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Preserved thenar muscles in non‐ambulant Duchenne muscular dystrophy patients

BACKGROUND: Clinical trials in Duchenne muscular dystrophy (DMD) focus primarily on ambulant patients. Results cannot be extrapolated to later disease stages due to a decline in targeted muscle tissue. In non‐ambulant DMD patients, hand function is relatively preserved and crucial for daily‐life act...

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Autores principales: Naarding, Karin J., Keene, Kevin R., Sardjoe Mishre, Aashley S.D., Veeger, Thom T.J., van de Velde, Nienke M., Prins, Arina J., Burakiewicz, Jedrzej, Verschuuren, Jan J.G.M., van der Holst, Menno, Niks, Erik H., Kan, Hermien E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8200430/
https://www.ncbi.nlm.nih.gov/pubmed/33963807
http://dx.doi.org/10.1002/jcsm.12711
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author Naarding, Karin J.
Keene, Kevin R.
Sardjoe Mishre, Aashley S.D.
Veeger, Thom T.J.
van de Velde, Nienke M.
Prins, Arina J.
Burakiewicz, Jedrzej
Verschuuren, Jan J.G.M.
van der Holst, Menno
Niks, Erik H.
Kan, Hermien E.
author_facet Naarding, Karin J.
Keene, Kevin R.
Sardjoe Mishre, Aashley S.D.
Veeger, Thom T.J.
van de Velde, Nienke M.
Prins, Arina J.
Burakiewicz, Jedrzej
Verschuuren, Jan J.G.M.
van der Holst, Menno
Niks, Erik H.
Kan, Hermien E.
author_sort Naarding, Karin J.
collection PubMed
description BACKGROUND: Clinical trials in Duchenne muscular dystrophy (DMD) focus primarily on ambulant patients. Results cannot be extrapolated to later disease stages due to a decline in targeted muscle tissue. In non‐ambulant DMD patients, hand function is relatively preserved and crucial for daily‐life activities. We used quantitative MRI (qMRI) to establish whether the thenar muscles could be valuable to monitor treatment effects in non‐ambulant DMD patients. METHODS: Seventeen non‐ambulant DMD patients (range 10.2–24.1 years) and 13 healthy controls (range 9.5–25.4 years) underwent qMRI of the right hand at 3 T at baseline. Thenar fat fraction (FF), total volume (TV), and contractile volume (CV) were determined using 4‐point Dixon, and T2(water) was determined using multiecho spin‐echo. Clinical assessments at baseline (n = 17) and 12 months (n = 13) included pinch strength (kg), performance of the upper limb (PUL) 2.0, DMD upper limb patient reported outcome measure (PROM), and playing a video game for 10 min using a game controller. Group differences and correlations were assessed with non‐parametric tests. RESULTS: Total volume was lower in patients compared with healthy controls (6.9 cm(3), 5.3–9.0 cm(3) vs. 13.0 cm(3), 7.6–15.8 cm(3), P = 0.010). CV was also lower in patients (6.3 cm(3), 4.6–8.3 cm(3) vs. 11.9 cm(3), 6.9–14.6 cm(3), P = 0.010). FF was slightly elevated (9.7%, 7.3–11.4% vs. 7.7%, 6.6–8.4%, P = 0.043), while T2(water) was higher (31.5 ms, 30.0–32.6 ms vs. 28.1 ms, 27.8–29.4 ms, P < 0.001). Pinch strength and PUL decreased over 12 months (2.857 kg, 2.137–4.010 to 2.243 kg, 1.930–3.339 kg, and 29 points, 20–36 to 23 points, 17–30, both P < 0.001), while PROM did not (49 points, 36–57 to 44 points, 30–54, P = 0.041). All patients were able to play for 10 min at baseline or follow‐up, but some did not comply with the study procedures regarding this endpoint. Pinch strength correlated with TV and CV in patients (rho = 0.72 and rho = 0.68) and controls (both rho = 0.89). PUL correlated with TV, CV, and T2(water) (rho = 0.57, rho = 0.51, and rho = −0.59). CONCLUSIONS: Low thenar FF, increased T2(water), correlation of muscle size with strength and function, and the decrease in strength and function over 1 year indicate that the thenar muscles are a valuable and quantifiable target for therapy in later stages of DMD. Further studies are needed to relate these data to the loss of a clinically meaningful milestone.
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spelling pubmed-82004302021-06-15 Preserved thenar muscles in non‐ambulant Duchenne muscular dystrophy patients Naarding, Karin J. Keene, Kevin R. Sardjoe Mishre, Aashley S.D. Veeger, Thom T.J. van de Velde, Nienke M. Prins, Arina J. Burakiewicz, Jedrzej Verschuuren, Jan J.G.M. van der Holst, Menno Niks, Erik H. Kan, Hermien E. J Cachexia Sarcopenia Muscle Original Articles BACKGROUND: Clinical trials in Duchenne muscular dystrophy (DMD) focus primarily on ambulant patients. Results cannot be extrapolated to later disease stages due to a decline in targeted muscle tissue. In non‐ambulant DMD patients, hand function is relatively preserved and crucial for daily‐life activities. We used quantitative MRI (qMRI) to establish whether the thenar muscles could be valuable to monitor treatment effects in non‐ambulant DMD patients. METHODS: Seventeen non‐ambulant DMD patients (range 10.2–24.1 years) and 13 healthy controls (range 9.5–25.4 years) underwent qMRI of the right hand at 3 T at baseline. Thenar fat fraction (FF), total volume (TV), and contractile volume (CV) were determined using 4‐point Dixon, and T2(water) was determined using multiecho spin‐echo. Clinical assessments at baseline (n = 17) and 12 months (n = 13) included pinch strength (kg), performance of the upper limb (PUL) 2.0, DMD upper limb patient reported outcome measure (PROM), and playing a video game for 10 min using a game controller. Group differences and correlations were assessed with non‐parametric tests. RESULTS: Total volume was lower in patients compared with healthy controls (6.9 cm(3), 5.3–9.0 cm(3) vs. 13.0 cm(3), 7.6–15.8 cm(3), P = 0.010). CV was also lower in patients (6.3 cm(3), 4.6–8.3 cm(3) vs. 11.9 cm(3), 6.9–14.6 cm(3), P = 0.010). FF was slightly elevated (9.7%, 7.3–11.4% vs. 7.7%, 6.6–8.4%, P = 0.043), while T2(water) was higher (31.5 ms, 30.0–32.6 ms vs. 28.1 ms, 27.8–29.4 ms, P < 0.001). Pinch strength and PUL decreased over 12 months (2.857 kg, 2.137–4.010 to 2.243 kg, 1.930–3.339 kg, and 29 points, 20–36 to 23 points, 17–30, both P < 0.001), while PROM did not (49 points, 36–57 to 44 points, 30–54, P = 0.041). All patients were able to play for 10 min at baseline or follow‐up, but some did not comply with the study procedures regarding this endpoint. Pinch strength correlated with TV and CV in patients (rho = 0.72 and rho = 0.68) and controls (both rho = 0.89). PUL correlated with TV, CV, and T2(water) (rho = 0.57, rho = 0.51, and rho = −0.59). CONCLUSIONS: Low thenar FF, increased T2(water), correlation of muscle size with strength and function, and the decrease in strength and function over 1 year indicate that the thenar muscles are a valuable and quantifiable target for therapy in later stages of DMD. Further studies are needed to relate these data to the loss of a clinically meaningful milestone. John Wiley and Sons Inc. 2021-05-08 2021-06 /pmc/articles/PMC8200430/ /pubmed/33963807 http://dx.doi.org/10.1002/jcsm.12711 Text en © 2021 The Authors. Journal of Cachexia, Sarcopenia and Muscle published by John Wiley & Sons Ltd on behalf of Society on Sarcopenia, Cachexia and Wasting Disorders. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Naarding, Karin J.
Keene, Kevin R.
Sardjoe Mishre, Aashley S.D.
Veeger, Thom T.J.
van de Velde, Nienke M.
Prins, Arina J.
Burakiewicz, Jedrzej
Verschuuren, Jan J.G.M.
van der Holst, Menno
Niks, Erik H.
Kan, Hermien E.
Preserved thenar muscles in non‐ambulant Duchenne muscular dystrophy patients
title Preserved thenar muscles in non‐ambulant Duchenne muscular dystrophy patients
title_full Preserved thenar muscles in non‐ambulant Duchenne muscular dystrophy patients
title_fullStr Preserved thenar muscles in non‐ambulant Duchenne muscular dystrophy patients
title_full_unstemmed Preserved thenar muscles in non‐ambulant Duchenne muscular dystrophy patients
title_short Preserved thenar muscles in non‐ambulant Duchenne muscular dystrophy patients
title_sort preserved thenar muscles in non‐ambulant duchenne muscular dystrophy patients
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8200430/
https://www.ncbi.nlm.nih.gov/pubmed/33963807
http://dx.doi.org/10.1002/jcsm.12711
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