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Published on: October 23, 2013
Prospective study of Chlamydia pneumoniae IgG seropositivity and risks of future myocardial infarction
P M Ridker1, R B Kundsin, M J Stampfer
1Divisions of Cardiology, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA. pmridker@bics.bwh.harvard.edu
Insights
This study found no link between Chlamydia pneumoniae infection and future myocardial infarction (MI) risk in men. Chlamydia pneumoniae seropositivity did not increase the likelihood of experiencing a first MI in this large prospective cohort.
Area of Science:
- Cardiovascular disease research
- Infectious disease epidemiology
- Microbiology
Background:
- Chlamydia pneumoniae is a suspected contributor to atherothrombosis.
- Limited prospective data exists on Chlamydia pneumoniae exposure and future myocardial infarction (MI) risk.
Purpose of the Study:
- To investigate the association between Chlamydia pneumoniae infection and the risk of future myocardial infarction (MI).
Main Methods:
- Prospective cohort study of nearly 15,000 healthy men.
- Measured IgG antibodies against Chlamydia pneumoniae in baseline blood samples.
- Compared 343 men who had a first MI with matched controls over a 12-year follow-up.
Main Results:
- Chlamydia pneumoniae IgG seropositivity rates were similar between men who later had an MI and control subjects.
- No significant relative risks for future MI were found across various Chlamydia pneumoniae IgG titers.
- No association was observed after adjusting for cardiovascular risk factors or with C-reactive protein levels.
Conclusions:
- In a large, socioeconomically homogeneous male cohort, Chlamydia pneumoniae IgG seropositivity was not associated with an increased risk of future MI.
- Findings controlled for age, smoking, and other cardiovascular risk factors.
- This study provides no evidence supporting Chlamydia pneumoniae's role in MI development.
Background:
Chlamydia pneumoniae has been hypothesized to play a role in atherothrombosis. However, prospective data relating exposure to Chlamydia pneumoniae and risks of future myocardial infarction (MI) are sparse.
Methods And Results:
In a prospective cohort of nearly 15 000 healthy men, we measured IgG antibodies directed against Chlamydia pneumoniae in blood samples collected at baseline from 343 study participants who subsequently reported a first MI and from an equal number of age- and smoking-matched control subjects who did not report vascular disease during a 12-year follow-up period. The proportion of study subjects with IgG antibodies directed against Chlamydia increased with age and cigarette consumption. However, prevalence rates of Chlamydia IgG seropositivity were virtually identical at baseline among men who subsequently reported first MI compared with age- and smoking-matched control subjects. Specifically, the relative risks of future MI associated with Chlamydia pneumoniae IgG titers >/=1:16, 1:32, 1:64, 1:128, and 1:256 were 1.1, 1.0, 1.1, 1.0, and 0.8, respectively (all probability values not significant). There was no association in analyses adjusted for other risk factors, evaluating early as compared with late events, or among nonsmokers. Further, there was no association between seropositivity and concentration of C-reactive protein, a marker of inflammation that predicts MI risk in this cohort.
Conclusions:
In a large-scale study of socioeconomically homogeneous men that controlled for age, smoking, and other cardiovascular risk factors, we found no evidence of association between Chlamydia pneumoniae IgG seropositivity and risks of future MI.
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