Increased risk of chronic fatigue syndrome following herpes zoster: a population-based study

被引:0
|
作者
S.-Y. Tsai
T.-Y. Yang
H.-J. Chen
C.-S. Chen
W.-M. Lin
W.-C. Shen
C.-N. Kuo
C.-H. Kao
机构
[1] Mackay Memorial Hospital,Department of Laboratory Medicine
[2] Johns Hopkins University,Department of Health Policy and Management, Bloomberg School of Public Health
[3] China Medical University Hospital,Molecular and Genomic Epidemiology Center
[4] China Medical University,Management Office for Health Data
[5] China Medical University Hospital,Department of Public Health
[6] China Medical University,Division of Chinese Trauma
[7] China Medical University Hospital,Department of Diagnostic Radiology
[8] China Medical University,Department of Computer Science and Information Engineering
[9] Chang Gung Memorial Hospital,Department of Nuclear Medicine and PET Center
[10] Chang Gung University,Graduate Institute of Clinical Medicine Science and School of Medicine, College of Medicine
[11] Asia University,undefined
[12] Kau-Tang Traditional Medical Hospital,undefined
[13] China Medical University Hospital,undefined
[14] China Medical University,undefined
来源
European Journal of Clinical Microbiology & Infectious Diseases | 2014年 / 33卷
关键词
Chronic Fatigue Syndrome; Herpes Zoster; Varicella Zoster Virus; Antiviral Treatment; Chronic Fatigue Syndrome Patient;
D O I
暂无
中图分类号
学科分类号
摘要
Chronic fatigue syndrome (CFS) is a complex disorder accompanied by unexplainable persistent fatigue, in which several etiological factors exist, such as viral infections. Using the National Health Insurance Research Database (NHIRD) of Taiwan, this study evaluated the association between herpes zoster (HZ) infection and the risk of CFS, and examined the possibility of patients developing postviral fatigue effects, including the possibility of developing other unexplainable chronic fatigue conditions. In this prospective cohort study using the NHIRD, we identified 9,205 patients with HZ infection [ICD-9 (International Classification of Disease, Ninth Revision), code 053] and 36,820 patients without HZ infection (non-HZ) from 2005 to 2007, and followed up to the end of 2010. The incidence rate of CFS was higher in the HZ cohort than in the non-HZ cohort (4.56 vs. 3.44 per 1,000 person-years), with an adjusted hazard ratio of 1.29 [95 % confidence interval (CI) = 1.09–1.53]. It was shown that the risk of CFS without comorbidity for each patient increased from 1.25- to 1.36-fold between the CFS and non-CFS cohorts; with long-term follow-up, the HZ cohort showed a significantly higher cumulative incidence rate of developing CFS than the non-HZ patients. We propose that patients with chronic fatigue might exist in a subset of patients that would be associated with HZ infection. The actual mechanism of development of CFS that is attributed to HZ infection remains unclear. The findings of this population cohort study provide pivotal evidence of postviral fatigue among patients with HZ infection.
引用
收藏
页码:1653 / 1659
页数:6
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