TY - JOUR
T1 - Upper and lower extremities in Duchenne muscular dystrophy evaluated with quantitative MRI and proton MR spectroscopy in a multicenter cohort
AU - Forbes, Sean C.
AU - Arora, Harneet
AU - Willcocks, Rebecca J.
AU - Triplett, William T.
AU - Rooney, William D.
AU - Barnard, Alison M.
AU - Alabasi, Umar
AU - Wang, Dah Jyuu
AU - Lott, Donovan J.
AU - Senesac, Claudia R.
AU - Harrington, Ann T.
AU - Finanger, Erika L.
AU - Tennekoon, Gihan I.
AU - Brandsema, John
AU - Daniels, Michael J.
AU - Lee Sweeney, H.
AU - Walter, Glenn A.
AU - Vandenborne, Krista
N1 - Funding Information:
Study supported by the National Institute of Neurological Disorders and Stroke and the National Institute of Arthritis and Musculoskeletal and Skin Diseases (R01AR056973); study supported in part by NIH shared instrument grant (NIH S10OD021701 and NIH S10OD018224). A portion of this work was performed in the McKnight Brain Institute at the National High Magnetic Field Laboratory’s AMRIS Facility, which is supported by National Science Foundation Cooperative (DMR-1644779) and the State of Florida.
Publisher Copyright:
© RSNA, 2020.
PY - 2020/6
Y1 - 2020/6
N2 - Background: Upper extremity MRI and proton MR spectroscopy are increasingly considered to be outcome measures in Duchenne muscular dystrophy (DMD) clinical trials. Purpose: To demonstrate the feasibility of acquiring upper extremity MRI and proton (1H) MR spectroscopy measures of T2 and fat fraction in a large, multicenter cohort (ImagingDMD) of ambulatory and nonambulatory individuals with DMD; compare upper and lower extremity muscles by using MRI and 1H MR spectroscopy; and correlate upper extremity MRI and 1H MR spectroscopy measures to function. Materials and Methods: In this prospective cross-sectional study, MRI and 1H MR spectroscopy and functional assessment data were acquired from participants with DMD and unaffected control participants at three centers (from January 28, 2016, to April 24, 2018). T2 maps of the shoulder, upper arm, forearm, thigh, and calf were generated from a spin-echo sequence (repetition time msec/echo time msec, 3000/20-320). Fat fraction maps were generated from chemical shift-encoded imaging (eight echo times). Fat fraction and 1HO T2 in the deltoid and biceps brachii were measured from single-voxel 1H MR spectroscopy (9000/11-243). Groups were compared by using Mann-Whitney test, and relationships between MRI and 1H MR spectroscopy and arm function were assessed by using Spearman correlation. Results: This study evaluated 119 male participants with DMD (mean age, 12 years ± 3 [standard deviation]) and 38 unaffected male control participants (mean age, 12 years ± 3). Deltoid and biceps brachii muscles were different in participants with DMD versus control participants in all age groups by using quantitative T2 MRI (P <.001) and 1H MR spectroscopy fat fraction (P <.05). The deltoid, biceps brachii, and triceps brachii were afected to the same extent (P >.05) as the soleus and medial gastrocnemius. Negative correlations were observed between arm function and MRI (T2: range among muscles, r = 20.53 to 20.73 [P <.01]; fat fraction, r = 20.49 to 20.70 [P <.01]) and 1H MR spectroscopy fat fraction (r = 20.64 to 20.71; P <.01). Conclusion: This multicenter study demonstrated early and progressive involvement of upper extremity muscles in Duchenne muscular dystrophy (DMD) and showed the feasibility of MRI and 1H MR spectroscopy to track disease progression over a wide range of ages in participants with DMD.
AB - Background: Upper extremity MRI and proton MR spectroscopy are increasingly considered to be outcome measures in Duchenne muscular dystrophy (DMD) clinical trials. Purpose: To demonstrate the feasibility of acquiring upper extremity MRI and proton (1H) MR spectroscopy measures of T2 and fat fraction in a large, multicenter cohort (ImagingDMD) of ambulatory and nonambulatory individuals with DMD; compare upper and lower extremity muscles by using MRI and 1H MR spectroscopy; and correlate upper extremity MRI and 1H MR spectroscopy measures to function. Materials and Methods: In this prospective cross-sectional study, MRI and 1H MR spectroscopy and functional assessment data were acquired from participants with DMD and unaffected control participants at three centers (from January 28, 2016, to April 24, 2018). T2 maps of the shoulder, upper arm, forearm, thigh, and calf were generated from a spin-echo sequence (repetition time msec/echo time msec, 3000/20-320). Fat fraction maps were generated from chemical shift-encoded imaging (eight echo times). Fat fraction and 1HO T2 in the deltoid and biceps brachii were measured from single-voxel 1H MR spectroscopy (9000/11-243). Groups were compared by using Mann-Whitney test, and relationships between MRI and 1H MR spectroscopy and arm function were assessed by using Spearman correlation. Results: This study evaluated 119 male participants with DMD (mean age, 12 years ± 3 [standard deviation]) and 38 unaffected male control participants (mean age, 12 years ± 3). Deltoid and biceps brachii muscles were different in participants with DMD versus control participants in all age groups by using quantitative T2 MRI (P <.001) and 1H MR spectroscopy fat fraction (P <.05). The deltoid, biceps brachii, and triceps brachii were afected to the same extent (P >.05) as the soleus and medial gastrocnemius. Negative correlations were observed between arm function and MRI (T2: range among muscles, r = 20.53 to 20.73 [P <.01]; fat fraction, r = 20.49 to 20.70 [P <.01]) and 1H MR spectroscopy fat fraction (r = 20.64 to 20.71; P <.01). Conclusion: This multicenter study demonstrated early and progressive involvement of upper extremity muscles in Duchenne muscular dystrophy (DMD) and showed the feasibility of MRI and 1H MR spectroscopy to track disease progression over a wide range of ages in participants with DMD.
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U2 - 10.1148/radiol.2020192210
DO - 10.1148/radiol.2020192210
M3 - Article
C2 - 32286193
AN - SCOPUS:85084884950
SN - 0033-8419
VL - 295
SP - 616
EP - 625
JO - RADIOLOGY
JF - RADIOLOGY
IS - 3
ER -