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Helicobacter pylori Infection Maybe a Risk Factor for Cardiac Syndrome X
Dong-Hong Zhang1, Chen Yuan2, Bei-Bei Wang3
1Department of Infection Disease, Shanghai Fifth People's Hospital, Shanghai, China.
Insights
Helicobacter pylori (H. pylori) infection is linked to a higher risk of Cardiac Syndrome X (CSX). This association is more pronounced in middle-aged individuals and in developing countries.
Area of Science:
- Cardiology
- Gastroenterology
- Infectious Diseases
Background:
- Cardiac Syndrome X (CSX) presents as angina pectoris despite normal coronary angiography.
- Chronic inflammation from Helicobacter pylori (H. pylori) infection is a potential contributor to CSX pathogenesis.
Approach:
- A meta-analysis was performed, systematically searching major scientific databases up to October 2021.
- Ten case-control studies comprising 703 CSX patients and 731 controls were analyzed using R software.
Key Points:
- H. pylori infection was significantly associated with an increased risk of CSX (OR: 8.29).
- The association was stronger in middle-aged individuals (40-50 years, OR: 11.27) and those over 50 (OR: 7.18).
- A notable link was observed in developing countries like Iran (OR: 12.99) and China (OR: 5.14), but not in Italy.
Conclusions:
- H. pylori infection may be associated with an increased risk of CSX.
- The pathogenicity appears stronger in middle-aged populations and certain developing nations.
- Further research is required to determine if H. pylori eradication can reduce CSX incidence, particularly in these demographics.
Purpose:
Cardiac syndrome X (CSX) is a condition with normal coronary angiography but angina pectoris. Chronic inflammation caused by Helicobacter pylori (H. pylori) infection may play a pathogenic role in CSX. Therefore, we conducted a meta-analysis to explore the relationship between H. pylori infection and risk of CSX.
Methods:
A systematic search in the Web of Science, Medline, Embase and Chinese databases (CNKI and Wanfang) was conducted up to October 2021. Articles on the association between H. pylori infection and the risk of CSX were included and were analyzed by R software (version 4.1.0).
Results:
Ten case-control studies involving 703 CSX patients and 731 healthy controls were included. H. pylori infection was associated with an increased risk of CSX (OR: 8.29, 95% CI: 4.64-14.82). We also found a significant association in those 25-40 years of age (OR: 1.34, 95% CI: 1.04-1.72), those 40-50 years of age (OR: 11.27, 95% CI: 4.29-29.61), those over 50 years of age (OR: 7.18, 95% CI: 3.59-14.36), those in developing countries [Iran (OR: 12.99, 95% CI: 8.61-19.60) and China (OR: 5.14, 95% CI: 3.09-8.56)]. However, this association was not apparent in a developed country [Italy (OR: 0.93, 95% CI: 0.37-2.33)].
Conclusions:
Our study suggested a possible association between H. pylori infection and the risk of CSX. Its pathogenicity is stronger in middle-aged individuals and some developing countries. However, more studies are needed to further investigate whether early eradication of H. pylori can reduce the incidence rate of CSX, especially in middle-aged individuals and some developing countries.
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