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A Mouse Model for Pathogen-induced Chronic Inflammation at Local and Systemic Sites
Published on: August 8, 2014
Chronic infections and the risk of carotid atherosclerosis: prospective results from a large population study
1Departments of Neurology, University Clinic Innsbruck, Innsbruck, Austria.
Insights
Chronic infections significantly increase atherosclerosis risk, particularly in individuals without existing risk factors. This suggests infections play a key role in the development of atherosclerosis through inflammation.
Area of Science:
- Cardiovascular Research
- Infectious Diseases
- Epidemiology
Background:
- The link between chronic infections and atherosclerosis pathogenesis is debated.
- Epidemiological evidence remains controversial.
Purpose of the Study:
- To investigate the association between chronic infections and atherosclerosis development.
- To assess the impact of chronic infections on carotid atherosclerosis progression.
Main Methods:
- Prospective population-based survey (Bruneck Study) of 826 adults aged 40-79.
- High-resolution duplex scanning to assess carotid atherosclerosis over 5 years.
- Standard diagnostic criteria to identify chronic respiratory, urinary tract, and dental infections.
Main Results:
- Chronic infections significantly amplified atherosclerosis risk (OR 4.08, P<0.0001), especially in those without baseline atherosclerosis.
- This association held true for all chronic bacterial infections and remained significant after adjusting for traditional risk factors.
- Elevated markers of systemic inflammation, bacterial endotoxin, and heat-shock proteins were linked to higher atherosclerosis risk in infected individuals.
Conclusions:
- Provides robust evidence for chronic infections contributing to human atherogenesis.
- Systemic inflammation and autoimmunity are potential mechanisms linking infections to atherosclerosis.
Background:
Chronic infections have been implicated in the pathogenesis of atherosclerosis, yet from an epidemiological perspective, this concept remains controversial.
Methods And Results:
The Bruneck Study is a prospective population-based survey on the pathogenesis of atherosclerosis. In 826 men and women 40 to 79 years old (1990 baseline), 5-year changes in carotid atherosclerosis were thoroughly assessed by high-resolution duplex scanning. The presence of chronic respiratory, urinary tract, dental, and other infections was ascertained by standard diagnostic criteria. Chronic infections amplified the risk of atherosclerosis development in the carotid arteries. The association was most pronounced in subjects free of carotid atherosclerosis at baseline (age-/sex-adjusted odds ratio [95% CI] for any chronic infection versus none, 4.08 [2.42 to 6.85]; P:<0.0001) and applied to all types of chronic (bacterial) infections. It remained independently significant after adjustment for classic vascular risk attributes and extended to low-risk individuals free of conventional risk factors. Among subjects with chronic infections, atherosclerosis risk was highest in those with a prominent inflammatory response. Markers of systemic inflammation, such as soluble adhesion molecules and circulating bacterial endotoxin, and levels of soluble human heat-shock protein 60 and antibodies to mycobacterial heat-shock protein 65 were elevated in subjects with chronic infections and predictive of an increased risk of atherosclerosis.
Conclusions:
The present study provides solid evidence for a role of common chronic infections in human atherogenesis. Induction of systemic inflammation and autoimmunity may be potential pathophysiological links.
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