Evidence map›Paper›PMID 36828644›Full record

ArticleRMD open2023

Adipokine profile in long-term juvenile dermatomyositis, and associations with adipose tissue distribution and cardiac function: a cross-sectional study.

Henriette Schermacher Marstein, Birgit Nomeland Witczak, Kristin Godang, Nicoleta Christina Olarescu, Thomas Schwartz, Berit Flatø, Øyvind Molberg, Jens Bollerslev, Ivar Sjaastad, Helga Sanner

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Article in RMD open, 2023. 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
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

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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.

  1. Article
4 · The record

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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

10 authors.

Henriette Schermacher MarsteinInstitute of Experimental Medical Research, Oslo University Hospital Ullevaal, Oslo, Norway henriette.marstein@medisin.uio.no.ORCID 0000-0003-3490-5601
Birgit Nomeland WitczakInstitute of Experimental Medical Research, Oslo University Hospital Ullevaal, Oslo, Norway.
Kristin GodangSection of Specialized Endocrinology, Department of Endocrinology, Morbid Obesity and Preventive Medicine, Medical Clinic, Oslo University Hospital, Oslo, Norway.
Nicoleta Christina OlarescuSection of Specialized Endocrinology, Department of Endocrinology, Morbid Obesity and Preventive Medicine, Medical Clinic, Oslo University Hospital, Oslo, Norway.
Thomas SchwartzInstitute of Experimental Medical Research, Oslo University Hospital Ullevaal, Oslo, Norway.
Berit FlatøInstitute for Clinical Medicine, Medical Faculty, University of Oslo, Oslo, Norway.
Øyvind MolbergDepartment of Rheumatology, Oslo University Hospital, Oslo, Norway.
Jens BollerslevSection of Specialized Endocrinology, Department of Endocrinology, Morbid Obesity and Preventive Medicine, Medical Clinic, Oslo University Hospital, Oslo, Norway.
Ivar SjaastadInstitute of Experimental Medical Research, Oslo University Hospital Ullevaal, Oslo, Norway.
Helga SannerDepartment of Health Sciences, Oslo New University College, Oslo, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesIn long-term juvenile dermatomyositis (JDM), altered adipose tissue distribution and subclinical cardiac dysfunction have been described. Our aims were to compare adipokine levels in patients with JDM after long-term disease with controls, and explore associations between adipokines and (1) adipose tissue distribution and (2) cardiac function.

methodsThe study cohort included 59 patients with JDM (60% female, mean age 25.2 years, mean disease duration 16.9 years), and 59 age/sex-matched controls. Updated Pediatric Rheumatology International Trials Organization criteria for clinically inactive JDM were used to stratify patients into active (JDM-active) or inactive (JDM-inactive) disease groups. Lipodystrophy was clinically assessed in all patients. In all study participants, we measured adipose tissue distribution by dual-energy X-ray absorptiometry and cardiac function by echocardiography. Serum adipokines (adiponectin, apelin-12, lipocalin-2, leptin, visfatin and resistin) were analysed using ELISA.

resultsPatients with JDM had higher leptin levels compared with controls (p≤0.01). In JDM-active, apelin-12 and visfatin were higher compared with JDM-inactive (p≤0.05). In JDM-total and JDM-active, lower adiponectin correlated with lipodystrophy and total fat mass. Also, systolic dysfunction correlated with: lower adiponectin in JDM-total, JDM-inactive and JDM-active, and with lower apelin-12 in JDM-total and JDM-active and resistin in JDM-active (all p≤0.05). Lower adiponectin correlated with diastolic dysfunction in JDM-total and JDM-active.

conclusionAfter long-term disease, leptin levels were unfavourably regulated in patients with JDM compared with controls, and apelin-12 and visfatin in JDM-active versus JDM-inactive. We found associations between adipokines and both adipose tissue distribution and cardiac systolic function in all patients with JDM, which was most prominent in patients with active disease.

Indexed as

DermatomyositisLipodystrophyAdipokinesAdiponectinAdultChildCross-Sectional StudiesFemaleHumansLeptinMaleNicotinamide PhosphoribosyltransferaseResistinTissue DistributionAdipokinesAdiponectinLeptinNicotinamide PhosphoribosyltransferaseResistinautoimmune diseasescardiovascular diseasescytokinesdermatomyositisinflammation

Identifiers

PMID36828644
PMCPMC9972436

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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.