Quantitative muscle MRI biomarkers in Duchenne muscular dystrophy: cross-sectional correlations with age and functional tests

被引:19
作者
Sherlock, Sarah P. [1 ]
Zhang, Yao [1 ]
Binks, Michael [1 ]
Marraffino, Shannon [1 ]
机构
[1] Pfizer Inc, Cambridge, MA 02139 USA
关键词
four-stair climb; MRI; DMD; domagrozumab; Duchenne muscular dystrophy; functional test; imaging; SKELETAL-MUSCLE; DISEASE PROGRESSION; BOYS; TISSUE; QUANTIFICATION; STRENGTH;
D O I
10.2217/bmm-2020-0801
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Aim: Using baseline data from a clinical trial of domagrozumab in Duchenne muscular dystrophy, we evaluated the correlation between functional measures and quantitative MRI assessments of thigh muscle. Patients & methods: Analysis included timed functional tests, knee extension/strength and North Star Ambulatory Assessment. Patients (n = 120) underwent examinations of one thigh, with MRI sequences to enable measurements of muscle volume (MV), MV index, mean T2 relaxation time via T2-mapping and fat fraction. Results: MV was moderately correlated with strength assessments. MV index, fat fraction and T2-mapping measures had moderate correlations (r similar to 0.5) to all functional tests, North Star Ambulatory Assessment and age. Conclusion: The moderate correlation between functional tests, age and baseline MRI measures supports MRI as a biomarker in Duchenne muscular dystrophy clinical trials. Lay abstract: Clinical trials in Duchenne muscular dystrophy have proven to be challenging, due in part to the lack of robust biomarkers that are sensitive to detecting disease progression. While physical function, such as walking or climbing stairs, will be critical to demonstrating the long-term efficacy of a therapeutic, MRI may be a more objective approach that could detect subtle changes in disease status and offer earlier signals of clinical efficacy. In this study, researchers used baseline data from a Phase II clinical study (NCT02310763) to evaluate the relationship between measures of physical function and quantitative MRI assessments. They found that many MRI measures were moderately correlated with physical function, and muscle volume measurements were correlated with measures of strength. This study supports the use of MRI as a biomarker in Duchenne muscular dystrophy clinical trials.
引用
收藏
页码:761 / 773
页数:13
相关论文
共 50 条
  • [21] Gastrocnemius medialis muscle architecture and physiological cross sectional area in adult males with Duchenne muscular dystrophy
    Morse, C. I.
    Smith, J.
    Denny, A.
    Tweedale, J.
    Searle, N. D.
    JOURNAL OF MUSCULOSKELETAL & NEURONAL INTERACTIONS, 2015, 15 (02) : 154 - 160
  • [22] Quantitative muscle MRI and ultrasound for facioscapulohumeral muscular dystrophy: complementary imaging biomarkers
    Karlien Mul
    Corinne G. C. Horlings
    Sanne C. C. Vincenten
    Nicol C. Voermans
    Baziel G. M. van Engelen
    Nens van Alfen
    Journal of Neurology, 2018, 265 : 2646 - 2655
  • [23] Functional muscle ischemia in Duchenne and Becker muscular dystrophy
    Thomas, Gail D.
    FRONTIERS IN PHYSIOLOGY, 2013, 4
  • [24] Quantitative MRI and loss of free ambulation in Duchenne muscular dystrophy
    Fischmann, Arne
    Hafner, Patricia
    Gloor, Monika
    Schmid, Maurice
    Klein, Andrea
    Pohlman, Urs
    Waltz, Tanja
    Gonzalez, Rocio
    Haas, Tanja
    Bieri, Oliver
    Fischer, Dirk
    JOURNAL OF NEUROLOGY, 2013, 260 (04) : 969 - 974
  • [25] A Longitudinal Study of Quantitative Muscle Strength and Functional Motor Ability in Ambulatory Boys with Duchenne Muscular Dystrophy
    Buckon, Cathleen E.
    Sienko, Susan E.
    Fowler, Eileen G.
    Bagley, Anita M.
    Staudt, Loretta A.
    Sison-Williamson, Mitell
    Heberer, Kent R.
    McDonald, Craig M.
    Sussman, Michael D.
    JOURNAL OF NEUROMUSCULAR DISEASES, 2022, 9 (02) : 321 - 334
  • [26] Quantitative MRI and loss of free ambulation in Duchenne muscular dystrophy
    Arne Fischmann
    Patricia Hafner
    Monika Gloor
    Maurice Schmid
    Andrea Klein
    Urs Pohlman
    Tanja Waltz
    Rocio Gonzalez
    Tanja Haas
    Oliver Bieri
    Dirk Fischer
    Journal of Neurology, 2013, 260 : 969 - 974
  • [27] Longitudinal measurements of MRI-T2 in boys with Duchenne muscular dystrophy: Effects of age and disease progression
    Willcocks, R. J.
    Arpan, I. A.
    Forbes, S. C.
    Lott, D. J.
    Senesac, C. R.
    Senesac, E.
    Deol, J.
    Triplett, W. T.
    Baligand, C.
    Daniels, M. J.
    Sweeney, H. L.
    Walter, G. A.
    Vandenborne, K.
    NEUROMUSCULAR DISORDERS, 2014, 24 (05) : 393 - 401
  • [28] T2 mapping provides multiple approaches for the characterization of muscle involvement in neuromuscular diseases: a cross-sectional study of lower leg muscles in 5-15-year-old boys with Duchenne muscular dystrophy
    Arpan, Ishu
    Forbes, Sean C.
    Lott, Donovan J.
    Senesac, Claudia R.
    Daniels, Michael J.
    Triplett, William T.
    Deol, Jasjit K.
    Sweeney, H. Lee
    Walter, Glenn A.
    Vandenborne, Krista
    NMR IN BIOMEDICINE, 2013, 26 (03) : 320 - 328
  • [29] Using MRI to quantify skeletal muscle pathology in Duchenne muscular dystrophy: A systematic mapping review
    Alic, Lejla
    Griffin, John F.
    Eresen, Aydin
    Kornegay, Joe N.
    Ji, Jim X.
    MUSCLE & NERVE, 2021, 64 (01) : 8 - 22
  • [30] QUANTITATIVE MUSCLE ULTRASOUND IN DUCHENNE MUSCULAR DYSTROPHY: A COMPARISON OF TECHNIQUES
    Shklyar, Irina
    Geisbush, Tom R.
    Mijialovic, Aleksandar S.
    Pasternak, Amy
    Darras, Basil T.
    Wu, Jim S.
    Rutkove, Seward B.
    Zaidman, Craig M.
    MUSCLE & NERVE, 2015, 51 (02) : 207 - 213