Evidence map›Paper›PMID 42045807›Full record

ArticleArthritis & rheumatology (Hoboken, N.J.)2026

Differences in SARS-CoV-2 Antigen Persistence in Individuals With Systemic Autoimmune Rheumatic Diseases Compared to the General Population: A RECOVER-Adult Cohort Study.

Naomi J Patel, Zoe Swank, Jiaqi Wang, Xiaosong Wang, Lauren A O'Keeffe, Madison Negron, Liya S Getachew, Louise L Hansen, Grace Qian, Alene A Saavedra and 9 more

Abstract read
In one paragraph

Article in Arthritis & rheumatology (Hoboken, N.J.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

19 authors.

Naomi J PatelDivision of Rheumatology, Inflammation, and Immunity, Mass General Brigham, Boston, Massachusetts.ORCID https://orcid.org/0000-0002-6038-0346
Zoe SwankHarvard Medical School, Boston, Massachusetts.
Jiaqi WangRheumatology and Allergy Clinical Epidemiology Research Center, Mongan Institute, Department of Medicine, Massachusetts General Hospital, Boston.
Xiaosong WangDivision of Rheumatology, Inflammation, and Immunity, Mass General Brigham, Boston, Massachusetts.
Lauren A O'KeeffeDivision of Rheumatology, Inflammation, and Immunity, Mass General Brigham, Boston, Massachusetts.
Madison NegronRheumatology and Allergy Clinical Epidemiology Research Center, Mongan Institute, Department of Medicine, Massachusetts General Hospital, Boston.
Liya S GetachewDivision of Rheumatology, Inflammation, and Immunity, Mass General Brigham, Boston, Massachusetts.
Louise L HansenHarvard Medical School, Boston, Massachusetts.
Grace QianDivision of Rheumatology, Inflammation, and Immunity, Mass General Brigham, Boston, Massachusetts.
Alene A SaavedraDivision of Rheumatology, Inflammation, and Immunity, Mass General Brigham, Boston, Massachusetts.
Kevin T MuellerDivision of Rheumatology, Inflammation, and Immunity, Mass General Brigham, Boston, Massachusetts.
Natalie A DavisDivision of Rheumatology, Inflammation, and Immunity, Mass General Brigham, Boston, Massachusetts.
Kathleen M M VanniDivision of Rheumatology, Inflammation, and Immunity, Mass General Brigham, Boston, Massachusetts.ORCID https://orcid.org/0000-0003-0839-9661
Sandria SavageRECOVER Patient Representative, New York, New York.
Julie S LamRECOVER Community Representative, New York, New York.
Zachary S WallaceDivision of Rheumatology, Inflammation, and Immunity, Mass General Brigham, Boston, Massachusetts.
David R WaltHarvard Medical School, Boston, Massachusetts.
Jeffrey A SparksDivision of Rheumatology, Inflammation, and Immunity, Mass General Brigham, Boston, Massachusetts.ORCID https://orcid.org/0000-0002-5556-4618
RECOVER‐Adult

Funding

The Harvard Clinical and Translational Science CenterUL1TR002541 · NCATS · HARVARD MEDICAL SCHOOL · PI NADLER, LEE MARSHALL · 2018 to 2022
$93.0M
VERITY: Value and Evidence in Rheumatology using bioInformaTics, and advanced analYticsP30AR072577 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI Daniel Hal Solomon · 2017 to 2026
$9.8M
Joint Biology Consortium Resource-based CenterP30AR070253 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI Peter A Nigrovic, Jeffrey Andrew Sparks · 2016 to 2026
$9.4M
Rheumatoid Arthritis-Related Autoantibodies, Articular Inflammation, and RA-Associated Interstitial Lung DiseaseR01AR077607 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI SPARKS, JEFFREY ANDREW · 2021 to 2025
$3.7M
Rheumatoid Arthritis-associated Parenchymal Lung Disease: Clinical and Molecular PhenotypesR01HL155522 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI Jeffrey Andrew Sparks, George R Washko · 2022 to 2026
$3.5M
Immunologic and Clinical Sequelae after COVID-19 in Patients with Systemic Autoimmune Rheumatic DiseasesR01AR080659 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI Jeffrey Andrew Sparks · 2023 to 2026
$2.9M
NCATS NIH HHS UL1 TR002541NCRR NIH HHS 1UL1TR002541-01NHLBI NIH HHS R01 HL155522NIAMS NIH HHS P30 AR070253NIAMS NIH HHS P30 AR072577NIAMS NIH HHS R01 AR077607NIAMS NIH HHS R01 AR080659
6 · The paper itself

Abstract

objectiveIndividuals with systemic autoimmune rheumatic diseases (SARDs) are at risk for worse acute and post-acute COVID-19 outcomes, though whether individuals with SARDs have longer persistence of viral antigens after COVID-19 has not been studied.

methodsThis retrospective cohort study evaluated post-COVID-19 differences in SARS-CoV-2 antigen (spike, spike protein that contains the receptor-binding domain, and nucleocapsid) positivity between individuals with SARDs (COVID-19 and Rheumatic Diseases [RheumCARD]) and without SARDs (Researching COVID to Enhance Recovery [RECOVER]-Adult). SARS-CoV-2 antigens were measured in collected samples using a validated ultrasensitive single molecule array. This digital enzyme-linked immunosorbent assay used antibody-coated magnetic beads to capture antigen molecules, which were loaded into microwell arrays and detected through enzymatic cleavage of a fluorescent substrate. We used logistic regression to estimate unadjusted and adjusted (for age, sex, infection year, vaccination status, and COVID-19 treatment) odds ratios for SARS-CoV-2 antigen positivity at months 3 and 6 following COVID-19.

resultsAmong 210 individuals with SARDs in RheumCARD and 348 individuals without SARDs in RECOVER-Adult, any SARS-CoV-2 antigen positivity was more common in those with SARDs (36.7% in RheumCARD vs 18.9% in RECOVER-Adult; P < 0.001). Those with SARDs had higher odds of nucleocapsid antigen positivity (adjusted odds ratio [aOR] 3.73, 95% confidence interval [CI] 1.28-10.85) or any antigen positivity (aOR 2.89, 95% CI 1.43-5.85) three months after COVID-19 infection and higher odds of nucleocapsid antigen positivity (aOR 6.62, 95% CI 1.09-40.30) six months after COVID-19 infection.

conclusionIndividuals with SARDs were more likely to have SARS-CoV-2 antigen positivity at months 3 and 6 following COVID-19 infection compared with individuals without SARDs, not explained by demographics, variant, vaccination, or treatment.

Identifiers

PMID42045807
PMCPMC13598665

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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.