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Excess pneumonia and influenza mortality attributable to seasonal influenza in subtropical Shanghai, China

BACKGROUND: Disease burden attributable to influenza is substantial in subtropical regions. Our study aims to estimate excess pneumonia and influenza (P&I) mortality associated with influenza by subtypes/lineages in Shanghai, China, 2010–2015. METHODS: Quasi-Poisson regression models were fitted...

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Autores principales: Yu, Xinchun, Wang, Chunfang, Chen, Tao, Zhang, Wenyi, Yu, Huiting, Shu, Yuelong, Hu, Wenbiao, Wang, Xiling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5719671/
https://www.ncbi.nlm.nih.gov/pubmed/29212467
http://dx.doi.org/10.1186/s12879-017-2863-1
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author Yu, Xinchun
Wang, Chunfang
Chen, Tao
Zhang, Wenyi
Yu, Huiting
Shu, Yuelong
Hu, Wenbiao
Wang, Xiling
author_facet Yu, Xinchun
Wang, Chunfang
Chen, Tao
Zhang, Wenyi
Yu, Huiting
Shu, Yuelong
Hu, Wenbiao
Wang, Xiling
author_sort Yu, Xinchun
collection PubMed
description BACKGROUND: Disease burden attributable to influenza is substantial in subtropical regions. Our study aims to estimate excess pneumonia and influenza (P&I) mortality associated with influenza by subtypes/lineages in Shanghai, China, 2010–2015. METHODS: Quasi-Poisson regression models were fitted to weekly numbers of deaths from causes coded as P&I for Shanghai general and registered population. Three proxies for influenza activity were respectively used as an explanatory variable. Long-term trend, seasonal trend and absolute humidity were adjusted for as confounding factors. The outcome measurements of excess P&I mortality associated with influenza subtypes/lineages were derived by subtracting the baseline mortality from fitted mortality. RESULTS: Excess P&I mortality associated with influenza were 0.22, 0.30, and 0.23 per 100,000 population for three different proxies in Shanghai general population, lower than those in registered population (0.34, 0.48, and 0.36 per 100,000 population). Influenza B (Victoria) lineage did not contribute to excess P&I mortality (P = 0.206) while influenza B (Yamagata) lineage did (P = 0.044). Influenza-associated P&I mortality was high in the elderly population. CONCLUSIONS: Seasonal influenza A virus had a higher P&I mortality than influenza B virus, while B (Yamagata) lineage is the dominant lineage attributable to P&I mortality. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12879-017-2863-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-57196712017-12-08 Excess pneumonia and influenza mortality attributable to seasonal influenza in subtropical Shanghai, China Yu, Xinchun Wang, Chunfang Chen, Tao Zhang, Wenyi Yu, Huiting Shu, Yuelong Hu, Wenbiao Wang, Xiling BMC Infect Dis Research Article BACKGROUND: Disease burden attributable to influenza is substantial in subtropical regions. Our study aims to estimate excess pneumonia and influenza (P&I) mortality associated with influenza by subtypes/lineages in Shanghai, China, 2010–2015. METHODS: Quasi-Poisson regression models were fitted to weekly numbers of deaths from causes coded as P&I for Shanghai general and registered population. Three proxies for influenza activity were respectively used as an explanatory variable. Long-term trend, seasonal trend and absolute humidity were adjusted for as confounding factors. The outcome measurements of excess P&I mortality associated with influenza subtypes/lineages were derived by subtracting the baseline mortality from fitted mortality. RESULTS: Excess P&I mortality associated with influenza were 0.22, 0.30, and 0.23 per 100,000 population for three different proxies in Shanghai general population, lower than those in registered population (0.34, 0.48, and 0.36 per 100,000 population). Influenza B (Victoria) lineage did not contribute to excess P&I mortality (P = 0.206) while influenza B (Yamagata) lineage did (P = 0.044). Influenza-associated P&I mortality was high in the elderly population. CONCLUSIONS: Seasonal influenza A virus had a higher P&I mortality than influenza B virus, while B (Yamagata) lineage is the dominant lineage attributable to P&I mortality. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12879-017-2863-1) contains supplementary material, which is available to authorized users. BioMed Central 2017-12-07 /pmc/articles/PMC5719671/ /pubmed/29212467 http://dx.doi.org/10.1186/s12879-017-2863-1 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Yu, Xinchun
Wang, Chunfang
Chen, Tao
Zhang, Wenyi
Yu, Huiting
Shu, Yuelong
Hu, Wenbiao
Wang, Xiling
Excess pneumonia and influenza mortality attributable to seasonal influenza in subtropical Shanghai, China
title Excess pneumonia and influenza mortality attributable to seasonal influenza in subtropical Shanghai, China
title_full Excess pneumonia and influenza mortality attributable to seasonal influenza in subtropical Shanghai, China
title_fullStr Excess pneumonia and influenza mortality attributable to seasonal influenza in subtropical Shanghai, China
title_full_unstemmed Excess pneumonia and influenza mortality attributable to seasonal influenza in subtropical Shanghai, China
title_short Excess pneumonia and influenza mortality attributable to seasonal influenza in subtropical Shanghai, China
title_sort excess pneumonia and influenza mortality attributable to seasonal influenza in subtropical shanghai, china
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5719671/
https://www.ncbi.nlm.nih.gov/pubmed/29212467
http://dx.doi.org/10.1186/s12879-017-2863-1
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