Evidence map›Paper›PMID 39579597›Full record

ArticleNeuromuscular disorders : NMD2025

Respiratory function and evaluation in individuals with facioscapulohumeral muscular dystrophy in the Muscular Dystrophy Surveillance, Tracking and Research Network.

Katherine D Mathews, Jonathan Suhl, Kristin M Conway, Amy Moore, Joyce T Alese, Russell J Butterfield, Paul A Romitti, Muscular Dystrophy Surveillance, Tracking and Research Network (MD STARnet)

Abstract read
In one paragraph

Article in Neuromuscular disorders : NMD, 2025. 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. Observational
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

8 authors.

Katherine D MathewsDepartment of Pediatrics, Roy J and Lucille A Carver College of Medicine, The University of Iowa, Iowa City, Iowa, United States.
Jonathan SuhlDepartment of Epidemiology, College of Public Health, University of Iowa, S416 CPHB, 145 N Riverside Dr, Iowa City, Iowa 52242, United States.
Kristin M ConwayDepartment of Epidemiology, College of Public Health, University of Iowa, S416 CPHB, 145 N Riverside Dr, Iowa City, Iowa 52242, United States.
Amy MooreRTI International, Research Triangle Park, North Carolina, United States.
Joyce T AleseDivision of Birth Defects and Infant Disorders, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, GA, United States; McKing Consulting Corporation, Atlanta, GA, United States.
Russell J ButterfieldDepartment of Pediatrics, University of Utah, Salt Lake City, Utah 84108, United States.
Paul A RomittiDepartment of Epidemiology, College of Public Health, University of Iowa, S416 CPHB, 145 N Riverside Dr, Iowa City, Iowa 52242, United States. Electronic address: paul-romitti@uiowa.edu.
Muscular Dystrophy Surveillance, Tracking and Research Network (MD STARnet)

Funding

Therapeutic Potential of ESC-Derived Myogenic PrecursorsU54NS053672 · NINDS · UNIVERSITY OF IOWA · PI MOORE, STEVEN A · 2005 to 2019
$22.0M
The University of Iowa's NeuroNEXT Clinical Research SiteU24NS107181 · NINDS · UNIVERSITY OF IOWA · PI MATHEWS, KATHERINE DIANNE, SHY, MICHAEL E. · 2018 to 2022
$1.5M
Component C: Iowa MD STARnet Site Data DisseminationU01DD001247 · DD · UNIVERSITY OF IOWA · PI ROMITTI, PAUL A · 2019 to 2023
$400k
Intramural CDC HHS CC999999NCBDD CDC HHS U01 DD001116NCBDD CDC HHS U01 DD001117NCBDD CDC HHS U01 DD001119NCBDD CDC HHS U01 DD001123NCBDD CDC HHS U01 DD001126NCBDD CDC HHS U01 DD001247NCBDD CDC HHS U01 DD001248NCBDD CDC HHS U01 DD001253NINDS NIH HHS U24 NS107181NINDS NIH HHS U54 NS053672
6 · The paper itself

Abstract

Using data from the US population-based, multisite Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet), we describe respiratory testing and insufficiency among people with facioscapulohumeral muscular dystrophy (FSHD) diagnosed during 2008-2016. We calculated frequencies and proportions for selected outpatient respiratory assessments (pulmonary function tests [PFTs], forced vital capacity (FVC), inspiratory/expiratory pressure, and polysomnograms) and abnormal test results. We examined frequencies by disease characteristics (FSHD type, ages of onset, non-ambulatory status, scoliosis, lordosis), obesity, and number of health encounters. Of 170 people with FSHD, 20.0% underwent PFTs during 2008-2016. Polysomnograms were infrequent (14.1%). FVC <80% predicted was recorded for 64.7% of people tested; additional respiratory outcomes were rare (<5%). Frequency of evaluations and respiratory insufficiency were higher among those with known risk factors and longer follow-up. We observed low proportions of respiratory testing among all confirmed cases of FSHD, but relatively high proportions of mild respiratory insufficiency among those tested. The higher proportions of testing among people with conditions that increase risk of respiratory complications suggest targeted monitoring. Broad implementation of the FSHD guidelines recommending all individuals receive baseline respiratory evaluation at diagnosis could identify respiratory insufficiency as a complication of FSHD.

Indexed as

Muscular Dystrophy, FacioscapulohumeralRespiratory InsufficiencyAdolescentAdultAgedChildFemaleHumansMaleMiddle AgedPolysomnographyRespiratory Function TestsUnited StatesYoung AdultFacioscapulohumeral respiratory insufficiencyGuidelinesMuscular dystrophySurveillance

Identifiers

PMID39579597
PMCPMC11911087

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.