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遗传性血色素沉着症患者经超声心动图检测心功能改善。

Improvements in cardiac function detected using echocardiography in patients with hereditary haemochromatosis.

机构信息

Department of Cardiology, St James Hospital, Dublin 8, Ireland.

Department of Neuroradiology, Vancouver General Hospital, 899 W 12th Ave., Vancouver, BC, V5Z 1M9, Canada.

出版信息

Ir J Med Sci. 2020 Feb;189(1):109-117. doi: 10.1007/s11845-019-02032-5. Epub 2019 May 20.

DOI:10.1007/s11845-019-02032-5
PMID:31111347
Abstract

BACKGROUND

Hereditary haemochromatosis is often not diagnosed until adulthood. Iron overload cardiomyopathy initially results in diastolic dysfunction and can result in arrhythmias and irreversible cardiac failure if untreated. The aim of this study was to investigate whether patients with newly diagnosed hereditary haemochromatosis without signs of heart failure exhibit subclinical alterations of cardiac function and to determine if cardiac function improved after 1 year of venesection.

METHODS

Baseline echocardiography was performed on 25 patients with newly diagnosed hereditary haemochromatosis with elevated serum ferritin levels. The test was repeated after 1 year of treatment with venesection. Tissue Doppler imaging (TDI) and deformation (strain) imaging using speckle tracking were performed. Left atrial force was measured according to the Newtonian principle, in which force (dynes) = mass × acceleration. Left atrial force was calculated by the Manning method expressed as ρ × 0.53 × mitral annular orifice area × (peak A velocity).

RESULTS

Radial strain showed a significant improvement after 1 year of venesection (increase from 38.8 to 52.6). The LAF showed a significant decrease after 1 year of venesection (median decrease = 0.6 (IQR 0, 1.60), p = 0.0004). Iso-volumetric relaxation time (IVRT) decreased significantly in patients after 1 year of venesection (decrease from 107.4 ± 16.2 to 97.68 ± 15.4 ms, p (0.0187)).

CONCLUSION

Among all measurements, radial strain, IVRT and left atrial force were shown to significantly improve following a 1-year course of venesection, suggesting that these parameters could be used to identify subclinical cardiac dysfunction in patients with iron overload secondary to hereditary haemochromatosis and to guide intensification of venesection therapy.

摘要

背景

遗传性血色素沉着症通常直到成年后才被诊断出来。铁过载性心肌病最初导致舒张功能障碍,如果未经治疗,可导致心律失常和不可逆性心力衰竭。本研究旨在探讨新诊断的遗传性血色素沉着症患者在没有心力衰竭迹象的情况下是否存在亚临床心脏功能改变,并确定静脉放血治疗 1 年后心脏功能是否改善。

方法

对 25 例血清铁蛋白水平升高的新诊断遗传性血色素沉着症患者进行基线超声心动图检查。在静脉放血治疗 1 年后重复该检查。进行组织多普勒成像(TDI)和斑点追踪的变形(应变)成像。根据牛顿定律测量左心房力,其中力(达因)=质量×加速度。左心房力通过曼宁法计算,用ρ×0.53×二尖瓣瓣环口面积×(峰值 A 速度)表示。

结果

静脉放血 1 年后,径向应变明显改善(从 38.8 增加到 52.6)。静脉放血 1 年后左心房力明显下降(中位数下降 0.6(IQR 0,1.60),p=0.0004)。静脉放血 1 年后等容舒张时间(IVRT)显著降低(从 107.4±16.2 降至 97.68±15.4ms,p(0.0187))。

结论

在所有测量指标中,径向应变、IVRT 和左心房力在静脉放血 1 年后均显著改善,提示这些参数可用于识别铁过载性遗传性血色素沉着症患者亚临床心脏功能障碍,并指导静脉放血治疗的强化。

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