The relationship between Helicobacter pylori seropositivity and COPD.



Thorax, 2015; 70 (10) doi:10.1136/thoraxjnl-2015-207059

Authors: Sze Marc A, Chen Yu-Wei Roy, Tam Sheena, Tashkin Donald, Wise Robert A et al.(3)

Affiliation: University of British Columbia, Canada; University of British Columbia, Canada; University of British Columbia, Canada; David Geffen School of Medicine at UCLA, Los Angeles, CA, United States; Johns Hopkins University School of Medicine, Baltimore, MD, United States (show more (3))

Sample size: 4765

Abstract: RATIONALE: Chronic systemic infections such as those with Helicobacter pylori (H. pylori) may contribute to the evolution and progression of chronic obstructive pulmonary disease (COPD). Using data from the Lung Health Study (LHS), we determined the relationship of H. pylori infection with the severity and progression of COPD.
METHODS: Using an immunoassay, we measured H. pylori immunoglobulin G (IgG) antibody titres in serum samples of 4765 patients with mild-to-moderate COPD. We then determined their relationship with the individual's FEV1 and the rate of decline in FEV1 and mortality over 11 years using multiple regression analysis.
RESULTS: Approximately 18% of the patients were seropositive to H. pylori and these individuals demonstrated lower FEV1 (L) values at every study visit compared with individuals who were seronegative for H. pylori (p value=0.00012). However, patients with seropositivity to H. pylori were on average 0.012 m shorter than those with seronegativity (p value=0.0015). The significant relationship between FEV1 and H. pylori seropositivity disappeared when FEV1 per cent predicted (FEV1pp) was used (p value=0.45). H. pylori seropositive individuals had greater circulating C reactive protein (CRP) levels compared with H. pylori seronegative individuals (p value=0.012), and had increased risk of cardiovascular mortality (relative risk 1.61, p=0.05).
CONCLUSIONS: H. pylori infection was associated with reduced lung function that is most likely due to the effect of the bacterium on lung growth earlier in life. It is also associated with systemic inflammation and increased risk of cardiovascular mortality in patients with COPD.
TRIAL REGISTRATION NUMBERS: NCT00000568 and NCT00000569.














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