clinical and Experimental Cardiology, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.

Netherlands Heart Institute (Nl-HI), Utrecht, the Netherlands.

出版信息

Eur Heart J Cardiovasc Imaging. 2019 Jan 1;20(1):92-100. doi: 10.1093/ehjci/jey047.

Abstract

AIMS

The p.Arg14del founder mutation in the gene encoding phospholamban (PLN) is associated with an increased risk of malignant ventricular arrhythmia (VA) and heart failure. It has been shown to lead to calcium overload, cardiomyocyte damage, and eventually to myocardial fibrosis. This study sought to investigate ventricular function, the extent and localization of myocardial fibrosis and the associations with ECG features and VA in PLN p.Arg14del mutation carriers.

METHODS AND RESULTS

Cardiovascular magnetic resonance (CMR) data of 150 mutation carriers were analysed retrospectively. Left ventricular (LV) and right ventricular (RV) volumes, mass, and ejection fraction were measured. The extent of late gadolinium enhancement (LGE) was expressed as a percentage of myocardial mass. All standard ECG parameters were measured. Occurrence of VA was analysed on ambulatory 24-h and/or exercise electrocardiography, if available. Mean age was 40 ± 15 years, 42% males, and 7% were index patients while 93% were pre-symptomatic carriers identified after family cascade screening. Mean LV ejection fraction (LVEF) and RV ejection fraction were 58 ± 9% and 55 ± 9%, respectively. LV-LGE was present in 91% of mutation carriers with reduced LVEF (<45%) and in 30% of carriers with preserved LVEF. In carriers with positive LV-LGE, its median extent was 5.9% (interquartile range 3.2-12.7). LGE was mainly observed in the inferolateral wall. Carriers with inverted T-waves in the lateral ECG leads more often had LV-LGE (P < 0.01) than carriers without. Finally, the presence of LV-LGE, but not attenuated R-waves and inverted lateral T-waves, was independently associated with VA.

CONCLUSION

LV myocardial fibrosis is present in many PLN p.Arg14del mutation carriers, and who still have a preserved LVEF. It is seen predominantly in the LV inferolateral wall and corresponds with electrocardiographic repolarization abnormalities. Although preliminary, myocardial fibrosis was found to be independently associated with VA. Our findings support the use of CMR with LGE early in the diagnostic work-up.

摘要

目的

编码肌浆网磷蛋白(PLN)的基因中 p.Arg14del 突变与恶性室性心律失常(VA)和心力衰竭的风险增加相关。该突变已被证实可导致钙超载、心肌细胞损伤,最终导致心肌纤维化。本研究旨在探讨 PLN p.Arg14del 突变携带者的心室功能、心肌纤维化的程度和定位,以及与心电图特征和 VA 的关系。

方法和结果

回顾性分析了 150 名突变携带者的心血管磁共振(CMR)数据。测量左心室(LV)和右心室(RV)容积、质量和射血分数。用心肌质量的百分比表示晚期钆增强(LGE)的程度。测量所有标准心电图参数。如果有条件,通过动态 24 小时和/或运动心电图分析 VA 的发生情况。平均年龄为 40±15 岁,男性占 42%,7%为首发患者,93%为经家族级联筛查发现的无症状携带者。平均 LV 射血分数(LVEF)和 RV 射血分数分别为 58±9%和 55±9%。91%的突变携带者 LVEF 降低(<45%),30%的携带者 LVEF 正常,存在 LV-LGE。在 LVEF 阳性的携带者中,LGE 的中位数程度为 5.9%(四分位距 3.2-12.7)。LGE 主要发生在下外侧壁。心电图外侧导联 T 波倒置的携带者更常出现 LV-LGE(P<0.01),而非携带者则无。最后,LV-LGE 的存在,而不是 R 波衰减和外侧 T 波倒置,与 VA 独立相关。

结论

许多 PLN p.Arg14del 突变携带者存在 LV 心肌纤维化,且 LVEF 仍保持正常。它主要发生在 LV 下外侧壁,与心电图复极异常相对应。尽管初步研究,心肌纤维化被发现与 VA 独立相关。我们的发现支持在诊断工作中早期使用 LGE 的 CMR。

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