| PANOVSKÝ, Roman, Martin PEŠL, Tomáš HOLEČEK, Jan MÁCHAL, Věra FEITOVÁ, Lenka MRÁZOVÁ, Jana HABERLOVÁ, Alžběta SLABÁ, Pavel VÍT, Veronika STARÁ and Vladimír KINCL. Cardiac profile of the Czech population of Duchenne muscular dystrophy patients: a cardiovascular magnetic resonance study with T1 mapping. ORPHANET JOURNAL OF RARE DISEASES. LONDON: BMC, 2019, vol. 14, No 10, p. 1-10. ISSN 1750-1172. Available from: https://dx.doi.org/10.1186/s13023-018-0986-0. |
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@article{1498676,
author = {Panovský, Roman and Pešl, Martin and Holeček, Tomáš and Máchal, Jan and Feitová, Věra and Mrázová, Lenka and Haberlová, Jana and Slabá, Alžběta and Vít, Pavel and Stará, Veronika and Kincl, Vladimír},
article_location = {LONDON},
article_number = {10},
doi = {http://dx.doi.org/10.1186/s13023-018-0986-0},
keywords = {Cardiac magnetic resonance Duchene muscular dystrophy T1 mapping; extracellular volume Cardiomyopathy},
language = {eng},
issn = {1750-1172},
journal = {ORPHANET JOURNAL OF RARE DISEASES},
title = {Cardiac profile of the Czech population of Duchenne muscular dystrophy patients: a cardiovascular magnetic resonance study with T1 mapping},
url = {https://ojrd.biomedcentral.com/articles/10.1186/s13023-018-0986-0},
volume = {14},
year = {2019}
}
TY - JOUR
ID - 1498676
AU - Panovský, Roman - Pešl, Martin - Holeček, Tomáš - Máchal, Jan - Feitová, Věra - Mrázová, Lenka - Haberlová, Jana - Slabá, Alžběta - Vít, Pavel - Stará, Veronika - Kincl, Vladimír
PY - 2019
TI - Cardiac profile of the Czech population of Duchenne muscular dystrophy patients: a cardiovascular magnetic resonance study with T1 mapping
JF - ORPHANET JOURNAL OF RARE DISEASES
VL - 14
IS - 10
SP - 1-10
EP - 1-10
PB - BMC
SN - 17501172
KW - Cardiac magnetic resonance Duchene muscular dystrophy T1 mapping
KW - extracellular volume Cardiomyopathy
UR - https://ojrd.biomedcentral.com/articles/10.1186/s13023-018-0986-0
L2 - https://ojrd.biomedcentral.com/articles/10.1186/s13023-018-0986-0
N2 - BackgroundThe 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.MethodsThe 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).ResultsCompared 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 (104131ms and 1043 +/- 37ms vs. 983 +/- 15ms, 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.
ER -
PANOVSKÝ, Roman, Martin PEŠL, Tomáš HOLEČEK, Jan MÁCHAL, Věra FEITOVÁ, Lenka MRÁZOVÁ, Jana HABERLOVÁ, Alžběta SLABÁ, Pavel VÍT, Veronika STARÁ and Vladimír KINCL. Cardiac profile of the Czech population of Duchenne muscular dystrophy patients: a cardiovascular magnetic resonance study with T1 mapping. \textit{ORPHANET JOURNAL OF RARE DISEASES}. LONDON: BMC, 2019, vol.~14, No~10, p.~1-10. ISSN~1750-1172. Available from: https://dx.doi.org/10.1186/s13023-018-0986-0.
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