Cardiovascular Magnetic Resonance Imaging Tissue Characterization in Non-ischemic Cardiomyopathies

被引:1
作者
Rodriguez-Ortiz, J. [1 ]
Abuzaid, A. [2 ]
Brian, Agbor-Etang [3 ]
Ordovas, K. [4 ]
机构
[1] Orlando Hlth Heart Inst, Orlando, FL USA
[2] Alaska Heart & Vasc Inst, Anchorage, AK 99508 USA
[3] Univ Calif San Francisco, Dept Cardiol, San Francisco, CA 94115 USA
[4] Univ Calif San Francisco, Dept Radiol, San Francisco, CA 94115 USA
关键词
Cardiac magnetic resonance; Non-ischemic cardiomyopathy; Late gadolinium enhancement; T1; mapping; Extracellular volume; Dilated cardiomyopathy; T2; Strain; LATE GADOLINIUM ENHANCEMENT; VENTRICULAR NON-COMPACTION; SUDDEN CARDIAC DEATH; IDIOPATHIC DILATED CARDIOMYOPATHY; EXTRACELLULAR VOLUME FRACTION; IMPROVES RISK STRATIFICATION; HYPERTROPHIC CARDIOMYOPATHY; MYOCARDIAL FIBROSIS; PROGNOSTIC VALUE; DELAYED-ENHANCEMENT;
D O I
10.1007/s11936-020-00813-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of review In this review, we will focus the role of CMR in dilated cardiomyopathy and genetic cardiomyopathy. Recent findings Non-invasive imaging plays a crucial rule in the diagnostic workup of cardiomyopathies. In these entities, echocardiography is the first-line imaging tool for diagnostic assessment, but CMR has the unique capability to identify and differentiate the underlying pathology, mainly through tissue characterization, even if the EF is preserved. Myocardial tissue characterization is crucial for adequate prognostication and guiding of therapy. Visual, semi-quantitative, and quantitative methods allow the accurate description of myocardial pathologies such as edema, hyperemia, hypoperfusion, and fibrosis. Basic CMR protocols and standardized post-processing methods are well established and routinely performed. CMR has the ability to characterize concomitantly the myocardial tissue characteristics using techniques such as LGE, T1 mapping with ECV measurements, and T2 mapping, and also deformation functional parameters (i.e., strain) and thus provides important insights into the underlying etiology of cardiomyopathy and prognosis. The results of several studies show that CMR findings are associated with clinical outcomes and can inform the management of these patients, including longitudinal assessment of treatment response. CMR should be routinely used in the workup of patients with non-ischemic cardiomyopathy for both diagnostic and prognostic applications. The presence of LV dilatation and systolic dysfunction in the absence of significant coronary artery disease together with valvular diseases represents a significant etiology to cause cardiomyopathy in cardiology practices. Additionally, other etiologies as infiltrative heart diseases, channelopathy/genetic cardiomyopathy and cardiac involvement in systemic diseases and oncologic process complete the spectrum that may range from isolated LV involvement or biventricular failure. Non-invasive imaging plays a crucial rule in the diagnostic workup of cardiomyopathies. In these entities, echocardiography is the first-line imaging tool for diagnostic assessment, but CMR has the unique capability to identify and differentiate the underlying pathology, mainly through tissue characterization, even if the EF is preserved. Myocardial tissue characterization is crucial for adequate prognostication and guiding of therapy. Visual, semi-quantitative, and quantitative methods allow the accurate description of myocardial pathologies such as edema, hyperaemia, hypoperfusion, and fibrosis. Basic CMR protocols and standardized post-processing methods are well established and routinely performed.
引用
收藏
页数:16
相关论文
共 109 条
  • [1] Occurrence and frequency of arrhythmias in hypertrophic cardiomyopathy on relation to delayed enhancement on cardiovascular magnetic resonance
    Adabag, A. Selcuk
    Maron, Barry J.
    Appelbaum, Evan
    Harrigan, Caltlin J.
    Buros, Jacqueline L.
    Gibson, C. Michael
    Lesser, John R.
    Hanna, Constance A.
    Udelson, James E.
    Manning, Warren J.
    Maron, Martin S.
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2008, 51 (14) : 1369 - 1374
  • [2] Relationship between Extension or Texture Features of Late Gadolinium Enhancement and Ventricular Tachyarrhythmias in Hypertrophic Cardiomyopathy
    Amano, Yasuo
    Suzuki, Yasuyuki
    Yanagisawa, Fumi
    Omori, Yuko
    Matsumoto, Naoya
    [J]. BIOMED RESEARCH INTERNATIONAL, 2018, 2018
  • [3] Reference values for left and right ventricular trabeculation and non-compacted myocardium
    Andre, Florian
    Burger, Astrid
    Lossnitzer, Dirk
    Buss, Sebastian J.
    Abdel-Aty, Hassan
    Gianntisis, Evangelos
    Steen, Henning
    Katus, Hugo A.
    [J]. INTERNATIONAL JOURNAL OF CARDIOLOGY, 2015, 185 : 240 - 247
  • [4] Long-Term Prognostic Value of Cardiac Magnetic Resonance in Left Ventricle Noncompaction A Prospective Multicenter Study
    Andreini, Daniele
    Pontone, Gianluca
    Bogaert, Jan
    Roghi, Alberto
    Barison, Andrea
    Schwitter, Juerg
    Mushtaq, Saima
    Vovas, Georgios
    Sormani, Paola
    Aquaro, Giovanni D.
    Monney, Pierre
    Segurini, Chiara
    Guglielmo, Marco
    Conte, Edoardo
    Fusini, Laura
    Dello Russo, Antonio
    Lombardi, Massimo
    Gripari, Paola
    Baggiano, Andrea
    Fiorentini, Cesare
    Lombardi, Federico
    Bartorelli, Antonio L.
    Pepi, Mauro
    Masci, Pier Giorgio
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2016, 68 (20) : 2166 - 2181
  • [5] Right ventricular systolic function and mechanical dispersion identify patients with arrhythmogenic right ventricular cardiomyopathy
    Aneq, Meriam Astrom
    Maret, Eva
    Brudin, Lars
    Svensson, Anneli
    Engvall, Jan
    [J]. CLINICAL PHYSIOLOGY AND FUNCTIONAL IMAGING, 2018, 38 (05) : 779 - 787
  • [6] Cardiac Phenotypes in Hereditary Muscle Disorders JACC State-of-the-Art Review
    Arbustini, Eloisa
    Di Toro, Alessandro
    Giuliani, Lorenzo
    Favalli, Valentina
    Narula, Nupoor
    Grasso, Maurizia
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2018, 72 (20) : 2485 - 2506
  • [7] Occult cardiac contractile dysfunction in dystrophin-deficient children revealed by cardiac magnetic resonance strain imaging
    Ashford, MW
    Liu, W
    Lin, SJ
    Abraszewski, P
    Caruthers, SD
    Connolly, AM
    Yu, X
    Wickline, SA
    [J]. CIRCULATION, 2005, 112 (16) : 2462 - 2467
  • [8] Prediction of the estimated 5-year risk of sudden cardiac death and syncope or non-sustained ventricular tachycardia in patients with hypertrophic cardiomyopathy using late gadolinium enhancement and extracellular volume CMR
    Avanesov, Maxim
    Muench, Julia
    Weinrich, Julius
    Well, Lennart
    Saering, Dennis
    Stehning, Christian
    Tahir, Enver
    Bohnen, Sebastian
    Radunski, Ulf K.
    Muellerleile, Kai
    Adam, Gerhard
    Patten, Monica
    Lund, Gunnar
    [J]. EUROPEAN RADIOLOGY, 2017, 27 (12) : 5136 - 5145
  • [9] Differences in the extent of fibrosis in obstructive and nonobstructive hypertrophic cardiomyopathy
    Avegliano, Gustavo
    Politi, Maria T.
    Costabel, Juan P.
    Kuschnir, Paola
    Trivi, Marcelo
    Ronderos, Ricardo
    [J]. JOURNAL OF CARDIOVASCULAR MEDICINE, 2019, 20 (06) : 389 - 396
  • [10] Barison A, 2019, EUROPEAN HEART J S2, V20, pjez102002