Evidence map›Paper›PMID 42085372›Full record

ArticlePloS one2026

Association between coronavirus disease 2019 and new-onset autoimmune diseases during the early phase of the pandemic.

Joung Ha Park, Min-Taek Lee, Sun-Young Jung, Sang Tae Choi, Seong-Ho Choi

Abstract read
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Joung Ha ParkDivision of Infectious Diseases, Department of Internal Medicine, Chung-Ang University Gwangmyeong Hospital, Gwangmyeong-si, South Korea.
Min-Taek LeeCollege of Pharmacy, Chung-Ang University, Seoul, South Korea.
Sun-Young JungCollege of Pharmacy, Chung-Ang University, Seoul, South Korea.
Sang Tae ChoiDivision of Rheumatology, Department of Internal Medicine, Chung-Ang University College of Medicine, Seoul, South Korea.
Seong-Ho ChoiDivision of Infectious Diseases, Department of Internal Medicine, Chung-Ang University Hospital, Seoul, South Korea.ORCID https://orcid.org/0000-0001-8108-2412

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Emerging evidence suggests that viral infections, including SARS-CoV-2, may trigger autoimmunity. This study investigated the risk of developing autoimmune diseases following coronavirus disease 2019 (COVID-19) using sequence symmetry analysis. We utilized nationwide population-based data from South Korea by linking the National Health Insurance Service database with the Korea Centers for Disease Control and Prevention Agency COVID-19 registry. This study included 2,678 patients with COVID-19 and 92,725 patients without COVID-19 identified between 01/10/2020 and 30/06/2021, during the early phase of the pandemic. Both groups consisted of individuals who were diagnosed with autoimmune diseases within 180 days before or after the index date. We calculated the adjusted sequence ratio (aSR) to compare the incidence of autoimmune diseases within 180 days before and from 14 to 180 days after the index date (the COVID-19 diagnosis date for the COVID-19 group and the first medical visit for the non-COVID-19 group). The differences in autoimmune disease incidence between the groups were evaluated using the ratio of aSR (RaSR). The incidence of newly diagnosed autoimmune diseases-Behcet's disease (RaSR, 2.03), ankylosing spondylitis (2.04), ulcerative colitis (1.15), Crohn's disease (2.22), psoriasis (1.27), type 1 diabetes mellitus (1.61), and Graves' disease (1.14)-was significantly higher in the COVID-19 group than in the non-COVID-19 group after the index date. Subgroup analysis comparing patients with non-severe COVID-19 with those without COVID-19 yielded consistent findings. Furthermore, the incidence of inflammatory bowel diseases was higher in the non-severe COVID-19 group after the index date (RaSR, 1.29). These findings reinforce growing evidence that COVID-19 could induce autoimmunity and increase the risk of developing autoimmune diseases. Therefore, clinicians should remain vigilant for potential autoimmune complications in patients with a history of COVID-19 when clinically indicated.

Indexed as

Autoimmune DiseasesCOVID-19AdultAgedFemaleHumansIncidenceMaleMiddle AgedPandemicsRepublic of KoreaSARS-CoV-2

Identifiers

PMID42085372
PMCPMC13143056

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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.