Evidence map›Paper›PMID 29145499›Full record

ArticlePloS one2017

Clinical tool for disease phenotyping in granulomatous lung disease.

Lori J Silveira, Matthew Strand, Michael V Van Dyke, Margaret M Mroz, Anna V Faino, Dana M Dabelea, Lisa A Maier, Tasha E Fingerlin

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 80% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

8 authors at 3 institutions in 1 country.

Lori J SilveiraDivision of Biostatistics and Informatics, National Jewish Health, Denver, Colorado, United States of America.
Matthew StrandDivision of Biostatistics and Informatics, National Jewish Health, Denver, Colorado, United States of America.
Michael V Van DykeColorado Department of Public Health and Environment, Denver, Colorado, United States of America.
Margaret M MrozDivision of Environmental and Occupational Health, National Jewish Health, Denver, Colorado, United States of America.
Anna V FainoDivision of Biostatistics and Informatics, National Jewish Health, Denver, Colorado, United States of America.
Dana M DabeleaColorado School of Public Health, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States of America.
Lisa A MaierColorado School of Public Health, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States of America.
Tasha E FingerlinColorado School of Public Health, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States of America.ORCID http://orcid.org/0000-0002-6405-3705
Colorado School of Public Health · USNational Jewish Health · USColorado Department of Public Health and Environment · US

Funding

Colorado Clinical and Translational Science Institute (UL1)UL1TR000154 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2012 to 2013
$20.4M
T Cells in Beryllium Sensitization and DiseaseP01ES011810 · NIEHS · UNIVERSITY OF COLORADO DENVER · PI NEWMAN, LEE S · 2002 to 2013
$14.0M
NCATS NIH HHS UL1 TR000154NIEHS NIH HHS P01 ES011810
6 · The paper itself

Abstract

backgroundExposure to beryllium may lead to granuloma formation and fibrosis in those who develop chronic beryllium disease (CBD). Although disease presentation varies from mild to severe, little is known about CBD phenotypes. This study characterized CBD disease phenotypes using longitudinal measures of lung function.

methodsUsing a case-only study of 207 CBD subjects, subject-specific trajectories over time were estimated from longitudinal pulmonary function and exercise-tolerance tests. To estimate linear combinations of the 30-year values that define underlying patterns of lung function, we conducted factor analysis. Cluster analysis was then performed on all the predicted lung function values at 30 years. These estimates were used to identify underlying features and subgroups of CBD.

resultsTwo factors, or composite measures, explained nearly 70% of the co-variation among the tests; one factor represented pulmonary function in addition to oxygen consumption and workload during exercise, while the second factor represented exercise tests related to gas exchange. Factors were associated with granulomas on biopsy, exposure, steroid use and lung inflammation. Three clusters of patients (n = 53, n = 59 and, n = 95) were identified based on the collection of test values. Lower levels of each of the factor composite scores and cluster membership were associated with baseline characteristics of patients.

conclusionsUsing factor analysis and cluster analysis, we identified disease phenotypes that were associated with baseline patient characteristics, suggesting that CBD is a heterogeneous disease with varying severity. These clinical tools may be used in future basic and clinical studies to help define the mechanisms and risk factors for disease severity.

Indexed as

Adrenal Cortex HormonesAdultBiopsyFemaleGranulomaHumansLongitudinal StudiesLung DiseasesMaleMiddle AgedPhenotypeRespiratory Function TestsAdrenal Cortex Hormones

Identifiers

PMID29145499
PMCPMC5690625
OpenAlexW2768377257

What OpenQuestion 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 OpenQuestion graph.