Chlamydia pneumoniae serological status is not associated with asthma in children or young adults

Background The factors that cause the allergic sensitization and inflammation in asthma still remain to be clarified. A role for Chlamydia pneumoniae has been suggested although serological studies have produced conflicting findings. This study aims to clarify the relationship between asthmatic vari...

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Veröffentlicht in:International journal of epidemiology 2000-04, Vol.29 (2), p.280-284
Hauptverfasser: Mills, Graham D, Lindeman, Jennifer A, Fawcett, J Paul, Herbison, G Peter, Sears, Malcolm R
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container_end_page 284
container_issue 2
container_start_page 280
container_title International journal of epidemiology
container_volume 29
creator Mills, Graham D
Lindeman, Jennifer A
Fawcett, J Paul
Herbison, G Peter
Sears, Malcolm R
description Background The factors that cause the allergic sensitization and inflammation in asthma still remain to be clarified. A role for Chlamydia pneumoniae has been suggested although serological studies have produced conflicting findings. This study aims to clarify the relationship between asthmatic variables and C. pneumoniae serological status. Methods A case-control study was undertaken on an asthma-enriched subset from a longitudinal birth cohort. In all, 198 subjects (96 with self-reported asthma) had C. pneumoniae serology (microimmunofluorescence [MIF] IgG, IgA) undertaken at age 11 and age 21 and assessment made in relation to a number of asthma variables. Results The only statistically significant finding was in subjects self-reporting asthma at age 21 who had evidence of lower IgG titres (P = 0.046), a finding in the opposite direction to that expected from the hypothesis. Subjects with high IgG titres (≥128) were less likely to have reported ever having asthma; odds ratio (OR) = 0.29, (95% CI : 0.10–0.87). No association existed between symptoms suggestive of asthma in the previous 12 months and either IgG (P = 0.127) or IgA (P = 0.189) antibody titres at age 21. Likewise, no association was found between symptoms suggestive of asthma in the previous two years and C. pneumoniae IgG antibody titre (P = 0.81) at age 11. There was no evidence of an association with any of the other variables examined at either age 11 or age 21. These included use of inhaled steroids, serum IgE levels, airway responsiveness, skin test evidence of atopy, or smoking status. Conclusion The results of this study suggest that C. pneumoniae infection when diagnosed by MIF serology is not a major risk factor for the development of asthma in children and young adults. The study has not, however, addressed the role this organism may play in specific asthmatic subsets or asthma exacerbations.
doi_str_mv 10.1093/ije/29.2.280
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A role for Chlamydia pneumoniae has been suggested although serological studies have produced conflicting findings. This study aims to clarify the relationship between asthmatic variables and C. pneumoniae serological status. Methods A case-control study was undertaken on an asthma-enriched subset from a longitudinal birth cohort. In all, 198 subjects (96 with self-reported asthma) had C. pneumoniae serology (microimmunofluorescence [MIF] IgG, IgA) undertaken at age 11 and age 21 and assessment made in relation to a number of asthma variables. Results The only statistically significant finding was in subjects self-reporting asthma at age 21 who had evidence of lower IgG titres (P = 0.046), a finding in the opposite direction to that expected from the hypothesis. Subjects with high IgG titres (≥128) were less likely to have reported ever having asthma; odds ratio (OR) = 0.29, (95% CI : 0.10–0.87). No association existed between symptoms suggestive of asthma in the previous 12 months and either IgG (P = 0.127) or IgA (P = 0.189) antibody titres at age 21. Likewise, no association was found between symptoms suggestive of asthma in the previous two years and C. pneumoniae IgG antibody titre (P = 0.81) at age 11. There was no evidence of an association with any of the other variables examined at either age 11 or age 21. These included use of inhaled steroids, serum IgE levels, airway responsiveness, skin test evidence of atopy, or smoking status. Conclusion The results of this study suggest that C. pneumoniae infection when diagnosed by MIF serology is not a major risk factor for the development of asthma in children and young adults. The study has not, however, addressed the role this organism may play in specific asthmatic subsets or asthma exacerbations.</description><identifier>ISSN: 0300-5771</identifier><identifier>EISSN: 1464-3685</identifier><identifier>DOI: 10.1093/ije/29.2.280</identifier><identifier>PMID: 10817126</identifier><identifier>CODEN: IJEPBF</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>adolescence ; Adolescent ; Adult ; Antibodies, Bacterial - blood ; Asthma ; Asthma - epidemiology ; Asthma - immunology ; Asthma - microbiology ; Biological and medical sciences ; Bronchial Provocation Tests ; Case-Control Studies ; Child ; Child, Preschool ; Chlamydia Infections - epidemiology ; Chlamydia Infections - immunology ; Chlamydia Infections - microbiology ; Chlamydia pneumoniae ; Chlamydophila pneumoniae - immunology ; Chronic obstructive pulmonary disease, asthma ; Diagnosis, Differential ; Female ; Fluorescent Antibody Technique ; Humans ; Immunoglobulin A - analysis ; Immunoglobulin G - analysis ; Male ; Medical sciences ; Pneumology ; Prevalence ; Prospective Studies ; Risk Factors ; serology</subject><ispartof>International journal of epidemiology, 2000-04, Vol.29 (2), p.280-284</ispartof><rights>2000 INIST-CNRS</rights><rights>Copyright Oxford University Press(England) Apr 2000</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c381t-949b8672c45edef39da046ec29b4431e6377651ccba2284b10b56b76d1bc4923</citedby><cites>FETCH-LOGICAL-c381t-949b8672c45edef39da046ec29b4431e6377651ccba2284b10b56b76d1bc4923</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=1326617$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10817126$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mills, Graham D</creatorcontrib><creatorcontrib>Lindeman, Jennifer A</creatorcontrib><creatorcontrib>Fawcett, J Paul</creatorcontrib><creatorcontrib>Herbison, G Peter</creatorcontrib><creatorcontrib>Sears, Malcolm R</creatorcontrib><title>Chlamydia pneumoniae serological status is not associated with asthma in children or young adults</title><title>International journal of epidemiology</title><addtitle>Int. J. Epidemiol</addtitle><description>Background The factors that cause the allergic sensitization and inflammation in asthma still remain to be clarified. A role for Chlamydia pneumoniae has been suggested although serological studies have produced conflicting findings. This study aims to clarify the relationship between asthmatic variables and C. pneumoniae serological status. Methods A case-control study was undertaken on an asthma-enriched subset from a longitudinal birth cohort. In all, 198 subjects (96 with self-reported asthma) had C. pneumoniae serology (microimmunofluorescence [MIF] IgG, IgA) undertaken at age 11 and age 21 and assessment made in relation to a number of asthma variables. Results The only statistically significant finding was in subjects self-reporting asthma at age 21 who had evidence of lower IgG titres (P = 0.046), a finding in the opposite direction to that expected from the hypothesis. Subjects with high IgG titres (≥128) were less likely to have reported ever having asthma; odds ratio (OR) = 0.29, (95% CI : 0.10–0.87). No association existed between symptoms suggestive of asthma in the previous 12 months and either IgG (P = 0.127) or IgA (P = 0.189) antibody titres at age 21. Likewise, no association was found between symptoms suggestive of asthma in the previous two years and C. pneumoniae IgG antibody titre (P = 0.81) at age 11. There was no evidence of an association with any of the other variables examined at either age 11 or age 21. These included use of inhaled steroids, serum IgE levels, airway responsiveness, skin test evidence of atopy, or smoking status. Conclusion The results of this study suggest that C. pneumoniae infection when diagnosed by MIF serology is not a major risk factor for the development of asthma in children and young adults. 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J. Epidemiol</addtitle><date>2000-04-01</date><risdate>2000</risdate><volume>29</volume><issue>2</issue><spage>280</spage><epage>284</epage><pages>280-284</pages><issn>0300-5771</issn><eissn>1464-3685</eissn><coden>IJEPBF</coden><abstract>Background The factors that cause the allergic sensitization and inflammation in asthma still remain to be clarified. A role for Chlamydia pneumoniae has been suggested although serological studies have produced conflicting findings. This study aims to clarify the relationship between asthmatic variables and C. pneumoniae serological status. Methods A case-control study was undertaken on an asthma-enriched subset from a longitudinal birth cohort. In all, 198 subjects (96 with self-reported asthma) had C. pneumoniae serology (microimmunofluorescence [MIF] IgG, IgA) undertaken at age 11 and age 21 and assessment made in relation to a number of asthma variables. Results The only statistically significant finding was in subjects self-reporting asthma at age 21 who had evidence of lower IgG titres (P = 0.046), a finding in the opposite direction to that expected from the hypothesis. Subjects with high IgG titres (≥128) were less likely to have reported ever having asthma; odds ratio (OR) = 0.29, (95% CI : 0.10–0.87). No association existed between symptoms suggestive of asthma in the previous 12 months and either IgG (P = 0.127) or IgA (P = 0.189) antibody titres at age 21. Likewise, no association was found between symptoms suggestive of asthma in the previous two years and C. pneumoniae IgG antibody titre (P = 0.81) at age 11. There was no evidence of an association with any of the other variables examined at either age 11 or age 21. These included use of inhaled steroids, serum IgE levels, airway responsiveness, skin test evidence of atopy, or smoking status. Conclusion The results of this study suggest that C. pneumoniae infection when diagnosed by MIF serology is not a major risk factor for the development of asthma in children and young adults. The study has not, however, addressed the role this organism may play in specific asthmatic subsets or asthma exacerbations.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>10817126</pmid><doi>10.1093/ije/29.2.280</doi><tpages>5</tpages></addata></record>
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source Oxford University Press Journals All Titles (1996-Current); MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
subjects adolescence
Adolescent
Adult
Antibodies, Bacterial - blood
Asthma
Asthma - epidemiology
Asthma - immunology
Asthma - microbiology
Biological and medical sciences
Bronchial Provocation Tests
Case-Control Studies
Child
Child, Preschool
Chlamydia Infections - epidemiology
Chlamydia Infections - immunology
Chlamydia Infections - microbiology
Chlamydia pneumoniae
Chlamydophila pneumoniae - immunology
Chronic obstructive pulmonary disease, asthma
Diagnosis, Differential
Female
Fluorescent Antibody Technique
Humans
Immunoglobulin A - analysis
Immunoglobulin G - analysis
Male
Medical sciences
Pneumology
Prevalence
Prospective Studies
Risk Factors
serology
title Chlamydia pneumoniae serological status is not associated with asthma in children or young adults
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