Evidence map›Paper›PMID 31250334›Full record

ArticleJournal of clinical immunology2019

Cellular Defects in CVID Patients with Chronic Lung Disease in the USIDNET Registry.

Erinn S Kellner, Ramsay Fuleihan, Charlotte Cunningham-Rundles, USIDNET Consortium, Joshua B Wechsler

Open access · greenAbstract read
In one paragraph

Article in Journal of clinical immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

16 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Interstitial Lung Disease in Immunocompromised Children.Diagnostics (Basel, Switzerland) · 2022
    Article
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  9. Article
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  11. Article
  12. Review
  13. Review
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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

5 authors at 3 institutions in 1 country.

Erinn S KellnerDivision of Allergy and Immunology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA. erinn.kellner@cchmc.org.ORCID 0000-0002-5609-3256
Ramsay FuleihanDivision of Allergy-Immunology, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA.
Charlotte Cunningham-RundlesDivision of Allergy and Immunology, Department of Medicine, The Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
USIDNET Consortium
Joshua B WechslerDivision of Allergy and Immunology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA. j-wechsler@northwestern.edu.
Northwestern University · USIcahn School of Medicine at Mount Sinai · USLurie Children's Hospital · US

Funding

Regulation of Ulcerative Colitis by mast cells and histamineK08DK097721 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI WECHSLER, JOSHUA BRIAN · 2015 to 2019
$792k
TRANSCRIPTION FACTOR EKLF--REGULATION BY PHOSPHORYLATIONF32DK009772 · NIDDK · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI OUYANG, LIAOHAN · 1998 to 1999
–
NIDDK NIH HHS F32 DK009772NIDDK NIH HHS K08 DK097721
6 · The paper itself

Abstract

purposeChronic lung disease is the most common cause of morbidity and mortality in patients with common variable immunodeficiency (CVID). While biomarkers exist to predict non-infectious complications, the unique features that define CVID patients with chronic lung disease are not well understood.

methodsWe analyzed data from CVID patients from the retrospective USIDNET (United States Immunodeficiency Network) patient database. Patients were categorized into 3 phenotypes for comparison: (1) CVID without chronic lung disease, (2) CVID with bronchiectasis only, and (3) CVID with interstitial lung disease (ILD) with or without bronchiectasis. Among these groups, differences were assessed in demographics, comorbidities, infections, treatments, and peripheral blood immune measures. We analyzed 1518 CVID patients which included 1233 (81.2%) without chronic lung disease, 147 (9.7%) with bronchiectasis only, and 138 (9.1%) with interstitial lung disease.

resultsPatients with ILD had lower CD3

conclusionThis analysis suggests that patients with chronic lung disease may be more likely to have lower peripheral T cell counts and complications of those defects compared with CVID patients without chronic lung disease.

Indexed as

AdolescentAdultAutoimmunityChildChild, PreschoolChronic DiseaseCommon Variable ImmunodeficiencyDatabases, FactualDisease SusceptibilityFemaleHumansInfantLung DiseasesLung Diseases, InterstitialMaleMiddle AgedautoimmunityCommon variable immunodeficiencyCVIDGLILDgranulomatous lymphocytic interstitial lung diseaseUSIDNET

Identifiers

PMID31250334
PMCPMC6903687
OpenAlexW2954110681

What OpenQuestion holds

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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.