Chlamydia pneumoniae and cytomegalovirus seropositivity, inflammatory markers, and the risk of myocardial infarction at a young age

Citation
M. Gattone et al., Chlamydia pneumoniae and cytomegalovirus seropositivity, inflammatory markers, and the risk of myocardial infarction at a young age, AM HEART J, 142(4), 2001, pp. 633-640
Citations number
35
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Journal title
AMERICAN HEART JOURNAL
ISSN journal
00028703 → ACNP
Volume
142
Issue
4
Year of publication
2001
Pages
633 - 640
Database
ISI
SICI code
0002-8703(200110)142:4<633:CPACSI>2.0.ZU;2-O
Abstract
Background Pathogens causing chronic infections may promote atherosclerosis . The aim of our study was to evaluate the association of Chlamydia pneumon iae (Cp) and cytomegalovirus (CMV) infection and of inflammatory activation with premature myocardial infarction (MI). Methods Specific anti-Cp and anti-CMV immunoglobulin G (IgG), fibrinogen, w hite blood cells (WBC), and C-reactive protein (CRP) were measured in 120 p ost-Ml patients less than or equal to 50 years old and in 120 age-matched c ontrols. Results Seropositivity to Cp and elevated concentrations of anti-Cp and ant i-CMV IgGs were more frequent (P = .01) in patients than in control subject s, and fibrinogen, CRP, and WBC levels (P = .02) were more elevated. After adjustment for coronary risk factors and socioeconomic status, the odds rat ios (95% confidence intervals) for premature MI were 2.4 (1.3-4.6) for Cp i nfection and 2.9 (1.5-5.8) for CMV. The risk of Cp infection was greater in smokers (3.7, 1.8-7.6). When both infections were present (35% of patients vs 8% of controls, P = .001), CRP was higher (P = .01) and the risk increa sed by 12 times (12.5, 4-38.9) compared with that in subjects without any i nfection and by 5 times (4.9, 2.2-10.9) if only one was present. Conclusions After adjustment for confounders, seropositivity to both Cp and CMV infections is associated with the diagnosis of premature MI. The combi nation of both infections is associated with an enhanced inflammatory respo nse and a markedly increased risk of premature MI.