Evidence map›Paper›PMID 27894310›Full record

ArticlePediatric rheumatology online journal2016

Monitoring change in volume of calcifications in juvenile idiopathic inflammatory myopathy: a pilot study using low dose computed tomography.

Maria Ibarra, Cynthia Rigsby, Gabrielle A Morgan, Christina L Sammet, Chiang-Ching Huang, Dong Xu, Ira N Targoff, Lauren M Pachman

Open access · goldAbstract readEvaluation Study
In one paragraph

Article in Pediatric rheumatology online journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
0.5field-weighted citation impact, top 28% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Juvenile Dermatomyositis: New Clues to Diagnosis and Therapy.Current treatment options in rheumatology · 2021
    Article
  6. Review
  7. 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

8 authors at 5 institutions in 1 country.

Maria IbarraDivision of Pediatric Rheumatology, Children's Mercy Hospital , 2401 Gillham Road, Kansas City, Missouri, 64108-4619, USA.
Cynthia RigsbyDepartment of Medical Imaging, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA.
Gabrielle A MorganCure JM Center of Excellence, Stanley Manne Research Institute affiliated with Ann & Robert H. Lurie Children's Hospital of Chicago, 225 East Chicago Avenue, Box 212, Chicago, IL, 60611, USA.
Christina L SammetDepartment of Medical Imaging, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA.
Chiang-Ching HuangJoseph J. Zilber School of Public Health, University of Wisconsin, Milwaukee, WI, USA.
Dong XuCure JM Center of Excellence, Stanley Manne Research Institute affiliated with Ann & Robert H. Lurie Children's Hospital of Chicago, 225 East Chicago Avenue, Box 212, Chicago, IL, 60611, USA.
Ira N TargoffThe Department of Internal Medicine, The University of Oklahoma, Norman, OK, USA.
Lauren M PachmanCure JM Center of Excellence, Stanley Manne Research Institute affiliated with Ann & Robert H. Lurie Children's Hospital of Chicago, 225 East Chicago Avenue, Box 212, Chicago, IL, 60611, USA. pachman@northwestern.edu.
Lurie Children's Hospital · USNorthwestern University · USChildren's Mercy Hospital · USUniversity of Oklahoma · USUniversity of Wisconsin–Milwaukee · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDystrophic calcifications may occur in patients with J uvenile Idiopathic Inflammatory Myopathy (JIIM) as well as other connective tissue and metabolic diseases, but a reliable method of measuring the volume of these calcifications has not been established. The purpose of this study is to determine the feasibility of low dose, limited slice, Computed Tomography (CT) to measure objectively in-situ calcification volumes in patients with JIIM over time.

methodsTen JIIM patients (eight JDM, two Overlap) with calcifications were prospectively recruited over a 2-year period to undergo two limited, low dose, four-slice CT scans. Calculation of the volume of calcifications used a CT post processing workstation. Additional patient data included: Disease Activity Scores (DAS), Childhood Myositis Assessment Scale (CMAS), myositis specific antibodies (MSA), and the TNFα-308 promoter region A/G polymorphism. Statistical analysis utilized the Pearson correlation coefficient, the paired t-test and descriptive statistics.

resultsTen JIIM, mean age 14.54 ± 4.54 years, had a duration of untreated disease of 8.68 ± 5.65 months  MSA status: U1RNP (1), PM-Scl (1), Ro (1, 4 indeterminate), p155/140 (2), MJ (3), Mi-2 indeterminate (1), negative (3). 4/8 JDM (50%) were TNF-α-308 A+. Overall, the calcification volumes tended to decrease from the first to the second CT study by 0.5 cm

conclusionWe conclude: 1) the limited low dose CT technique provides objective data about volume of the calcifications in JIIM; 2) measuring the volume of calcifications in an extremity is associated with minimal radiation exposure; 3) This method may be useful to evaluate the efficacy of therapies for JIIM dystrophic calcification.

Indexed as

AdolescentCalcinosisChildFeasibility StudiesFemaleHumansMaleMyositisPilot ProjectsRadiation DosageTomography, X-Ray ComputedYoung AdultCalcificationCalcification volumeComputed Tomography (CT)Juvenile idiopathic inflammatory myopathyOverlap syndrome

Identifiers

PMID27894310
PMCPMC5127038
OpenAlexW2558825042

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.