Evidence map›Paper›PMID 39003346›Full record

ArticleRheumatology international2024

COVID-19 severity, breakthrough infections and vaccine safety in young individuals with autoimmune diseases: insights from the COVAD study.

Alessia Alunno, Francesco Carubbi, Ai Lyn Tan, Parikshit Sen, Lorenzo Cavagna, Mrudula Joshi, Jessica Day, Sreoshy Saha, Carlos Enrique Toro Gutiérrez, Carlo Vinicio Caballero-Uribe and 6 more

Abstract read
In one paragraph

Article in Rheumatology international, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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

16 authors.

Alessia Alunno *Internal Medicine and Nephrology Division, Department of Clinical Medicine, Life, Health and Environmental Sciences, University of L'Aquila and San Salvatore Hospital, Piazzale Salvatore Tommasi 1, 67100, L'Aquila, Italy. alessia.alunno82@gmail.com.ORCID 0000-0003-1105-5640
Francesco Carubbi *Internal Medicine and Nephrology Division, Department of Clinical Medicine, Life, Health and Environmental Sciences, University of L'Aquila and San Salvatore Hospital, Piazzale Salvatore Tommasi 1, 67100, L'Aquila, Italy.ORCID 0000-0003-1958-5136
Ai Lyn TanNIHR Leeds Biomedical Research Centre, Leeds Teaching Hospitals Trust, Leeds, UK.ORCID 0000-0002-9158-7243
Parikshit SenMaulana Azad Medical College, 2-Bahadurshah Zafar Marg, New Delhi, Delhi, 110002, India.ORCID 0000-0002-1630-6026
Lorenzo CavagnaRheumatology Unit, Dipartimento di Medicine Interna e Terapia Medica, Università degli Studi di Pavia, Pavia, Lombardy, Italy.ORCID 0000-0003-3292-1528
Mrudula JoshiByramjee Jeejeebhoy Government Medical College and Sassoon General Hospitals, Pune, India.ORCID 0000-0001-7312-351X
Jessica DayDepartment of Rheumatology, Royal Melbourne Hospital, Parkville, VIC, 3050, Australia.ORCID 0000-0001-8528-4361
Sreoshy SahaMymensingh Medical College, Mymensingh, Bangladesh.ORCID 0000-0001-6745-9770
Carlos Enrique Toro GutiérrezReference Center for Osteoporosis, Rheumatology and Dermatology, Pontifica Universidad Javeriana Cali, Cali, Colombia.ORCID 0000-0002-6084-7049
Carlo Vinicio Caballero-UribeDepartment of Medicine, Hospital Universidad del Norte, Barranquilla, Atlantico, Colombia.ORCID 0000-0002-9845-8620
Oliver DistlerDepartment of Rheumatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.ORCID 0000-0002-0546-8310
Hector ChinoyDivision of Musculoskeletal and Dermatological Sciences, Centre for Musculoskeletal Research, School of Biological Sciences, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, The University of Manchester, Manchester, UK.ORCID 0000-0001-6492-1288
Rohit AggarwalDivision of Rheumatology and Clinical Immunology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.ORCID 0000-0002-4508-1233
Vikas Agarwal *Department of Clinical Immunology and Rheumatology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India.
Latika GuptaDivision of Musculoskeletal and Dermatological Sciences, Centre for Musculoskeletal Research, School of Biological Sciences, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, The University of Manchester, Manchester, UK.ORCID 0000-0003-2753-2990
COVAD Study Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Notwithstanding the wealth of literature on COVID-19, studies focusing on young adults with autoimmune diseases (AD) are lacking. To determine early (within 7 days) and late (after 7 days) anti-SARS-CoV-2 vaccine-related adverse events (AEs), post-vaccine disease flares, COVID-19 severity and breakthrough infections (B-INFs) in young people with rheumatic diseases (RMDs) and non-rheumatic autoimmune diseases (nr-ADs) compared to healthy controls (HC). Data were captured through the international COVID-19 vaccination in autoimmune diseases (COVAD) 1 and 2 questionnaires. Of 20,685 complete responses, we identified 6010 from patients aged 18-35 years (1692 RMD, 400 nrADs, 3918 HC) who received up to 4 vaccine doses. BNT162b2 was the most frequently administered vaccine and prior to vaccination, 7% of people with nrAD were taking immunosuppressants (IS) versus 80% in RMDs. Early mild AEs were more frequent in RMDs (93%) and nr-ADs (92%) compared to HC (85%). The frequency of late mild AEs was < 20% in all groups. Severe AEs were rare. SARS-CoV-2 infection rates were similar across all groups, however, RMD patients reported a single episode of infection more frequently than nrADs and HC, while nrADs reported multiple infections more frequently than RMD. Self-reported disease flares were reported by 10% or RMD and 7% of nrAD patients. Our study reinforces the safety of anti-SARS-CoV-2 vaccine also in young people with ADs, but it also highlights that among young individuals the number and clinical picture of SARS-CoV-2 infections is affected more by the type of AD rather than by coexisting IS therapy.

Indexed as

Autoimmune DiseasesCOVID-19COVID-19 VaccinesSARS-CoV-2Severity of Illness IndexAdolescentAdultBNT162 VaccineBreakthrough InfectionsFemaleHumansMaleRheumatic DiseasesVaccinationYoung AdultBNT162 VaccineCOVID-19 VaccinesAdverse eventsAutoimmune diseasesCOVID-19Vaccine

Identifiers

PMID39003346
PMCPMC11343807

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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.