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Relationship between human herpesvirus 6 infection and inflammatory bowel disease using novel biomarker

OBJECTIVE: Inflammatory bowel disease (IBD) is closely related to stress and fatigue. Human herpesvirus 6B (HHV‐6B) is reactivated by stress and fatigue and is associated with IBD. This study aimed to clarify the relationship between IBD and HHV‐6B. METHODS: Antibody titers to SITH‐1, a protein spec...

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Autores principales: Matsumoto, Satohiro, Otaki, Yuzo, Yoshida, Yukio, Kobayashi, Nobuyuki, Oka, Naomi, Yanagisawa, Hiroyuki, Kondo, Kazuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Publishing Asia Pty Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10684980/
https://www.ncbi.nlm.nih.gov/pubmed/38034055
http://dx.doi.org/10.1002/jgh3.12992
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author Matsumoto, Satohiro
Otaki, Yuzo
Yoshida, Yukio
Kobayashi, Nobuyuki
Oka, Naomi
Yanagisawa, Hiroyuki
Kondo, Kazuhiro
author_facet Matsumoto, Satohiro
Otaki, Yuzo
Yoshida, Yukio
Kobayashi, Nobuyuki
Oka, Naomi
Yanagisawa, Hiroyuki
Kondo, Kazuhiro
author_sort Matsumoto, Satohiro
collection PubMed
description OBJECTIVE: Inflammatory bowel disease (IBD) is closely related to stress and fatigue. Human herpesvirus 6B (HHV‐6B) is reactivated by stress and fatigue and is associated with IBD. This study aimed to clarify the relationship between IBD and HHV‐6B. METHODS: Antibody titers to SITH‐1, a protein specific to HHV‐6B latent infection, were measured in 163 patients with IBD (107 with ulcerative colitis [UC] and 56 with Crohn's disease [CD]); clinical and endoscopic scores and depression scores of UC and CD were analyzed to examine the relationship between SITH‐1 and IBD. The SITH‐1 cut‐off value was set as 1.96, according to known reports. RESULTS: In patients with UC, C‐reactive protein (CRP) level was significantly higher (1.5 vs 0.6 mg/L, P = 0.006) and disease exacerbation within 6 months after entry was significantly more common in the SITH‐1 (+) group (20% vs 0%, P < 0.001). In the subanalysis comparing with and without UC exacerbation, the optimal cut‐off value for SITH‐1 to detect UC exacerbation was 3.44 (area under the curve: 0.81; 95% confidence interval: 0.72–0.90). CRP levels, SITH‐1 levels, and disease activity scores by the clinical or endoscopic index were significantly higher in the exacerbation group than in the non‐exacerbation group (2.6 vs 0.9 mg/L, P = 0.03; 4.90 vs 1.71, P < 0.001; 4 vs 3, P = 0.03; 5 vs 3, P = 0.02; respectively). CONCLUSION: Patients with UC with high titers of SITH‐1 have high disease activity and frequent disease exacerbation. SITH‐1 can be associated with UC disease activity.
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spelling pubmed-106849802023-11-30 Relationship between human herpesvirus 6 infection and inflammatory bowel disease using novel biomarker Matsumoto, Satohiro Otaki, Yuzo Yoshida, Yukio Kobayashi, Nobuyuki Oka, Naomi Yanagisawa, Hiroyuki Kondo, Kazuhiro JGH Open Original Articles OBJECTIVE: Inflammatory bowel disease (IBD) is closely related to stress and fatigue. Human herpesvirus 6B (HHV‐6B) is reactivated by stress and fatigue and is associated with IBD. This study aimed to clarify the relationship between IBD and HHV‐6B. METHODS: Antibody titers to SITH‐1, a protein specific to HHV‐6B latent infection, were measured in 163 patients with IBD (107 with ulcerative colitis [UC] and 56 with Crohn's disease [CD]); clinical and endoscopic scores and depression scores of UC and CD were analyzed to examine the relationship between SITH‐1 and IBD. The SITH‐1 cut‐off value was set as 1.96, according to known reports. RESULTS: In patients with UC, C‐reactive protein (CRP) level was significantly higher (1.5 vs 0.6 mg/L, P = 0.006) and disease exacerbation within 6 months after entry was significantly more common in the SITH‐1 (+) group (20% vs 0%, P < 0.001). In the subanalysis comparing with and without UC exacerbation, the optimal cut‐off value for SITH‐1 to detect UC exacerbation was 3.44 (area under the curve: 0.81; 95% confidence interval: 0.72–0.90). CRP levels, SITH‐1 levels, and disease activity scores by the clinical or endoscopic index were significantly higher in the exacerbation group than in the non‐exacerbation group (2.6 vs 0.9 mg/L, P = 0.03; 4.90 vs 1.71, P < 0.001; 4 vs 3, P = 0.03; 5 vs 3, P = 0.02; respectively). CONCLUSION: Patients with UC with high titers of SITH‐1 have high disease activity and frequent disease exacerbation. SITH‐1 can be associated with UC disease activity. Wiley Publishing Asia Pty Ltd 2023-11-02 /pmc/articles/PMC10684980/ /pubmed/38034055 http://dx.doi.org/10.1002/jgh3.12992 Text en © 2023 The Authors. JGH Open published by Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Matsumoto, Satohiro
Otaki, Yuzo
Yoshida, Yukio
Kobayashi, Nobuyuki
Oka, Naomi
Yanagisawa, Hiroyuki
Kondo, Kazuhiro
Relationship between human herpesvirus 6 infection and inflammatory bowel disease using novel biomarker
title Relationship between human herpesvirus 6 infection and inflammatory bowel disease using novel biomarker
title_full Relationship between human herpesvirus 6 infection and inflammatory bowel disease using novel biomarker
title_fullStr Relationship between human herpesvirus 6 infection and inflammatory bowel disease using novel biomarker
title_full_unstemmed Relationship between human herpesvirus 6 infection and inflammatory bowel disease using novel biomarker
title_short Relationship between human herpesvirus 6 infection and inflammatory bowel disease using novel biomarker
title_sort relationship between human herpesvirus 6 infection and inflammatory bowel disease using novel biomarker
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10684980/
https://www.ncbi.nlm.nih.gov/pubmed/38034055
http://dx.doi.org/10.1002/jgh3.12992
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