Evidence map›Paper›PMID 36388923›Full record

ArticleFrontiers in medicine2022

Biochemical and genomic identification of novel biomarkers in progressive sarcoidosis: HBEGF, eNAMPT, and ANG-2.

Nancy G Casanova, Vivian Reyes-Hernon, Taylor Gregory, Belinda Sun, Tadeo Bermudez, Matthew K Hufford, Radu C Oita, Sara M Camp, Gabriela Hernandez-Molina, Jorge Rojas Serrano and 6 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

  1. Metabolomic signaling in sarcoidosis pathogenesis.Current opinion in immunology · 2026
    Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Phenotypes and Serum Biomarkers in Sarcoidosis.Diagnostics (Basel, Switzerland) · 2024
    Review
  7. Review
  8. Article
  9. 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

16 authors at 4 institutions in 2 countries.

Nancy G CasanovaDepartment of Medicine, University of Arizona Health Sciences, Tucson, AZ, United States.
Vivian Reyes-HernonDepartment of Medicine, University of Arizona Health Sciences, Tucson, AZ, United States.
Taylor GregoryDepartment of Medicine, University of Arizona Health Sciences, Tucson, AZ, United States.
Belinda SunDepartment of Pathology, University of Arizona Health Sciences, Tucson, AZ, United States.
Tadeo BermudezDepartment of Medicine, University of Arizona Health Sciences, Tucson, AZ, United States.
Matthew K HuffordDepartment of Medicine, University of Arizona Health Sciences, Tucson, AZ, United States.
Radu C OitaDepartment of Medicine, University of Arizona Health Sciences, Tucson, AZ, United States.
Sara M CampDepartment of Medicine, University of Arizona Health Sciences, Tucson, AZ, United States.
Gabriela Hernandez-MolinaInstituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, México City, Mexico.
Jorge Rojas SerranoInstituto Nacional de Enfermedades Respiratorias, México City, Mexico.
Xiaoguang SunDepartment of Medicine, University of Arizona Health Sciences, Tucson, AZ, United States.
Jocelyn FimbresInstituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, México City, Mexico.
Mehdi MirsaeidiDepartment of Medicine, College of Medicine, University of Florida, Jacksonville, FL, United States.
Saad SammaniDepartment of Medicine, University of Arizona Health Sciences, Tucson, AZ, United States.
Christian BimeDepartment of Medicine, University of Arizona Health Sciences, Tucson, AZ, United States.
Joe G N GarciaDepartment of Medicine, University of Arizona Health Sciences, Tucson, AZ, United States.
University of Arizona · USInstituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán · MXFlorida College · USInstituto Nacional de Enfermedades Respiratorias · MX

Funding

SELPLG as a candidate gene in Acute Respiratory Distress SyndromeK08HL141623 · NHLBI · UNIVERSITY OF ARIZONA · PI BIME, CHRISTIAN · 2018 to 2022
$863k
NHLBI NIH HHS K08 HL141623
6 · The paper itself

Abstract

Background: Progressive pulmonary fibrosis is a serious complication in subjects with sarcoidosis. The absence of reliable, non-invasive biomarkers that detect early progression exacerbates the difficulty in predicting sarcoidosis severity. To potentially address this unmet need, we evaluated a panel of markers for an association with sarcoidosis progression (HBEGF, NAMPT, IL1-RA, IL-6, IL-8, ANG-2). This panel encompasses proteins related to inflammation, vascular injury, cell proliferation, and fibroblast mitogenesis processes. Methods: Plasma biomarker levels and biomarker protein expression in lung and lymph nodes tissues (immunohistochemical studies) from sarcoidosis subjects with limited disease and progressive (complicated) sarcoidosis were performed. Gene expression of the protein-coding genes included in this panel was analyzed using RNAseq in sarcoidosis granulomatous tissues from lung and lymph nodes. Results: Except for IL-8, plasma levels of each biomarker-eNAMPT, IL-1RA, IL-6, ANG-2, and HBEGF-were significantly elevated in sarcoidosis subjects compared to controls. In addition, plasma levels of HBEGF were elevated in complicated sarcoidosis, while eNAMPT and ANG-2 were observed to serve as markers of lung fibrosis in a subgroup of complicated sarcoidosis. Genomic studies corroborated Conclusion: These findings suggest HBEGF, eNAMPT, and ANG-2 may serve as potential novel indicators of the clinical severity of sarcoidosis disease.

Indexed as

biomarkerfibrosisgene expressionplasmasarcoidosis

Identifiers

PMID36388923
PMCPMC9640603
OpenAlexW4307371954

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.