Literature DB >> 31469921

Longitudinal reliability of outcome measures in patients with Duchenne muscular dystrophy.

Sara Nagy1,2, Sabine Schädelin3, Patricia Hafner1, Ulrike Bonati1,2, Delia Scherrer1, Selina Ebi1, Simone Schmidt1, Anna-Lena Orsini1,2, Oliver Bieri4, Dirk Fischer1.   

Abstract

INTRODUCTION: The definition of reliable outcome measures is of increasing interest in patients with Duchenne muscular dystrophy (DMD).
METHODS: In this retrospective study, we analyzed the longitudinal reliability of clinical and radiological endpoints in 29 ambulant patients with DMD. Clinical outcome measures included motor function measure (MFM) and timed function tests, while quantitative MRI data were mean fat fraction (MFF) and T2 relaxation time of thigh muscles. Statistical analysis was based on 3-, 6-, and 12-month follow-up data.
RESULTS: Quantitative MRI using the MFF was the most sensitive and powerful marker of disease progression with a sample size of four at 1-year follow-up, followed by the D1 domain of MFM (standing and transfer function) with a sample size of 12. DISCUSSION: Our data support the longitudinal design of clinical trials over at least 12 months and the combinational use of clinical and radiological surrogate outcome measures.
© 2019 Wiley Periodicals, Inc.

Entities:  

Keywords:  Duchenne muscular dystrophy; clinical outcome measure; longitudinal analysis; motor function measure; quantitative muscle MRI; sample size

Year:  2019        PMID: 31469921     DOI: 10.1002/mus.26690

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  6 in total

1.  Ambulatory Duchenne muscular dystrophy children: cross-sectional correlation between function, quantitative muscle ultrasound and MRI.

Authors:  Hala Abdulhady; Hossam M Sakr; Nermine S Elsayed; Tamer A El-Sobky; Nagia Fahmy; Amr M Saadawy; Heba Elsedfy
Journal:  Acta Myol       Date:  2022-03-31

2.  Upper and Lower Extremities in Duchenne Muscular Dystrophy Evaluated with Quantitative MRI and Proton MR Spectroscopy in a Multicenter Cohort.

Authors:  Sean C Forbes; Harneet Arora; Rebecca J Willcocks; William T Triplett; William D Rooney; Alison M Barnard; Umar Alabasi; Dah-Jyuu Wang; Donovan J Lott; Claudia R Senesac; Ann T Harrington; Erika L Finanger; Gihan I Tennekoon; John Brandsema; Michael J Daniels; H Lee Sweeney; Glenn A Walter; Krista Vandenborne
Journal:  Radiology       Date:  2020-04-14       Impact factor: 11.105

3.  Translation and cross-cultural adaptation of the Charcot-Marie-Tooth disease Pediatric Scale to Brazilian Portuguese and determination of its measurement properties.

Authors:  Karoliny Lisandra Teixeira Cruz; Ana Cristina Resende Camargos; Juliana Cardoso; Cyntia Rogean de Jesus Alves de Baptista; Aline Duprat Ramos; Ana Claudia Mattiello-Sverzut; Joshua Burns; Hércules Ribeiro Leite
Journal:  Braz J Phys Ther       Date:  2020-08-07       Impact factor: 3.377

4.  Baseline fat fraction is a strong predictor of disease progression in Becker muscular dystrophy.

Authors:  Thom T J Veeger; Nienke M van de Velde; Kevin R Keene; Erik H Niks; Melissa T Hooijmans; Andrew G Webb; Jurriaan H de Groot; Hermien E Kan
Journal:  NMR Biomed       Date:  2022-02-05       Impact factor: 4.478

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

Authors:  Sarah P Sherlock; Yao Zhang; Michael Binks; Shannon Marraffino
Journal:  Biomark Med       Date:  2021-06-22       Impact factor: 2.851

6.  Selection Approach to Identify the Optimal Biomarker Using Quantitative Muscle MRI and Functional Assessments in Becker Muscular Dystrophy.

Authors:  Nienke M van de Velde; Melissa T Hooijmans; Aashley S D Sardjoe Mishre; Kevin R Keene; Zaïda Koeks; Thom T J Veeger; Iris Alleman; Erik W van Zwet; Jan-Willem M Beenakker; Jan J G M Verschuuren; Hermien E Kan; Erik H Niks
Journal:  Neurology       Date:  2021-06-23       Impact factor: 9.910

  6 in total

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