Evidence map›Paper›PMID 23831963›Full record

ArticleAnnals of the rheumatic diseases2014

MxA as a clinically applicable biomarker for identifying systemic interferon type I in primary Sjogren's syndrome.

Naomi I Maria, Zana Brkic, Matti Waris, Cornelia G van Helden-Meeuwsen, Kim Heezen, Joop P van de Merwe, Paul L van Daele, Virgil A S H Dalm, Hemmo A Drexhage, Marjan A Versnel

Open access · bronzeAbstract read
In one paragraph

Article in Annals of the rheumatic diseases, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed, 2 pooled it
3.9field-weighted citation impact, top 6% 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

73 citing papers in PubMed, 2 syntheses or guidelines pooled it, 123 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. UnravelingFrontiers in oncology · 2024
    Review
  20. Article

13 more citing papers are in PubMed but not listed here.

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

10 authors at 2 institutions in 2 countries.

Naomi I MariaDepartment of Immunology, Erasmus MC, , Rotterdam, Zuid-holland, The Netherlands.
Zana Brkic
Matti Waris
Cornelia G van Helden-Meeuwsen
Kim Heezen
Joop P van de Merwe
Paul L van Daele
Virgil A S H Dalm
Hemmo A Drexhage
Marjan A Versnel
Erasmus MC · NLUniversity of Turku · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo establish an easy and practical assay for identifying systemic interferon (IFN) type I bioactivity in patients with primary Sjögren's syndrome (pSS). The IFN type I signature is present in over half of the pSS patients and identifies a subgroup with a higher disease activity. This signature is currently assessed via laborious expression profiles of multiple IFN type I-inducible genes.

methodsIn a cohort of 35 pSS patients, myxovirus-resistance protein A (MxA) was assessed as a potential biomarker for type I IFN activity, using an enzyme immunoassay (EIA) on whole-blood and flow cytometric analyses (fluorescence-activated cell sorting, FACS) of isolated CD14 monocytes. In addition, potential biomarkers such as CD64, CD169 and B cell-activating factor (BAFF) were simultaneously analysed in CD14 monocytes using FACS. The IFNscore, a measure for total type I IFN bioactivity, was calculated using expression values of the IFN type I signature genes--IFI44, IFI44L, IFIT3, LY6E and MX1--in CD14 monocytes, determined by real-time quantitative PCR.

resultsIFNscores correlated the strongest with monocyte MxA protein (r=0.741, p<0.001) and whole-blood MxA levels (r=0.764, p<0.001), weaker with CD169 (r=0.495, p<0.001) and CD64 (r=0.436, p=0.007), and not at all with BAFF protein. In particular, whole blood MxA levels correlated with EULAR Sjögren's Syndrome Disease Activity Index scores and numerous clinical pSS parameters. Interestingly, patients on hydroxychloroquine showed reduced MxA levels (EIA, p=0.04; FACS p=0.001).

conclusionsThe MxA assays were excellent tools to assess IFN type I activity in pSS, MxA-EIA being the most practical. MxA levels associate with features of active disease and are reduced in hydroxychloroquine-treated patients, suggesting the clinical applicability of MxA in stratifying patients according to IFN positivity.

Indexed as

AdultAgedAged, 80 and overAntigensAntigens, SurfaceBiomarkersCohort StudiesCytoskeletal ProteinsFemaleGene Expression ProfilingGPI-Linked ProteinsHumansImmunoenzyme TechniquesInterferon Type IIntracellular Signaling Peptides and ProteinsMaleAntigensAntigens, SurfaceBiomarkersCytoskeletal ProteinsGPI-Linked ProteinsIFI44 protein, humanIFIT3 protein, humanInterferon Type IIntracellular Signaling Peptides and ProteinsLY6E protein, humanMX1 protein, humanMyxovirus Resistance ProteinsRNA, MessengerDisease ActivitySjøgren's SyndromeTreatment

Identifiers

PMID23831963
PMCPMC4033122
OpenAlexW2167981267

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.