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Risk of Herpes Zoster and Family History: A Meta-analysis of Case-control Studies

BACKGROUND: Herpes zoster (HZ) results from the reactivation of latent varicella zoster virus (VZV) residing in dorsal root and cranial nerve ganglia. Advanced age and dysfunctional cell-mediated immune responses are well-established risk factors for VZV reactivation. There have been recent interest...

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Autores principales: Lai, Yi Chun, Yew, Yik Weng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4817439/
https://www.ncbi.nlm.nih.gov/pubmed/27057014
http://dx.doi.org/10.4103/0019-5154.177748
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author Lai, Yi Chun
Yew, Yik Weng
author_facet Lai, Yi Chun
Yew, Yik Weng
author_sort Lai, Yi Chun
collection PubMed
description BACKGROUND: Herpes zoster (HZ) results from the reactivation of latent varicella zoster virus (VZV) residing in dorsal root and cranial nerve ganglia. Advanced age and dysfunctional cell-mediated immune responses are well-established risk factors for VZV reactivation. There have been recent interests in whether there is an increased risk of the disease associated with a positive family history. AIMS AND OBJECTIVES: We aimed to conduct a meta-analysis to evaluate the association between HZ infection and family history. In addition, we investigated the dose-response relationship between HZ infection and the number of relatives with a history of HZ. MATERIALS AND METHODS: Observational studies were searched from MEDLINE, EMBASE, and Cochrane Central Register from inception to April 15, 2015. The Meta-analysis of Observational Studies in Epidemiology guidelines were followed in conducting this study. To estimate the pooled odds ratio, random-effects model of DerSimonian and Laird was used. Heterogeneity between studies was assessed using the I(2) statistic. A dose-response meta-analysis with studies that reported appropriate data were done using the generalized least squares for trend method. RESULTS: Five studies, yielding a total of 4169 subjects, were identified for meta-analysis. Cases with HZ were 3.03 (95% confidence interval [CI]: 1.86–4.94, P < 0.001) and 3.27 (95% CI: 1.75–6.10, P < 0.001) times more likely to report the first-degree relatives and total relatives with a history of HZ, respectively. A significant positive dose-response relationship between the risk of HZ infection and the number of relatives with a history of HZ was also demonstrated (P < 0.001). CONCLUSIONS: This meta-analysis demonstrated that family history is a significant risk factor for HZ infection. This risk has a dose-response relationship with the number of relatives with a history of HZ.
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spelling pubmed-48174392016-04-07 Risk of Herpes Zoster and Family History: A Meta-analysis of Case-control Studies Lai, Yi Chun Yew, Yik Weng Indian J Dermatol Original Article BACKGROUND: Herpes zoster (HZ) results from the reactivation of latent varicella zoster virus (VZV) residing in dorsal root and cranial nerve ganglia. Advanced age and dysfunctional cell-mediated immune responses are well-established risk factors for VZV reactivation. There have been recent interests in whether there is an increased risk of the disease associated with a positive family history. AIMS AND OBJECTIVES: We aimed to conduct a meta-analysis to evaluate the association between HZ infection and family history. In addition, we investigated the dose-response relationship between HZ infection and the number of relatives with a history of HZ. MATERIALS AND METHODS: Observational studies were searched from MEDLINE, EMBASE, and Cochrane Central Register from inception to April 15, 2015. The Meta-analysis of Observational Studies in Epidemiology guidelines were followed in conducting this study. To estimate the pooled odds ratio, random-effects model of DerSimonian and Laird was used. Heterogeneity between studies was assessed using the I(2) statistic. A dose-response meta-analysis with studies that reported appropriate data were done using the generalized least squares for trend method. RESULTS: Five studies, yielding a total of 4169 subjects, were identified for meta-analysis. Cases with HZ were 3.03 (95% confidence interval [CI]: 1.86–4.94, P < 0.001) and 3.27 (95% CI: 1.75–6.10, P < 0.001) times more likely to report the first-degree relatives and total relatives with a history of HZ, respectively. A significant positive dose-response relationship between the risk of HZ infection and the number of relatives with a history of HZ was also demonstrated (P < 0.001). CONCLUSIONS: This meta-analysis demonstrated that family history is a significant risk factor for HZ infection. This risk has a dose-response relationship with the number of relatives with a history of HZ. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC4817439/ /pubmed/27057014 http://dx.doi.org/10.4103/0019-5154.177748 Text en Copyright: © 2016 Indian Journal of Dermatology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Lai, Yi Chun
Yew, Yik Weng
Risk of Herpes Zoster and Family History: A Meta-analysis of Case-control Studies
title Risk of Herpes Zoster and Family History: A Meta-analysis of Case-control Studies
title_full Risk of Herpes Zoster and Family History: A Meta-analysis of Case-control Studies
title_fullStr Risk of Herpes Zoster and Family History: A Meta-analysis of Case-control Studies
title_full_unstemmed Risk of Herpes Zoster and Family History: A Meta-analysis of Case-control Studies
title_short Risk of Herpes Zoster and Family History: A Meta-analysis of Case-control Studies
title_sort risk of herpes zoster and family history: a meta-analysis of case-control studies
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4817439/
https://www.ncbi.nlm.nih.gov/pubmed/27057014
http://dx.doi.org/10.4103/0019-5154.177748
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