Evidence map›Paper›PMID 27103383›Full record

ArticleThe European respiratory journal2016

Beryllium-induced lung disease exhibits expression profiles similar to sarcoidosis.

Li Li, Lori J Silveira, Nabeel Hamzeh, May Gillespie, Peggy M Mroz, Annyce S Mayer, Tasha E Fingerlin, Lisa A Maier

Open access · bronzeAbstract read
In one paragraph

Article in The European respiratory journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

19 citing papers in PubMed, 28 citations in OpenAlex.

  1. Immune regulation by CD55 in chronic beryllium disease.American journal of respiratory cell and molecular biology · 2026
    Article
  2. Article
  3. Overview of multi-omics approaches for pulmonary sarcoidosis.EC pulmonology and respiratory medicine · 2025
    Article
  4. Review
  5. Review
  6. Article
  7. The Role ofMicroorganisms · 2022
    Review
  8. Innate and Adaptive Immunity in Noninfectious Granulomatous Lung Disease.Journal of immunology (Baltimore, Md. : 1950) · 2022
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Age-associated B Cells Appear in Patients with Granulomatous Lung Diseases.American journal of respiratory and critical care medicine · 2020
    Article
  14. Article
  15. Review
  16. Article
  17. DNA Methylation Changes in Lung Immune Cells Are Associated with Granulomatous Lung Disease.American journal of respiratory cell and molecular biology · 2019
    Article
  18. Article
  19. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Li LiDept of Medicine, National Jewish Health, Denver, CO, USA Division of Pulmonary and Critical Care Sciences, Dept of Medicine, School of Medicine, Denver, CO, USA lil@njhealth.org.
Lori J SilveiraDept of Medicine, National Jewish Health, Denver, CO, USA.
Nabeel HamzehDept of Medicine, National Jewish Health, Denver, CO, USA Division of Pulmonary and Critical Care Sciences, Dept of Medicine, School of Medicine, Denver, CO, USA.
May GillespieDept of Medicine, National Jewish Health, Denver, CO, USA.
Peggy M MrozDept of Medicine, National Jewish Health, Denver, CO, USA.
Annyce S MayerDept of Medicine, National Jewish Health, Denver, CO, USA Division of Pulmonary and Critical Care Sciences, Dept of Medicine, School of Medicine, Denver, CO, USA Environmental Occupational Health Dept, School of Public Health, University of Colorado, Denver, CO, USA.
Tasha E FingerlinDept of Medicine, National Jewish Health, Denver, CO, USA.
Lisa A MaierDept of Medicine, National Jewish Health, Denver, CO, USA Division of Pulmonary and Critical Care Sciences, Dept of Medicine, School of Medicine, Denver, CO, USA Environmental Occupational Health Dept, School of Public Health, University of Colorado, Denver, CO, USA.
University of Colorado Denver · USNational Jewish Health · USColorado School of Public Health · US

Funding

Colorado Clinical and Translational Sciences InstituteUL1TR001082 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2013 to 2017
$48.0M
T Cells in Beryllium Sensitization and DiseaseP01ES011810 · NIEHS · UNIVERSITY OF COLORADO DENVER · PI NEWMAN, LEE S · 2002 to 2013
$14.0M
Exposure in Epigenetic Regulation of Immune Response in CBDR01ES023826 · NIEHS · NATIONAL JEWISH HEALTH · PI MAIER, LISA A, YANG, IVANA V · 2015 to 2019
$2.3M
Colorado Career Development Program in the Genetics and Genomics of Lung DiseasesK12HL090147 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI GERACI, MARK W · 2007 to 2012
$2.0M
Functional Genomics Approach to the Role of the JAK/STAT and MAPK Pathway in CBDK01ES020857 · NIEHS · UNIVERSITY OF COLORADO DENVER · PI LI, LI · 2011 to 2013
$382k
NCATS NIH HHS UL1 TR001082NHLBI NIH HHS K12 HL090147NIEHS NIH HHS K01 ES020857NIEHS NIH HHS P01 ES011810NIEHS NIH HHS R01 ES023826
6 · The paper itself

Abstract

A subset of beryllium-exposed workers develop beryllium sensitisation (BeS) which precedes chronic beryllium disease (CBD). We conducted an in-depth analysis of differentially expressed candidate genes in CBD.We performed Affymetrix GeneChip 1.0 ST array analysis on peripheral blood mononuclear cells (PBMCs) from 10 CBD, 10 BeS and 10 beryllium-exposed, nondiseased controls stimulated with BeSO4 or medium. The differentially expressed genes were validated by high-throughput real-time PCR in this group and in an additional group of cases and nonexposed controls. The functional roles of the top candidate genes in CBD were assessed using a pharmacological inhibitor. CBD gene expression data were compared with whole blood and lung tissue in sarcoidosis from the Gene Expression Omnibus.We confirmed almost 450 genes that were significantly differentially expressed between CBD and controls. The top enrichment of genes was for JAK (Janus kinase)-STAT (signal transducer and activator of transcription) signalling. A JAK2 inhibitor significantly decreased tumour necrosis factor-α and interferon-γ production. Furthermore, we found 287 differentially expressed genes overlapped in CBD/sarcoidosis. The top shared pathways included cytokine-cytokine receptor interactions, and Toll-like receptor, chemokine and JAK-STAT signalling pathways.We show that PBMCs demonstrate differentially expressed gene profiles relevant to the immunnopathogenesis of CBD. CBD and sarcoidosis share similar differential expression of pathogenic genes and pathways.

Indexed as

Gene Expression ProfilingGene Expression RegulationAdultAgedAged, 80 and overBerylliosisBerylliumChronic DiseaseFemaleHumansInterferon-gammaLeukocytes, MononuclearLung DiseasesMaleMiddle AgedOccupational ExposureBerylliumInterferon-gammaTumor Necrosis Factor-alpha

Identifiers

PMID27103383
PMCPMC5134922
OpenAlexW2336397951

What OpenQuestion holds

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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.