Evidence map›Paper›PMID 34787322›Full record

Observational studyMuscle & nerve2022

A population-based study of scoliosis among males diagnosed with a dystrophinopathy identified by the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet).

Kristin M Conway, Amber Gedlinske, Katherine D Mathews, Seth Perlman, Nicholas Johnson, Russell Butterfield, Man Hung, Jerry Bounsanga, Dennis Matthews, Joyce Oleszek and 1 more

Erratum issuedOpen access · greenAbstract readObservational Study
In one paragraph

Observational study in Muscle & nerve, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 43% 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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 6 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 7 institutions in 1 country.

Kristin M ConwayDepartment of Epidemiology, The University of Iowa, Iowa City, Iowa, USA.ORCID 0000-0001-8633-966X
Amber GedlinskeDepartment of Internal Medicine, The University of Iowa, Iowa City, Iowa, USA.
Katherine D MathewsDepartments of Pediatrics and Neurology, The University of Iowa, Iowa City, Iowa, USA.
Seth PerlmanDepartment of Neurology, Seattle Children's Hospital, Seattle, Washington, USA.
Nicholas JohnsonDepartment of Neurology, Virginia Commonwealth University, Richmond, Virginia, USA.ORCID 0000-0002-3917-4257
Russell ButterfieldDepartments of Pediatrics and Neurology, University of Utah, Salt Lake City, Utah, USA.ORCID 0000-0002-8452-7189
Man HungCollege of Dental Medicine, Roseman University of Health Sciences, South Jordan, Utah, USA.
Jerry BounsangaUtah Medical Education Council, Salt Lake City, Utah, USA.
Dennis MatthewsDepartment of Physical Medicine and Rehabilitation, University of Colorado and Children's Hospital, Denver, Colorado, USA.
Joyce OleszekDepartment of Physical Medicine and Rehabilitation, University of Colorado and Children's Hospital, Denver, Colorado, USA.
Paul A RomittiDepartment of Epidemiology, The University of Iowa, Iowa City, Iowa, USA.
University of Iowa · USChildren's Hospital Colorado · USHealth Education Council · USRoseman University of Health Sciences · USSeattle Children's Hospital · USUniversity of Utah · USVirginia Commonwealth University · US

Funding

Therapeutic Potential of ESC-Derived Myogenic PrecursorsU54NS053672 · NINDS · UNIVERSITY OF IOWA · PI CAMPBELL, KEVIN P. · 2005 to 2019
$22.0M
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
Surveillance and Epidemiologic Research of Duchenne and Becker Muscular DystrophyU01DD000189 · DD · UNIVERSITY OF IOWA · PI ROMITTI, PAUL A · 2006 to 2011
$4.1M
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
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
Component A: Iowa MD STARnet Core SiteU01DD001248 · DD · UNIVERSITY OF IOWA · PI MATHEWS, KATHERINE DIANNE, ROMITTI, PAUL A · 2019 to 2023
$2.0M
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
Development and validation of clinical outcome assessments in LGMD2AR21TR003184 · NCATS · VIRGINIA COMMONWEALTH UNIVERSITY · PI JOHNSON, NICHOLAS ELWOOD, STATLAND, JEFFREY · 2020 to 2021
$452k
Component C: Iowa MD STARnet Site Data DisseminationU01DD001247 · DD · UNIVERSITY OF IOWA · PI ROMITTI, PAUL A · 2019 to 2023
$400k
ACL HHS U01DD001248FDA HHS R01 FD006071NCATS NIH HHS R21 TR003184NCBDD CDC HHS U01 DD000187NCBDD CDC HHS U01 DD000189NCBDD CDC HHS U01 DD000190NCBDD CDC HHS U01 DD000191NCBDD CDC HHS U01 DD001242NCBDD CDC HHS U01 DD001247NCBDD CDC HHS U01 DD001248NINDS NIH HHS R01 NS104010NINDS NIH HHS U24 NS107181NINDS NIH HHS U54 NS053672
6 · The paper itself

Abstract

INTRODUCTION/

aimsScoliosis is a common comorbidity among individuals diagnosed with a dystrophinopathy. We examined associations between clinical predictors and scoliosis in childhood-onset dystrophinopathy.

methodsThe progression and treatment of scoliosis were obtained from data collected by the US population-based Muscular Dystrophy Surveillance, Tracking, and Research Network. Associations between loss of independent ambulation (LoA) and corticosteroid use and scoliosis outcomes (ages at or exceeding Cobb angle thresholds [10°, 20°, 30°]; surgery) were estimated using Kaplan-Meier curve estimation and extended Cox regression modeling.

resultsWe analyzed curvature data for 513 of 1054 individuals ascertained. Overall, approximately one-half had at least one radiograph and one-quarter had a curvature of at least 20°. The average maximum curvature was 25.0° (SD = 21.5°) among all individuals and 42.8° (SD = 18.8°) among those recommended for surgery. Higher adjusted hazards ratio of curvature (aHR DISCUSSION: Our retrospective observational study suggests corticosteroids may delay spinal curvature progression and need for scoliosis surgery. Continuing corticosteroids after LoA also showed potential benefits of delaying curvature progression, additional studies are needed to confirm this finding or address the magnitude of benefit.

Indexed as

Muscular Dystrophy, DuchenneScoliosisAdrenal Cortex HormonesHumansMaleProportional Hazards ModelsRetrospective StudiesAdrenal Cortex HormonescorticosteroidDuchenne muscular dystrophydystrophinopathyscoliosis

Identifiers

PMID34787322
PMCPMC8752499
OpenAlexW3214002282

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.