TY - JOUR
T1 - A prospective study of periodontal disease and risk of gastric and duodenal ulcer in male health professionals
AU - Boylan, Matthew R.
AU - Khalili, Hamed
AU - Huang, Edward S.
AU - Michaud, Dominique S.
AU - Izard, Jacques
AU - Joshipura, Kaumudi J.
AU - Chan, Andrew T.
N1 - Funding Information:
E.S.H. conceived and designed the study. M.R.B., H.K., A.T.C., E.S.H., D.S.M., K.J., and J.I. analyzed the data. A.T.C. supervised the study. M.R.B., A.T.C., H.K., E.S.H., K.J., and J.I. wrote the paper. Financial Support: Funded by UM1 CA167552 (Willett) and R21 CA139193 (J.I.) from NCI/NIH and K24 DK098311 (A.T.C.) from the NIDDK/NIH. A.T.C. is a Damon Runyon Cancer Research Foundation Clinical Investigator. H.K. is supported by a career development award from the Crohn’s and Colitis Foundation of America (CCFA). Potential Competing interests: A.T. Chan has served as a consultant for Bayer HealthCare, Millennium Pharmaceuticals, Inc., Pfizer, Inc., and Pozen, Inc. The other authors declare no conflict of interest.
PY - 2014
Y1 - 2014
N2 - OBJECTIVES: Periodontal disease has been associated with higher circulating levels of inflammatory markers and conditions associated with chronic inflammation, including vascular disease, diabetes mellitus, and cancer. Limited data exist on the relationship between periodontal disease and gastric and duodenal ulcer. METHODS: We conducted a prospective cohort study of 49,120 men in the Health Professionals Follow-up Study, aged 40-75 years at enrollment in 1986. Biennially, we assessed periodontal disease, tooth loss, and other risk factors for gastric and duodenal ulcer. We validated diagnoses of gastric and duodenal ulcer through medical record review. We used Cox proportional hazards modeling, adjusting for potential confounders, to estimate hazard ratios (HRs) and 95% confidence intervals (CIs). RESULTS: We documented 138 cases of gastric ulcer and 124 cases of duodenal ulcer with available information on Helicobacter pylori status over 24 years of follow-up. After adjustment for risk factors, including smoking and regular use of aspirin and nonsteroidal anti-inflammatory drugs, men with periodontal disease with bone loss had a multivariate HR of ulcer of 1.62 (95% CI, 1.24-2.12). Periodontal disease appeared to be associated with a similar risk of developing ulcers that were H. pylori negative (HR 1.75; 95% CI, 1.26-2.43) than H. pylori positive (HR 1.40; 95% CI, 0.87-2.24), as well as ulcers in the stomach (HR 1.75; 95% CI, 1.21-2.53) than ulcers in the duodenum (HR 1.47; 95% CI, 0.98-2.19). CONCLUSIONS: Periodontal disease is associated with an increased risk of incident gastric and duodenal ulcer. This relationship may be mediated by alterations in the oral and gastrointestinal microbiome and/or systemic inflammatory factors.
AB - OBJECTIVES: Periodontal disease has been associated with higher circulating levels of inflammatory markers and conditions associated with chronic inflammation, including vascular disease, diabetes mellitus, and cancer. Limited data exist on the relationship between periodontal disease and gastric and duodenal ulcer. METHODS: We conducted a prospective cohort study of 49,120 men in the Health Professionals Follow-up Study, aged 40-75 years at enrollment in 1986. Biennially, we assessed periodontal disease, tooth loss, and other risk factors for gastric and duodenal ulcer. We validated diagnoses of gastric and duodenal ulcer through medical record review. We used Cox proportional hazards modeling, adjusting for potential confounders, to estimate hazard ratios (HRs) and 95% confidence intervals (CIs). RESULTS: We documented 138 cases of gastric ulcer and 124 cases of duodenal ulcer with available information on Helicobacter pylori status over 24 years of follow-up. After adjustment for risk factors, including smoking and regular use of aspirin and nonsteroidal anti-inflammatory drugs, men with periodontal disease with bone loss had a multivariate HR of ulcer of 1.62 (95% CI, 1.24-2.12). Periodontal disease appeared to be associated with a similar risk of developing ulcers that were H. pylori negative (HR 1.75; 95% CI, 1.26-2.43) than H. pylori positive (HR 1.40; 95% CI, 0.87-2.24), as well as ulcers in the stomach (HR 1.75; 95% CI, 1.21-2.53) than ulcers in the duodenum (HR 1.47; 95% CI, 0.98-2.19). CONCLUSIONS: Periodontal disease is associated with an increased risk of incident gastric and duodenal ulcer. This relationship may be mediated by alterations in the oral and gastrointestinal microbiome and/or systemic inflammatory factors.
UR - http://www.scopus.com/inward/record.url?scp=84893913152&partnerID=8YFLogxK
U2 - 10.1038/ctg.2013.14
DO - 10.1038/ctg.2013.14
M3 - Article
AN - SCOPUS:84893913152
SN - 2155-384X
VL - 5
JO - Clinical and Translational Gastroenterology
JF - Clinical and Translational Gastroenterology
M1 - e49
ER -