Background: () is a common cause of widespread bacterial infections and has been associated with the stabilization of the microbiome. The microbiome, through modulating systemic inflammation with possible upregulation of the NLRP3 inflammasome, may potentiate the development of breast cancer (BC). The purpose of this study was to therefore evaluate the correlation between previous infection and the incidence of BC.

Methods: A large national database was used to collect International Classification of Disease Ninth and Tenth Codes to evaluate the incidence of BC between January 2010 and December 2019 in patients with and without history. A retrospective cohort study was performed where these groups of individuals were matched by age range, Charlson Comorbidity Index (CCI), and antibiotic treatment exposure. Significance and relative risk were obtained using standard statistical procedures.

Results: A total of 13,599 patients were matched by age range and CCI in both the experimental and control groups. BC incidence was 259 (1.905%) in the group compared to 686 (5.044%) in the control group (P < 2.2 × 10; odds ratio (OR) = 0.604, 95% confidence interval (CI): 0.553 - 0.660). Matching by antibiotic treatment exposure resulted in two groups of 3,189 patients, in which BC incidence was 98 (3.073 %) in the group compared to 171 (5.362%) in the control group (P < 2.2 × 10; OR = 0.584, 95% CI: 0.515 - 0.661).

Conclusion: The study shows a statistically significant correlation between and a reduced incidence of BC. These results warrant further research regarding 's role in upregulating the NLRP3 inflammasome and its potential role in BC prevention and treatment.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10409556PMC
http://dx.doi.org/10.14740/wjon1617DOI Listing

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