Antibodies to Chlamydia pneumoniae and clinical course in patients with unstable angina pectoris
Inflammation is one of the most important mechanisms that contribute to coronary artery disease (CAD). One of the micro-organisms that is mentioned as a source of the inflammation is Chlamydia pneumoniae. In this study, we investigated the relationship between titres of IgG and IgA antibodies to C....
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Published in: | Atherosclerosis Vol. 153; no. 2; pp. 499 - 504 |
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01-12-2000
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Abstract | Inflammation is one of the most important mechanisms that contribute to coronary artery disease (CAD). One of the micro-organisms that is mentioned as a source of the inflammation is
Chlamydia
pneumoniae. In this study, we investigated the relationship between titres of IgG and IgA antibodies to
C.
pneumoniae and the clinical course, during hospitalisation and during an 18-month follow-up, in 211 patients admitted to hospital with unstable angina pectoris. Slightly more patients who were refractory during their hospitalisation were positive for
C.
pneumoniae antibodies than patients who could be stabilised by drug treatment (53 vs. 43%, for IgG and 16 vs. 11% for IgA, respectively)(n.s.). In logistic regression analysis no significant predictive values were observed for the relationship between antibody titres and clinical course. The antibody titres to
C.
pneumoniae were lower in the unstable angina patients who had plasma levels of interleukin-10 (IL-10) above 5 pg/ml than in the patients with levels below 5 pg/ml, and higher in smokers than in non-smokers. No associations were observed between antibody titres to
C.
pneumoniae and C-reactive protein (CRP), interleukin-6 (IL-6), age, total cholesterol levels, fibrin degradation products (FDP), plasminogen activator inhibitor-1 (PAI-1) and erythrocyte sedimentation rate (ESR). In conclusion, there was no significant association between antibody titres to
C.
pneumoniae and risk of events during hospitalisation and the 18-month follow-up period in patients admitted for unstable angina pectoris. |
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AbstractList | Inflammation is one of the most important mechanisms that contribute to coronary artery disease (CAD). One of the micro-organisms that is mentioned as a source of the inflammation is Chlamydia pneumoniae. In this study, we investigated the relationship between titres of IgG and IgA antibodies to C. pneumoniae and the clinical course, during hospitalisation and during an 18-month follow-up, in 211 patients admitted to hospital with unstable angina pectoris. Slightly more patients who were refractory during their hospitalisation were positive for C. pneumoniae antibodies than patients who could be stabilised by drug treatment (53 vs. 43%, for IgG and 16 vs. 11% for IgA, respectively)(n.s.). In logistic regression analysis no significant predictive values were observed for the relationship between antibody titres and clinical course. The antibody titres to C. pneumoniae were lower in the unstable angina patients who had plasma levels of interleukin-10 (IL-10) above 5 pg/ml than in the patients with levels below 5 pg/ml, and higher in smokers than in non-smokers. No associations were observed between antibody titres to C. pneumoniae and C-reactive protein (CRP), interleukin-6 (IL-6), age, total cholesterol levels, fibrin degradation products (FDP), plasminogen activator inhibitor-1 (PAI-1) and erythrocyte sedimentation rate (ESR). In conclusion, there was no significant association between antibody titres to C. pneumoniae and risk of events during hospitalisation and the 18-month follow-up period in patients admitted for unstable angina pectoris. Inflammation is one of the most important mechanisms that contribute to coronary artery disease (CAD). One of the micro-organisms that is mentioned as a source of the inflammation is Chlamydia pneumoniae. In this study, we investigated the relationship between titres of IgG and IgA antibodies to C. pneumoniae and the clinical course, during hospitalisation and during an 18-month follow-up, in 211 patients admitted to hospital with unstable angina pectoris. Slightly more patients who were refractory during their hospitalisation were positive for C. pneumoniae antibodies than patients who could be stabilised by drug treatment (53 vs. 43%, for IgG and 16 vs. 11% for IgA, respectively)(n.s.). In logistic regression analysis no significant predictive values were observed for the relationship between antibody titres and clinical course. The antibody titres to C. pneumoniae were lower in the unstable angina patients who had plasma levels of interleukin-10 (IL-10) above 5 pg/ml than in the patients with levels below 5 pg/ml, and higher in smokers than in non-smokers. No associations were observed between antibody titres to C. pneumoniae and C-reactive protein (CRP), interleukin-6 (IL-6), age, total cholesterol levels, fibrin degradation products (FDP), plasminogen activator inhibitor-1 (PAI-1) and erythrocyte sedimentation rate (ESR). In conclusion, there was no significant association between antibody titres to C. pneumoniae and risk of events during hospitalisation and the 18-month follow-up period in patients admitted for unstable angina pectoris. |
Author | Ossewaarde, Jacobus M. de Maat, Moniek P.M. Haverkate, Frits Kluft, Cornelis Manger Cats, Volkert Verheggen, Peter W.H.M. |
Author_xml | – sequence: 1 givenname: Moniek P.M. surname: de Maat fullname: de Maat, Moniek P.M. email: mpm.demaat@pg.tno.nl organization: Division of Vascular and Connective Tissue Research, Gaubius Laboratory TNO-PG, PO Box 2215, 2301 CE, Leiden, The Netherlands – sequence: 2 givenname: Jacobus M. surname: Ossewaarde fullname: Ossewaarde, Jacobus M. organization: Research Laboratory for Infectious Diseases, National Institute of Public Health and the Environment, Bilthoven, The Netherlands – sequence: 3 givenname: Peter W.H.M. surname: Verheggen fullname: Verheggen, Peter W.H.M. organization: Department of Cardiology, Leiden University Medical Centre, Leiden, The Netherlands – sequence: 4 givenname: Cornelis surname: Kluft fullname: Kluft, Cornelis organization: Division of Vascular and Connective Tissue Research, Gaubius Laboratory TNO-PG, PO Box 2215, 2301 CE, Leiden, The Netherlands – sequence: 5 givenname: Volkert surname: Manger Cats fullname: Manger Cats, Volkert organization: Department of Cardiology, Leiden University Medical Centre, Leiden, The Netherlands – sequence: 6 givenname: Frits surname: Haverkate fullname: Haverkate, Frits organization: Division of Vascular and Connective Tissue Research, Gaubius Laboratory TNO-PG, PO Box 2215, 2301 CE, Leiden, The Netherlands |
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Keywords | Chlamydia pneumoniae Inflammation C-reactive protein Interleukin-10 Unstable angina Infection Human Prognosis Chlamydiaceae Interleukin 10 Chlamydiales Cardiovascular disease Bacteria Coronary heart disease Variant angina |
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SubjectTerms | Angina, Unstable - blood Angina, Unstable - immunology Angina, Unstable - physiopathology Antibodies, Bacterial - blood Antibodies, Bacterial - immunology Antigens, Bacterial - immunology Biological and medical sciences C-reactive protein Cardiology. Vascular system Chlamydia pneumoniae Chlamydophila Infections - immunology Chlamydophila Infections - physiopathology Chlamydophila pneumoniae - immunology Coronary heart disease Female Heart Humans Inflammation Interleukin-10 Male Medical sciences Unstable angina |
Title | Antibodies to Chlamydia pneumoniae and clinical course in patients with unstable angina pectoris |
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