Journal List > Korean J Gastroenterol > v.56(4) > 1006719

Kim, Kim, Lee, Kang, Seo, Lim, Kwon, Song, Lee, Lee, Park, Hwang, Kim, Jeong, Lee, Jung, and Song: Risk Factors for Development and Recurrence of Peptic Ulcer Disease

Abstract

Background/Aims

Peptic ulcer disease (PUD) is one of the common gastrointestinal diseases, and its medical management has been developed so much that the incidence of its serious complications, such as bleeding and perforation, are declining significantly. Its prevalence in Korea is not definitely decreased, probably due to increasing proportion of elderly patients and their rising usage of non-steroidal anti-inflammatory drugs (NSAIDs) and aspirins. This study was conducted to identify the risk factors for development and recurrence of peptic ulcer disease in Korea.

Methods

From 2003 to 2008, upper gastrointestinal endoscopy and detailed personal questionnaires were performed for patients who visited Department of Gastroenterology at Seoul National University Bundang Hospital. In total, 475 PUD patients and 335 non-ulcer dyspepsia patients were included. The results of questionnaires and repeated upper gastrointestinal endoscopy at initial diagnosis time and follow-up periods were analyzed.

Results

Multivariable analysis showed that male, H. pylori infection, NSAIDs use and smoking were risk factors for the development of PUD. The use of proton pump inhibitors (PPIs) and H2 receptor antagonists has significantly reduced the risk of PUD in patients who had taken NSAIDs and/or aspirins. H. pylori infection was found as the only risk factor for the recurrence of PUD.

Conclusions

For the old patients who are taking drugs, such as NSAIDs and aspirins, concomitant use of PPIs or H2 receptor antagonists should be considered to protect from the development of PUD. H. pylori eradication has been confirmed again to be essential for the treatment of PUD patients infected with H. pylori.

REFERENCES

1. Malfertheiner P, Chan FK, McColl KE. Peptic ulcer disease. Lancet. 2009; 374:1449–1461.
crossref
2. Herná ndez-Dí az S, Rodrí guez LA. Association between non-steroidal anti-inflammatory drugs and upper gastrointestinal tract bleeding/perforation: an overview of epidemiologic studies published in the 1990s. Arch Intern Med. 2000; 160:2093–2099.
3. Lanza LL, Walker AM, Bortnichak EA, Dreyer NA. Peptic ulcer and gastrointestinal hemorrhage associated with non-steroidal anti-inflammatory drug use in patients younger than 65 years. A large health maintenance organization cohort study. Arch Intern Med. 1995; 155:1371–1377.
crossref
4. Huang JQ, Sridhar S, Hunt RH. Role of Helicobacter pylori infection and non-steroidal anti-inflammatory drugs in pep-tic-ulcer disease: a metaanalysis. Lancet. 2002; 359:14–22.
5. Wang YR, Richter JE, Dempsey DT. Trends and outcomes of hospitalizations for peptic ulcer disease in the United States, 1993 to 2006. Ann Surg. 2010; 251:51–58.
crossref
6. Kim JI, Kim SG, Kim N, et al. Changing prevalence of upper gastrointestinal disease in 28 893 Koreans from 1995 to 2005. Eur J Gastroenterol Hepatol. 2009; 21:787–793.
7. Kwon JH, Choi MG, Lee SW, et al. Trends of gastrointestinal diseases at a single institution in Korea over the past two decades. Gut Liver. 2009; 3:252–258.
crossref
8. Kim SH, Kang HW, Yoon WJ, et al. Clinical characteristics of peptic ulcer in the aged in Korea. Korean J Med. 2004; 66:19–25.
9. Yu KD, Kim NY, Park YS, et al. Clinical characteristics of elderly Korean patients with peptic ulcer. Korean J Med. 2006; 71:501–510.
10. Kurata JH, Nogawa AN. Meta-analysis of risk factors for peptic ulcer. Nonsteroidal antiinflammatory drugs, Helicobacter pylori, and smoking. J Clin Gastroenterol. 1997; 24:2–17.
11. Marshall BJ, Warren JR. Unidentified curved bacilli in the stomach of patients with gastritis and peptic ulceration. Lancet. 1984; 1:1311–1315.
crossref
12. Vu C, Ng YY. Prevalence of Helicobacter pylori in peptic ulcer disease in a Singapore hospital. Singapore Med J. 2000; 41:478–481.
13. Kuipers EJ, Thijs JC, Festen HP. The prevalence of Helicobacter pylori in peptic ulcer disease. Aliment Pharmacol Ther. 1995; 9(suppl 2):59–69.
14. Sung JJ, Kuipers EJ, EL-Serag HB. Systematic review: the global incidence and prevalence of peptic ulcer disease. Aliment Pharmacol Ther. 2009; 29:938–946.
crossref
15. Wong SN, Sollano JD, Chan MM, et al. Changing trends in peptic ulcer prevalence in a tertiary care setting in the Philip-pines: a seven-year study. J Gastroenterol Hepatol. 2005; 20:628–632.
crossref
16. Xia HH, Phung N, Altiparmak E, et al. Reduction of peptic ulcer disease and Helicobacter pylori infection but increase of reflux esophagitis in Western Sydney between 1990 and 1998. Dig Dis Sci. 2001; 46:2716–2723.
17. Lee EJ, Gham CW, Park TW, et al. The effect of Helicobacter pylori eradication on the improvement of the symptoms in patients with functional dyspepsia and peptic ulcer disease. Korean J Med. 2006; 71:141–148.
18. Yim JY, Kim N, Choi SH, et al. Seroprevalence of Helicobacter pylori in South Korea. Helicobacter. 2007; 12:333–340.
19. Jang HJ, Choi MH, Shin WG, et al. Has peptic ulcer disease changed during the past ten years in Korea? A prospective multicenter study. Dig Dis Sci. 2008; 53:1527–1531.
crossref
20. Jang MK, Kim HY, Cho BD, et al. Prospective study for the prevalence of Helicobacter pylori infection in patients with gastric ulcer and duodenal ulcer among Korean population. Korean J Med. 1997; 52:457–464.
21. Ciociola AA, McSorley DJ, Turner K, Sykes D, Palmer JB. Helicobacter pylori infection rates in duodenal ulcer patients in the United States may be lower than previously estimated. Am J Gastroenterol. 1999; 94:1834–1840.
22. Tsuji H, Kohli Y, Fukumitsu S, et al. Helicobacter pylori -negative gastric and duodenal ulcers. J Gastroenterol. 1999; 34:455–460.
23. Meucci G, Di Battista R, Abbiati C, et al. Prevalence and risk factors of Helicobacter pylori-negative peptic ulcer: a multicenter study. J Clin Gastroenterol. 2000; 31:42–47.
24. Aalykke C, Lauritsen K. Epidemiology of NSAID-related gastroduodenal mucosal injury. Best Pract Res Clin Gastroenterol. 2001; 15:705–722.
crossref
25. Langman MJ, Weil J, Wainwright P, et al. Risks of bleeding peptic ulcer associated with individual non-steroidal anti-inflammatory drugs. Lancet. 1994; 343:1075–1078.
crossref
26. Hawkey CJ. Nonsteroidal anti-inflammatory drug gastropathy. Gastroenterology. 2000; 119:521–535.
crossref
27. Nishikawa K, Sugiyama T, Kato M, et al. Non-Helicobacter pylori and non-NSAID peptic ulcer disease in the Japanese population. Eur J Gastroenterol Hepatol. 2000; 12:635–640.
28. Arroyo MT, Forne M, de Argila CM, et al. The prevalence of peptic ulcer not related to Helicobacter pylori or non-steroidal anti-inflammatory drug use is negligible in southern Europe. Helicobacter. 2004; 9:249–254.
29. Garcí a Rodrí guez LA, Herná ndez-Dí az S. Risk of uncomplicated peptic ulcer among users of aspirin and non-aspirin nonsteroidal antiinflammatory drugs. Am J Epidemiol. 2004; 159:23–31.
30. Iwamoto J, Mizokami Y, Shimokobe K, et al. Clinical features of gastroduodenal ulcer in Japanese patients taking low-dose aspirin. Dig Dis Sci. 2010; 55:2270–2274.
crossref
31. Derry S, Loke YK. Risk of gastrointestinal hemorrhage with long term use of aspirin: metaanalysis. BMJ. 2000; 321:1183–1187.
32. Sturkenboom MC, Burke TA, Dieleman JP, Tangelder MJ, Lee F, Goldstein JL. Underutilization of preventive strategies in patients receiving NSAIDs. Rheumatology (Oxford). 2003; 42(suppl 3):iii23–31.
crossref
33. Steinman MA, McQuaid KR, Covinsky KE. Age and rising rates of cyclooxygenase-2 inhibitor use. Results from a national survey. J Gen Intern Med. 2006; 21:245–250.
34. Cai S, Garcí a Rodrí guez LA, Massó-Gonzá lez EL, Herná n-dez-Dí az S. Uncomplicated peptic ulcer in the UK: trends from 1997 to 2005. Aliment Pharmacol Ther. 2009; 30:1039–1048.
crossref

Table 1.
Comparisons of the Clinical Characteristics between Patients with Peptic Ulcer Disease and Controls
Controls
(n=335)
n (%)
Peptic ulcer disease
(n=475)
n (%)
p
Age (yr, mean± SD) 52.1±12.4 58.2±14.9 <0.001
Age over 70 19 (5.6) 106 (29.6) <0.001
Male 103 (30.7) 334 (70.3) <0.001
Female 232 (69.3) 141 (29.7)
Location of ulcer
Gastric ulcer 266 (56.0)
Duodenal ulcer 209 (44.0)
Current smoking 31 (9.3) 163 (34.3) <0.001
Male 25 (24.3) 158 (47.3) <0.001
Female 6 (2.6) 5 (3.5) 0.069
Current alcohol drinking 59 (17.6) 170 (35.8) <0.001
Male 42 (40.8) 164 (49.1) <0.001
Female 17 (7.3) 6 (4.3) 0.095
NSAIDs within 4 weeks 38 (11.3) 112 (23.6) <0.001
Aspirins within 4 weeks 36 (10.7) 107 (22.5) <0.001
H. pylori infection 200 (59.7) 345 (72.6) <0.001

  NSAIDs, non-steroidal inflammatory drugs; H. pylori, Helicobacter pylori.

Table 2.
Relationship between Peptic Ulcer Disease and Duration of NSAIDs and Aspirin Medication
Controls
(n=335)
n (%)
Peptic ulcer disease
(n=475)
n (%)
p
NSAIDs Within 4 weeks 38 (11.3) 112 (23.6) <0.001
From 4 to 8 weeks 36 (10.7) 58 (12.2) 0.507
Aspirins Within 4 weeks 36 (10.7) 107 (22.5) <0.001
From 4 to 8 weeks 11 (3.3) 33 (6.9) 0.023

  NSAIDs, non-steroidal anti-inflammatory drugs.

Table 3.
Multivariate Analysis for the Risk Factors of Peptic Ulcer Disease Development
Controls
(n=335)
n (%)
Peptic ulcer disease
(n=475)
n (%)
Odds ratio 95%
Confidence interval
p
Male 103 (30.7) 334 (70.3) 7.65 2.97-19.71 <0.001
H. pylori infection 200 (59.7) 345 (72.6) 5.59 2.35-13.26 <0.001
NSAIDs within 4 weeks 38 (11.3) 112 (23.6) 3.31 1.12-9.80 0.031
Current smoking 31 (9.3) 163 (34.3) 2.64 1.04-6.68 0.041

  H. pylori, Helicobacter pylori; NSAIDs, non-steroidal inflammatory drugs.

Table 4.
Comparisons of the Clinical Characteristics Depending on the Location of Peptic Ulcer Disease
Gastric ulcer
(n=265)
n (%)
Duodenal ulcer
(n=210)
n (%)
p
Age (yr, mean± SD) 61.9±13.7 53.3±15.1 <0.001
Age over 70 76 (28.6) 30 (14.2) <0.001
BMI over 25 kg/m2 30 (11.3) 36 (17.1) 0.038
Blood type n=154 n=137 0.028
A 51 (33.1) 34 (24.8)
B 40 (30.0) 32 (23.4)
AB 16 (10.4) 15 (10.9)
O 47 (30.5) 56 (40.9)
Monthly income
Below 1,000,000 won 20 (7.5) 11 (5.2) 0.011
Over 8,000,000 won 14 (5.3) 27 (12.9) 0.011
Above college graduation 57 (21.5) 64 (30.5) 0.007
Current smoking 101 (38.1) 62 (29.5) 0.010
H. pylori infection 180 (68.0) 165 (78.6) 0.007
Past history of 16 (6.0) 27 (12.9) 0.007
H. pylori eradication
NSAIDs within 4 weeks 69 (26.0) 43 (20.5) 0.168
Aspirin within 4 weeks 66 (24.9) 41 (19.5) 0.175

  BMI, Body mass index; H. pylori, Helicobacter pylori; NSAIDs, non-steroidal inflammatory drugs.

Table 5.
Peptic Ulcer Disease Development Depending on the Use of NSAIDs and Gastroprotective Agents
Control
(n=335)
n (%)
Peptic ulcer disease
(n=475)
n (%)
p
PPIs within 4 weeks (+) NSAIDs within 4 weeks (+) 4 (6.9) 54 (93.1) 0.334
(−) 18 (10.1) 161 (89.9)
(−) NSAIDs within 4 weeks (+) 34 (36.6) 59 (63.4) <0.001
(−) 277 (58.7) 196 (41.4)
H2 receptor antagonists within 4 weeks (+) NSAIDs within 4 weeks (+) 14 (23.0) 47 (77.0) 0.097
(−) 49 (33.1) 99 (66.9)
(−) NSAIDs within 4 weeks (+) 24 (26.7) 66 (73.3) <0.001
(−) 246 (48.8) 258 (51.2)

  PPIs, proton pump inhibitors; NSAIDs, non-steroidal inflammatory drugs.

Table 6.
Comparisons of Characteristics Depending on the Recurrence of Peptic Ulcer Disease
Recurrence
(n=37)
n (%)
No recurrence
(n=207)
n (%)
p
Age over 70 14 (37.8) 34 (16.4) 0.005
Location of ulcer
Gastric ulcer 20 (54.1) 115 (55.6) 0.921
Duodenal ulcer 17 (45.9) 92 (44.4)
Current smoking 11 (29.8) 69 (33.3) 0.821
Current alcohol drinking 12 (32.4) 69 (33.3) 0.825
H. pylori infection 19 (51.4) 168 (81.2) <0.001
H. pylori eradication 10 (27.0) 142 (68.6) <0.001
Number of H. pylori eradication trial 0.851
1 st 8 (21.6) 120 (58.0)
2 nd 1 (2.7) 14 (6.8)
3 rd 1 (2.7) 8 (3.9)
Chronic illness 20 (54.1) 65 (31.4) 0.034
Aspirins within 4 weeks 20 (54.1) 46 (22.2) <0.001
NSAIDs within 4 weeks 9 (24.3) 48 (23.2) 0.951
Time to recurrence
≤1 year 17 (45.9)
1-2 year 10 (27.1)
2-3 year 6 (16.2)
3-4 year 4 (10.8)

  H. pylori, Helicobacter pylori; NSAIDs, non-steroidal inflammatory drugs.

Recurrence was analyzed among 246 peptic ulcer patients who had showed scar in the follow-up endoscopy after ulcer medication.

Chronic illness includes diabetes mellitus, hypertension, hypercholesterolemia, ischemic heart disease, congestive heart failure, cerebrovascular attack, chronic hepatitis, liver cirrho-sis, inflammatory bowel disease, rheumatic arthritis, and chronic renal disease.

Table 7.
Multivariate Analysis for the Risk Factors of Peptic Ulcer Disease Recurrence
Recurrence
(n=37)
n (%)
No recurrence
(n=207)
n (%)
Odds ratio 95%
Confidence interval
p
Age over 70 14 (37.8) 34 (16.4) 0.334 0.065-1.723 0.190
H. pylori infection 19 (51.4) 168 (81.2) 1.000
H. pylori eradication 10 (27.0) 142 (68.6) 0.024 0.003-0.175 0.000
Chronic illness 20 (54.1) 65 (31.4) 0.642 0.133-3.112 0.582
Aspirins within 4 weeks 20 (54.1) 46 (22.2) 2.752 0.490-15.441 0.250

  H. pylori, Helicobacter pylori; NSAIDs, non-steroidal inflammatory drugs.

TOOLS
Similar articles