Evidence map›Paper›PMID 37432516›Full record

ArticleRheumatology international2024

Risk factors for developing calcinosis in juvenile dermatomyositis: subcutaneous and myofascial edema in initial magnetic resonance imaging.

Belina Y Yi, Joshua Marrs, Patricia Acharya, Amit Sura, Michal Cidon

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Article in Rheumatology international, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Calcinosis in dermatomyositis.Current opinion in rheumatology · 2024
    Review
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.

Belina Y YiDivision of Rheumatology, Children's Hospital Los Angeles, Los Angeles, CA, USA. yjbelina.yi@gmail.com.ORCID 0000-0003-2385-2591
Joshua MarrsDepartment of Pediatrics, Los Angeles General Medical Center, Los Angeles, CA, USA.ORCID 0009-0009-0600-5164
Patricia AcharyaDepartment of Radiology, Keck School of Medicine, Children's Hospital of Los Angeles, University of Southern California, Los Angeles, CA, USA.ORCID 0000-0002-4777-0542
Amit SuraDepartment of Radiology, Keck School of Medicine, Children's Hospital of Los Angeles, University of Southern California, Los Angeles, CA, USA.ORCID 0000-0002-4332-078X
Michal CidonDivision of Rheumatology, Keck School of Medicine, Children's Hospital of Los Angeles, University of Southern California, Los Angeles, CA, USA.ORCID 0000-0001-6581-7618

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Calcinosis is a sequela of Juvenile Dermatomyositis (JDM) with significant morbidity. A retrospective study observing risk factors for JDM calcinosis, including a possible association between higher intensity of subcutaneous and myofascial edema in initial magnetic resonance imaging (MRI) and development of calcinosis was performed at a tertiary pediatric medical center. Data from the past 20 years on JDM patients with MRIs at the time of JDM diagnosis were obtained. MRIs were individually evaluated by two pediatric musculoskeletal radiologists who blindly graded the intensity of edema on a 0-4 Likert scale. Clinical data and edema scores were compared between patients who developed calcinosis and who did not. Forty-three patients (14 with calcinosis and 29 without calcinosis) were identified. The calcinosis group contained more racial and ethnic minorities, younger ages of JDM onset and longer time to reach JDM diagnosis. Muscle enzyme levels at JDM diagnosis were lower in the calcinosis group, especially Creatinine Kinase (CK) (p = 0.047) and Alanine Aminotransferase (ALT) (p = 0.015). The median score for edema in both groups was 3 (p = 0.39) with an inter-rater reliability of 95%. There was no association between increased subcutaneous and myofascial edema in MRIs at the time of JDM diagnosis and development of calcinosis. Earlier age of JDM onset, racial and ethnic minority, and delay in JDM diagnosis could be risks for developing calcinosis. The calcinosis group presented with lower muscle enzyme levels at the time of JDM diagnosis, especially CK and ALT with statistical significance. This could reflect delay in diagnosis and treatment.

Indexed as

CalcinosisDermatomyositisEdemaMagnetic Resonance ImagingAdolescentChildChild, PreschoolFemaleHumansMaleRetrospective StudiesRisk FactorsCalcinosisEdemaJuvenile dermatomyositisMagnetic resonance imagingRisk factor

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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.