AI Article Synopsis

  • Rotavirus infection is a well-known cause of gastroenteritis in children, and it may trigger autoimmune diseases, but the relationship between these two is not fully understood.
  • A population-matched cohort study in South Korea analyzed data from over 86,000 children hospitalized for rotavirus from 2002 to 2017 to assess the risk of later developing autoimmune conditions.
  • The findings indicated that children who were hospitalized for rotavirus had a 24% higher risk of developing autoimmune diseases compared to those who were not exposed, with a follow-up period of around 12 years.

Article Abstract

Importance: Rotavirus infection is a common cause of gastroenteritis in children that can trigger autoimmune processes, but the nature of this interaction remains poorly understood.

Objective: To estimate the association of rotavirus infection with the risk of subsequent autoimmune disease.

Design, Setting, And Participants: This population-matched cohort study used data from children and adolescents (aged younger than 18 years) in South Korea (national registers from January 1, 2002, to December 31, 2017). The cohort consisted of 86 157 patients in the exposure group who had experienced rotavirus-associated hospitalization and the same number of matched patients in the unexposed group. Data analyses were from May 1, 2020, through October 20, 2022.

Exposures: Hospitalization for rotavirus infection.

Main Outcomes And Measures: The main outcome was childhood autoimmune diseases during the study defined by diagnoses according to the National Health Insurance Database. Hazard ratios (HRs) with 95% CIs for autoimmune diseases were estimated using a Cox model, with multiple confounding factors controlled.

Results: This cohort study consisted of 1 914 461 individuals born in South Korea from 2002 to 2005 who were potentially eligible. After exclusions, there were 86 517 individuals in the exposed group and 86 517 in the unexposed group after 1:1 incidence density sampling. The study included 49 072 (57.0%) male patients. The median (IQR) age at diagnosis of rotavirus-associated hospitalization was 1.5 (0.9-2.7) years, and the HR for autoimmune disease in the exposed group was 1.24 (95% CI, 1.19-1.28) for a mean (SD) follow-up time of 12.1 (3.2) years. The use of more stringent definitions for exposure and outcomes in a multivariable stratified analysis also indicated that rotavirus-associated hospitalization was associated with an increased risk of subsequent autoimmune disease (HR, 1.22 [95% CI, 1.16-1.28]). Sensitivity analysis showed that individuals with rotavirus-associated hospitalization was related to multiple autoimmune syndromes (2 or more: HR, 1. 51 [95% CI, 1. 31-1. 73]; 3 or more: HR, 1. 79 [95% CI, 1.18-2.72]) and that the number of rotavirus-associated hospitalization were associated with higher risks for autoimmune disease in a dose-dependent manner (single hospitalization event: HR, 1.20 [95% CI, 1.16-1.24]; multiple events HR, 1.60 [95% CI, 1.49-1.72]).

Conclusions And Relevance: Our results indicate that rotavirus-associated hospitalization is significantly associated with subsequent autoimmune disease during childhood. Clinicians should be aware of the heightened susceptibility to autoimmune disease in individuals with prior rotavirus-associated hospitalization.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10372702PMC
http://dx.doi.org/10.1001/jamanetworkopen.2023.24532DOI Listing

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