Evidence map›Paper›PMID 29746679›Full record

ReviewJournal of the Pediatric Infectious Diseases Society2018

Noninfectious Manifestations and Complications of Chronic Granulomatous Disease.

Sarah E Henrickson, Artemio M Jongco, Kelly F Thomsen, Elizabeth K Garabedian, Isaac P Thomsen

Registry-linked trialOpen access · bronzeAbstract readReview
In one paragraph

Review in Journal of the Pediatric Infectious Diseases Society, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05104723 (A Phase 1/2 Open-label Study to Evaluate the Safety and Efficacy of Tofacitinib for Chronic Granulomatous Disease With Inflammatory Complications), which is not on this map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
4.0field-weighted citation impact, top 6% 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.

NCT05104723 phase1 / phase2completednot on this mapstarted 2022, after this paper: background citation

A Phase 1/2 Open-label Study to Evaluate the Safety and Efficacy of Tofacitinib for Chronic Granulomatous Disease With Inflammatory Complications

TypeinterventionalSponsorNational Institute of Allergy and Infectious Diseases (NIAID)Ran2022 to 2026Enrolled10ConditionsChronic Granulomatous Disease, Inflammatory Gastrointestinal Disease, Inflammatory Skin Disease, Inflammatory Lung DiseaseArmsXELJANZ (tofacitinib)
3 · Its place in the literature

Who cites it

53 citing papers in PubMed, 74 citations in OpenAlex.

  1. Article
  2. Review
  3. How I Treat: Chronic granulomatous disease.Journal of human immunity · 2026
    Review
  4. Surgical Reconstruction of Ulcers in Chronic Granulomatous Disease.Plastic and reconstructive surgery. Global open · 2026
    Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. A LTBiScience · 2024
    Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. Article
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 4 institutions in 1 country.

Sarah E HenricksonDivision of Allergy and Immunology, Department of Pediatrics, Children's Hospital of Philadelphia, Pennsylvania.
Artemio M JongcoInstitute for Immunology, University of Pennsylvania, Philadelphia.
Kelly F ThomsenDivision of Gastroenterology, Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, Tennessee.
Elizabeth K GarabedianNational Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland.
Isaac P ThomsenDivision of Pediatric Infectious Diseases, Vanderbilt University School of Medicine, Nashville, Tennessee.
Vanderbilt University · USChildren's Hospital of Philadelphia · USNational Human Genome Research Institute · USUniversity of Pennsylvania · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic granulomatous disease (CGD), a primary immunodeficiency characterized by a deficient neutrophil oxidative burst and the inadequate killing of microbes, is well known to cause a significantly increased risk of invasive infection. However, infectious complications are not the sole manifestations of CGD; substantial additional morbidity is driven by noninfectious complications also. These complications can include, for example, a wide range of inflammatory diseases that affect the gastrointestinal tract, lung, skin, and genitourinary tract and overt autoimmune disease. These diseases can occur at any age and are especially problematic in adolescents and adults with CGD. Many of these noninfectious complications present a highly challenging therapeutic conundrum, wherein immunosuppression must be balanced against an already markedly increased risk of invasive fungal and bacterial infections. In this review, the myriad noninfectious complications of CGD are discussed, as are important gaps in our understanding of these processes, which warrant further investigation.

Indexed as

Autoimmune DiseasesDiagnosis, DifferentialGranulomaGranulomatous Disease, ChronicHumansInflammatory Bowel DiseasesLung Diseases

Identifiers

PMID29746679
PMCPMC5946858
OpenAlexW2802560068

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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.