Evidence map›Paper›PMID 24199653›Full record

ArticleRespiratory research2013

Interferon-inducible chemokines reflect severity and progression in sarcoidosis.

Robert Su, Michelle-Linh T Nguyen, Misha R Agarwal, Christopher Kirby, Christine P Nguyen, Joris Ramstein, Eli P Darnell, Antonio D Gomez, Melissa Ho, Prescott G Woodruff and 1 more

Open access · goldAbstract read
In one paragraph

Article in Respiratory research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

37 citing papers in PubMed, 84 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Increased proportions of circulating PD-1Respiratory research · 2024
    Article
  9. Sarcoidosis-associated pulmonary fibrosis: joining the dots.European respiratory review : an official journal of the European Respiratory Society · 2023
    Review
  10. Article
  11. Macrophage Biology in Human Granulomatous Skin Inflammation.International journal of molecular sciences · 2023
    Review
  12. Article
  13. Article
  14. Observational
  15. Article
  16. Review
  17. Epigenetics and sarcoidosis.European respiratory review : an official journal of the European Respiratory Society · 2021
    Review
  18. Article
  19. Inflammatory Pathways in Sarcoidosis.Advances in experimental medicine and biology · 2021
    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

11 authors at 1 institution in 1 country.

Robert Su
Michelle-Linh T Nguyen
Misha R Agarwal
Christopher Kirby
Christine P Nguyen
Joris Ramstein
Eli P Darnell
Antonio D Gomez
Melissa Ho
Prescott G Woodruff
Laura L KothDivision of Pulmonary, Critical Care, Sleep and Allergy, University of California San Francisco, 505 Parnassus Avenue, Box 0111, San Francisco, CA 94143, USA. laura.koth@ucsf.edu.
University of California, San Francisco · US

Funding

Immunophenotyping and Lymphocyte Effector Functions in SarcoidosisR56AI087652 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KOTH, LAURA L · 2010 to 2010
$386k
NIAID NIH HHS 1R56AI087652
6 · The paper itself

Abstract

backgroundIdentification of serum proteins that track with disease course in sarcoidosis may have clinical and pathologic importance. We previously identified up-regulated transcripts for interferon-inducible chemokines CXCL9, and CXCL10, in blood of sarcoidosis patients compared to controls. The objective of this study was to determine whether proteins encoded by these transcripts were elevated in serum and identified patients with remitting vs. chronic progressive sarcoidosis longitudinally.

methodsSerum levels of CXCL9, CXCL10, and proteins associated with inflammation and/or disease activity (sIL2R, ACE, ESR and CRP) were measured in a prospective cohort of sarcoidosis subjects and controls. Comparisons were made between groups and clinical course using pulmonary function measures and a severity score developed by Wasfi et al.

resultsIn a cross-sectional analysis of 36 non-immunosuppressed sarcoidosis subjects, serum CXCL9, CXCL10, and sIL2R were significantly elevated compared to 46 controls (p < 0.0001). CXCL9 and CXCL10 were strongly inter-correlated (p = 0.0009). CXCL10 and CXCL9 were inversely correlated with FVC% predicted and DLCO% predicted, respectively. CXCL10 and CXCL9 significantly correlated with sarcoidosis severity score. sIL2R, ESR, CRP, and ACE serum levels did not correlate with pulmonary function measures or severity score. In the longitudinal analysis of 26 subjects, changes in serum CXCL10 level over time corresponded with progression versus remission of disease.

conclusionsInterferon-γ-inducible chemokines, CXCL9 and CXCL10, are elevated in sarcoidosis and inter-correlated with each other. Chemokine levels correlated with measures of disease severity. Serial measurements of CXCL10 corresponded to clinical course.

Indexed as

Disease ProgressionSeverity of Illness IndexAdultBiomarkersBlood SedimentationCase-Control StudiesChemokine CXCL10Chemokine CXCL9Cohort StudiesC-Reactive ProteinCross-Sectional StudiesFemaleHumansLongitudinal StudiesMaleMiddle AgedBiomarkersChemokine CXCL10Chemokine CXCL9C-Reactive ProteinReceptors, Interleukin-2

Identifiers

PMID24199653
PMCPMC4176097
OpenAlexW2102372147

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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.