Cardiac profile of the Czech population of Duchenne muscular dystrophy patients: a cardiovascular magnetic resonance study with T1 mapping
Jazyk angličtina Země Velká Británie, Anglie Médium electronic
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
LQ1605
Ministerstvo Školství, Mládeže a Tělovýchovy - International
PubMed
30626423
PubMed Central
PMC6327529
DOI
10.1186/s13023-018-0986-0
PII: 10.1186/s13023-018-0986-0
Knihovny.cz E-zdroje
- Klíčová slova
- Cardiac magnetic resonance, Cardiomyopathy, Duchene muscular dystrophy, T1 mapping; extracellular volume,
- MeSH
- Duchennova muskulární dystrofie diagnostické zobrazování MeSH
- gadolinium analýza MeSH
- kardiomyopatie diagnostické zobrazování MeSH
- lidé MeSH
- magnetická rezonanční tomografie metody MeSH
- mladiství MeSH
- Check Tag
- lidé MeSH
- mladiství MeSH
- mužské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Geografické názvy
- Česká republika MeSH
- Názvy látek
- gadolinium MeSH
BACKGROUND: The progressive cardiomyopathy that develops in boys with Duchenne and Becker muscular dystrophy (DMD/BMD) is presumed to be a secondary consequence of the fibrosis within the myocardium. There are only limited data on using parametric imaging in these patients. The purpose of this study was to assess native T1 and extracellular volume (ECV) values in DMD patients. METHODS: The Czech population of males with DMD/BMD was screened. All eligible patients fulfilling the inclusion criteria were included. Forty nine males underwent cardiac magnetic resonance (MR) examination including T1 native and post-contrast mapping measurements. One DMD patient and all BMD patients were excluded from statistical analysis. Three groups were compared - Group D1 - DMD patients without late gadolinium enhancement (LGE) (n = 23), Group D2 - DMD patients with LGE (n = 20), and Group C - gender matched controls (n = 13). RESULTS: Compared to controls, both DMD groups had prolonged T1 native relaxation time. These results are concordant in all 6 segments as well as in global values (1041 ± 31 ms and 1043 ± 37 ms vs. 983 ± 15 ms, both p < 0.05). Group D2 had significantly increased global ECV (0.28 ± 0.044 vs. 0.243 ± 0.013, p < 0.05) and segmental ECV in inferolateral and anterolateral segments in comparison with controls. The results were also significant after adjustment for subjects' age. CONCLUSION: DMD males had increased native T1 relaxation time independent of the presence or absence of myocardial fibrosis. Cardiac MR may provide clinically useful information even without contrast media administration.
Department of Biology Faculty of Medicine Masaryk University Brno Czech Republic
Department of Medical Imaging St Anne's University Hospital Brno Czech Republic
Department of Pathophysiology Faculty of Medicine Masaryk University Brno Czech Republic
Department of Pediatric Neurology University Hospital Brno Brno Czech Republic
International Clinical Research Center St Anne's University Hospital Brno Czech Republic
Pediatric Clinic University Hospital Brno Brno Czech Republic
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Birnkrant DJ, Bushby K, Bann CM, et al. DMD care considerations working group. Diagnosis and management of Duchenne muscular dystrophy, part 2: respiratory, cardiac, bone health, and orthopaedic management. Lancet Neurol. 2018;17(4):347–361. doi: 10.1016/S1474-4422(18)30025-5. PubMed DOI PMC
McNally EM. New approaches in the therapy of cardiomyopathy in muscular dystrophy. Ann Rev Med. 2007;58:75–88. doi: 10.1146/annurev.med.58.011706.144703. PubMed DOI
Mu X, Tang Y, Lu A, et al. The role of notch signaling in muscle progenitor cell depletion and the rapid onset of histopathology in muscular dystrophy. Hum Mol Genet. 2015;24(10):2923–2937. doi: 10.1093/hmg/ddv055. PubMed DOI PMC
Berry SE, Andruszkiewicz P, Chun JL, Hong J. Nestin expression in end-stage disease in dystrophin-deficient heart: implications for regeneration from endogenous cardiac stem cells. Stem Cells Transl Med. 2013;2(11):848–861. doi: 10.5966/sctm.2012-0174. PubMed DOI PMC
Aartsma-Rus A, Van Deutekom JC, Fokkema IF, Van Ommen GJ, Den Dunnen JT. Entries in the Leiden Duchenne muscular dystrophy mutation database: an overview of mutation types and paradoxical cases that confirm the reading-frame rule. Muscle Nerve. 2006;34(2):135–144. doi: 10.1002/mus.20586. PubMed DOI
Bladen CL, Salgado D, Monges S, et al. The TREAT-NMD DMD global database: analysis of more than 7,000 Duchenne muscular dystrophy mutations. Hum Mutat. 2015;36(4):395–402. doi: 10.1002/humu.22758. PubMed DOI PMC
Cotton RG, Auerbach AD, Beckmann JS, et al. Recommendations for locus-specific databases and their curation. Hum Mutat. 2008;29(1):2–5. doi: 10.1002/humu.20650. PubMed DOI PMC
Li W, Liu W, Zhong J, Yu X. Early manifestation of alteration in cardiac function in dystrophin deficient MDX mouse using 3D CMR tagging. J Cardiovasc Magn Reson. 2009;11:40. doi: 10.1186/1532-429X-11-40. PubMed DOI PMC
Power A, Poonja S, Disler D, et al. Echocardiographic image quality deteriorates with age in children and young adults with Duchenne muscular dystrophy. Front Cardiovasc Med. 2017;4:82. doi: 10.3389/fcvm.2017.00082. PubMed DOI PMC
D'Amario D, Amodeo A, Adorisio R, et al. A current approach to heart failure in Duchenne muscular dystrophy. Heart. 2017;103(22):1770–1779. doi: 10.1136/heartjnl-2017-311269. PubMed DOI
Markham LW, Michelfelder EC, Border WL, et al. Abnormalities of diastolic function precede dilated cardiomyopathy associated with Duchenne muscular dystrophy. J Am Soc Echocardiogr. 2006;19(7):865–871. doi: 10.1016/j.echo.2006.02.003. PubMed DOI
Puchalski MD, Williams RV, Askovich B, et al. Late gadolinium enhancement: precursor to cardiomyopathy in Duchenne muscular dystrophy? Int J Cardiovasc Imaging. 2009;25(1):57–63. doi: 10.1007/s10554-008-9352-y. PubMed DOI PMC
Florian A, Ludwig A, Engelen M, et al. Left ventricular systolic function and the pattern of late-gadolinium-enhancement independently and additively predict adverse cardiac events in muscular dystrophy patients. J Cardiovasc Magn Reson. 2014;16:81. doi: 10.1186/s12968-014-0081-1. PubMed DOI PMC
Silva MC, Meira ZM, Gurgel Giannetti J, et al. Myocardial delayed enhancement by magnetic resonance imaging in patients with muscular dystrophy. J Am Coll Cardiol. 2007;49:1874–1879. doi: 10.1016/j.jacc.2006.10.078. PubMed DOI
Hor KN, Taylor MD, Al-Khalidi HR, et al. Prevalence and distribution of late gadolinium enhancement in a large population of patients with Duchenne muscular dystrophy: effect of age and left ventricular systolic function. J Cardiovasc Magn Reson. 2013;15:107. doi: 10.1186/1532-429X-15-107. PubMed DOI PMC
Tandon A, Villa CR, Hor KN, et al. Myocardial fibrosis burden predicts left ventricular ejection fraction and is associated with age and steroid treatment duration in Duchenne muscular dystrophy. J Am Heart Assoc. 2015;4:1–9. doi: 10.1161/JAHA.114.001338. PubMed DOI PMC
Silva MC, Magalhães TA, Meira ZM, et al. Myocardial fibrosis progression in Duchenne and Becker muscular dystrophy: a randomized clinical trial. JAMA Cardiol. 2017;2(2):190–199. doi: 10.1001/jamacardio.2016.4801. PubMed DOI
Coolen BF, Geelen T, Paulis LE, Nauerth A, Nicolay K, Strijkers GJ. Three-dimensional T1 mapping of the mouse heart using variable flip angle steady-state MR imaging. NMR Biomed. 2011;24(2):154–162. doi: 10.1002/nbm.1566. PubMed DOI
Florian A, Ludwig A, Rösch S, Yildiz H, Sechtem U, Yilmaz A. Myocardial fibrosis imaging based on T1-mapping and extracellular volume fraction (ECV) measurement in muscular dystrophy patients: diagnostic value compared with conventional late gadolinium enhancement (LGE) imaging. Eur Heart J Cardiovasc Imaging. 2014;15:1004–1012. doi: 10.1093/ehjci/jeu050. PubMed DOI
Soslow J, Damon S, Crum K, et al. Increased myocardial native T1 and extracellular volume in patients with Duchenne muscular dystrophy. J Cardiovasc Magn Reson. 2016;18:5. doi: 10.1186/s12968-016-0224-7. PubMed DOI PMC
Starc JJ, Moore RA, Rattan MS, et al. Elevated myocardial extracellular volume fraction in Duchenne muscular dystrophy. Pediatr Cardiol. 2017;38(7):1485–1492. doi: 10.1007/s00246-017-1690-x. PubMed DOI
Olivieri L, Kellman P, McCarter R, Cross R, Hansen M, Spurney C. Native T1 values identify myocardial changes and stratify disease severity in patients with Duchenne muscular dystrophy. J Cardiovasc Magn Reson. 2016;18:72. doi: 10.1186/s12968-016-0292-8. PubMed DOI PMC
Stehlíkova K, Skalova D, Zidkova J, et al. Muscular dystrophies and myopathies: the spectrum of mutated genes in the Czech Republic. Clin Genet. 2017;91:463–469. doi: 10.1111/cge.12839. PubMed DOI
Vry J, Gramsch K, Rodger S, et al. European Cross-sectional survey of current care practices for Duchenne muscular dystrophy reveals regional and age-dependent differences. J Neuromuscul Dis. 2016;3(4):517–527. doi: 10.3233/JND-160185. PubMed DOI PMC
Schulz-Menger J, Bluemke DA, Bremerich J, et al. Standardized image interpretation and post processing in cardiovascular magnetic resonance: Society for Cardiovascular Magnetic Resonance (SCMR). Board of Trustees Task Force on standardized post processing. J Cardiovasc Magn Reson. 2013;15:35. doi: 10.1186/1532-429X-15-35. PubMed DOI PMC
Cerqueira MD, Weissman NJ, Dilsizian V, et al. Standardized myocardial segmentation and nomenclature for tomographic imaging of the heart. A statement for healthcare professionals from the cardiac imaging committee of the council on clinical cardiology of the American Heart Association. Int J Cardiovasc Imaging. 2002;18:539–542. PubMed
Ashwath ML, Jacobs IB, Crowe CA, Ashwath RC, Super DM, Bahler RC. Left ventricular dysfunction in Duchenne muscular dystrophy and genotype. Am J Cardiol. 2014;114(2):284–289. doi: 10.1016/j.amjcard.2014.04.038. PubMed DOI PMC
Shah RV, Kato S, Roujol S, et al. Native myocardial T1 as a biomarker of cardiac structure in nonischemic cardiomyopathy. Am J Cardiol. 2016;117:282–288. doi: 10.1016/j.amjcard.2015.10.046. PubMed DOI
Puntmann VO, Arroyo Ucar E, Hinojar Baydes R, et al. Aortic stiffness and interstitial myocardial fibrosis by native T1 are independently associated with left ventricular remodeling in patients with dilated cardiomyopathy. Hypertension. 2014;64:762–768. doi: 10.1161/HYPERTENSIONAHA.114.03928. PubMed DOI
Puntmann VO, Carr-White G, Jabbour A, et al. T1-mapping and outcome in nonischemic cardiomyopathy. JACC Cardiovasc Imaging. 2016;9:40–50. doi: 10.1016/j.jcmg.2015.12.001. PubMed DOI
Flett AS, Hayward MP, Ashworth MT, et al. Equilibrium contrast cardiovascular magnetic resonance for the measurement of diffuse myocardial fibrosis: preliminary validation in humans. Circulation. 2010;122:138–144. doi: 10.1161/CIRCULATIONAHA.109.930636. PubMed DOI
Bilchick KC, Salerno M, Plitt D, et al. Prevalence and distribution of regional scar in dysfunctional myocardial segments in Duchenne muscular dystrophy. J Cardiovasc Magn Reson. 2011;13(1):20. doi: 10.1186/1532-429X-13-20. PubMed DOI PMC
Mavrogeni S, Papavasiliou A, Giannakopoulou K, et al. Oedema-fibrosis in Duchenne muscular dystrophy: role of cardiovascular magnetic resonance imaging. Eur J Clin Investig. 2017;47(12):e12843. doi: 10.1111/eci.12843. PubMed DOI
McNally EM, Kaltman JR, Benson DW, et al. Contemporary cardiac issues in Duchenne muscular dystrophy. Working Group of the National Heart, lung, and blood institute in collaboration with Parent Project Muscular Dystrophy. Circulation. 2015;131(18):1590–1598. doi: 10.1161/CIRCULATIONAHA.114.015151. PubMed DOI PMC
von Knobelsdorff-Brenkenhoff F, Prothmann M, Dieringer MA, et al. Myocardial T1 and T2 mapping at 3 T: reference values, influencing factors and implications. J Cardiovasc Magn Reson. 2013;15:53. doi: 10.1186/1532-429X-15-53. PubMed DOI PMC
D'Orsogna L, O'Shea JP, Miller G. Cardiomyopathy of Duchenne muscular dystrophy. Pediatr Cardiol. 1988;9(4):205–213. doi: 10.1007/BF02078410. PubMed DOI
Sarrazin E, von der Hagen M, Schara U, von Au K, Kaindl AM. Growth and psychomotor development of patients with Duchenne muscular dystrophy. Eur J Paediatr Neurol. 2014;18(1):38–44. doi: 10.1016/j.ejpn.2013.08.008. PubMed DOI
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