Evidence map›Paper›PMID 26939803›Full record

ArticleClinical and experimental immunology2016

NETosis-associated serum biomarkers are reduced in type 1 diabetes in association with neutrophil count.

J Qin, S Fu, C Speake, C J Greenbaum, J M Odegard

Open access · greenAbstract read
In one paragraph

Article in Clinical and experimental immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

36 citing papers in PubMed, 52 citations in OpenAlex.

  1. Review
  2. Target neutrophil heterogeneity and plasticity in cancer.Journal of hematology & oncology · 2025
    Review
  3. Review
  4. Article
  5. NETs: a new target for autoimmune disease.Frontiers in immunology · 2025
    Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Neutrophils in chronic inflammatory diseases.Cellular & molecular immunology · 2022
    Review
  14. Review
  15. Article
  16. Review
  17. Review
  18. Review
  19. Article
  20. 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

5 authors at 1 institution.

J QinDiabetes Clinical Research Program, Benaroya Research Institute at Virginia Mason, Seattle, WA, USA.
S FuDiabetes Clinical Research Program, Benaroya Research Institute at Virginia Mason, Seattle, WA, USA.
C SpeakeDiabetes Clinical Research Program, Benaroya Research Institute at Virginia Mason, Seattle, WA, USA.
C J GreenbaumDiabetes Clinical Research Program, Benaroya Research Institute at Virginia Mason, Seattle, WA, USA.
J M OdegardDiabetes Clinical Research Program, Benaroya Research Institute at Virginia Mason, Seattle, WA, USA.
Benaroya Research Institute

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As the immune pathways involved in the pathogenesis of type 1 diabetes (T1D) are not fully understood, biomarkers implicating novel mechanisms of disease are of great interest and call for independent evaluation. Recently, it was reported that individuals with T1D display dramatic elevations in circulating components of neutrophil extracellular traps (NETs), indicating a potential role for NETosis in T1D. Our aim was to evaluate further the potential of NET-associated proteins as novel circulating biomarkers in T1D. We tested serum from subjects with T1D (n = 44) with a median age of 26·5 years and a median duration of 2·2 years, along with 38 age-matched controls. T1D subjects did not show elevations in either neutrophil elastase (NE) or proteinase 3 (PR3), as reported previously. In fact, both NE and PR3 levels were reduced significantly in T1D subjects, particularly in subjects within 3 years of diagnosis, consistent with the known reduction in neutrophil counts in recent-onset T1D. Indeed, levels of both NE and PR3 correlated with absolute neutrophil counts. Therefore, while not ruling out potential local or transient spikes in NETosis activity, the levels of these serum markers do not support a role for systemically elevated NETosis in the T1D population we studied. Rather, a modest reduction in these markers may reflect other important aspects of disease activity associated with reduced neutrophil numbers.

Indexed as

AdultAge of OnsetBiomarkersCase-Control StudiesDiabetes Mellitus, Type 1Extracellular TrapsFemaleGene ExpressionHumansLeukocyte CountLeukocyte ElastaseMaleMyeloblastinNeutrophilsBiomarkersLeukocyte ElastaseMyeloblastinautoimmunitydiabetesneutrophils

Identifiers

PMID26939803
PMCPMC4872375
OpenAlexW2291524306

What OpenQuestion holds

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Read underepoch 390

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.