Myocardial native T1 mapping and extracellular volume quantification in asymptomatic female carriers of Duchenne muscular dystrophy gene mutations

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Authors

MASÁROVÁ Lucia PANOVSKÝ Roman PEŠL Martin LUZ Mojica-Pisciotti Mary HOLEČEK Tomáš KINCL Vladimír JUŘÍKOVÁ Lenka MÁCHAL Jan OPATŘIL Lukáš FEITOVA Vera

Year of publication 2023
Type Article in Periodical
Magazine / Source Orphanet Journal of Rare Diseases
MU Faculty or unit

Faculty of Medicine

Citation
web https://ojrd.biomedcentral.com/articles/10.1186/s13023-023-02899-9
Doi http://dx.doi.org/10.1186/s13023-023-02899-9
Keywords Cardiac magnetic resonance; Duchenne muscular dystrophy; Native T-1 mapping; Extracellular volume quantification; Late gadolinium enhancement
Attached files
Description Background Female carriers of dystrophin gene mutations (DMD-FC) were previously considered non-manifesting, but in recent decades, cardiomyopathy associated with muscular dystrophy and myocardial fibrosis has been described. Our study aimed to assess prospectively myocardial fibrosis in asymptomatic DMD-FC compared to a sex-matched control group (CG) with similar age distribution using native T1 mapping and extracellular volume (ECV) quantification by cardiovascular magnetic resonance (CMR) imaging. Materials and methods 38 DMD-FC with verified genetic mutation and 22 healthy volunteers were included. Using CMR, native T1 relaxation time and ECV quantification were determined in each group. Late gadolinium enhancement (LGE) was assessed in all cases. Results There were 38 DMD-FC (mean age 39.1 +/- 8.8 years) and 22 healthy volunteers (mean age 39.9 +/- 12.6 years) imagined by CMR. The mean global native T1 relaxation time was similar for DMD-FC and CG (1005.1 +/- 26.3 ms vs. 1003.5 +/- 25.0 ms; p-value = 0.81). Likewise, the mean global ECV value was also similar between the groups (27.92 +/- 2.02% vs. 27.10 +/- 2.89%; p-value = 0.20). The segmental analysis of mean ECV values according to the American Heart Association classification did not show any differences between DMD-FC and CG. There was a non-significant trend towards higher mean ECV values of DMD-FC in the inferior and inferolateral segments of the myocardium (p-value = 0.075 and 0.070 respectively). Conclusion There were no statistically significant differences in the mean global and segmental native T1 relaxation times and the mean global or segmental ECV values. There was a trend towards higher segmental mean ECV values of DMD-FC in the inferior and inferolateral walls of the myocardium.
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