Evidence map›Paper›PMID 29471675›Full record

ArticleAutoimmunity2018

Alterations in nucleotide-binding oligomerization domain-2 expression, pathway activation, and cytokine production in Yao syndrome.

Christine McDonald, Min Shen, Erin E Johnson, Amrita Kabi, Qingping Yao

Open access · greenAbstract read
In one paragraph

Article in Autoimmunity, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

26 citing papers in PubMed, 38 citations in OpenAlex.

  1. Multi-omics characterization of Yao syndrome identifies three pathophysiological axes and disease-specific divergence from Blau syndrome.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Article
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  3. Review
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  11. Yao syndrome in a child with C2 deficiency.The journal of allergy and clinical immunology. In practice · 2024
    Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Implications of combinedFrontiers in immunology · 2023
    Article
  17. Article
  18. Review
  19. Review
  20. New insights on multigenic autoinflammatory diseases.Therapeutic advances in musculoskeletal disease · 2022
    Review
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 3 institutions in 1 country.

Christine McDonalda Department of Pathobiology , Lerner Research Institute, Cleveland Clinic , Cleveland , OH , USA.ORCID 0000-0002-6745-9487
Min Shenb Department of Rheumatic and Immunologic Disease , Orthopaedic and Rheumatologic Institute, Cleveland Clinic , Cleveland , OH , USA.
Erin E Johnsonc Department of Biology , John Carroll University, University Heights , OH , USA.
Amrita Kabia Department of Pathobiology , Lerner Research Institute, Cleveland Clinic , Cleveland , OH , USA.
Qingping Yaob Department of Rheumatic and Immunologic Disease , Orthopaedic and Rheumatologic Institute, Cleveland Clinic , Cleveland , OH , USA.
Cleveland Clinic · USCleveland Clinic Lerner College of Medicine · USJohn Carroll University · US

Funding

Clinical and Translational Science Collaborative of ClevelandUL1TR000439 · NCATS · CASE WESTERN RESERVE UNIVERSITY · PI KONSTAN, MICHAEL W. · 2012 to 2016
$50.0M
NCATS NIH HHS UL1 TR000439
6 · The paper itself

Abstract

Yao syndrome (YAOS) is a systemic autoinflammatory disease (SAID), formerly termed nucleotide-binding oligomerization domain-2 (NOD2)-associated autoinflammatory disease. Due to the recent identification of YAOS, the molecular mechanisms underlying its disease pathogenesis are unclear. With specific NOD2 variants as characteristic genotypic features of YAOS, our study examined NOD2 expression, transcript splicing, signaling pathway activation, and cytokine profiles in peripheral blood mononuclear cells (PBMCs) from 10 YAOS patients and six healthy individuals. All participants were genotyped for NOD2 variants; all YAOS patients were heterozygous for the NOD2 IVS8

Indexed as

AdultAgedAntibodies, Monoclonal, HumanizedCytokinesFemaleGenetic Predisposition to DiseaseHereditary Autoinflammatory DiseasesHumansInterleukin-6Leukocytes, MononuclearMaleMiddle AgedNod2 Signaling Adaptor Proteinp38 Mitogen-Activated Protein KinasesSignal TransductionYoung AdultAntibodies, Monoclonal, HumanizedCytokinesIL6 protein, humanInterleukin-6NOD2 protein, humanNod2 Signaling Adaptor Proteinp38 Mitogen-Activated Protein Kinasestocilizumabanti-cytokine therapyAutoinflammatory diseasegeneticsNOD2Yao syndrome

Identifiers

PMID29471675
PMCPMC6036904
OpenAlexW2789409139

What OpenQuestion holds

Textmetadata
LicenceTDM
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.