Evidence map›Paper›PMID 40900969›Full record

ArticleNeurology. Genetics2025

Test-Retest Reliability of Motor Function and Myometry Outcomes From the Vamorolone Trials in Duchenne Muscular Dystrophy.

Rebecca A Tobin, Eric P Hoffman, Linda Johnson, Meredith K James, Paula R Clemens, Utkarsh J Dang, VBP15-LTE and VBP15-004 Investigators

Abstract read
In one paragraph

Article in Neurology. Genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Trial
  2. Trial
  3. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Rebecca A TobinCarleton University, Ottawa, Canada.ORCID https://orcid.org/0000-0001-7918-3193
Eric P HoffmanDepartment of Pharmaceutical Sciences, School of Pharmacy and Pharmaceutical Sciences, Binghamton University-State University of New York.ORCID https://orcid.org/0000-0001-6470-5139
Linda JohnsonTRiNDS LLC, Pittsburgh, PA.ORCID https://orcid.org/0009-0008-3815-2161
Meredith K JamesJohn Walton Muscular Dystrophy Research Centre, The Newcastle Upon Tyne Hospitals NHS Trust and Newcastle University, United Kingdom; and.ORCID https://orcid.org/0000-0001-8078-7744
Paula R ClemensUniversity of Pittsburgh School of Medicine and Department of Veterans Affairs Medical Center, Pittsburgh, PA.ORCID https://orcid.org/0000-0002-0652-6703
Utkarsh J DangCarleton University, Ottawa, Canada.ORCID https://orcid.org/0000-0003-4120-2015
VBP15-LTE and VBP15-004 Investigators

Funding

Biomarker Signatures for Duchenne Muscular DystrophyR61NS119639 · NINDS · STATE UNIVERSITY OF NY,BINGHAMTON · PI DANG, UTKARSH J, HATHOUT, YETRIB · 2022 to 2024
$1.6M
Clinical Trial Readiness for Monitoring Muscle Inflammation in Duchenne Muscular DystrophyR21TR004895 · NCATS · STATE UNIVERSITY OF NY,BINGHAMTON · PI HOFFMAN, ERIC P. · 2023 to 2024
$430k
NCATS NIH HHS R21 TR004895NINDS NIH HHS R61 NS119639
6 · The paper itself

Abstract

Background and Objectives: Understanding the reliability of outcomes used in clinical care and trials is important to delineate intervention-induced change from random variability. Reliability, sensitivity, and clinical meaningfulness of change are all key aspects of choosing the most appropriate outcome measure for a clinical trial. Common outcome measures to monitor progression and treatment effect in Duchenne muscular dystrophy (DMD) include measures of strength (myometry) and motor function tests: stand from supine velocity (STANDV), North Star Ambulatory Assessment (NSAA), 6-minute walk distance (6MWD), 10-m run/walk (RWV), and 4-stair climb velocity (CLIMBV). Our objective was to present test-retest reliability of common outcome measures using pretreatment measurements and to provide insights into missing measurements. Methods: Data were used on outcome measures in steroid-naïve, 4 to <7 years participants with DMD in 2 multisite, multicountry vamorolone trials (VBP15-002 [n = 48 participants] and VBP15-004 [n = 121 participants]). Bland-Altman analysis, the coefficient of variation, and the intraclass correlation coefficient (ICC) were used. Results: Based on the ICC, NSAA, RWV, and CLIMBV have good reliability, whereas the 6MWD and STANDV have moderate reliability. Two different techniques were used for myometry in VBP15-002 (CINRG Quantitative Measurement System [CQMS]) and VBP15-004 (MicroFET2 handheld digital muscle dynamometer [HHD]). Reliability of myometry ranged from poor to moderate, and CQMS did not show improved reliability over HHD. The 6MWD and myometry showed the highest rates of missingness. Because of similar age ranges and harmonized outcomes, our findings were compared with the FOR-DMD cohort. Myometry and CLIMBV were not in FOR-DMD; reliability findings were concordant for the 4 outcomes in common. For most outcomes, we found reduced reliability compared with previous studies in older age groups. Discussion: Reliable outcome measures, appropriate for the age of patients, are key to improving power in clinical trials, leading to fewer participants needed and reducing patient and site burden. We found NSAA, RWV, and CLIMBV to be the most reliable. This should be considered in the context of sensitivity to drug effect, and clinical meaningfulness of changes observed: all 5 motor outcomes were sensitive to drug effect of vamorolone and prednisone, whereas myometry was not.

Identifiers

PMID40900969
PMCPMC12401549

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.