Evidence map›Paper›PMID 36515466›Full record

ArticleRheumatology (Oxford, England)2023

Serum IFNα2 levels are associated with disease activity and outperform IFN-I gene signature in a longitudinal childhood-onset SLE cohort.

M Javad Wahadat, Hongchao Qi, Cornelia G van Helden-Meeuwsen, Erika Huijser, Lotte van den Berg, Annette van Dijk-Hummelman, Jens C Göpfert, Anne Heine, Marleen Verkaaik, Marco W J Schreurs and 3 more

Abstract read
In one paragraph

Article in Rheumatology (Oxford, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
–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

12 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  6. Observational
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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

13 authors.

M Javad WahadatDepartment of Immunology, Erasmus University Medical Center, Rotterdam, The Netherlands.ORCID 0000-0003-3961-1274
Hongchao QiDepartment of Biostatistics, Erasmus University Medical Center, Rotterdam, The Netherlands.
Cornelia G van Helden-MeeuwsenDepartment of Immunology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Erika HuijserDepartment of Immunology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Lotte van den BergDepartment of Paediatric Rheumatology, Sophia Children's hospital, Erasmus University Medical Center, Rotterdam, The Netherlands.
Annette van Dijk-HummelmanDepartment of Paediatric Rheumatology, Sophia Children's hospital, Erasmus University Medical Center, Rotterdam, The Netherlands.
Jens C GöpfertDepartment of Applied, Biomarkers and Immunoassays, NMI Natural and Medical Sciences Institute at the University of Tübingen, Reutlingen, Germany.
Anne HeineDepartment of Applied, Biomarkers and Immunoassays, NMI Natural and Medical Sciences Institute at the University of Tübingen, Reutlingen, Germany.
Marleen VerkaaikDepartment of Paediatric Rheumatology, Sophia Children's hospital, Erasmus University Medical Center, Rotterdam, The Netherlands.
Marco W J SchreursLaboratory Medical Immunology, Department of Immunology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Willem A DikLaboratory Medical Immunology, Department of Immunology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Sylvia KamphuisDepartment of Paediatric Rheumatology, Sophia Children's hospital, Erasmus University Medical Center, Rotterdam, The Netherlands.ORCID 0000-0002-1964-352X
Marjan A VersnelDepartment of Immunology, Erasmus University Medical Center, Rotterdam, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo study the association of serum IFNα2 levels measured by ultrasensitive single-molecule array (Simoa) and the IFN-I gene signature (IGS) with disease activity and determine whether these assays can mark disease activity states in a longitudinal cohort of childhood-onset SLE (cSLE) patients.

methodsSerum IFNα2 levels were measured in 338 samples from 48 cSLE patients and 67 healthy controls using an IFNα Simoa assay. Five-gene IGS was measured by RT-PCR in paired whole blood samples. Disease activity was measured by clinical SELENA-SLEDAI and BILAG-2004. Low disease activity was defined by Low Lupus Disease Activity State (LLDAS) and flares were characterized by SELENA-SLEDAI flare index. Analysis was performed using linear mixed models.

resultsA clear positive correlation was present between serum IFNα2 levels and the IGS (r = 0.78, P < 0.0001). Serum IFNα2 levels and IGS showed the same significant negative trend in the first 3 years after diagnosis. In this timeframe, mean baseline serum IFNα2 levels decreased by 55.1% (Δ 201 fg/ml, P < 0.001) to a mean value of 164 fg/ml, which was below the calculated threshold of 219.4 fg/ml that discriminated between patients and healthy controls. In the linear mixed model, serum IFNα2 levels were significantly associated with both cSELENA-SLEDAI and BILAG-2004, while the IGS did not show this association. Both IFN-I assays were able to characterize LLDAS and disease flare in receiver operating characteristic analysis.

conclusionsSerum IFNα2 levels measured by Simoa technology are associated with disease activity scores and characterize disease activity states in cSLE.

Indexed as

Interferon Type ILupus Erythematosus, SystemicHumansInterferon-alphaInterferon-alphaInterferon Type Idisease activityIFN signatureSimoaSLEtype I IFN

Identifiers

PMID36515466
PMCPMC10393436

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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.