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Unexpected myocarditis in thalassaemia major patient screened for iron load cardiomyopathy.在筛查铁负荷型心肌病的重型地中海贫血患者中发现意外的心肌炎。
BMJ Case Rep. 2009;2009. doi: 10.1136/bcr.08.2008.0811. Epub 2009 Feb 16.
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On T2* magnetic resonance and cardiac iron.T2* 磁共振与心脏铁沉积
Circulation. 2011 Apr 12;123(14):1519-28. doi: 10.1161/CIRCULATIONAHA.110.007641. Epub 2011 Mar 28.
3
Survival in a large cohort of Greek patients with transfusion-dependent beta thalassaemia and mortality ratios compared to the general population.在一个依赖输血的希腊β地中海贫血患者的大队列中进行生存分析,并与普通人群进行死亡率比较。
Eur J Haematol. 2011 Apr;86(4):332-8. doi: 10.1111/j.1600-0609.2011.01582.x.
4
Cardiac iron and cardiac disease in males and females with transfusion-dependent thalassemia major: a T2* magnetic resonance imaging study.输血依赖型重型地中海贫血患者的心脏铁与心脏疾病:一项 T2*磁共振成像研究。
Haematologica. 2011 Apr;96(4):515-20. doi: 10.3324/haematol.2010.025510. Epub 2011 Jan 12.
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International reproducibility of single breathhold T2* MR for cardiac and liver iron assessment among five thalassemia centers.五项地中海贫血中心单屏气 T2*MR 心脏和肝脏铁评估的国际可重复性。
J Magn Reson Imaging. 2010 Aug;32(2):315-9. doi: 10.1002/jmri.22245.
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Update on survival in thalassemia major.重型地中海贫血患者生存情况的最新进展
Hemoglobin. 2009;33 Suppl 1:S76-80. doi: 10.3109/03630260903347336.
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Efficacy of deferasirox in reducing and preventing cardiac iron overload in beta-thalassemia.地拉罗司降低和预防β-地中海贫血心脏铁过载的疗效。
Blood. 2010 Mar 25;115(12):2364-71. doi: 10.1182/blood-2009-04-217455. Epub 2009 Dec 8.
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Improved survival in thalassemia major patients on switching from desferrioxamine to combined chelation therapy with desferrioxamine and deferiprone.从去铁胺转换为去铁胺与地拉罗司联合螯合疗法后,重型地中海贫血患者的生存率得到提高。
Haematologica. 2009 Dec;94(12):1777-8. doi: 10.3324/haematol.2009.009118. Epub 2009 Oct 8.
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Cardiac T2* magnetic resonance for prediction of cardiac complications in thalassemia major.心脏T2*磁共振成像预测重型地中海贫血患者心脏并发症的研究
Circulation. 2009 Nov 17;120(20):1961-8. doi: 10.1161/CIRCULATIONAHA.109.874487. Epub 2009 Oct 2.
10
Deferasirox (Exjade) significantly improves cardiac T2* in heavily iron-overloaded patients with beta-thalassemia major.地拉罗司(Exjade)可显著改善重型β-地中海贫血患者的心脏 T2*。
Ann Hematol. 2010 Apr;89(4):405-9. doi: 10.1007/s00277-009-0838-z. Epub 2009 Oct 2.

β-地中海贫血症患者心脏 T2* 心血管磁共振的国际调查。

International survey of T2* cardiovascular magnetic resonance in β-thalassemia major.

机构信息

Royal Brompton and Harefield NHS Foundation Trust, London, UK.

出版信息

Haematologica. 2013 Sep;98(9):1368-74. doi: 10.3324/haematol.2013.083634. Epub 2013 Jun 28.

DOI:10.3324/haematol.2013.083634
PMID:23812939
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3762092/
Abstract

Accumulation of myocardial iron is the cause of heart failure and early death in most transfused thalassemia major patients. T2* cardiovascular magnetic resonance provides calibrated, reproducible measurements of myocardial iron. However, there are few data regarding myocardial iron loading and its relation to outcome across the world. A survey is reported of 3,095 patients in 27 worldwide centers using T2* cardiovascular magnetic resonance. Data on baseline T2* and numbers of patients with symptoms of heart failure at first scan (defined as symptoms and signs of heart failure with objective evidence of left ventricular dysfunction) were requested together with more detailed information about patients who subsequently developed heart failure or died. At first scan, 20.6% had severe myocardial iron (T2*≤ 10 ms), 22.8% had moderate myocardial iron (T2* 10-20 ms) and 56.6% of patients had no iron loading (T2*>20 ms). There was significant geographical variation in myocardial iron loading (24.8-52.6%; P<0.001). At first scan, 85 (2.9%) of 2,915 patients were reported to have heart failure (81.2% had T2* <10 ms; 98.8% had T2* <20 ms). During follow up, 108 (3.8%) of 2,830 patients developed new heart failure. Of these, T2* at first scan had been less than 10 ms in 96.3% and less than 20 ms in 100%. There were 35 (1.1%) cardiac deaths. Of these patients, myocardial T2* at first scan had been less than 10 ms in 85.7% and less than 20 ms in 97.1%. Therefore, in this worldwide cohort of thalassemia major patients, over 43% had moderate/severe myocardial iron loading with significant geographical differences, and myocardial T2* values less than 10 ms were strongly associated with heart failure and death.

摘要

心肌铁的积累是大多数输血地中海贫血患者心力衰竭和早期死亡的原因。T2心血管磁共振提供了经过校准、可重复的心肌铁测量。然而,关于全球范围内心肌铁负荷及其与结局的关系的数据很少。报告了一项对 27 个世界中心的 3095 例患者使用 T2心血管磁共振进行的调查。要求提供基线 T2数据和首次扫描时出现心力衰竭症状的患者数量(定义为心力衰竭症状和体征伴左心室功能障碍的客观证据),并提供随后出现心力衰竭或死亡的患者的更详细信息。首次扫描时,20.6%的患者有严重心肌铁(T2≤10ms),22.8%的患者有中度心肌铁(T210-20ms),56.6%的患者无铁负荷(T2>20ms)。心肌铁负荷存在显著的地域差异(24.8-52.6%;P<0.001)。首次扫描时,2915 例患者中有 85 例(2.9%)报告有心力衰竭(81.2%的 T2*<10ms;98.8%的 T2*<20ms)。在随访期间,2830 例患者中有 108 例(3.8%)新发心力衰竭。其中,96.3%的患者首次扫描时 T2小于 10ms,100%的患者首次扫描时 T2小于 20ms。有 35 例(1.1%)心脏死亡。这些患者中,85.7%的患者首次扫描时 T2小于 10ms,97.1%的患者首次扫描时 T2小于 20ms。因此,在这个全球地中海贫血患者队列中,超过 43%的患者有中度/重度心肌铁负荷,且存在显著的地域差异,T2*值小于 10ms与心力衰竭和死亡密切相关。