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Chlamydia pneumoniae infection and cerebrovascular disease: a systematic review and meta-analysis

BACKGROUND: A wealth of published studies have been published on association between Chlamydia pneumoniae (C.pneumoniae) infection and cerebrovascular (CV) disease, but the results were inconsistent. This meta-analysis provides a systematic review of the available evidence from all serological and p...

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Autores principales: Chen, Juan, Zhu, Meijia, Ma, Gaoting, Zhao, Zhangning, Sun, Zhongwen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4222774/
https://www.ncbi.nlm.nih.gov/pubmed/24261578
http://dx.doi.org/10.1186/1471-2377-13-183
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author Chen, Juan
Zhu, Meijia
Ma, Gaoting
Zhao, Zhangning
Sun, Zhongwen
author_facet Chen, Juan
Zhu, Meijia
Ma, Gaoting
Zhao, Zhangning
Sun, Zhongwen
author_sort Chen, Juan
collection PubMed
description BACKGROUND: A wealth of published studies have been published on association between Chlamydia pneumoniae (C.pneumoniae) infection and cerebrovascular (CV) disease, but the results were inconsistent. This meta-analysis provides a systematic review of the available evidence from all serological and pathological studies of CV disease and C.pneumoniae. METHODS: A comprehensive research was conducted of MEDLINE, EMBASE, CNKI, WanFang technological periodical database and reference lists of articles to identify eligible case-control and cohort studies. Odds radio (OR) was calculated for each study outcome. Random effect model was used as pooling method and publication bias was estimated for the results. RESULTS: Fifty-two published studies that met criteria were selected. In case control studies, an association between C.pneumoniae infection and CV disease was revealed by serum specific IgG (OR, 1.61; 95% CI: 1.34 to 1.94), serum IgA (OR, 2.33; 95% CI: 1.76 to 3.08) and PCR technique of C.pneumoniae in peripheral blood cells (OR, 1.90; 95% CI: 1.17 to 3.07). No significant association was found in serum anti-C.pneumonae IgM seropositivity or in-situ-detection of C.pneumoniae in arterial biopsies with CV disease. Subgroup analysis by available studies suggested that C.pneumoniae may paly a role in atherosclerotic stroke, but be less significant in stroke of cardioembolism or other etiologies. CONCLUSION: Association between C.pneumoniae infection and CV disease depends on the analytical method adopted, which seems stronger with stroke due to large artery atherosclerosis. Establishing a causal relationship between C.peumoniae infection and CV disease will require more prospective studies with combination of techniques and stratified by etiological subtypes.
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spelling pubmed-42227742014-11-07 Chlamydia pneumoniae infection and cerebrovascular disease: a systematic review and meta-analysis Chen, Juan Zhu, Meijia Ma, Gaoting Zhao, Zhangning Sun, Zhongwen BMC Neurol Research Article BACKGROUND: A wealth of published studies have been published on association between Chlamydia pneumoniae (C.pneumoniae) infection and cerebrovascular (CV) disease, but the results were inconsistent. This meta-analysis provides a systematic review of the available evidence from all serological and pathological studies of CV disease and C.pneumoniae. METHODS: A comprehensive research was conducted of MEDLINE, EMBASE, CNKI, WanFang technological periodical database and reference lists of articles to identify eligible case-control and cohort studies. Odds radio (OR) was calculated for each study outcome. Random effect model was used as pooling method and publication bias was estimated for the results. RESULTS: Fifty-two published studies that met criteria were selected. In case control studies, an association between C.pneumoniae infection and CV disease was revealed by serum specific IgG (OR, 1.61; 95% CI: 1.34 to 1.94), serum IgA (OR, 2.33; 95% CI: 1.76 to 3.08) and PCR technique of C.pneumoniae in peripheral blood cells (OR, 1.90; 95% CI: 1.17 to 3.07). No significant association was found in serum anti-C.pneumonae IgM seropositivity or in-situ-detection of C.pneumoniae in arterial biopsies with CV disease. Subgroup analysis by available studies suggested that C.pneumoniae may paly a role in atherosclerotic stroke, but be less significant in stroke of cardioembolism or other etiologies. CONCLUSION: Association between C.pneumoniae infection and CV disease depends on the analytical method adopted, which seems stronger with stroke due to large artery atherosclerosis. Establishing a causal relationship between C.peumoniae infection and CV disease will require more prospective studies with combination of techniques and stratified by etiological subtypes. BioMed Central 2013-11-21 /pmc/articles/PMC4222774/ /pubmed/24261578 http://dx.doi.org/10.1186/1471-2377-13-183 Text en Copyright © 2013 Chen et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Chen, Juan
Zhu, Meijia
Ma, Gaoting
Zhao, Zhangning
Sun, Zhongwen
Chlamydia pneumoniae infection and cerebrovascular disease: a systematic review and meta-analysis
title Chlamydia pneumoniae infection and cerebrovascular disease: a systematic review and meta-analysis
title_full Chlamydia pneumoniae infection and cerebrovascular disease: a systematic review and meta-analysis
title_fullStr Chlamydia pneumoniae infection and cerebrovascular disease: a systematic review and meta-analysis
title_full_unstemmed Chlamydia pneumoniae infection and cerebrovascular disease: a systematic review and meta-analysis
title_short Chlamydia pneumoniae infection and cerebrovascular disease: a systematic review and meta-analysis
title_sort chlamydia pneumoniae infection and cerebrovascular disease: a systematic review and meta-analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4222774/
https://www.ncbi.nlm.nih.gov/pubmed/24261578
http://dx.doi.org/10.1186/1471-2377-13-183
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