Evidence map›Paper›PMID 35616642›Full record

ArticleACR open rheumatology2022

Gene Expression Profiles of Treatment Response and Non-Response in Children With Juvenile Dermatomyositis.

Cory Stingl, Jeffrey A Dvergsten, Simon W M Eng, Rae S M Yeung, Marvin J Fritzler, Thomas Mason, Cynthia Crowson, Deepak Voora, Ann M Reed

Open access · goldAbstract read
In one paragraph

Article in ACR open rheumatology, 2022. 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
0.9field-weighted citation impact, top 26% 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, 6 citations in OpenAlex.

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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

9 authors at 4 institutions in 2 countries.

Cory StinglDuke University, Durham, North Carolina.
Jeffrey A DvergstenDuke University, Durham, North Carolina.ORCID https://orcid.org/0000-0002-3492-9665
Simon W M EngThe Hospital for Sick Children, Toronto, Ontario, Canada.
Rae S M YeungThe Hospital for Sick Children, Toronto, Ontario, Canada.
Marvin J FritzlerUniversity of Calgary, Calgary, Alberta, Canada.
Thomas MasonMayo Clinic, Rochester, Minnesota.
Cynthia CrowsonMayo Clinic, Rochester, Minnesota.ORCID https://orcid.org/0000-0001-5847-7475
Deepak VooraDuke University, Durham, North Carolina.
Ann M ReedDuke University, Durham, North Carolina.ORCID https://orcid.org/0000-0002-4521-7647
Duke University · USHospital for Sick Children · CAMayo Clinic · USUniversity of Calgary · CA

Funding

Preparing Genetic Counselors for Genomic Medicine ResearchT32HG008955 · NHGRI · DUKE UNIVERSITY · PI COONEY, KATHLEEN A, HAGA, SUSANNE · 2017 to 2021
$2.0M
Childhood Arthritis and Rheumatology Research AllianceCSR NIH HHS T32 HG008955NHGRI NIH HHS T32 HG008955
6 · The paper itself

Abstract

objectiveThe study objective was to identify differences in gene expression between treatment responders (TRs) and treatment non-responders (TNRs) diagnosed with juvenile dermatomyositis (JDM).

methodsGene expression analyses were performed using whole blood messenger RNA sequencing in patients with JDM (n = 17) and healthy controls (HCs; n = 10). Four analyses were performed (A1-4) comparing differential gene expression and pathways analysis exploiting the timing of sample acquisition and the treatments received to perform these comparative analyses. Analyses were done at diagnosis and follow-up, which averaged 7 months later in the cohort.

resultsAt diagnosis, the expression of 10 genes differed between TRs and TNRs. Hallmark and canonical pathway analysis revealed 11 and 60 pathways enriched in TRs and 3 and 21 pathways enriched in TNRs, respectively. Pathway enrichment at diagnosis in TRs was strongest in pathways involved in metabolism, complement activation, and cell signaling as mediated by IL-8, p38/microtubule associated protein kinases (MAPK)/extracellular signal-regulated kinases (ERK), Phosphatidylinositol 3 Kinase Gamma (PI3Kγ), and the B cell receptor. Follow-up hallmark and canonical pathway analysis showed that 2 and 14 pathways were enriched in TRs, whereas 24 and 123 pathways were enriched in treatment TNRs, respectively. Prior treatment with glucocorticoids significantly altered expression of 13 genes in the analysis of subjects at diagnosis with JDM as compared with HCs.

conclusionNumerous genes and pathways differ between TRs and TNRs at diagnosis and follow-up. Prior treatment with glucocorticoids prior to specimen acquisition had a small effect on the performed analyses.

Identifiers

PMID35616642
PMCPMC9374052
OpenAlexW4281568002

What OpenQuestion holds

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Registered trials

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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.