Evidence map›Paper›PMID 37483011›Full record

ArticleAnnals of clinical and translational neurology2023

A comprehensive study of skeletal muscle imaging in FHL1-related reducing body myopathy.

Payam Mohassel, Pomi Yun, Safoora Syeda, Abhinandan Batra, Andrew J Bradley, Sandra Donkervoort, Soledad Monges, Julie S Cohen, Doris G Leung, Francina Munell and 12 more

Open access · goldAbstract read
In one paragraph

Article in Annals of clinical and translational neurology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. 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

22 authors at 13 institutions in 8 countries.

Payam Mohassel *Neurogenetics Branch, National Institute of Neurological Disorders and Stroke, Bethesda, MD, USA.ORCID 0000-0001-5313-9514
Pomi Yun *Neurogenetics Branch, National Institute of Neurological Disorders and Stroke, Bethesda, MD, USA.ORCID 0000-0002-7304-7411
Safoora SyedaNeurogenetics Branch, National Institute of Neurological Disorders and Stroke, Bethesda, MD, USA.
Abhinandan BatraDepartment of Physical Therapy, University of Florida, Gainesville, FL, USA.
Andrew J BradleyAdvanced Cardiovascular Imaging Laboratory, NHLBI, NIH, Bethesda, MD, USA.
Sandra DonkervoortNeurogenetics Branch, National Institute of Neurological Disorders and Stroke, Bethesda, MD, USA.
Soledad MongesServicio de Neurología, Hospital de Pediatría J.P. Garrahan, Buenos Aires, Argentina.
Julie S CohenDepartment of Neurology, Kennedy Krieger Institute, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Doris G LeungDepartment of Neurology, Kennedy Krieger Institute, Johns Hopkins University School of Medicine, Baltimore, MD, USA.ORCID 0000-0002-2558-7798
Francina MunellPediatric Neurology, Vall d'Hebron University Hospital, Barcelona, Spain.
Carlos OrtezDepartment of Pediatric Neurology, Neuromuscular Unit, Hospital Sant Joan de Déu and Institut de Recerca Sant Joan de Déu, Barcelona, Spain.
Angel Sánchez-MontáñezPediatric Neuroradiology, Hospital Universitari Vall d'Hebron, Vall d'Hebron, Autonomous University of Barcelona, Barcelona, Spain.
Peter KarachunskiUniversity of Minnesota Medical School, Minneapolis, MN, USA.
John BrandsemaDivision of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Livija MedneDivision of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Vinay ChaudhryDepartment of Neurology, University of North Carolina, Chapel Hill, NC, USA.
Giorgio TascaUnità Operativa Complessa di Neurologia, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.ORCID 0000-0003-0849-9144
A Reghan FoleyNeurogenetics Branch, National Institute of Neurological Disorders and Stroke, Bethesda, MD, USA.ORCID 0000-0003-2168-1119
Bjarne UddFolkhalsan Research Center, Department of Medical Genetics, University of Helsinki, Helsinki, Finland.
Andrew E AraiAdvanced Cardiovascular Imaging Laboratory, NHLBI, NIH, Bethesda, MD, USA.
Glenn A WalterDepartment of Physiology and Functional Genomics, University of Florida, Gainesville, FL, USA.
Carsten G BönnemannNeurogenetics Branch, National Institute of Neurological Disorders and Stroke, Bethesda, MD, USA.ORCID 0000-0002-5930-2324
National Institute of Neurological Disorders and Stroke · USChildren's Hospital of Philadelphia · USKennedy Krieger Institute · USNational Institutes of Health · USUniversity of Florida · USGarrahan Hospital · ARHebron University · PSHospital Sant Joan de Déu Barcelona · ESNewcastle upon Tyne Hospitals NHS Foundation Trust · GBUniversitat Autònoma de Barcelona · ESUniversity of Helsinki · FIUniversity of Minnesota Medical Center · USUniversity of North Carolina at Chapel Hill · US

Funding

Molecular and Clinical Manifestations of Matrix and Aggregate MyopathiesZIANS003129 · NINDS · NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE · PI BÖNNEMANN, CARSTEN · 2011 to 2025
$52.8M
Sleep and Circadian Dysfunction, Brain and Neurobehavioral Development in AutismP50HD103538 · NICHD · HUGO W. MOSER RES INST KENNEDY KRIEGER · PI S. Ali Fatemi, Bradley L Schlaggar · 2020 to 2026
$9.9M
NHLBI NIH HHS 02-H-0050NICHD NIH HHS P50 HD103538NINDS NIH HHS 12-N-0095
6 · The paper itself

Abstract

objectiveFHL1-related reducing body myopathy is an ultra-rare, X-linked dominant myopathy. In this cross-sectional study, we characterize skeletal muscle ultrasound, muscle MRI, and cardiac MRI findings in FHL1-related reducing body myopathy patients.

methodsSeventeen patients (11 male, mean age 35.4, range 12-76 years) from nine independent families with FHL1-related reducing body myopathy underwent clinical evaluation, muscle ultrasound (n = 11/17), and lower extremity muscle MRI (n = 14/17), including Dixon MRI (n = 6/17). Muscle ultrasound echogenicity was graded using a modified Heckmatt scale. T1 and STIR axial images of the lower extremity muscles were evaluated for pattern and distribution of abnormalities. Quantitative analysis of intramuscular fat fraction was performed using the Dixon MRI images. Cardiac studies included electrocardiogram (n = 15/17), echocardiogram (n = 17/17), and cardiac MRI (n = 6/17). Cardiac muscle function, T1 maps, T2-weighted black blood images, and late gadolinium enhancement patterns were analyzed.

resultsMuscle ultrasound showed a distinct pattern of increased echointensity in skeletal muscles with a nonuniform, multifocal, and "geographical" distribution, selectively involving the deeper fascicles of muscles such as biceps and tibialis anterior. Lower extremity muscle MRI showed relative sparing of gluteus maximus, rectus femoris, gracilis, and lateral gastrocnemius muscles and an asymmetric and multifocal, "geographical" pattern of T1 hyperintensity within affected muscles. Cardiac studies revealed mild and nonspecific abnormalities on electrocardiogram and echocardiogram with unremarkable cardiac MRI studies.

interpretationSkeletal muscle ultrasound and muscle MRI reflect the multifocal aggregate formation in muscle in FHL1-related reducing body myopathy and are practical and informative tools that can aid in diagnosis and monitoring of disease progression.

Indexed as

Contrast MediaMuscular DiseasesAdolescentAdultAgedChildCross-Sectional StudiesGadoliniumHumansIntracellular Signaling Peptides and ProteinsLIM Domain ProteinsMaleMiddle AgedMuscle ProteinsMuscle, SkeletalYoung AdultContrast MediaFHL1 protein, humanGadoliniumIntracellular Signaling Peptides and ProteinsLIM Domain ProteinsMuscle Proteins

Identifiers

PMID37483011
PMCPMC10424657
OpenAlexW4385075081

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.