Evidence map›Paper›PMID 38551101›Full record

ArticleMuscle & nerve2024

Cross-sectional study of patients with VCP multisystem proteinopathy 1 using dual-energy x-ray absorptiometry.

Rod Carlo Agram Columbres, Vu Luu, Minh Nguyen, Virginia Kimonis

Open access · hybridAbstract read
In one paragraph

Article in Muscle & nerve, 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, top 95% 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

1 citing paper in PubMed, 0 citations in OpenAlex.

  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

4 authors at 2 institutions in 1 country.

Rod Carlo Agram ColumbresDivision of Genetics and Metabolism, Department of Pediatrics, School of Medicine, University of California, Irvine, California, USA.
Vu LuuDivision of Genetics and Metabolism, Department of Pediatrics, School of Medicine, University of California, Irvine, California, USA.
Minh NguyenDivision of Genetics and Metabolism, Department of Pediatrics, School of Medicine, University of California, Irvine, California, USA.
Virginia KimonisDivision of Genetics and Metabolism, Department of Pediatrics, School of Medicine, University of California, Irvine, California, USA.ORCID https://orcid.org/0000-0003-1567-4449
University of California, Irvine · USWilliam Carey University · US

Funding

Genetic basis of myopathy with Paget disease of boneR01AR050236 · NIAMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI KIMONIS, VIRGINIA EUNICE · 2004 to 2008
$1.3M
Translational Studies in VCP Inclusion Body Myopathy with Paget Disease of BoneR56AR050236 · NIAMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI KIMONIS, VIRGINIA EUNICE · 2009 to 2009
$437k
FDA HHS R01 FD007478NIAMS NIH HHS R01 AR050236NIAMS NIH HHS R56 AR050236
6 · The paper itself

Abstract

INTRODUCTION/

aimsVCP multisystem proteinopathy 1 (MSP1), encompassing inclusion body myopathy (IBM), Paget's disease of bone (PDB) and frontotemporal dementia (FTD) (IBMPFD), features progressive muscle weakness, fatty infiltration, and disorganized bone structure in Pagetic bones. The aim of this study is to utilize dual-energy x-ray absorptiometry (DXA) parameters to examine it as a biomarker of muscle and bone disease in MSP1.

methodsDXA scans were obtained in 28 patients to assess body composition parameters (bone mineral density [BMD], T-score, total fat, and lean mass) across different groups: total VCP disease (n = 19), including myopathy without Paget's ("myopathy"; n = 12) and myopathy with Paget's ("Paget"; n = 7), and unaffected first-degree relatives serving as controls (n = 6).

resultsIn the VCP disease group, significant declines in left hip BMD and Z-scores were noted versus the control group (p ≤ .03). The VCP disease group showed decreased whole body lean mass % (p = .04), and increased total body fat % (p = .04) compared to controls. Subgroup comparisons indicated osteopenia in 33.3% and osteoporosis in 8.3% of the myopathy group, with 14.3% exhibiting osteopenia in the Paget group. Moreover, the Paget group displayed higher lumbar L1-L4 T-score values than the myopathy group. DISCUSSION: In MSP1, DXA revealed reduced bone and lean mass, and increased fat mass. These DXA insights could aid in monitoring disease progression of muscle loss and secondary osteopenia/osteoporosis in MSP1, providing value both clinically and in clinical research.

Indexed as

Absorptiometry, PhotonBone DensityMuscular Dystrophies, Limb-GirdleMyositis, Inclusion BodyOsteitis DeformansAdenosine TriphosphatasesAdultAgedBody CompositionCross-Sectional StudiesFemaleFrontotemporal DementiaHumansMaleMiddle AgedValosin Containing ProteinAdenosine TriphosphatasesValosin Containing ProteinVCP protein, humanDXAIBMPFDMSP1myopathyVCP/p97

Identifiers

PMID38551101
PMCPMC11076161
OpenAlexW4393310906

What Socratic holds

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Registered trials

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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 Socratic graph.