Evidence map›Paper›PMID 38795602›Full record

ArticleNeuromuscular disorders : NMD2024

The Limb Girdle Muscular Dystrophy Health Index (LGMD-HI).

Joy A Stouffer, Kameron Bates, Leroy R Thacker, Chad Heatwole, Nicholas E Johnson

Abstract read
In one paragraph

Article in Neuromuscular disorders : NMD, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

5 authors.

Joy A StoufferVirginia Commonwealth University School of Medicine, 1201 E Marshall St #4-100, Richmond, VA 23298, United States.
Kameron BatesDepartment of Neurology, Virginia Commonwealth University School of Medicine, 417N 11th St, Richmond, VA 23298, United States.
Leroy R ThackerDepartment of Biostatistics, Virginia Commonwealth University, One Capital Square 830 East Main Street, Box 980032, Richmond, VA 23219, United States.
Chad HeatwoleDepartment of Neurology, University of Rochester, 601 Elmwood Ave., Box 673, Rochester, NY 14642, United States; Center for Health and Technology, University of Rochester, Saunders Research Building, 265 Crittenden Blvd, Rochester, NY 14642, United States.
Nicholas E JohnsonDepartment of Neurology, Virginia Commonwealth University School of Medicine, 417N 11th St, Richmond, VA 23298, United States. Electronic address: Nicholas.johnson@vcuhealth.org.

Funding

Identifying the RNA Splicing and Gene Expression Changes that Cause Congenital Myotonic Dystrophy (Renewal)R01NS104010 · NINDS · VIRGINIA COMMONWEALTH UNIVERSITY · PI Nicholas Elwood Johnson · 2018 to 2026
$4.4M
Establishing Biomarkers and Clinical Endpoints in Myotonic Dystrophy Type-1 (Renewal)R01FD006071 · FDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI Nicholas Elwood Johnson, CHARLES A THORNTON · 2017 to 2026
$3.7M
Health Endpoints and Longitudinal Progression in Congenital Myotonic Dystrophy (HELP-CDM)K23NS091511 · NINDS · VIRGINIA COMMONWEALTH UNIVERSITY · PI JOHNSON, NICHOLAS ELWOOD · 2015 to 2019
$997k
Development and validation of clinical outcome assessments in LGMD2AR21TR003184 · NCATS · VIRGINIA COMMONWEALTH UNIVERSITY · PI JOHNSON, NICHOLAS ELWOOD, STATLAND, JEFFREY · 2020 to 2021
$452k
FDA HHS R01 FD006071NCATS NIH HHS R21 TR003184NINDS NIH HHS K23 NS091511NINDS NIH HHS R01 NS104010
6 · The paper itself

Abstract

Limb girdle muscular dystrophy (LGMD) is a debilitating disease and the fourth most common muscular dystrophy. This study describes the development of the LGMD-Health Index (LGMD-HI). Participants were aged >18 years and recruited from three LGMD registries and GRASP-LGMD consortium. The initial instrument, comprised of 16 thematic subscales and 161 items, underwent expert review resulting in item removal as well as confirmatory factor analysis followed by inter-rater reliability and internal consistency of the subscales. Following expert review, one subscale and 59 items were eliminated. Inter-rater reliability was assessed and five items were removed due to Cohen's kappa <0.5. The final subscales had high internal consistencies with an average Cronbach alpha of 0.92. Test re-test reliability of the final instrument was high (intraclass correlation coefficient=0.97). Known groups validity testing showed a statistically significant difference in LGMD-HI scores amongst subjects based on ambulation status (28.7 vs 50.0, p < 0.0001), but not sex, employment status, or genetic subtype. The final instrument is comprised of 15 subscales and 97 items. The LGMD-HI is a disease-specific, patient-reported outcome measure designed in compliance with published FDA guidelines. This instrument is capable of measuring burden of disease with no significant variation based on LGMD subtype.

Indexed as

Muscular Dystrophies, Limb-GirdleAdultAgedFemaleHumansMaleMiddle AgedRegistriesReproducibility of ResultsSeverity of Illness IndexYoung AdultHealth indexLimb girdle muscular dystrophyMuscular dystrophiesPatient-reported outcome measureSymptom burden

Identifiers

PMID38795602
PMCPMC11176010

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.