Evidence map›Paper›PMID 37396005›Full record

ArticleAnnals of gastroenterology

Association of serum IgG4 and disease outcomes in patients with inflammatory bowel disease.

R Christopher Chase, Hani Tamim, Walaa G El Sheikh, Kristin Clift, David Bruining, Christina Ha, Francis A Farraye, Jana G Hashash

Abstract read
In one paragraph

Article in Annals of gastroenterology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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.

R Christopher ChaseDivision of Internal Medicine, Mayo Clinic, Jacksonville, Florida USA (R. Christopher Chase).
Hani TamimClinical Research Institute, American University of Beirut Medical Center, Beirut, Lebanon (Hani Tamim, Walaa G. El Sheikh).
Walaa G El SheikhClinical Research Institute, American University of Beirut Medical Center, Beirut, Lebanon (Hani Tamim, Walaa G. El Sheikh).
Kristin CliftDivision of Gastroenterology and Hepatology, Mayo Clinic, Jacksonville, Florida, USA (Kristin Clift, Francis A. Farraye, Jana G. Hashash).
David BruiningDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota USA (David Bruining).
Christina HaDivision of Gastroenterology and Hepatology, Mayo Clinic, Scottsdale, Arizona USA (Christina Ha).
Francis A FarrayeDivision of Gastroenterology and Hepatology, Mayo Clinic, Jacksonville, Florida, USA (Kristin Clift, Francis A. Farraye, Jana G. Hashash).
Jana G HashashDivision of Gastroenterology and Hepatology, Mayo Clinic, Jacksonville, Florida, USA (Kristin Clift, Francis A. Farraye, Jana G. Hashash).

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The etiology of inflammatory bowel disease (IBD) is multifactorial and thought to be influenced by inappropriate activation of the gut mucosal immune system. As the only immunoglobulin G (IgG) subclass unable to activate the classical complement cascade, the role of IgG4 in IBD pathophysiology as an immunomodulator is controversial. This study aimed to determine the association of low, normal and high IgG4 levels with the outcomes of IBD patients. Methods: This was a retrospective study of a multisite tertiary care center database evaluating patients with IBD who had an IgG4 level drawn between 2014 and 2021. Subjects were divided into low, normal, and high IgG4 level groups for evaluation of demographic and clinical indicators of IBD activity and severity. Results: Of 284 patients with IBD, 22 had low (7.7%), 16 high (5.6%), and 246 (86.6%) normal IgG4 levels. There was no difference in IBD subtype, mean age, age at IBD diagnosis, or smoking between the 3 groups. There was no difference in number of hospitalizations (P=0.20), C-reactive protein levels, need for intestinal resection (P=0.85), or presence of primary sclerosing cholangitis (P=0.15), pancreatitis (P=0.70), or perianal disease (P=0.68) between the groups. Significantly more patients in the low IgG4 group had previous exposure to vedolizumab compared to the other groups and more patients in the low IgG4 group received vedolizumab (P=0.04), azathioprine (P=0.04) and prednisone (P=0.03) during the 5-year follow up. Conclusion: In this study, a low serum IgG4 level was associated with higher rates of vedolizumab, azathioprine, and steroid use.

Indexed as

disease outcomesdisease severityIgG4inflammatory bowel disease

Identifiers

PMID37396005
PMCPMC10304528

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.