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John Danesh Clinical Trial
Service Unit and Epidemiological Studies Unit, Nuffield Department of
Clinical Medicine, University of Oxford, Radcliffe Infirmary, Oxford
OX2 6HE
Correspondence to: J Danesh
john.danesh{at}balliol.ox.ac.uk
Objectives:
To examine the association between
coronary heart disease and chronic Helicobacter pylori infection.
Design:
Case-control study of myocardial infarction at
young ages and study of sibling pairs with one member affected and the
other not.
Setting:
United Kingdom.
Participants:
1122 survivors of suspected acute
myocardial infarction at ages 30-49 (mean age 44 years) and 1122 age
and sex matched controls with no history of coronary heart disease; 510 age and sex matched pairs of siblings (mean age 59 years) in which one
sibling had survived myocardial infarction and one had no history of
coronary heart disease.
Main outcome measures:
Serological evidence of chronic
infection with H pylori.
Results:
472 (42%) of the 1122 cases with early onset myocardial infarction were seropositive for H pylori
antibodies compared with 272 (24%) of the 1122 age and sex matched
controls, giving an odds ratio of 2.28 (99% confidence interval 1.80 to 2.90). This odds ratio fell to 1.87 (1.42 to 2.47; P<0.0001) after smoking and indicators of socioeconomic status were adjusted for and to
1.75 (1.29 to 2.36) after additional adjustment for blood lipid
concentrations and obesity. Only 158 of the 510 pairs of siblings were
discordant for H pylori status; among these, 91 cases and 67 controls were seropositive (odds ratio 1.33 (0.86 to 2.05)). No strong
correlations were observed between H pylori seropositivity
and measurements of other risk factors for coronary heart disease
(plasma lipids, fibrinogen, C reactive protein, albumin, etc).
Conclusion:
In the context of results from other
relevant studies, these two studies suggest a moderate association
between coronary heart disease and H pylori
seropositivity that cannot be fully accounted for by other risk
factors. But even if this association is causal and largely reversible
by eradication of chronic infection, very large randomised trials would
be needed to show this.
Key messages
© BMJ 1999
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