Evidence map›Paper›PMID 34376205›Full record

ArticlePediatric rheumatology online journal2021

Changes in total body fat and body mass index among children with juvenile dermatomyositis treated with high-dose glucocorticoids.

Amer Khojah, Victoria Liu, Gabrielle Morgan, Richard M Shore, Lauren M Pachman

Open access · goldAbstract read
In one paragraph

Article in Pediatric rheumatology online journal, 2021. 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
1.1field-weighted citation impact, top 24% 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, 10 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. B Cell Lymphocytosis in Juvenile Dermatomyositis.Diagnostics (Basel, Switzerland) · 2023
    Article
  6. 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

5 authors at 2 institutions in 1 country.

Amer KhojahDivision of Pediatric Rheumatology, Department of Pediatric, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, 60611, USA. akhojah@luriechildrens.org.ORCID http://orcid.org/0000-0003-3357-4863
Victoria LiuCure JM Center of Excellence, Stanley Manne Research Center, Chicago, IL, USA.
Gabrielle MorganCure JM Center of Excellence, Stanley Manne Research Center, Chicago, IL, USA.
Richard M ShoreDepartment of Medical Imaging, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA.
Lauren M PachmanDivision of Pediatric Rheumatology, Department of Pediatric, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, 60611, USA.
Lurie Children's Hospital · USStanley Foundation · US

Funding

Northwestern University Clinical and Translational Science Institute (NUCATS)UL1TR001422 · NCATS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI D'AQUILA, RICHARD · 2015 to 2023
$56.8M
Mitochondrial calcification in juvenile dermatomyositisR21AR077565 · NIAMS · UNIVERSITY OF WASHINGTON · PI LOOD, JAN CHRISTIAN · 2020 to 2021
$432k
NCATS NIH HHS UL1 TR001422NIAMS NIH HHS R21 AR077565NIH HHS R-21 AR077565NIH HHS UL1TR001422
6 · The paper itself

Abstract

objectiveHigh-dose glucocorticoids (GC) remain the primary therapy to induce remission in Juvenile Dermatomyositis (JDM). Studies of the natural history of GC associated weight gain in children are very limited, especially in the JDM population. This study aims to measure BMI changes in a cohort of JDM subjects over 60 months and to examine the changes in body composition by DXA.

methodsWe included all subjects with JDM who had 5 years of follow-up data and multiple DXA studies. BMI and total body fat (TBF) percentiles were calculated based on the CDC published percentile charts. To study the natural history of weight gain and TBF, we assessed the data at four-time points (T0 = baseline, T1 > 1.5 years, T2 = 1.51-3.49 years, T3 = 3.5-5 years).

results68 subjects (78% female, 70% white) were included in this retrospective study. Paired T-test showed a significant increase in the mean BMI percentile by 17.5 points (P = 0.004) after the initiation of medical treatment, followed by a gradual decrease over the study period. However, the TBF percentile did not change over the study period. TBF in the last visit (T3) had a strong correlation with the T1 BMI, and T1 TBF percentile (correlation coefficients 0.63, 0.56 P < 0.001, 0.002 respectively). Also, there was a positive correlation (correlation coefficients 0.39, P = 0.002) between the TBF percentile and muscle DAS but not the skin DAS.

conclusionsAlthough the BMI percentile decreased throughout the study, the TBF percentile remained high until the end of the study (60 months). This finding raises the concern that some of the reduction in the BMI percentile could reflect a drop in the lean body mass from muscle wasting rather than actual fat loss.

Indexed as

Adipose TissueBody Mass IndexChild, PreschoolDermatomyositisFemaleGlucocorticoidsHumansInfantMaleRetrospective StudiesGlucocorticoidsAnd fat distributionDXA scanGlucocorticoidsJuvenile dermatomyositisPediatric obesity

Identifiers

PMID34376205
PMCPMC8353815
OpenAlexW3157053457

What OpenQuestion holds

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LicenceCC BY
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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.