Longitudinal 2-point dixon muscle magnetic resonance imaging in becker muscular dystrophy

被引:21
作者
Bonati, Ulrike [1 ]
Schmid, Maurice [1 ]
Hafner, Patricia [2 ]
Haas, Tanja [3 ]
Bieri, Oliver [3 ]
Gloor, Monika [3 ]
Fischmann, Arne [4 ]
Fischer, Dirk [1 ,2 ,5 ]
机构
[1] Univ Childrens Hosp Basel, Div Neuropaediat, CH-4031 Basel, Switzerland
[2] Univ Basel Hosp, Dept Neurol, CH-4031 Basel, Switzerland
[3] Univ Basel Hosp, Dept Radiol, Div Radiol Phys, CH-4031 Basel, Switzerland
[4] Univ Basel Hosp, Div Neuroradiol, CH-4031 Basel, Switzerland
[5] Kantonsspital Baselland, Univ Clin Internal Med, Bruderholz, Switzerland
关键词
2-point Dixon method; Becker muscular dystrophy; follow-up; muscle fat fraction; quantitative MRI; MOTOR FUNCTION MEASURE; GENE; MRI; DISEASES; PROTEIN;
D O I
10.1002/mus.24629
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: Quantitative MRI techniques detect disease progression in myopathies more sensitively than muscle function measures or conventional MRI. To date, only conventional MRI data using visual rating scales are available for measurement of disease progression in Becker muscular dystrophy (BMD). Methods: In 3 patients with BMD (mean age 36.8 years), the mean fat fraction (MFF) of the thigh muscles was assessed by MRI at baseline and at 1-year follow-up using a 2-point Dixon approach (2PD). The motor function measurement scale (MFM) was used for clinical assessment. Results: The mean MFF of all muscles at baseline was 61.6% (SD 7.6). It increased by 3.7% to 65.3% (SD 4.7) at follow-up. The severity of muscle involvement varied between various muscle groups. Conclusions: As in other myopathies, 2PD can quantify fatty muscle degeneration in BMD and can detect disease progression in a small sample size and at relatively short imaging intervals. Muscle Nerve51: 918-921, 2015
引用
收藏
页码:918 / 921
页数:4
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