Evidence map›Paper›PMID 36264970›Full record

ArticlePloS one2022

Autoantibody profile in sarcoidosis, analysis from the GRADS sarcoidosis cohort.

Basheer Khassawneh, Chengsong Zhu, Briana Barkes, Brian Vestal, Sarah Shrock, May Gillespie, Karin Pacheco, Kevin D Deane, Lisa A Maier, Quan-Zhen Li and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

7 citing papers in PubMed, 5 citations in OpenAlex.

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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

12 authors at 5 institutions in 2 countries.

Basheer KhassawnehJordan University of Science and Technology, Irbid, Jordan.ORCID 0000-0003-2160-4498
Chengsong ZhuUniversity of Texas Southwestern Medical Center, Dallas, TX, United States of America.
Briana BarkesNational Jewish Health, Denver, CO, United States of America.
Brian VestalNational Jewish Health, Denver, CO, United States of America.
Sarah ShrockNational Jewish Health, Denver, CO, United States of America.
May GillespieNational Jewish Health, Denver, CO, United States of America.
Karin PachecoNational Jewish Health, Denver, CO, United States of America.
Kevin D DeaneUniversity of Colorado, Aurora, CO, United States of America.
Lisa A MaierNational Jewish Health, Denver, CO, United States of America.
Quan-Zhen LiUniversity of Texas Southwestern Medical Center, Dallas, TX, United States of America.
Nabeel HamzehNational Jewish Health, Denver, CO, United States of America.ORCID 0000-0001-7296-8975
GRADS investigators
National Jewish Health · USThe University of Texas Southwestern Medical Center · USJordan University of Science and Technology · JOUniversity of Colorado Anschutz Medical Campus · USUniversity of Iowa · US

Funding

Sarcoidosis and A1AT Genomics & Informatics CenterU01HL112707 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BECICH, MICHAEL JOHN, KAMINSKI, NAFTALI · 2012 to 2015
$8.5M
Immunologic and Molecular Phenotypes in AATD and SarcoidosisU01HL112695 · NHLBI · NATIONAL JEWISH HEALTH · PI MAIER, LISA A · 2012 to 2014
$465k
NHLBI NIH HHS HHSN268201000021CNHLBI NIH HHS HHSN268201600001CNHLBI NIH HHS HHSN268201600002CNHLBI NIH HHS U01 HL112695NHLBI NIH HHS U01 HL112707
6 · The paper itself

Abstract

backgroundSarcoidosis, a multi-systemic granulomatous disease, is a predominantly T-cell disease but evidence for a role for humoral immunity in disease pathogenesis is growing. Utilizing samples from the Genomic Research in Alpha-1 anti-trypsin Deficiency and Sarcoidosis (GRADS) study, we examined the prevalence of autoantibodies in sarcoidosis patients with pulmonary-only and extra-pulmonary organ involvement compared to normal controls. STUDY DESIGN AND

methodsWe analyzed serum samples from sarcoidosis patients who participated in the GRADS study utilizing an autoantigen microarray platform for both IgM and IgG antibodies. The cohort included sarcoidosis patients with pulmonary-only disease (POS, n = 106), sarcoidosis patients with extra-pulmonary disease (EPS, n = 120) and a normal control cohort (NC, n = 101). Organ involvement was assessed following a standardized format across all GRADS participating centers.

resultsSarcoidosis patients overall had increased levels of IgM and IgG autoantibodies compared to normal controls. In addition, several autoantibodies were elevated in the POS and EPS cohorts compared to the NC cohort. Differences in autoantibody levels were also noted between the POS and the EPS cohorts. When comparing organ involvement with sarcoidosis, bone, spleen and ear, nose and throat involvement had higher IgM expression than other organs.

conclusionSarcoidosis patients have elevated IgM and IgG autoantibody levels compared to normal controls. In addition, individuals with pulmonary as well as additional organ involvement had higher IgM expression. Further research is needed focusing on specific organ-autoantibody pairs and role of autoantibodies in disease pathogenesis.

Indexed as

Lung DiseasesSarcoidosisAutoantibodiesAutoantigensHumansImmunoglobulin GImmunoglobulin MAutoantibodiesAutoantigensImmunoglobulin GImmunoglobulin M

Identifiers

PMID36264970
PMCPMC9584415
OpenAlexW4306896990

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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.