Please use this identifier to cite or link to this item:
http://localhost:8080/xmlui/handle/123456789/9535
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Marutani, Kentaro | - |
dc.contributor.author | Murata, Kenji | - |
dc.contributor.author | Mizuno, Yumi | - |
dc.contributor.author | dkk. | - |
dc.date.accessioned | 2025-01-06T04:04:27Z | - |
dc.date.available | 2025-01-06T04:04:27Z | - |
dc.date.issued | 2024-10 | - |
dc.identifier.issn | 1684-1182 | - |
dc.identifier.uri | http://localhost:8080/xmlui/handle/123456789/9535 | - |
dc.description.abstract | Background/Purpose: Recent large-scale epidemiological studies have revealed significant temporal associations between certain viral infections and the subsequent development of Kawasaki disease (KD). Despite these associations, definitive laboratory evidence linking acute or recent viral infections to KD cases remains elusive. The objective of this study is to employ a molecular epidemiological approach to investigate the temporal association between viral infections and the development of KD. Methods: We analyzed 2460 patients who underwent the FilmArray Respiratory Panel test between April 2020 and September 2021. Results: Following the application of inclusion criteria, 2402 patients were categorized into KD (n Z 148), respiratory tract infection (n Z 1524), and control groups (n Z 730). The KD group exhibited higher positive rates for respiratory syncytial virus (RSV), human rhinovirus/enterovirus (hRV/EV), parainfluenza virus (PIV) 3, and adenovirus (AdV) compared to the control group. Additionally, coinfections involving two or more viruses were significantly more prevalent in the KD group. Notably, RSV-positive, hRV/EV-positive, and PIV3-positive KD patients exhibited a one-month delay in peak occurrence compared to non-KD patients positive for corresponding viruses. In contrast, AdV-positive KD cases did not show a one-month delay in peak occurrence. Moreover, anti-RSV, anti-PIV3, and anti-AdV antibody-positive rates or antibody titers were higher in RSV-, PIV3-, and AdV-positive KD cases, respectively, compared to non-KD cases with the same viral infections. Conclusion: Recent infection with RSV, PIV3, or AdV, occasionally in conjunction with other viruses, may contribute to the pathogenesis of KD as infrequent complications. | en_US |
dc.language.iso | en_US | en_US |
dc.publisher | Journal of Microbiology, Immunology and Infection | en_US |
dc.relation.ispartofseries | Original Article;691-699 | - |
dc.subject | Epidemiology | en_US |
dc.subject | Kawasaki disease | en_US |
dc.subject | Pathogenesis | en_US |
dc.subject | PCR | en_US |
dc.subject | Viral infections | en_US |
dc.title | Respiratory viral infections and Kawasaki disease: A molecular epidemiological analysis | en_US |
dc.type | Article | en_US |
Appears in Collections: | Vol. 57 No. 5 (2024) |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
691-699.pdf | 720.09 kB | Adobe PDF | View/Open |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.