Evidence map›Paper›PMID 37682255›Full record

ArticleLa Tunisie medicale2023

Sarcopenia: a new issue in juvenile idiopathic arthritis. A study Protocol.

Hanene Lassoued Ferjani, Fatma Majdoub, Dorra Ben Nessib, Dhia Kaffel, Wafa Triki, Kaouther Maatallah, Wafa Hamdi

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in La Tunisie medicale, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05291416 (Sarcopenia; a New Issue in Juvenile Idiopathic Arthritis), which is not on this map. Not yet cited in PubMed.

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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.

NCT05291416 unknown statusnot on this map

Sarcopenia; a New Issue in Juvenile Idiopathic Arthritis

TypeobservationalSponsorUniversity Tunis El ManarRan2022 to 2022Enrolled60ConditionsSarcopenia, Juvenile Idiopathic ArthritisArmsdensitometry/ handgrip dynamometer
3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

7 authors at 1 institution in 1 country.

Hanene Lassoued FerjaniService de rhumatologie, Institut Mohamed Kassab d'orthopédie- Manouba/ Faculté de Médecine de Tunis/ Université Tunis El Manar/ Unité de recherche UR17SP04.
Fatma MajdoubService de rhumatologie, Institut Mohamed Kassab d'orthopédie- Manouba/ Faculté de Médecine de Tunis/ Université Tunis El Manar/ Unité de recherche UR17SP04.
Dorra Ben NessibService de rhumatologie, Institut Mohamed Kassab d'orthopédie- Manouba/ Faculté de Médecine de Tunis/ Université Tunis El Manar/ Unité de recherche UR17SP04.
Dhia KaffelService de rhumatologie, Institut Mohamed Kassab d'orthopédie- Manouba/ Faculté de Médecine de Tunis/ Université Tunis El Manar/ Unité de recherche UR17SP04.
Wafa TrikiService de rhumatologie, Institut Mohamed Kassab d'orthopédie- Manouba/ Faculté de Médecine de Tunis/ Université Tunis El Manar/ Unité de recherche UR17SP04.
Kaouther MaatallahService de rhumatologie, Institut Mohamed Kassab d'orthopédie- Manouba/ Faculté de Médecine de Tunis/ Université Tunis El Manar/ Unité de recherche UR17SP04.
Wafa HamdiService de rhumatologie, Institut Mohamed Kassab d'orthopédie- Manouba/ Faculté de Médecine de Tunis/ Université Tunis El Manar/ Unité de recherche UR17SP04.
Tunis El Manar University · TN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe decrease in muscle function and mass is defined as sarcopenia. Known for a long time as an age-related disorder, sarcopenia is nowadays well recognized in childhood. Juvenile idiopathic arthritis (JIA), a chronic inflammatory joint disease may be associated with loss of skeletal mass.

aimThis protocol aims to evaluate the prevalence rate of sarcopenia and its associated factors in JIA.

methodsTo evaluate the prevalence rate and factors associated with sarcopenia in juvenile idiopathic arthritis, we are enrolling 30 children with JIA and 30 healthy children aged between 4-and 16 years. Clinical data will report: age, sex, body mass index, disease duration, and therapeutic management. All participants will undergo the Whole-body Dual-energy X-ray absorptiometry to assess the skeletal muscle mass. The muscle strength will be measured using the handgrip dynamometer and adjusted to the body mass index. Data will be analyzed and compared to age and sex reference curves.

resultsThis study aims to detect sarcopenia in JIA children and identify subsequently the main associated factors. By collecting anthropometric data and extracting the main features of the disease, specific metrics will be extracted. Body composition will be obtained using the DXA scans, including appendicular lean mass and skeletal muscle mass. Muscle strength will also be assessed.

conclusionThis study aims to assess sarcopenia in JIA patients, using the sarcopenia update definition. If we will provide conclusive results, it will be possible to better identify the associated factors of sarcopenia and to prevent children from this complication. Clinical trials registration NCT05291416.

Indexed as

Arthritis, JuvenileSarcopeniaAbsorptiometry, PhotonAdolescentChildChild, PreschoolHand StrengthHumansMuscle Strength

Identifiers

PMID37682255
PMCPMC11099933
OpenAlexW4386529958

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LicenceCC BY-NC-ND
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Registered trials

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.