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Korean J Intern Med > Volume 30(6); 2015 > Article
Bang and Baik: Time to learn from the past and prepare for the future in Helicobacter pylori eradication
See Article on Page 801-807
Helicobacter pylori is still prevalent in Korea, although the prevalence has decreased from 66.9% in 1998 to 54.4% in 2013 [1-5]. Sanitary improvements and wide application of eradication therapy have contributed to this. However, it is still a great socioeconomic and national healthcare burden [6]. This bacterial pathogen is involved in various gastrointestinal diseases, including gastritis, peptic ulcer, mucosa-associated lymphoid tissue lymphoma, and gastric cancer [7,8]. Although only 1% to 15% of patients with H. pylorii infection develop the clinical disease, even asymptomatic H. pylorii gastritis should be considered an infectious disease and treated to prevent severe complications, such as gastric cancer, as reported by the Kyoto Global Consensus conference [4]. This suggests a paradigm shift in the eradication of H. pylorii from treatment to prevention [4].
Standard triple therapy (standard dose proton pump inhibitor, amoxicillin 1 g, and clarithromycin 500 mg twice daily for 7 to 14 days) is the recommended first-line regimen for eradication of H. pylorii in Korea [9]. Over the past decade, studies of the trend in H. pylorii eradication rates in Korea have shown a constant or decreasing trend [10]. Concerns about changing the first-line regimen have been growing, because studies indicating a constant trend also showed eradication rates below 90% in per-protocol analyses [10]. Particularly, a recent meta-analysis revealed a decreasing trend in the eradication rate (from 1998 to 2013) in Korea, which has an overall eradication rate of 74.6% (95% confidence interval [CI], 72.1 to 77.2) with intention-to-treat and 82.0% (95% CI, 80.8 to 83.2) by per-protocol analysis [11].
In this issue, Kim et al. [12] reported a trend in the H. pylorii eradication rate using first-line triple therapy in Metropolitan Busan, which is the second largest city in Korea after Seoul. This retrospective study included 1,413 patients who were treated with the standard triple regimen for 7 days between 2003 and 2012 [12]. The overall eradication rate was 84.9% (per-protocol analysis), which is an unacceptable level for the currently recommended regimen. Moreover, the most recent eradication rate was 78.8% in 2012, which has decreased significantly during the last 10 years [12]. These results are consistent with those of the recent meta-analysis and indicate the need for a novel therapeutic regimen in Korea. If the treatment duration had been extended to 14 days, the expected improvement in the eradication rate would have been approximately 5%, which is still an unacceptable level [13].
High clarithromycin resistance in Korea is suspected to be a cause of treatment failure. Although data are scarce, the clarithromycin resistance rate was estimated to be 17.2% to 23.7% in 2012 [14]. Another study reported a resistance rate of 38.5% in 2009, which falls into the category of high clarithromycin resistance [13,15]. The Korean guideline recommends a bismuth-containing quadruple regimen (standard dose proton pump inhibitor twice daily, metronidazole 500 mg three times daily, and bismuth 120 mg and tetracycline 500 mg four times daily for 7 to 14 days) in areas where clarithromycin resistance is high [9]. It is difficult to determine when to change the first-line regimen in an area, because only a few studies have reported data on antibiotic resistance in H. pylorii eradication. However, time trend data continuously indicate the need for a novel regimen. If possible, a susceptibility test-based combination of drugs is the ideal regimen for eradication of an infectious pathogen. However, it is nearly impossible to perform culture and susceptibility tests for H. pylorii in hospitals. With the increase in geographical antibiotic resistance data, it should be possible to determine the preferred regimen among the potential candidates according to the geographic area.
Kim et al. [12] also reported that smoking and female gender are associated with treatment failure. Smoking is a well-known risk factor for treatment failure. As the authors described, a reduction in antibiotic delivery due to decreased gastric blood flow is suspected to be the main mechanism [13]. However, it is not clear why female gender is associated with treatment failure. The high prevalence of H. pylorii infection in carriers of the A2143G mutation in 23S rRNA, which is associated with treatment failure, is presumed to be a possible cause [12,16]. However, another Korean study did not show a preponderance of the A2143G mutation in women [17].
In brief, time trend data indicate decreasing efficacy of standard triple therapy in the eradication of H. pylorii. However, no superior regimen has been found to be more effective than standard triple therapy in Korea. The combination of existing drugs, based on the results of antibiotic susceptibility tests, is the ideal method. Without geographic antibiotic resistance data, it is impossible to compare or interpret the clinical trials of novel regimens [18]. In the setting of a culture and susceptibility test-based regimen choice or with the accumulation of local antibiotic resistance data, it may be possible to determine the best regimen or find novel therapies.

Conflict of interest

No potential conflict of interest relevant to this article was reported.


1. Kim JH, Kim HY, Kim NY, et al. Seroepidemiological study of Helicobacter pylori infection in asymptomatic people in South Korea. J Gastroenterol Hepatol 2001;16:969–975.
crossref pmid
2. Yim JY, Kim N, Choi SH, et al. Seroprevalence of Helicobacter pylori in South Korea. Helicobacter 2007;12:333–340.
crossref pmid
3. Lim SH, Kwon JW, Kim N, et al. Prevalence and risk factors of Helicobacter pylori infection in Korea: nation-wide multicenter study over 13 years. BMC Gastroenterol 2013;13:104.
crossref pmid pmc pdf
4. Lee JY, Kim N. Future trends of Helicobacter pylori eradication therapy in Korea. Korean J Gastroenterol 2014;63:158–170.
crossref pmid
5. Kim NY. Helicobacter pylori. Seoul: Daehanuihak, 2015.

6. Jung KW, Won YJ, Kong HJ, et al. Cancer statistics in Korea: incidence, mortality, survival, and prevalence in 2012. Cancer Res Treat 2015;47:127–141.
crossref pmid pmc pdf
7. McColl KE. Clinical practice: Helicobacter pylori infection. N Engl J Med 2010;362:1597–1604.
crossref pmid
8. Cheung DY, Kim TH. Helicobacter pylori in human stomach: can it be called mutualism or a disease? Korean J Gastroenterol 2012;59:329–337.
crossref pmid
9. Kim SG, Jung HK, Lee HL, et al. Guidelines for the diagnosis and treatment of Helicobacter pylori infection in Korea, 2013 revised edition. Korean J Gastroenterol 2013;62:3–26.
crossref pmid
10. Jo Y. Decreased eradication rates of Helicobacter pylori and problem solving. Korean J Gastroenterol 2014;63:63–65.
crossref pmid
11. Gong EJ, Yun SC, Jung HY, et al. Meta-analysis of first-line triple therapy for helicobacter pylori eradication in Korea: is it time to change? J Korean Med Sci 2014;29:704–713.
crossref pmid pmc
12. Kim SE, Park MI, Park SJ, et al. Trends in Helicobacter pylori eradication rates by first-line triple therapy and related factors in eradication therapy. Korean J Intern Med 2015;30:801–807.
crossref pmid pmc
13. Malfertheiner P, Megraud F, O’Morain CA, et al. Management of Helicobacter pylori infection: the Maastricht IV/ Florence Consensus Report. Gut 2012;61:646–664.
crossref pmid
14. Lee JW, Kim N, Kim JM, et al. Prevalence of primary and secondary antimicrobial resistance of Helicobacter pylori in Korea from 2003 through 2012. Helicobacter 2013;18:206–214.
crossref pmid
15. Hwang TJ, Kim N, Kim HB, et al. Change in antibiotic resistance of Helicobacter pylori strains and the effect of A2143G point mutation of 23S rRNA on the eradication of H. pylorii in a single center of Korea. J Clin Gastroenterol 2010;44:536–543.
crossref pmid
16. De Francesco V, Margiotta M, Zullo A, et al. Clarithromycin-resistant genotypes and eradication of Helicobacter pylori. Ann Intern Med 2006;144:94–100.
crossref pmid
17. Jung MK, Lee JK, Heo J, Kang EJ, Lee YR. The effect of concomittent therarpy and quadruple therapy for patients who had 23S ribosomal ribonucleic acid mutated Helicobacter pylori in Daegu and Kyoungpook area. Korean J Helicobacter Up Gastrointest Res 2014;14:249–254.
18. Graham DY. Editorial: avoiding unethical Helicobacter pylori clinical trials: susceptibility-based studies and probiotics as adjuvants. Helicobacter 2015;20:321–325.
crossref pmid pmc
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