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Increased risk of chronic fatigue syndrome following infection: a 17-year population-based cohort study

BACKGROUND: Previous serological studies have indicated an association between viruses and atypical pathogens and Chronic Fatigue Syndrome (CFS). This study aims to investigate the correlation between infections from common pathogens, including typical bacteria, and the subsequent risk of developing...

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Autores principales: Chang, Hsun, Kuo, Chien-Feng, Yu, Teng-Shun, Ke, Liang-Yin, Hung, Chung-Lieh, Tsai, Shin-Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10638797/
https://www.ncbi.nlm.nih.gov/pubmed/37951920
http://dx.doi.org/10.1186/s12967-023-04636-z
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author Chang, Hsun
Kuo, Chien-Feng
Yu, Teng-Shun
Ke, Liang-Yin
Hung, Chung-Lieh
Tsai, Shin-Yi
author_facet Chang, Hsun
Kuo, Chien-Feng
Yu, Teng-Shun
Ke, Liang-Yin
Hung, Chung-Lieh
Tsai, Shin-Yi
author_sort Chang, Hsun
collection PubMed
description BACKGROUND: Previous serological studies have indicated an association between viruses and atypical pathogens and Chronic Fatigue Syndrome (CFS). This study aims to investigate the correlation between infections from common pathogens, including typical bacteria, and the subsequent risk of developing CFS. The analysis is based on data from Taiwan’s National Health Insurance Research Database. METHODS: From 2000 to 2017, we included a total of 395,811 cases aged 20 years or older newly diagnosed with infection. The cases were matched 1:1 with controls using a propensity score and were followed up until diagnoses of CFS were made. RESULTS: The Cox proportional hazards regression analysis was used to estimate the relationship between infection and the subsequent risk of CFS. The incidence density rates among non-infection and infection population were 3.67 and 5.40 per 1000 person‐years, respectively (adjusted hazard ratio [HR] = 1.5, with a 95% confidence interval [CI] 1.47–1.54). Patients infected with Varicella-zoster virus, Mycobacterium tuberculosis, Escherichia coli, Candida, Salmonella, Staphylococcus aureus and influenza virus had a significantly higher risk of CFS than those without these pathogens (p < 0.05). Patients taking doxycycline, azithromycin, moxifloxacin, levofloxacin, or ciprofloxacin had a significantly lower risk of CFS than patients in the corresponding control group (p < 0.05). CONCLUSION: Our population-based retrospective cohort study found that infection with common pathogens, including bacteria, viruses, is associated with an increased risk of developing CFS.
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spelling pubmed-106387972023-11-11 Increased risk of chronic fatigue syndrome following infection: a 17-year population-based cohort study Chang, Hsun Kuo, Chien-Feng Yu, Teng-Shun Ke, Liang-Yin Hung, Chung-Lieh Tsai, Shin-Yi J Transl Med Research BACKGROUND: Previous serological studies have indicated an association between viruses and atypical pathogens and Chronic Fatigue Syndrome (CFS). This study aims to investigate the correlation between infections from common pathogens, including typical bacteria, and the subsequent risk of developing CFS. The analysis is based on data from Taiwan’s National Health Insurance Research Database. METHODS: From 2000 to 2017, we included a total of 395,811 cases aged 20 years or older newly diagnosed with infection. The cases were matched 1:1 with controls using a propensity score and were followed up until diagnoses of CFS were made. RESULTS: The Cox proportional hazards regression analysis was used to estimate the relationship between infection and the subsequent risk of CFS. The incidence density rates among non-infection and infection population were 3.67 and 5.40 per 1000 person‐years, respectively (adjusted hazard ratio [HR] = 1.5, with a 95% confidence interval [CI] 1.47–1.54). Patients infected with Varicella-zoster virus, Mycobacterium tuberculosis, Escherichia coli, Candida, Salmonella, Staphylococcus aureus and influenza virus had a significantly higher risk of CFS than those without these pathogens (p < 0.05). Patients taking doxycycline, azithromycin, moxifloxacin, levofloxacin, or ciprofloxacin had a significantly lower risk of CFS than patients in the corresponding control group (p < 0.05). CONCLUSION: Our population-based retrospective cohort study found that infection with common pathogens, including bacteria, viruses, is associated with an increased risk of developing CFS. BioMed Central 2023-11-11 /pmc/articles/PMC10638797/ /pubmed/37951920 http://dx.doi.org/10.1186/s12967-023-04636-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Chang, Hsun
Kuo, Chien-Feng
Yu, Teng-Shun
Ke, Liang-Yin
Hung, Chung-Lieh
Tsai, Shin-Yi
Increased risk of chronic fatigue syndrome following infection: a 17-year population-based cohort study
title Increased risk of chronic fatigue syndrome following infection: a 17-year population-based cohort study
title_full Increased risk of chronic fatigue syndrome following infection: a 17-year population-based cohort study
title_fullStr Increased risk of chronic fatigue syndrome following infection: a 17-year population-based cohort study
title_full_unstemmed Increased risk of chronic fatigue syndrome following infection: a 17-year population-based cohort study
title_short Increased risk of chronic fatigue syndrome following infection: a 17-year population-based cohort study
title_sort increased risk of chronic fatigue syndrome following infection: a 17-year population-based cohort study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10638797/
https://www.ncbi.nlm.nih.gov/pubmed/37951920
http://dx.doi.org/10.1186/s12967-023-04636-z
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