Skip to main content
Log in

Equivalent Helicobacter pylori infection rates in Lynch syndrome mutation carriers with and without a first-degree relative with gastric cancer

  • Original Article
  • Published:
International Journal of Colorectal Disease Aims and scope Submit manuscript

Abstract

Background

Patients with Lynch syndrome (LS) are at an increased risk of developing gastric cancer. In 2010, a guideline that recommended to screen all patients for Helicobacter pylori was implemented in the Netherlands. H. pylori is an important risk factor in the development of gastric cancer in the general population, and eradication of the bacterium reduces this risk. We aimed to assess the proportion of LS patients being tested and the yield and also addressed the question whether H. pylori infection is more prevalent in LS families with known cases of gastric cancer.

Methods

Proven mutation carriers from five different Dutch hospitals were included. The implementation of H. pylori screening and its outcome was examined. The observation period was 2008–2013. The presence of first-degree family members with gastric cancer was noted, and it was observed if H. pylori infection was more prevalent in Lynch families with known cases of gastric cancer. Obtainable endoscopy reports were reviewed.

Results

Four hundred forty-three (male, 184) proven mutation carriers were included. The proportion of patients screened increased after 2010, from 37 to 68 %. Twenty percent of the patients were infected. The 25 patients who had a first-degree family member with gastric cancer did not have a higher infection rate. In 30 % of cases, an endoscopy was performed; in four patients, intestinal metaplasia and in eight patients, gastric cancer was found.

Conclusion

The recommendation to screen for H. pylori is increasingly followed. The prevalence of infection in this patient group does not differ from the general population. Patients who had a first-degree family member with gastric cancer did not have a higher infection rate.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Lynch HT, de la Chapelle A (2003) Hereditary colorectal cancer. N Engl J Med 348:919–32

    Article  CAS  PubMed  Google Scholar 

  2. Aarnio M, Sankila R, Pukkala E et al (1999) Cancer risk in mutation carriers of DNA-mismatch-repair genes. Int J Cancer 12:214–8

    Article  Google Scholar 

  3. Koornstra JJ, Mourits MJ, Sijmons RH et al (2009) Management of extracolonic tumours in patients with Lynch syndrome. Lancet Oncol 10:400–8

    Article  CAS  PubMed  Google Scholar 

  4. Maul JS, Warner NR, Kuwada SK et al (2006) Extracolonic cancers associated with hereditary nonpolyposis colorectal cancer in the Utah Population Database. Am J Gastroenterol 101:1591–1596

    Article  PubMed  Google Scholar 

  5. Aarnio M, Salovaara R, Aaltonen LA et al (1997) Features of gastric cancer in hereditary non-polyposis colorectal cancer syndrome. Int J Cancer 21:551–5

    Article  Google Scholar 

  6. Capelle LG, Van Grieken NC, Lingsma HF et al (2010) Risk and epidemiological time trends of gastric cancer in Lynch syndrome carriers in the Netherlands. Gastroenterology 138:487–492

    Article  PubMed  Google Scholar 

  7. Watson P, Vasen HF, Mecklin JP et al (2008) The risk of extra-colonic, extra-endometrial cancer in the Lynch syndrome. Int J Cancer 123:444–449

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  8. Park YJ, Shin KH, Park JG (2000) Risk of gastric cancer in hereditary nonpolyposis colorectal cancer in Korea. Clin Cancer Res 6:2994–8

    CAS  PubMed  Google Scholar 

  9. Renkonen-Sinisalo L, Sipponen P, Aarnio M et al (2002) No support for endoscopic surveillance for gastric cancer in hereditary non-polyposis colorectal cancer. Scand J Gastroenterol 37:574–7

    Article  CAS  PubMed  Google Scholar 

  10. Correa P (1992) Human gastric carcinogenesis: a multistep and multifactorial process—First American Cancer Society Award Lecture on Cancer Epidemiology and Prevention. Cancer Res 52:6735–6740

    CAS  PubMed  Google Scholar 

  11. IARC Working Group on the Evaluation of Carcinogenic Risks to Humans (1994) Schistosomes, liver flukes, and Helicobacter pylori. IARC Monogr Eval Carcinog Risks Hum June 61:1–241

    Google Scholar 

  12. Vasen HF, Blanco I, Aktan-Collan K et al (2013) Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts. Gut 62:812–23

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. 13) www.oncoline.nl, erfelijke tumoren, Lynch syndrome, consensus based, 1-7-2010

  14. Numans ME, De Wit NJ, Dirven JAM et al (2013) NHG-standaard Maagklachten(Derde herziening). Huisarts Wet 56:26–35

    Google Scholar 

  15. Blankenstein V, van Vuuren L et al (2013) The prevalence of Helicobacter pylori infection in the Netherlands. Scand J Gastroenterol 48(7):794–800

    Article  PubMed  Google Scholar 

  16. Demirel BB, Akkas BE, Vural GU (2013) Clinical factors associated with H. pylori infection—is there an association with gastric cancer history in first-degree family members? Asian Pacific J Cancer Prev 14:1797–1802

    Article  Google Scholar 

  17. Rokkas T, Sechopoulos P, Pistiolas D et al (2010) H. pylori infection and gastric histology in first-degree relatives of gastric cancer patients: a meta-analysis. Eu J Gastroen Hepat 22:1128–1133

    Article  Google Scholar 

  18. Lansdorp-Vogelaar I, Sharp L (2013) Cost-effectiveness of screening and treating H. pylori for gastric cancer prevention. Best Pract Res Clin Gastroenterol 27:933–947

    Article  PubMed  Google Scholar 

  19. Engel C, Loeffler M, Steinke V et al (2012) Risks of less common cancers in proven mutation carriers with Lynch syndrome. J Clin Onc 30:4409–4415

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Eline C. Soer.

Ethics declarations

The study was approved by the ethics committees of the respective centers.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Soer, E.C., Leicher, L.W., Langers, A.M.J. et al. Equivalent Helicobacter pylori infection rates in Lynch syndrome mutation carriers with and without a first-degree relative with gastric cancer. Int J Colorectal Dis 31, 693–697 (2016). https://doi.org/10.1007/s00384-016-2524-7

Download citation

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00384-016-2524-7

Keywords

Navigation