Evidence map›Paper›PMID 35275556›Full record

ArticleJournal of neuromuscular diseases2022

Role Attainment in Emerging Adulthood: Subjective Evaluation by Male Adolescents and Adults with Duchenne and Becker Muscular Dystrophy.

Holly L Peay, Barbara T Do, Neil Khosla, Pangaja Paramsothy, Stephen W Erickson, Molly M Lamb, Nedra Whitehead, Deborah J Fox, Shree Pandya, Kathi Kinnett and 2 more

Open access · greenAbstract read
In one paragraph

Article in Journal of neuromuscular diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 37% of its field
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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Healthcare Self-Management, Executive Functioning, and Social Determinants of Health in Young Adults with Pediatric-Onset Disabilities: a Pilot Study.Archives of clinical neuropsychology : the official journal of the National Academy of Neuropsychologists · 2025
    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

12 authors at 9 institutions in 1 country.

Holly L PeayGenomics, Bioinformatics, and Translational Research Center, RTI International, Research Triangle Park, NC, USA.
Barbara T DoClinical Research Network Center, RTI International, Research Triangle Park, NC, USA.
Neil KhoslaOak Ridge Institute for Science and Education (ORISE) Fellowship, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Pangaja ParamsothyNational Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta GA, USA.
Stephen W EricksonGenomics, Bioinformatics, and Translational Research Center, RTI International, Research Triangle Park, NC, USA.
Molly M LambDepartment of Epidemiology, Colorado School of Public Health, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Nedra WhiteheadApplied Public Health Research Center, RTI International, Research Triangle Park, NC, USA.
Deborah J FoxNew York State Department of Health, Albany, NY, USA.
Shree PandyaSchool of Medicine and Dentistry, University of Rochester, Rochester, NY, USA.
Kathi KinnettParent Project Muscular Dystrophy, Hackensack, NJ, USA.
Jodi WolffSanthera Pharmaceuticals, Burlington, MA, USA.
James F HowardDepartment of Neurology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
RTI International · USCenters for Disease Control and Prevention · USColorado School of Public Health · USNew York State Department of Health · USParent Project Muscular Dystrophy · USResearch Network (United States) · USTriangle · USUniversity of North Carolina at Chapel Hill · USUniversity of Rochester · US

Funding

Surveillance and Epidemiologic Research of Duchenne and Becker Muscular DystrophyU01DD000189 · DD · UNIVERSITY OF IOWA · PI ROMITTI, PAUL A · 2006 to 2011
$4.1M
Arizona Muscular Dystrophy Surveillance and Research ProgramU01DD000187 · DD · UNIVERSITY OF ARIZONA · PI CUNNIFF, CHRISTOPHER MCCORD · 2006 to 2010
$2.9M
Surveillance and Epidemiologic Research of Duchenne and Becker Muscular DystrophyU01DD000190 · DD · NYSDOH/HEALTH RESEARCH, INC. · PI DRUSCHEL, CHARLOTTE MARIE · 2006 to 2010
$2.7M
Sureillance and Epidemiologic Research of Duchenne and Becker Muscular DystrophyU01DD000191 · DD · COLORADO STATE DEPT/PUB HLTH & ENVIRONMT · PI MILLER, LISA ANN · 2006 to 2010
$2.5M
Comp A-NY State Surveillance and Research of MD and Neuromuscular DisordersU01DD001123 · DD · CENTER OF ENVIRONMENTAL HEALTH · PI SOIM, AIDA · 2014 to 2018
$2.4M
Comp A-Surveillance and Research of Muscular Dystrophies and Neuromuscular DisordersU01DD001126 · DD · COLORADO STATE DEPT/PUB HLTH & ENVIRONMT · PI RUTTENBER, MARGARET · 2014 to 2018
$2.4M
Comp B-Surveillance and Res of MD and Neuromuscular DisordersU01DD001116 · DD · RESEARCH TRIANGLE INSTITUTE · PI WHITEHEAD, NEDRA SHARON · 2014 to 2018
$2.2M
The Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet): Component A - Core-Current SiteU01DD001255 · DD · RESEARCH TRIANGLE INSTITUTE · PI MOORE, AMY · 2019 to 2023
$2.0M
Intramural CDC HHS CC999999NCBDD CDC HHS U01 DD000187NCBDD CDC HHS U01 DD000189NCBDD CDC HHS U01 DD000190NCBDD CDC HHS U01 DD000191NCBDD CDC HHS U01 DD001116NCBDD CDC HHS U01 DD001123NCBDD CDC HHS U01 DD001126NCBDD CDC HHS U01 DD001255
6 · The paper itself

Abstract

backgroundYouth with Duchenne and Becker muscular dystrophy (DBMD) experience challenges in attaining adult roles, which may impact quality of life. New interventions and treatments may facilitate adult role attainment through improved function. Historical data on adult role attainment is important to assess the impact of new interventions on teens and young adults with DBMD. This study assesses medical knowledge, independence and employment, and relationships among adolescents and young adults with DBMD.

methodsThis study uses data from a 2013 Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet) survey on adult transition. Males with DBMD aged 16-30 years were included.

resultsSixty-five of 258 eligible males participated; we report results on 60 participants with an MD STARnet case definition of DMD or BMD. Individuals with BMD reported higher rates than those with DMD of frequently staying home without supervision (50% BMD; 14% DMD), independently performing daily physical needs (93% BMD; 7% DMD) and being employed full or part time (33% BMD; 4% DMD). Most participants understood medication and physical therapy goals; less than half indicated being often or always responsible for scheduling DMBD-related management and refilling medications. Most had not been in a romantic relationship but reported desiring such relationships.

conclusionsOur data reinforce the impact of DMD (and to a lesser extent, BMD) on transition to adult roles. These results provide an important historical comparator for teen and adult patients who are trying new interventions and therapies. Such data are important for assessing the quality-of-life impact of new treatments and to inform support and training programs for people with DBMD as they transition to new adult roles and responsibilities.

Indexed as

Muscular Dystrophy, DuchenneAdolescentAdultHumansMaleQuality of LifeSurveys and QuestionnairesYoung AdultadolescentMuscular dystrophiesself-caretransfer from pediatric to adult caretransition to adult care

Identifiers

PMID35275556
PMCPMC9126318
OpenAlexW4220941266

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.