Duchenne Dilated Cardiomyopathy: Cardiac Management from Prevention to Advanced Cardiovascular Therapies

被引：36

作者：

Adorisio, Rachele ^{[1
]}

Mencarelli, Erica ^{[1
]}

Cantarutti, Nicoletta ^{[2
]}

Calvieri, Camilla ^{[2
]}

Amato, Liliana ^{[1
]}

Cicenia, Marianna ^{[2
]}

Silvetti, Massimo ^{[2
]}

D'Amico, Adele ^{[3
]}

Grandinetti, Maria ^{[1
,4
]}

Drago, Fabrizio ^{[2
]}

Amodeo, Antonio ^{[1
]}

机构：

[1] Bambino Gesu Pediat Hosp, Dept Pediat Cardiol & Cardiac Surg Heart & Lung T, Heart Failure Heart Transplant Mech Circulatory S, Heart Failure Clin,IRCCS, I-00165 Rome, Italy

[2] Bambino Gesu Pediat Hosp, Dept Pediat Cardiol & Cardiac Surg, Syncope Unit, Pediat Cardiol & Cardiac Arrhythmias,IRCCS, I-00165 Rome, Italy

[3] Bambino Gesu Pediat Hosp, IRCCS, Genet & Rare Dis Res Area, Neuromuscolar Dis, I-00165 Rome, Italy

[4] Fdn Policlin Univ A, Dept Cardiovasc & Thorac Sci, Gemelli IRCCS, I-20097 Rome, Italy

来源：

JOURNAL OF CLINICAL MEDICINE | 2020年 / 9卷 / 10期

关键词：

duchenne muscular distrophy; dilated cardiomyopathy; heart failure; VENTRICULAR ASSIST DEVICE; CONVERTING ENZYME-INHIBITORS; BECKER MUSCULAR-DYSTROPHY; MECHANICAL CIRCULATORY SUPPORT; HEART-FAILURE; DESTINATION THERAPY; ECHOCARDIOGRAPHIC MEASURES; SYSTOLIC DYSFUNCTION; MYOCARDIAL FIBROSIS; PEDIATRIC-PATIENTS;

D O I：

10.3390/jcm9103186

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Duchenne muscular dystrophy (DMD) cardiomyopathy (DCM) is characterized by a hypokinetic, dilated phenotype progressively increasing with age. Regular cardiac care is crucial in DMD care. Early recognition and prophylactic use of angiotensin converting enzyme inhibitors (ACEi) are the main stay therapeutic strategy to delay incidence of DMD-DCM. Pharmacological treatment to improve symptoms and left ventricle (LV) systolic function, have been widely implemented in the past years. Because of lack of DMD specific drugs, actual indications for established DCM include current treatment for heart failure (HF). This review focuses on current HF strategies to identify, characterize, and treat DMD-DCM.

引用

页码：1 / 18

页数：18

共 113 条

[1] Heart rate reduction strategy using ivabradine in end-stage Duchenne cardiomyopathy [J].

Adorisio, Rachele ;

Calvieri, Camilla ;

Cantarutti, Nicoletta ;

D'Amico, Adele ;

Catteruccia, Michela ;

Bertini, Enrico ;

Baban, Anwar ;

Filippelli, Sergio ;

Perri, Gianluigi ;

Amodeo, Antonio ;

Drago, Fabrizio .

INTERNATIONAL JOURNAL OF CARDIOLOGY, 2019, 280 :99-103

[2] Comment on: 'Implantation of a left ventricular assist device to provide long term support for end-stage Duchenne muscular dystrophy-associated cardiomyopathy' by Stoller et al. [J].

Adorisio, Rachele ;

D'Amario, Domenico ;

Perri, Gianluigi ;

Amodeo, Antonio .

ESC HEART FAILURE, 2018, 5 (04) :651-652

[3] Progressive left ventricular dysfunction and myocardial fibrosis in Duchenne and Becker muscular dystrophy: a longitudinal cardiovascular magnetic resonance study [J].

Aikawa, Tadao ;

Takeda, Atsuhito ;

Oyama-Manabe, Noriko ;

Naya, Masanao ;

Yamazawa, Hirokuni ;

Koyanagawa, Kazuhiro ;

Ito, Yoichi M. ;

Anzai, Toshihisa .

PEDIATRIC CARDIOLOGY, 2019, 40 (02) :384-392

[4]

Allen Hugh D, 2013, PLoS Curr, V5, DOI 10.1371/currents.md.2cc69a1dae4be7dfe2bcb420024ea865

[5]

Altemose GT, 1997, J HEART LUNG TRANSPL, V16, P765

[6] Speckle-Tracking Echocardiography in Children With Duchenne Muscular Dystrophy: A Prospective Multicenter Controlled Cross-Sectional Study [J].

Amedro, Pascal ;

Vincenti, Marie ;

De La Villeon, Gregoire ;

Lavastre, Kathleen ;

Barrea, Catherine ;

Guillaumont, Sophie ;

Bredy, Charlene ;

Gamon, Lucie ;

Meli, Albano C. ;

Cazorla, Olivier ;

Fauconnier, Jeremy ;

Meyer, Pierre ;

Rivier, Francois ;

Adda, Jerome ;

Mura, Thibault ;

Lacampagne, Alain .

JOURNAL OF THE AMERICAN SOCIETY OF ECHOCARDIOGRAPHY, 2019, 32 (03) :412-422

[7] Left ventricular assist device in Duchenne Cardiomyopathy: Can we change the natural history of cardiac disease? [J].

Amodeo, Antonio ;

Adorisio, Rachele .

INTERNATIONAL JOURNAL OF CARDIOLOGY, 2012, 161 (03) :E43-E43

[8] Cardiac Phenotypes in Hereditary Muscle Disorders JACC State-of-the-Art Review [J].

Arbustini, Eloisa ;

Di Toro, Alessandro ;

Giuliani, Lorenzo ;

Favalli, Valentina ;

Narula, Nupoor ;

Grasso, Maurizia .

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2018, 72 (20) :2485-2506

[9] Comparison of right and left ventricular responses to left ventricular assist device support in patients with severe heart failure - A primary role of mechanical unloading underlying reverse remodeling [J].

Barbone, A ;

Holmes, JW ;

Heerdt, PM ;

The', AHS ;

Naka, Y ;

Joshi, N ;

Daines, M ;

Marks, AR ;

Oz, MC ;

Burkhoff, D .

CIRCULATION, 2001, 104 (06) :670-675

[10] Prednisone/prednisolone and deflazacort regimens in the CINRG Duchenne Natural History Study [J].

Bello, Luca ;

Gordish-Dressman, Heather ;

Morgenroth, Lauren P. ;

Henricson, Erik K. ;

Tina Duong ;

Hoffman, Eric P. ;

Cnaan, Avital ;

McDonald, Craig M. .

NEUROLOGY, 2015, 85 (12) :1048-1055

← 1 2 3 4 5 6 7 8 9 10 →