Evidence map›Paper›PMID 39460324›Full record

ArticleVaccines2024

Did We Overreact? Insights on COVID-19 Disease and Vaccination in a Large Cohort of Immune-Mediated Inflammatory Disease Patients during Sequential Phases of the Pandemic (The BELCOMID Study).

Jeroen Geldof, Marie Truyens, João Sabino, Marc Ferrante, Jo Lambert, Hilde Lapeere, Tom Hillary, An Van Laethem, Kurt de Vlam, Patrick Verschueren and 3 more

Abstract read
In one paragraph

Article in Vaccines, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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. 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

13 authors.

Jeroen GeldofDepartment of Gastroenterology and Hepatology, Ghent University Hospital, 9000 Ghent, Belgium.ORCID 0000-0003-0126-2929
Marie TruyensDepartment of Gastroenterology and Hepatology, Ghent University Hospital, 9000 Ghent, Belgium.ORCID 0000-0002-1264-4319
João SabinoDepartment of Gastroenterology and Hepatology, University Hospitals Leuven, 3000 Leuven, Belgium.
Marc FerranteDepartment of Gastroenterology and Hepatology, University Hospitals Leuven, 3000 Leuven, Belgium.
Jo LambertDepartment of Dermatology, Ghent University Hospital, 9000 Ghent, Belgium.ORCID 0000-0001-5303-9310
Hilde LapeereDepartment of Dermatology, Ghent University Hospital, 9000 Ghent, Belgium.
Tom HillaryDepartment of Dermatology, University Hospitals Leuven, 3000 Leuven, Belgium.
An Van LaethemDepartment of Dermatology, University Hospitals Leuven, 3000 Leuven, Belgium.
Kurt de VlamDepartment of Rheumatology, University Hospitals Leuven, 3000 Leuven, Belgium.
Patrick VerschuerenDepartment of Rheumatology, University Hospitals Leuven, 3000 Leuven, Belgium.ORCID 0000-0002-0340-3580
Triana LobatonDepartment of Gastroenterology and Hepatology, Ghent University Hospital, 9000 Ghent, Belgium.ORCID 0000-0003-1817-7704
Elizaveta PadalkoDepartment of Laboratory Medicine, Ghent University Hospital, 9000 Ghent, Belgium.
Séverine VermeireDepartment of Gastroenterology and Hepatology, University Hospitals Leuven, 3000 Leuven, Belgium.ORCID 0000-0001-9942-3019

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAs the COVID-19 pandemic becomes an endemic state, still many questions remain regarding the risks and impact of SARS-CoV-2 infection and vaccination in patients with immune-mediated inflammatory diseases (IMIDs) who were excluded from the phase 3 COVID-19 vaccination trials.

methodsThe BELCOMID study collected patient data and serological samples from a large, multicentric IMID patient cohort that was prospectively followed during sequential stages of the pandemic. Patients were stratified according to vaccination status into five groups across three sampling periods. Interactions between SARS-CoV-2 infection, COVID-19 vaccination status, IMID-treatment modalities and IMID course were explored.

resultsIn total, 2165 patients with IBD, a dermatological or rheumatological IMID participated. SARS-CoV-2 infection rates increased over the course of the pandemic and were highest in IMID patients that had refused every vaccine. After baseline COVID-19 vaccination, serologic spike (S)-antibody responses were attenuated by particular types of immune-modulating treatment: anti-TNF, rituximab, JAKi, systemic steroids, combined biologic/immunomodulator treatment. Nonetheless, S-antibody concentration increased progressively in patients who received a booster vaccination, reaching 100% seroconversion rate in patients who had received two booster vaccines. Previous SARS-CoV-2 infection was found as a predictor of higher S-antibody response. Patients who had refused every vaccine showed the lowest rates of S-seroconversion (53.8%). Multiple logistic regression did not identify previous SARS-CoV-2 infection as a risk factor for IMID flare-up. Furthermore, no increased risk of IMID flare-up was found with booster vaccination.

conclusionsAltogether, the BELCOMID study provides evidence for the efficacy and safety of COVID-19 vaccination and confirms the importance of repeated booster vaccination in IMID patients.

Indexed as

boosterCOVID-19IMIDreal worldvaccination

Identifiers

PMID39460324
PMCPMC11510991

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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.