» Articles » PMID: 31165513

Systematic Review with Meta-analysis: Association Between Helicobacter Pylori CagA Seropositivity and Odds of Inflammatory Bowel Disease

Overview
Date 2019 Jun 6
PMID 31165513
Citations 21
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Accumulating data support a protective role of Helicobacter pylori against inflammatory bowel diseases (IBD), which might be mediated by strain-specific constituents, specifically cagA expression.

Aim: To perform a systematic review and meta-analysis to more clearly define the association between CagA seropositivity and IBD.

Methods: We identified comparative studies that included sufficient detail to determine the odds or risk of IBD, Crohn's disease (CD) or ulcerative colitis (UC) amongst individuals with vs without evidence of cagA expression (eg CagA seropositivity). Estimates were pooled using a random effects model.

Results: Three clinical studies met inclusion criteria. cagA expression was represented by CagA seropositivity in all studies. Compared to CagA seronegativity overall, CagA seropositivity was associated with lower odds of IBD (OR 0.31, 95% CI 0.21-0.44) and CD (OR 0.25, 95% CI 0.17-0.38), and statistically nonsignificant lower odds for UC (OR 0.68, 95% CI 0.35-1.32). Similarly, compared to H pylori non-exposed individuals, H pylori exposed, CagA seropositive individuals had lower odds of IBD (OR 0.26, 95% CI 0.16-0.41) and CD (OR 0.23, 95% CI 0.15-0.35), but not UC (OR 0.66, 0.34-1.27). However, there was no significant difference in the odds of IBD, CD or UC between H pylori exposed, CagA seronegative and H pylori non-exposed individuals.

Conclusion: We found evidence for a significant association between CagA seropositive H pylori exposure and reduced odds of IBD, particularly CD, but not for CagA seronegative H pylori exposure. Additional studies are needed to confirm these findings and define underlying mechanisms.

Citing Articles

Role of gut microbiota and in inflammatory bowel disease through immune-mediated synergistic actions.

Deng Z, Li X, Liu L, Zeng H, Chen B, Peng J World J Gastroenterol. 2024; 30(47):5097-5103.

PMID: 39713161 PMC: 11612865. DOI: 10.3748/wjg.v30.i47.5097.


Debate on the relationship between infection and inflammatory bowel disease: a bibliometric analysis.

Wang Z, Zhao S, Zhong X, Su Y, Song Y, Li J Front Microbiol. 2024; 15:1479941.

PMID: 39569001 PMC: 11576472. DOI: 10.3389/fmicb.2024.1479941.


Impact of Eradication on Inflammatory Bowel Disease Onset and Disease Activity: To Eradicate or Not to Eradicate?.

Gravina A, Pellegrino R, Iascone V, Palladino G, Federico A, Zagari R Diseases. 2024; 12(8).

PMID: 39195178 PMC: 11353643. DOI: 10.3390/diseases12080179.


Roles of the components of the -pathogenicity island encoded type IV secretion system in .

Gou L, Yang X, Yun J, Ma Z, Zheng X, Du H Future Microbiol. 2024; 19(14):1253-1267.

PMID: 39171625 PMC: 11633423. DOI: 10.1080/17460913.2024.2383514.


Bibliometric analysis of the correlation between H. pylori and inflammatory bowel disease.

Li Y, Li L, Yin W, Wan J, Zhong X JGH Open. 2024; 8(8):e70014.

PMID: 39148512 PMC: 11325047. DOI: 10.1002/jgh3.70014.


References
1.
Burisch J, Pedersen N, Cukovic-Cavka S, Brinar M, Kaimakliotis I, Duricova D . East-West gradient in the incidence of inflammatory bowel disease in Europe: the ECCO-EpiCom inception cohort. Gut. 2013; 63(4):588-97. DOI: 10.1136/gutjnl-2013-304636. View

2.
Engler D, Leonardi I, Hartung M, Kyburz A, Spath S, Becher B . Helicobacter pylori-specific protection against inflammatory bowel disease requires the NLRP3 inflammasome and IL-18. Inflamm Bowel Dis. 2015; 21(4):854-61. DOI: 10.1097/MIB.0000000000000318. View

3.
Torres J, Camorlinga-Ponce M, Perez-Perez G, Munoz L, Munoz O . Specific serum immunoglobulin G response to urease and CagA antigens of Helicobacter pylori in infected children and adults in a country with high prevalence of infection. Clin Diagn Lab Immunol. 2002; 9(1):97-100. PMC: 119889. DOI: 10.1128/cdli.9.1.97-100.2002. View

4.
Ng W, Wong S, Ng S . Changing epidemiological trends of inflammatory bowel disease in Asia. Intest Res. 2016; 14(2):111-9. PMC: 4863044. DOI: 10.5217/ir.2016.14.2.111. View

5.
Wehkamp J, Harder J, Weichenthal M, Mueller O, Herrlinger K, Fellermann K . Inducible and constitutive beta-defensins are differentially expressed in Crohn's disease and ulcerative colitis. Inflamm Bowel Dis. 2003; 9(4):215-23. DOI: 10.1097/00054725-200307000-00001. View