Evidence map›Paper›PMID 35474226›Full record

ArticleMuscle & nerve2022

Body composition and myokines in a cohort of patients with Becker muscular dystrophy.

Andrea Barp, Elena Carraro, Giovanni Goggi, Andrea Lizio, Alice Zanolini, Carmelo Messina, Silvia Perego, Chiara Verdelli, Giovanni Lombardi, Valeria Ada Sansone and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Muscle & nerve, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.4field-weighted citation impact, top 42% 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

6 citing papers in PubMed, 5 citations in OpenAlex.

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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

11 authors at 2 institutions in 2 countries.

Andrea BarpNeurorehabilitation Unit, NeMO Clinical Center, University of Milan, Milan, Italy.ORCID 0000-0001-8015-2597
Elena CarraroNeurorehabilitation Unit, NeMO Clinical Center, University of Milan, Milan, Italy.
Giovanni GoggiEndocrinology and Diabetology Service, IRCCS Istituto Ortopedico Galeazzi, Milan, Italy.
Andrea LizioNeurorehabilitation Unit, NeMO Clinical Center, University of Milan, Milan, Italy.
Alice ZanoliniNeurorehabilitation Unit, NeMO Clinical Center, University of Milan, Milan, Italy.
Carmelo MessinaIRCCS Istituto Ortopedico Galeazzi, Milan, Italy.
Silvia PeregoLaboratory of Experimental Biochemistry & Molecular Biology, IRCCS Istituto Ortopedico Galeazzi, Milan, Italy.
Chiara VerdelliLaboratory of Experimental Endocrinology, IRCCS Istituto Ortopedico Galeazzi, Milan, Italy.
Giovanni LombardiLaboratory of Experimental Biochemistry & Molecular Biology, IRCCS Istituto Ortopedico Galeazzi, Milan, Italy.
Valeria Ada Sansone *Neurorehabilitation Unit, NeMO Clinical Center, University of Milan, Milan, Italy.
Sabrina Corbetta *Endocrinology and Diabetology Service, IRCCS Istituto Ortopedico Galeazzi, Milan, Italy.
University of Milan · ITIstituto Ortopedico Galeazzi · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

INTRODUCTION/

aimsBecker muscular dystrophy (BMD) is an X-linked disease leading to muscle wasting and weakness. The decrease in lean body mass (LBM) in Duchenne muscular dystrophy, has shown correlation with loss of muscle function and bone density (BD). Myokines (including irisin) are hormones secreted by skeletal muscle that allow crosstalk between muscle and bone. The present study analyzed body composition and circulating myokine levels in a cohort of BMD patients; moreover, the association between dual energy X-ray absorptiometry (DXA) parameters, functional motor assessments, and myokine levels was investigated.

methodsAll patients underwent DXA, blood samples for myokine assays, and functional motor assessments. A group of healthy controls (HCs) was also included.

resultsThirty BMD patients, median age at evaluation 36.0 y [26.0-41.0], were included. Twenty-nine patients underwent whole-body DXA. Median value of total body Z-score was -0.70. The prevalence of low skeletal muscle mass defined as appendicular skeletal muscle mass index (ASMMI) < 7.59 kg/m DISCUSSION: DXA is a useful tool to evaluate body composition in BMD patients; the decrease in BD and LBM is associated with a reduction of motor function in BMD.

Indexed as

Muscular Dystrophy, DuchenneAbsorptiometry, PhotonBody CompositionBone DensityFibronectinsHumansMuscle, SkeletalFibronectinsBecker muscular dystrophybone mineral densityDuchenne muscular dystrophyDXAIrisin

Identifiers

PMID35474226
PMCPMC9321020
OpenAlexW4224951212

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.