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本文引用的文献

1
Myocardial T1 mapping in pediatric and congenital heart disease.小儿及先天性心脏病的心肌T1 mapping成像
Circ Cardiovasc Imaging. 2015 Feb;8(2):e002504. doi: 10.1161/CIRCIMAGING.114.002504.
2
Left ventricular systolic function and the pattern of late-gadolinium-enhancement independently and additively predict adverse cardiac events in muscular dystrophy patients.左心室收缩功能和延迟钆增强模式可独立且相加地预测肌营养不良患者的不良心脏事件。
J Cardiovasc Magn Reson. 2014 Sep 25;16(1):81. doi: 10.1186/s12968-014-0081-1.
3
T1 mapping in dilated cardiomyopathy with cardiac magnetic resonance: quantification of diffuse myocardial fibrosis and comparison with endomyocardial biopsy.扩张型心肌病的心脏磁共振 T1 mapping:弥漫性心肌纤维化的定量分析及与心内膜心肌活检的比较。
Eur Heart J Cardiovasc Imaging. 2015 Feb;16(2):210-6. doi: 10.1093/ehjci/jeu183. Epub 2014 Sep 22.
4
T1 Mapping for Characterization of Intracellular and Extracellular Myocardial Diseases in Heart Failure.用于心力衰竭中细胞内和细胞外心肌疾病特征描述的T1映射
Curr Cardiovasc Imaging Rep. 2014;7(9):9287. doi: 10.1007/s12410-014-9287-8.
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Myocardial fibrosis in Eisenmenger syndrome: a descriptive cohort study exploring associations of late gadolinium enhancement with clinical status and survival.艾森曼格综合征心肌纤维化:一项描述性队列研究,探讨晚期钆增强与临床状况和生存的关系。
J Cardiovasc Magn Reson. 2014 May 14;16(1):32. doi: 10.1186/1532-429X-16-32.
6
Post-contrast myocardial T(1) and ECV disagree in a longitudinal canine study.在一项纵向犬类研究中,对比剂增强后的心肌T(1)值和细胞外容积(ECV)结果不一致。
NMR Biomed. 2014 Aug;27(8):988-95. doi: 10.1002/nbm.3135. Epub 2014 May 28.
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In-vivo T1 cardiovascular magnetic resonance study of diffuse myocardial fibrosis in hypertrophic cardiomyopathy.肥厚型心肌病弥漫性心肌纤维化的体内 T1 心血管磁共振研究。
J Cardiovasc Magn Reson. 2014 Apr 25;16(1):28. doi: 10.1186/1532-429X-16-28.
8
Myocardial extracellular remodeling is associated with ventricular diastolic dysfunction in children and young adults with congenital aortic stenosis.心肌细胞外基质重构与先天性主动脉瓣狭窄患儿和青年人心室舒张功能障碍相关。
J Am Coll Cardiol. 2014 May 6;63(17):1778-85. doi: 10.1016/j.jacc.2013.11.066. Epub 2014 Mar 13.
9
CMR quantification of myocardial scar provides additive prognostic information in nonischemic cardiomyopathy.CMR 定量评估心肌瘢痕有助于提供非缺血性心肌病的预后信息。
JACC Cardiovasc Imaging. 2013 Sep;6(9):944-54. doi: 10.1016/j.jcmg.2013.05.013. Epub 2013 Aug 8.
10
Association of fibrosis with mortality and sudden cardiac death in patients with nonischemic dilated cardiomyopathy.非缺血性扩张型心肌病患者纤维化与死亡率和心源性猝死的关系。
JAMA. 2013 Mar 6;309(9):896-908. doi: 10.1001/jama.2013.1363.

再谈心肌因子:心肌纤维化在成人先天性心脏病中的重要性。

Myocardial factor revisited: The importance of myocardial fibrosis in adults with congenital heart disease.

作者信息

Broberg Craig S, Burchill Luke J

机构信息

Adult Congenital Heart Program, Knight Cardiovascular Institute, Oregon Health & Science University, Portland, OR, USA.

Adult Congenital Heart Program, Knight Cardiovascular Institute, Oregon Health & Science University, Portland, OR, USA.

出版信息

Int J Cardiol. 2015 Jun 15;189:204-10. doi: 10.1016/j.ijcard.2015.04.064. Epub 2015 Apr 10.

DOI:10.1016/j.ijcard.2015.04.064
PMID:25897907
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4446173/
Abstract

Pioneers in congenital heart surgery observed that exercise capacity did not return to normal levels despite successful surgical repair, leading some to cite a "myocardial factor" playing a role. They conjectured that residual alterations in myocardial function would be significant for patients' long-term outlook. In fulfillment of their early observations, today's adult congenital heart disease (ACHD) population shows well-recognized features of heart failure, even among patients without clear residual anatomic or hemodynamic abnormalities, demonstrating the vital role of the myocardium in their morbidity and mortality. Whereas the 'myocardial factor' was an elusive concept in the early history of congenital heart care, we now have imaging techniques to detect and quantify one such factor--myocardial fibrosis. Understanding the importance of myocardial fibrosis as a final common pathway in a variety of congenital lesions provides a framework for both the study and treatment of clinical heart failure in this context. While typical heart failure pharmacology should reduce or attenuate fibrogenesis, efforts to show meaningful improvements with standard pharmacotherapy in ACHD repeatedly fall short. This paper considers the importance of myocardial fibrosis and function, the current body of evidence for myocardial fibrosis in ACHD, and its implications for research and treatment.

摘要

先天性心脏病手术的先驱者们观察到,尽管手术修复成功,但运动能力并未恢复到正常水平,这使得一些人认为存在“心肌因素”在起作用。他们推测,心肌功能的残留改变对患者的长期预后具有重要意义。为了证实他们早期的观察结果,如今的成人先天性心脏病(ACHD)患者群体表现出了公认的心力衰竭特征,即使在没有明显残留解剖或血流动力学异常的患者中也是如此,这表明心肌在其发病和死亡中起着至关重要的作用。虽然在先天性心脏病治疗的早期历史中,“心肌因素”是一个难以捉摸的概念,但我们现在拥有成像技术来检测和量化这样一个因素——心肌纤维化。了解心肌纤维化作为多种先天性病变的最终共同途径的重要性,为在此背景下临床心力衰竭的研究和治疗提供了一个框架。虽然典型的心力衰竭药理学应该减少或减弱纤维生成,但在ACHD中,用标准药物疗法显示出有意义改善的努力屡屡失败。本文探讨了心肌纤维化和功能的重要性、目前关于ACHD中心肌纤维化的证据以及它对研究和治疗的影响。