Dilated Cardiomyopathy: New Distinct Phenotypes or Temporal Phases of Disease?
作者信息
Hershberger Ray E, Zareba Karolina M
机构信息
Division of Human Genetics, Department of Internal Medicine, Ohio State University Wexner Medical Center, Columbus, Ohio, USA; Division of Cardiovascular Medicine, Department of Internal Medicine, Ohio State University Wexner Medical Center, Columbus, Ohio, USA; Dorothy M. Davis Heart and Lung Research Institute, Ohio State University Wexner Medical Center, Columbus, Ohio, USA.
Division of Cardiovascular Medicine, Department of Internal Medicine, Ohio State University Wexner Medical Center, Columbus, Ohio, USA; Dorothy M. Davis Heart and Lung Research Institute, Ohio State University Wexner Medical Center, Columbus, Ohio, USA. Electronic address: https://twitter.com/ZarebaCMR.
出版信息
J Am Coll Cardiol. 2022 Jun 7;79(22):2233-2235. doi: 10.1016/j.jacc.2022.04.008.
Abstract
摘要
相似文献
1
Dilated Cardiomyopathy: New Distinct Phenotypes or Temporal Phases of Disease?扩张型心肌病：是新的独特表型还是疾病的不同阶段？
J Am Coll Cardiol. 2022 Jun 7;79(22):2233-2235. doi: 10.1016/j.jacc.2022.04.008.
2
Short QT and dilated cardiomyopathy. A phenotype with a good prognosis?短QT间期与扩张型心肌病。一种预后良好的表型？
Int J Cardiol. 2011 Sep 15;151(3):356-7. doi: 10.1016/j.ijcard.2011.06.069. Epub 2011 Jul 26.
3
Imaging phenotype vs genotype in nonhypertrophic heritable cardiomyopathies: dilated cardiomyopathy and arrhythmogenic right ventricular cardiomyopathy.遗传性非肥厚型心肌病的影像学表型与基因型：扩张型心肌病和致心律失常性右室心肌病。
Circ Cardiovasc Imaging. 2010 Nov;3(6):753-65. doi: 10.1161/CIRCIMAGING.110.957563.
4
Familial apical dilated cardiomyopathy in a young man: a novel phenotype of Takatsubo syndrome or a new entity altogether?一名年轻男性的家族性心尖部扩张型心肌病：是Takotsubo综合征的一种新表型还是一种全新的疾病实体？
BMJ Case Rep. 2019 Jul 27;12(7):e231302. doi: 10.1136/bcr-2019-231302.
5
Familial dilated cardiomyopathy.家族性扩张型心肌病
Rev Port Cardiol. 2002 Dec;21(12):1487-503.
6
Clinical diabetic cardiomyopathy: a two-faced disease with restrictive and dilated phenotypes.临床糖尿病性心肌病：一种具有限制型和扩张型表型的两面性疾病。
Eur Heart J. 2015 Jul 14;36(27):1718-27, 1727a-1727c. doi: 10.1093/eurheartj/ehv134. Epub 2015 Apr 17.
7
Implications of Genetic Testing in Dilated Cardiomyopathy.扩张型心肌病的基因检测意义。
Circ Genom Precis Med. 2020 Oct;13(5):476-487. doi: 10.1161/CIRCGEN.120.003031. Epub 2020 Sep 3.
8
A new discovered gene mutation in a child with dilated cardiomyopathy.一个患有扩张型心肌病的儿童中发现的新基因突变。
Cardiol Young. 2021 Sep;31(9):1530-1531. doi: 10.1017/S1047951121001104. Epub 2021 Apr 5.
9
Lamin A/C mutations in dilated cardiomyopathy.扩张型心肌病中的核纤层蛋白A/C突变
Cardiol J. 2014;21(4):331-42. doi: 10.5603/CJ.a2014.0037. Epub 2014 May 20.
10
Diagnostic challenge in desmin cardiomyopathy with transformation of clinical phenotypes.伴有临床表型转变的结蛋白心肌病的诊断挑战
Pediatr Cardiol. 2013 Feb;34(2):467-70. doi: 10.1007/s00246-012-0312-x. Epub 2012 Apr 7.
引用本文的文献
1
Identifying novel phenotypes of elevated left ventricular end diastolic pressure using hierarchical clustering of features derived from electromechanical waveform data.利用从机电波形数据得出的特征进行分层聚类，识别左心室舒张末期压力升高的新表型。
Front Cardiovasc Med. 2022 Sep 23;9:980625. doi: 10.3389/fcvm.2022.980625. eCollection 2022.
本文引用的文献
1
2022 AHA/ACC/HFSA Guideline for the Management of Heart Failure: A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines.2022年美国心脏协会/美国心脏病学会/美国心力衰竭学会心力衰竭管理指南：美国心脏病学会/美国心脏协会临床实践指南联合委员会报告
J Am Coll Cardiol. 2022 May 3;79(17):e263-e421. doi: 10.1016/j.jacc.2021.12.012. Epub 2022 Apr 1.
2
Prevalence and Cumulative Risk of Familial Idiopathic Dilated Cardiomyopathy.家族性特发性扩张型心肌病的患病率和累积风险。
JAMA. 2022 Feb 1;327(5):454-463. doi: 10.1001/jama.2021.24674.
3
Improved Risk Stratification for Ventricular Arrhythmias and Sudden Death in Patients With Nonischemic Dilated Cardiomyopathy.非缺血性扩张型心肌病患者室性心律失常和猝死的风险分层改善。
J Am Coll Cardiol. 2021 Jun 15;77(23):2890-2905. doi: 10.1016/j.jacc.2021.04.030.
4
The Complex and Diverse Genetic Architecture of Dilated Cardiomyopathy.扩张型心肌病的复杂多样的遗传结构。
Circ Res. 2021 May 14;128(10):1514-1532. doi: 10.1161/CIRCRESAHA.121.318157. Epub 2021 May 13.
5
Outcome in Dilated Cardiomyopathy Related to the Extent, Location, and Pattern of Late Gadolinium Enhancement.扩张型心肌病的转归与晚期钆增强的范围、部位和模式有关。
JACC Cardiovasc Imaging. 2019 Aug;12(8 Pt 2):1645-1655. doi: 10.1016/j.jcmg.2018.07.015. Epub 2018 Sep 12.
6
T1-Mapping and Outcome in Nonischemic Cardiomyopathy: All-Cause Mortality and Heart Failure.T1 映射与非缺血性心肌病的转归：全因死亡率和心力衰竭。
JACC Cardiovasc Imaging. 2016 Jan;9(1):40-50. doi: 10.1016/j.jcmg.2015.12.001.
7
Profibrotic Role for Interleukin-4 in Cardiac Remodeling and Dysfunction.白细胞介素-4在心脏重塑和功能障碍中的促纤维化作用。
Hypertension. 2015 Sep;66(3):582-9. doi: 10.1161/HYPERTENSIONAHA.115.05627. Epub 2015 Jul 20.
Zotero 插件