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Physiological and pathological skeletal muscle T1 changes quantified using a fast inversion-recovery radial NMR imaging sequence
by
Marty, Benjamin
, Carlier, Pierre G.
in
59/57
/ 692/308/53
/ 692/617/375/374
/ Aged
/ Becker's muscular dystrophy
/ Bone mineral density
/ Dystrophy
/ Exercise - physiology
/ Healthy Volunteers
/ Humanities and Social Sciences
/ Humans
/ Magnetic Resonance Imaging - methods
/ Male
/ Middle Aged
/ multidisciplinary
/ Muscle, Skeletal - diagnostic imaging
/ Muscle, Skeletal - physiology
/ Muscles
/ Muscular Dystrophy, Duchenne - diagnostic imaging
/ Muscular Dystrophy, Duchenne - pathology
/ Musculoskeletal system
/ Myositis
/ NMR
/ Nuclear magnetic resonance
/ Physiology
/ Science
/ Science (multidisciplinary)
/ Skeletal muscle
/ Thigh - diagnostic imaging
/ Thigh - physiology
/ Variation
2019
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Physiological and pathological skeletal muscle T1 changes quantified using a fast inversion-recovery radial NMR imaging sequence
by
Marty, Benjamin
, Carlier, Pierre G.
in
59/57
/ 692/308/53
/ 692/617/375/374
/ Aged
/ Becker's muscular dystrophy
/ Bone mineral density
/ Dystrophy
/ Exercise - physiology
/ Healthy Volunteers
/ Humanities and Social Sciences
/ Humans
/ Magnetic Resonance Imaging - methods
/ Male
/ Middle Aged
/ multidisciplinary
/ Muscle, Skeletal - diagnostic imaging
/ Muscle, Skeletal - physiology
/ Muscles
/ Muscular Dystrophy, Duchenne - diagnostic imaging
/ Muscular Dystrophy, Duchenne - pathology
/ Musculoskeletal system
/ Myositis
/ NMR
/ Nuclear magnetic resonance
/ Physiology
/ Science
/ Science (multidisciplinary)
/ Skeletal muscle
/ Thigh - diagnostic imaging
/ Thigh - physiology
/ Variation
2019
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Physiological and pathological skeletal muscle T1 changes quantified using a fast inversion-recovery radial NMR imaging sequence
by
Marty, Benjamin
, Carlier, Pierre G.
in
59/57
/ 692/308/53
/ 692/617/375/374
/ Aged
/ Becker's muscular dystrophy
/ Bone mineral density
/ Dystrophy
/ Exercise - physiology
/ Healthy Volunteers
/ Humanities and Social Sciences
/ Humans
/ Magnetic Resonance Imaging - methods
/ Male
/ Middle Aged
/ multidisciplinary
/ Muscle, Skeletal - diagnostic imaging
/ Muscle, Skeletal - physiology
/ Muscles
/ Muscular Dystrophy, Duchenne - diagnostic imaging
/ Muscular Dystrophy, Duchenne - pathology
/ Musculoskeletal system
/ Myositis
/ NMR
/ Nuclear magnetic resonance
/ Physiology
/ Science
/ Science (multidisciplinary)
/ Skeletal muscle
/ Thigh - diagnostic imaging
/ Thigh - physiology
/ Variation
2019
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Physiological and pathological skeletal muscle T1 changes quantified using a fast inversion-recovery radial NMR imaging sequence
Journal Article
Physiological and pathological skeletal muscle T1 changes quantified using a fast inversion-recovery radial NMR imaging sequence
2019
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Overview
We investigated the response of skeletal muscle global T1 under different physiological and pathological conditions using an inversion-recovery radial T1 mapping sequence. Thirty five healthy volunteers, seven patients with Becker muscular dystrophy (BMD) and seven patients with sporadic inclusion body myositis (IBM) were investigated in order to evaluate the effects of gender, age, muscle group, exercise and pathological processes on global T1 values. In addition, the intramuscular fat content was measured using 3-point Dixon and the global T2 and water T2 (T2
H2O
) were determined with a multi-spin-echo sequence. In the muscles of healthy volunteers, there was no impact of age on global T1. However, we measured a significant effect of sex and muscle group. After exercise, a significant 7.7% increase of global T1 was measured in the recruited muscles, and global T1 variations were highly correlated to T2
H2O
variations (R = 0.91). In pathologies, global T1 values were reduced in fat infiltrated muscles. When fat fraction was taken into account, global T1 values were higher in IBM patients compared to BMD. Global T1 variations are a sensitive indicator of tissue changes in skeletal muscle related to several physiological and pathological events.
Publisher
Nature Publishing Group UK,Nature Publishing Group
Subject
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