A systematic approach for the diagnosis and treatment of idiopathic peptic ulcers

Article information

Korean J Intern Med. 2015;30(5):559-570

Publication date (electronic) : 2015 August 27

doi : https://doi.org/10.3904/kjim.2015.30.5.559

Chen-Shuan Chung ¹, Tsung-Hsien Chiang ², Yi-Chia Lee ²

¹Department of Internal Medicine, Far Eastern Memorial Hospital, New Taipei City, Taiwan

²Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan

Correspondence to Yi-Chia Lee, M.D. Department of Internal Medicine, National Taiwan University Hospital, National Taiwan University College of Medicine, No.7, Chung Shan South Road, Zhongzheng Dist., Taipei 10002, Taiwan Tel: +886-2-23123456 ext.63351 Fax: +886-2-23412775 E-mail: yichialee@ntu.edu.tw

Received 2015 January 22; Accepted 2015 June 20.

Abstract

An idiopathic peptic ulcer is defined as an ulcer with unknown cause or an ulcer that appears to arise spontaneously. The first step in treatment is to exclude common possible causes, including Helicobacter pylori infection, infection with other pathogens, ulcerogenic drugs, and uncommon diseases with upper gastrointestinal manifestations. When all known causes are excluded, a diagnosis of idiopathic peptic ulcer can be made. A patient whose peptic ulcer is idiopathic may have a higher risk for complicated ulcer disease, a poorer response to gastric acid suppressants, and a higher recurrence rate after treatment. Risk factors associated with this disease may include genetic predisposition, older age, chronic mesenteric ischemia, smoking, concomitant diseases, a higher American Society of Anesthesiologists score, and higher stress. Therefore, the diagnosis and management of emerging disease should systematically explore all known causes and treat underlying disease, while including regular endoscopic surveillance to confirm ulcer healing and the use of proton-pump inhibitors on a case-by-case basis.

Keywords: Idiopathic peptic ulcer; Helicobacter pylori infection; Endoscopy

INTRODUCTION

Helicobacter pylori infection and non-steroidal anti-inflammatory drugs (NSAIDs) are common causes of peptic ulcer disease (PUD). However, in recent years, the global occurrence of non-H. pylori, non-NSAID PUD has increased. Management of this emerging disease is increasingly important. Although clinicians tend to describe non-H. pylori, non-NSAID PUD as idiopathic, the term “idiopathic” refers to a disease whose cause is not known or appears to arise spontaneously. Therefore, in addition to a missed diagnosis of H. pylori and the unrecognized use of NSAIDs/aspirin, a diagnosis of idiopathic peptic ulcer disease (IPUD) should also exclude all other recognized etiologies of PUD, which requires a systematic approach that considers all possible causes.

IS THE PROPORTION OR ABSOLUTE NUMBER OF IDIOPATHIC PEPTIC ULCERS INCREASING?

The management of PUD changed dramatically after the discovery of H. pylori as a major cause of chronic gastritis, peptic ulcer, and gastric cancer. Over half of the world’s population is infected with H. pylori, especially in developing countries [1,2]. Historically, H. pylori infection was found in 90% to 100% of patients with duodenal ulcer (DU) and 60% to 100% of patients with gastric ulcer (GU) [3]. A test-and-treat strategy for H. pylori infection has been adopted as first-line management for patients with PUD, while a screen-and-treat strategy for H. pylori infection in the asymptomatic population has been considered as an effective approach to decrease future risk of gastric cancer [4,5]. These strategies have led to a continuous decline in the incidence of H. pylori-related peptic ulcers. Studies in Asia have also found that the incidence of H. pylori infection in younger patients has decreased [6-10], probably due to improved sanitation and hygiene. Conversely, the global use of NSAIDs/aspirin is increasingly prevalent in an aging population and medical comorbidities are frequent. Thus, non-H. pylori PUD is relatively more common because of increased use of ulcerogenic drugs [11].

Graham [12] proposed a model to illustrate the changing proportion of H. pylori-positive and -negative ulcer disease. If the H. pylori prevalence were to decline from 80% to 40%, and the risk of PUD from causes other than H. pylori were to remain stable at about 250 per 100,000 persons, the total number of ulcers would decrease from 1,050 to 650 per 100,000 persons, but the proportion of H. pylori-negative PUD would increase from 24% to 38% [12]. Epidemiological studies have consistently reported an increasing proportion of H. pylori-negative PUD, especially in Asian countries. Studies in the 1990s in the United States found that only about 6% of DUs were not associated with H. pylori infection, particularly in Caucasians [13]. However, later studies contradicted these results. A study in Orlando, Florida, found that only 32% of DU patients were H. pylori-positive, and only 25% of bleeding ulcers were associated with H. pylori [14]. A larger scale study including 305 cases showed that ~35% of PUD was not associated with H. pylori or NSAIDs [15], while a multicenter French study found that about 21.6% of patients with PUD had neither H. pylori infection nor a history of using ulcerogenic drugs [16]. Thus, it appears that the incidence of idiopathic ulcer remains stable in Western countries, in contrast to the increasing trend in Asian countries in recent years (Fig. 1) [15-43].

Figure 1.

(A) Global incidence of clinical idiopathic peptic ulcer disease from 1991 to 2013 reported in large-scale studies with a sample size > 300 patients. (B) Reports of idiopathic peptic ulcer disease in Asian countries, excluding studies on bleeding peptic ulcers.

In Asian countries, a study published in 1991 revealed that only 6% of DUs were H. pylori negative, and when ulcerogenic agents were excluded the incidence was as low as 0.3% [17]. In a 2006 Japanese study, DU was idiopathic in one third of cases [38], and the proportion of idiopathic ulcers was found to be as high as 40.6% in a Korean study conducted in 2007 [31]. The trend of increasing idiopathic ulcers appears to follow an exponential curve if we focus on large-scale studies with a study population > 300) (Fig. 1A) and exclude studies that included bleeding PUD (Fig. 1B). As further evidence for the changing etiology, research conducted in Hong Kong found that only the absolute number of H. pylori-related bleeding ulcer was declining, while the number of H. pylori-negative bleeding ulcers remained stable [33,44-46]. Thus, the accumulated evidence supports the concept proposed by Graham [12]: non-H. pylori- and non-NSAIDs-related ulcer diseases are more likely to be found in older, sicker patients, are more resistant to acid suppression therapy, and are associated with a greater risk of bleeding and recurrence and a greater overall mortality rate as compared with traditional H. pylori-positive PUD [44,45].

IDIOPATHIC PEPTIC ULCER DISEASE: A DIAGNOSIS OF EXCLUSION

Because IPUD is defined as PUD that arises without an identifiable cause, it is a diagnosis of exclusion. Possible etiologies to be excluded are shown in the Table 1 (upper panel), which may include missed H. pylori infection, unidentified use of ulcerogenic medications, rare systemic diseases with upper gastrointestinal tract manifestations, hyperacidity of the stomach, and other rare infections involving the upper gastrointestinal tract.

Table 1.

Etiologies to be excluded for the diagnosis of idiopathic peptic ulcer and associated risk factors

Incorrect diagnosis of H. pylori

There are several methods available to detect H. pylori infection. These methods are characterized according to whether a mucosal specimen is needed for analysis. Biopsy-based tests include histological evaluation, culture, polymerase chain reaction, and the rapid urease test (RUT). Alternatively, non-invasive methods may include the urea breath test (UBT), serology, and the stool antigen test (SAT). A meta-analysis has revealed the following pooled sensitivity and specificity for different methods: RUT 0.67 and 0.93; histology 0.70 and 0.90; culture 0.45 and 0.98; UBT 0.93 and 0.92; SAT 0.87 and 0.70; and serology 0.88 and 0.69 [46], respectively, which clearly demonstrates that each of the different tests has its own limitations, and a single negative test does not exclude H. pylori infection.

Current or recent use of antibiotics or proton pump inhibitors (PPIs) is known to influence the accuracy of H. pylori tests. Bacterial concentrations are decreased by these medications, leading to false-negative results. A number of studies have demonstrated a lower yield in testing for H. pylori infection in patients receiving antibiotic therapy. Borody et al. [17] showed that ~22% of H. pylori-negative DU patients were reported to have used antibiotics recently. Gisbert et al. [33] also found a lower prevalence of H. pylori in DU patients who had prior antibiotic therapy compared with those who did not (78% vs. 96%). In another study, the prevalence of H. pylori-negative DU was shown to be much lower when patients taking antibiotics within 4 weeks of testing were excluded [47]. In addition, the use of PPIs and histamine-2 receptor antagonists (H2RAs) can also cause false-negative results by reducing gastric acid secretion and inhibiting the growth of H. pylori. Approximately one-third of patients who remained positive for H. pylori infection had a negative UBT result while receiving PPIs [48]. The study even showed that the proportion of patients whose UBT results turned out to be positive after completion of PPIs therapy were 91% at 3 days, 97% at 7 days, and 100% at 14 days [48]. Chey et al. [49] also demonstrated that both PPIs and H2RAs could affect the sensitivity of UBT, with an equivocal or false-negative result of 61% and 18%, respectively.

RUT can also yield a false-negative result during an actively bleeding stage of PUD. Lee et al. [50] have found that the prevalence of H. pylori infection in patients presenting with bleeding DU was 72.7%, which was lower than the prevalence of 92.8% in those with non-bleeding peptic ulcers (p < 0.05). The false-negative rate of RUT for bleeding ulcer has been reported to be up to 25% [50]. In another study, 55.1% of patients with bleeding ulcers with an initially negative RUT result were discovered to have a positive result at follow-up endoscopy [23]. Lee et al. [51] have demonstrated that the low sensitivity of RUT (61%) for diagnosis of H. pylori infection during bleeding peptic ulcer can be overcome by increasing the number of biopsies from the gastric antrum to 74% or from the gastric body to 73%. Some investigators speculate that these results reflect a buffering effect of serum albumin on the pH indicator of the RUT [52].

The location and number of biopsies taken are also important for the diagnostic accuracy of both RUTs and histological results [33,45,53,54]. The distribution of H. pylori can be sporadic and variable in the stomach when intestinal metaplasia or atrophic gastritis develops. By histological examination, < 3% of antral biopsy specimens yielded a false-negative interpretation, compared with 6% to 9% of those from the corpus (p = 0.02) [54]. Another study based on 1,000 biopsy specimens has shown that the area of H. pylori colonization was larger than the area of active chronic gastritis, suggesting that H. pylori colonization may precede the development of active chronic gastritis [53]. In the presence of atrophic gastritis or intestinal metaplasia, H. pylori is prone to disappear from the gastric mucosa with such a histological change [55]. Therefore, it is postulated that H. pylori may migrate proximally from the antrum to the corpus because of lack of acid in the atrophic antrum. A meta-analysis has suggested that the sensitivities of RUT and histology could be improved to 78% and 83%, respectively, if biopsies were taken from both the antrum and the corpus of the stomach [46].

Unrecognized use of ulcerogenic drugs

Surreptitious use of medications or lack of medication history with regard to ulcerogenic drugs may be of paramount importance when encountering H. pylori-negative PUD. By testing the blood for drugs, some studies have shown that a substantial number of users of ulcerogenic drugs cannot provide a correct description of their medication history [56,57]. Using the platelet cyclo-oxygenase activity test, 12.7% more users of aspirin could be identified than the number obtained by clinical history alone. Sixty-six percent of NSAID users were actually taking aspirin, alone or in combination with other NSAIDS, and 59.3% of patients who claimed no (non-aspirin) NSAID use were actually using NSAIDs [57]. Blood salicylic acid concentrations revealed that about half of patients with intractable PUD who denied using aspirin were actually aspirin users [56]. Ong et al. [27] also found that when serum thromboxane B2 levels were checked, more than 30% of patients who were thought to have IPUD were found to have taken NSAIDs. Other possible non-NSAID, non-aspirin, ulcer-related drugs include steroids, potassium chloride, nitrogen-containing bisphosphonates, and some immunosuppressive medications [58,59]. Visible gastric mucosal damage was found in 38% of patients who received alendronate as compared to 13% in the placebo group [59]. The results demonstrate that a valid review of medication history is mandatory before making the diagnosis of IPUD.

Excluding malignancies

Follow-up endoscopy is necessary in IPUD, especially in those patients who have alarming symptoms or recurrent ulcers, to determine whether there are secondary causes or undiscovered malignancies (Fig. 2). In fact, ~5% of endoscopically benign-appearing GUs are malignant [60,61]. Endoscopic surveillance of the gastric pre-malignant condition has been useful in identifying early-stage malignancy at 3- to 6-month follow-up visits scheduled to confirm that the GU is healed [62,63]. Although the optimal interval for endoscopic surveillance remains to be determined, repeat endoscopic biopsies, obtaining sufficient tissue involving submucosa, or targeted optical biopsy by image-enhanced endoscopy is a reasonable approach for IPUD [64].

Figure 2.

A case of gastric ulcer with a missed diagnosis of gastric cancer. (A) One healing gastric ulcer was seen at the lesser curvature of the lower body. A biopsy showed only chronic inf lammation. (B) The ulcer remained present on follow-up endoscopy at 3 months despite continuous proton-pump inhibitor treatment. A repeated biopsy showed a well-differentiated adenocarcinoma. (C) An image of the tumor margin delineated by arrows under chromoendoscopy with indigo carmine spraying before endoscopic resection. (D) An image of the en bloc resected specimen.

Excluding rare etiologies

Rare etiologies for PUD may include unusual systemic diseases and unusual infectious pathogens. Uncommon systemic diseases, such as Crohn’s disease (Fig. 3), mastocytosis, amyloidosis, sarcoidosis, vasculitis, eosinophilic gastroenteritis, and Zollinger-Ellison syndrome (Fig. 4), are possible sources of the upper gastrointestinal manifestations of PUD. Screening of the lower gastrointestinal tract for Crohn’s disease and specific laboratory and radiological tests (such as repeated measurement of serum fasting gastrin, secretin stimulation test, quantification of gastric acid secretion, measurement of serum chromogranin A, radiological studies, and endoscopic ultrasound for Zollinger-Ellison syndrome) are needed to exclude these uncommon diseases. Rare infectious causes of PUD may include Helicobacter heilmanii, tuberculosis, syphilis, cytomegalovirus (Fig. 5), herpes simplex virus, and fungal infection (Fig. 6).

Figure 3.

A case of Crohn’s disease with upper gastrointestinal manifestations. (A) One oral ulcer was found on the soft palate. (B) One gastric ulcer was noted on the posterior wall of the antrum. (C) Upon colonoscopic examination, multiple colonic ulcers were seen with a cobblestone appearance over the ascending colon and (D) descending colon.

Figure 4.

A case of hyperacidity of the stomach due to Zollinger-Ellison syndrome. (A) Repeat upper endoscopy showed poorly healed duodenal ulcers and (B) reflux erosive esophagitis, suggestive of gastric acid over-production. (C) Upon abdominal sonography, a pancreatic tumor originating from the uncinate process of the pancreas was noted. (D) The pancreatic tumor specimen was confirmed as a neuroendocrine tumor (circle).

Figure 5.

A case of gastric and duodenal ulcers due to cytomegalovirus infection. Multiple areas of erythema were found over the lower body (A) and antrum of the stomach (B) with a negative Helicobacter pylori test. (C) A bleeding ulcer was noted on the posterior wall of the gastric antrum. (D) Diffuse ulcerations in the jejunum found by the balloon-assisted enteroscopy. A biopsy was positive for cytomegalovirus inclusion bodies.

Figure 6.

A case of a mucormycosis-related gastric ulcer. (A) Upon upper endoscopy, a gastric ulcer with greenish coating was noted in the greater curvature of the middle body. (B) Pathology showed numerous right-angled, pauci-septated, and ribbon-like hyphae (arrows), indicating a fungal infection (H&E, ×100).

In summary, accurate diagnosis of classic IPUD requires a systematic approach as outlined in Table 2. Confirmation of H. pylori infection status of the stomach and duodenum by at least three parallel tests is recommended to decrease the risk of a false-negative result. Thorough review of medication history is important to identify the use of potential ulcerogenic drugs. Moreover, a complete histological study of a benign-appearing ulcerative lesion is crucial to rule out the possibility of malignancy. Repeat endoscopic biopsies, optical targeted biopsy, or obtaining tissues deeper than the mucosal layer may improve diagnostic accuracy. Zollinger-Ellison syndrome should always be kept in mind when encountering poorly-healed peptic ulcers. Finally, rare infectious agents should be considered in the differential diagnosis, especially in immunocompromised subjects.

Table 2.

Considerations to review prior to making a diagnosis of idiopathic peptic ulcer

RISK FACTORS AND THE CLINICAL COURSE OF CLASSICAL IPUD

Risk factors for classical IPUD may include demographic risk factors, use of psychoactive substances, genetic risk factors, comorbid diseases, chronic mesenteric ischemia, and higher psychological stress (Table 1, lower panel).

Demographic factors, such as being Caucasian and older age, are associated with IPUD. A greater prevalence of H. pylori-negative ulcers was found in whites than in non-whites in previous studies [13,15]. In multi-racial studies, a greater prevalence of H. pylori-negative DUs was found in Malays and Chinese than in Indians [7,65]. Molecular changes in gastric protective factors, such as mucin, are also hypothesized to be associated with risk of ulcers. The gastric protective layer, which prevents enzymatic attachment by gastric acid, pepsin, and other aggressive factors, is created by secreted mucin. Structural changes of membrane-bound mucin and glycan side-chain sialic acids are associated with protective efficiency against offending factors. Based on an immunochemical study of ulcer tissues, cytoplasmic MUC17 staining intensity was significantly lower in patients with IPUD than in those with H. pylori-related peptic ulcer [66]. In addition to genetic or epigenetic changes in the gastric mucin molecule, the HLA-DQA1*0102 allele was associated with increased risk of IPUD [67,68]. Ethnic differences in the prevalence of H. pylori-negative PUD may correlate with different lifestyles or unknown genetic factors. Several studies in different areas have demonstrated that patients with IPUD are significantly older than those with PUD associated with H. pylori or NSAID use [23,26,27,34,69].

Older age was associated with a significantly lower level of prostaglandin concentration in the fundus, antrum, and post-bulbar duodenum [70]. Because prostaglandins protect the gastric mucosa from damage, diminished synthesis in elderly subjects makes their mucosa more susceptible to aggressive factors, followed by the ulcerogenic process. Moreover, older patients have higher risk for vascular disease, especially chronic mesenteric ischemia [71]. A combination of risk factors, including reduced blood flow, decreased production of prostaglandins by the stomach, a higher prevalence of concomitant diseases, and a higher American Society of Anesthesiologists score in the elderly render the mucosa more fragile and, thus, PUD is more likely to develop [16,72,73]. Cigarette smoking also increases xanthine oxidase activity, production of leukotrienes and nitric oxide, and neutrophil infiltration into the gastric mucosa [72]. An association between psychological stress and PUD has long been suggested. Two recent studies of Japanese victims of the Great East Japan Earthquake and Tsunami that occurred in 2011 have found that the incidence of PUD increased significantly after the psychological trauma [74,75]. In the first 3 months after the earthquake, the incidence of PUD was increased 1.5 fold, and the incidence of bleeding PUD was increased 2.2 fold [74,75]. Furthermore, after the earthquake, the proportion of IPUD doubled from 13% in 2010 to 24% in 2011 (p < 0.05) [75]. A population-based study of 3,379 Danish adults in 1982 to 1983 revealed a greater incidence of ulcers among subjects in the highest tertile of stress scores (3.5%) than in those in the lowest tertile (1.6%; p < 0.01) and high psychological stress has been identified as an independent risk factor for PUD on multivariate analysis (odds ratio, 1.12 per point increment of stress index; 95% confidence interval [CI], 1.01 to 1.23; p = 0.03) [76].

The clinical course of IPUD remains poorly understood because of the heterogeneity of diagnostic methods and populations recruited for studies. Nevertheless, idiopathic ulcer disease tends to cause longer-lasting ulceration, a greater recurrence rate and mortality rate, and greater symptoms of dyspepsia. In addition, it is more refractory to treatment than H. pylori-positive ulcer disease [26,77-84]. Furthermore, IPUD is also more likely to present with hemorrhage, and multiple and larger ulcers [84]. After a bleeding episode, the risk of recurrent ulcer complications within 12 months was higher in patients with H. pylori-negative PUD than in those with H. pylori-related PUD after eradication therapy (13.4% vs. 2.5%, p < 0.001) [26]. In Hong Kong, a 7-year cohort study has shown that the cumulative incidence of recurrent bleeding from ulcers was higher in the H. pylori-negative ulcer cohort than in the positive cohort (42.3% vs. 11.2%, p < 0.0001), and more patients died in the H. pylori-negative ulcer cohort than in the H. pylori-positive ulcer cohort (87.6% vs. 37.3%, p < 0.0001) [84]. A randomized trial with a 2-year follow-up period consistently showed that the prognosis of H. pylori-negative ulcers was poorer [81]. The rates of recurrent ulcer or ulcer that has not healed (35% vs. 26%), and relapse of dyspepsia symptoms (16% vs. 7%) were higher in those with H. pylori-negative ulcers than in those with H. pylori-positive ulcers [81].

MANAGEMENT OF IDIOPATHIC PEPTIC ULCER DISEASE

As IPUD is increasingly encountered, whether we should modify the standard treatment of PUD, including short-term PPI therapy and once-off H. pylori eradication, is of clinical significance. Based on present knowledge regarding a poorer response to acid-suppressing therapy in IPUD than in H. pylori-positive ulcers, anti-secretory medication remains the mainstay of treatment [77]. In a Danish study, outcomes in PPI-treated patients with DU did not differ according to H. pylori status, which suggested that PPI therapy was effective in the prevention of recurrence of IPUD [81]. In contrast, another study from Hong Kong demonstrated that the risk of re-bleeding (2.9 per 100 person-years vs. 1.1 per 100 person-years, p < 0.001) and mortality (hazard ratio, 1.1; 95% CI, 0.6 to 1.7) were not reduced by gastro-protective agents in patients with bleeding IPUD [30]. Gillen et al. [85] found that H. pylori infection may potentiate the anti-secretory effect of PPIs. During PPI administration, median basal intragastric pH was higher in the H. pylori-positive (7.95) versus -negative (3.75) subjects (p < 0.002) [85]. The poorer response to the anti-secretory therapy and altered gastric physiology of IPUD could indicate the necessity of longer duration and higher dose of acid-suppressing agents. Quan and Talley [45] have proposed a flow chart for the management of IPUD (Fig. 7). After excluding gastric H. pylori infection (by multiple testing with a parallel interpretation of results) and the use of common ulcerogenic medications, the diagnosis of clinical IPUD is made. PPIs administration for 4 to 8 weeks is recommended, and a longer duration of therapy may be needed for complicated ulcer (e.g., bleeding or perforated). Otherwise, patients with uncomplicated ulcer disease may wean off therapy with a wait-and-see strategy, or receive on-demand/maintenance PPI therapy if symptoms recur. Re-evaluation of IPUD by endoscopy should be considered. If healing is slow or absent, items listed in Table 2 should be re-evaluated to confirm whether classic IPUD is the correct diagnosis.

Figure 7.

A f low chart for the diagnosis and management of an idiopathic peptic ulcer disease. H. pylori, Helicobacter pylori; NSAID, nonsteroidal anti-inflammatory drug; ASA, acetylsalicylic acid (aspirin); H2RA, histamine-2 receptor antagonists; PPI, proton pump inhibitor. Adapted from Quan et al. [45], with permission from Nature Publishing Group.

CONCLUSIONS

An increase in the proportion of idiopathic ulcers has been confirmed worldwide, and peptic ulcer, once considered to be an infectious disease after the discovery of H. pylori, has gradually reverted to the original “no acid, no ulcer” theory. Given that the prognosis of IPUD is poorer than that of PUD associated with H. pylori or NSAIDs, careful evaluation of H. pylori infection by multiple parallel tests, detailed review of medication history, and thorough exclusion of other possible causes are of paramount importance before making the diagnosis of IPUD. Further well-designed clinical trials are needed to elucidate the natural history of IPUD, and to optimize the treatment strategy for this emerging disease.

Notes

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

References

1. Infection with Helicobacter pylori. IARC Monogr Eval Carcinog Risks Hum 1994;61:177–240.

2. Torres J, Lopez L, Lazcano E, Camorlinga M, Flores L, Munoz O. Trends in Helicobacter pylori infection and gastric cancer in Mexico. Cancer Epidemiol Biomarkers Prev 2005;14:1874–1877.

3. Kuipers EJ, Thijs JC, Festen HP. The prevalence of Helicobacter pylori in peptic ulcer disease. Aliment Pharmacol Ther 1995;9 Suppl 2:59–69.

4. Lee YC, Chen TH, Chiu HM, et al. The benefit of mass eradication of Helicobacter pylori infection: a community-based study of gastric cancer prevention. Gut 2013;62:676–682.

5. IARC Helicobacter pylori Working Group. Helicobacter pylori eradication as a strategy for gastric cancer prevention (IARC Working Group Reports, No. 8) [Internet]. Lyon (FR): International Agency for Research on Cancer; c2015. [cited 2015 Jun 22]. Available from: http://www.iarc.fr/en/publications/pdfs-online/wrk/wrk8/index.php.

6. Xia B, Xia HH, Ma CW, et al. Trends in the prevalence of peptic ulcer disease and Helicobacter pylori infection in family physician-referred uninvestigated dyspeptic patients in Hong Kong. Aliment Pharmacol Ther 2005;22:243–249.

7. Uyub AM, Raj SM, Visvanathan R, et al. Helicobacter pylori infection in north-eastern peninsular Malaysia: evidence for an unusually low prevalence. Scand J Gastroenterol 1994;29:209–213.

8. Sugiyama T, Nishikawa K, Komatsu Y, et al. Attributable risk of H. pylori in peptic ulcer disease: does declining prevalence of infection in general population explain increasing frequency of non-H. pylori ulcers? Dig Dis Sci 2001;46:307–310.

9. Singh V, Trikha B, Nain CK, Singh K, Vaiphei K. Epidemiology of Helicobacter pylori and peptic ulcer in India. J Gastroenterol Hepatol 2002;17:659–665.

10. Asaka M, Kimura T, Kudo M, et al. Relationship of Helicobacter pylori to serum pepsinogens in an asymptomatic Japanese population. Gastroenterology 1992;102:760–766.

11. Musumba C, Jorgensen A, Sutton L, et al. The relative contribution of NSAIDs and Helicobacter pylori to the aetiology of endoscopically-diagnosed peptic ulcer disease: observations from a tertiary referral hospital in the UK between 2005 and 2010. Aliment Pharmacol Ther 2012;36:48–56.

12. Graham DY, Large U.S. clinical trials report a high proportion of H. pylori negative duodenal ulcers at study entry as well as a high recurrence rate after cure of the infection: have we all been wrong? Gastroenterology 1998;114(Suppl 1):A17.

13. Nensey YM, Schubert TT, Bologna SD, Ma CK. Helicobacter pylori-negative duodenal ulcer. Am J Med 1991;91:15–18.

14. Sprung DJ, Apter MN. What is the role of Helicobacter pylori in peptic ulcer and gastric cancer outside the big cities? J Clin Gastroenterol 1998;26:60–63.

15. Jyotheeswaran S, Shah AN, Jin HO, Potter GD, Ona FV, Chey WY. Prevalence of Helicobacter pylori in peptic ulcer patients in greater Rochester, NY: is empirical triple therapy justified? Am J Gastroenterol 1998;93:574–578.

16. Charpignon C, Lesgourgues B, Pariente A, et al. Peptic ulcer disease: one in five is related to neither Helicobacter pylori nor aspirin/NSAID intake. Aliment Pharmacol Ther 2013;38:946–954.

17. Borody TJ, George LL, Brandl S, et al. Helicobacter pylori-negative duodenal ulcer. Am J Gastroenterol 1991;86:1154–1157.

18. Higuchi K, Arakawa T, Fujiwara Y, et al. Is Helicobacter pylori-negative duodenal ulcer masked by the high prevalence of H. pylori infection in the general population? Am J Gastroenterol 1999;94:3083–3084.

19. Tsuji H, Kohli Y, Fukumitsu S, et al. Helicobacter pylori-negative gastric and duodenal ulcers. J Gastroenterol 1999;34:455–460.

20. Arakawa T1, Higuchi K, Fujiwara Y, et al. Helicobacter pylori: criminal or innocent bystander? J Gastroenterol 2000;35 Suppl 12:42–46.

21. Aoyama N, Shinoda Y, Matsushima Y, et al. Helicobacter pylori-negative peptic ulcer in Japan: which contributes most to peptic ulcer development, Helicobacter pylori, NSAIDS or stress? J Gastroenterol 2000;35 Suppl 12:33–37.

22. 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.

23. Chan HL, Wu JC, Chan FK, et al. Is non-Helicobacter pylori, non-NSAID peptic ulcer a common cause of upper GI bleeding? A prospective study of 977 patients. Gastrointest Endosc 2001;53:438–442.

24. Kamada T, Haruma K, Kusunoki H, et al. Significance of an exaggerated meal-stimulated gastrin response in pathogenesis of Helicobacter pylori-negative duodenal ulcer. Dig Dis Sci 2003;48:644–651.

25. Chu KM, Kwok KF, Law S, Wong KH. Patients with Helicobacter pylori positive and negative duodenal ulcers have distinct clinical characteristics. World J Gastroenterol 2005;11:3518–3522.

26. Hung LC, Ching JY, Sung JJ, et al. Long-term outcome of Helicobacter pylori-negative idiopathic bleeding ulcers: a prospective cohort study. Gastroenterology 2005;128:1845–1850.

27. Ong TZ, Hawkey CJ, Ho KY. Nonsteroidal anti-inflammatory drug use is a significant cause of peptic ulcer disease in a tertiary hospital in Singapore: a prospective study. J Clin Gastroenterol 2006;40:795–800.

28. Jang HJ, Choi MH, Shin WG, et al. Has peptic ulcer disease changed during the past ten years in Korea? A prospective multi-center study. Dig Dis Sci 2008;53:1527–1531.

29. Chen TS, Luo JC, Chang FY. Prevalence of Helicobacter pylori infection in duodenal ulcer and gastro-duodenal ulcer diseases in Taiwan. J Gastroenterol Hepatol 2010;25:919–922.

30. Wong GL, Au KW, Lo AO, et al. Gastroprotective therapy does not improve outcomes of patients with Helicobacter pylori-negative idiopathic bleeding ulcers. Clin Gastroenterol Hepatol 2012;10:1124–1129.

31. Kim JJ, Kim N, Park HK, et al. Clinical characteristics of patients diagnosed as peptic ulcer disease in the third referral center in 2007. Korean J Gastroenterol 2012;59:338–346.

32. 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.

33. Gisbert JP, Blanco M, Mateos JM, et al. H. pylori-negative duodenal ulcer prevalence and causes in 774 patients. Dig Dis Sci 1999;44:2295–2302.

34. 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.

35. Arents NL, Thijs JC, van Zwet AA, Kleibeuker JH. Does the declining prevalence of Helicobacter pylori unmask patients with idiopathic peptic ulcer disease? Trends over an 8 year period. Eur J Gastroenterol Hepatol 2004;16:779–783.

36. Sbrozzi-Vanni A, Zullo A, Di Giulio E, et al. Low prevalence of idiopathic peptic ulcer disease: an Italian endoscopic survey. Dig Liver Dis 2010;42:773–776.

37. Vu C, Ng YY. Prevalence of Helicobacter pylori in peptic ulcer disease in a Singapore hospital. Singapore Med J 2000;41:478–481.

38. Yakoob J, Jafri W, Jafri N, et al. Prevalence of non-Helicobacter pylori duodenal ulcer in Karachi, Pakistan. World J Gastroenterol 2005;11:3562–3565.

39. Ootani H, Iwakiri R, Shimoda R, et al. Role of Helicobacter pylori infection and nonsteroidal anti-inflammatory drug use in bleeding peptic ulcers in Japan. J Gastroenterol 2006;41:41–46.

40. Goenka MK, Majumder S, Sethy PK, Chakraborty M. Helicobacter pylori negative, non-steroidal anti-inflammatory drug-negative peptic ulcers in India. Indian J Gastroenterol 2011;30:33–37.

41. Kang JM, Seo PJ, Kim N, et al. Analysis of direct medical care costs of peptic ulcer disease in a Korean tertiary medical center. Scand J Gastroenterol 2012;47:36–42.

42. Uyanikoglu A, Danalioglu A, Akyuz F, et al. Etiological factors of duodenal and gastric ulcers. Turk J Gastroenterol 2012;23:99–103.

43. Yoon H, Kim SG, Jung HC, Song IS. High recurrence rate of idiopathic peptic ulcers in long-term follow-up. Gut Liver 2013;7:175–181.

44. Chow DK, Sung JJ. Non-NSAID non-H. pylori ulcer disease. Best Pract Res Clin Gastroenterol 2009;23:3–9.

45. Quan C, Talley NJ. Management of peptic ulcer disease not related to Helicobacter pylori or NSAIDs. Am J Gastroenterol 2002;97:2950–2961.

46. Gisbert JP, Abraira V. Accuracy of Helicobacter pylori diagnostic tests in patients with bleeding peptic ulcer: a systematic review and meta-analysis. Am J Gastroenterol 2006;101:848–863.

47. Raj SM, Yap K, Haq JA, Singh S, Hamid A. Further evidence for an exceptionally low prevalence of Helicobacter pylori infection among peptic ulcer patients in north-eastern peninsular Malaysia. Trans R Soc Trop Med Hyg 2001;95:24–27.

48. Laine L, Estrada R, Trujillo M, Knigge K, Fennerty MB. Effect of proton-pump inhibitor therapy on diagnostic testing for Helicobacter pylori. Ann Intern Med 1998;129:547–550.

49. Chey WD, Woods M, Scheiman JM, Nostrant TT, DelValle J. Lansoprazole and ranitidine affect the accuracy of the 14C-urea breath test by a pH-dependent mechanism. Am J Gastroenterol 1997;92:446–450.

50. Lee JM, Breslin NP, Fallon C, O’Morain CA. Rapid urease tests lack sensitivity in Helicobacter pylori diagnosis when peptic ulcer disease presents with bleeding. Am J Gastroenterol 2000;95:1166–1170.

51. Lee TH, Lin CC, Chung CS, Lin CK, Liang CC, Tsai KC. Increasing biopsy number and sampling from gastric body improve the sensitivity of rapid urease test in patients with peptic ulcer bleeding. Dig Dis Sci 2015;60:454–457.

52. Leung WK, Sung JJ, Siu KL, Chan FK, Ling TK, Cheng AF. False-negative biopsy urease test in bleeding ulcers caused by the buffering effects of blood. Am J Gastroenterol 1998;93:1914–1918.

53. Bayerdorffer E, Oertel H, Lehn N, et al. Topographic association between active gastritis and Campylobacter pylori colonisation. J Clin Pathol 1989;42:834–839.

54. Genta RM, Graham DY. Comparison of biopsy sites for the histopathologic diagnosis of Helicobacter pylori: a topographic study of H. pylori density and distribution. Gastrointest Endosc 1994;40:342–345.

55. Craanen ME, Dekker W, Blok P, Ferwerda J, Tytgat GN. Intestinal metaplasia and Helicobacter pylori: an endoscopic bioptic study of the gastric antrum. Gut 1992;33:16–20.

56. Hirschowitz BI, Lanas A. Intractable upper gastrointestinal ulceration due to aspirin in patients who have undergone surgery for peptic ulcer. Gastroenterology 1998;114:883–892.

57. Lanas A, Serrano P, Bajador E, Esteva F, Benito R, Sainz R. Evidence of aspirin use in both upper and lower gastrointestinal perforation. Gastroenterology 1997;112:683–689.

58. Blank MA, Ems BL, Gibson GW, et al. Nonclinical model for assessing gastric effects of bisphosphonates. Dig Dis Sci 1997;42:281–288.

59. Graham DY, Malaty HM. Alendronate gastric ulcers. Aliment Pharmacol Ther 1999;13:515–519.

60. Pruitt RE, Truss CD. Endoscopy, gastric ulcer, and gastric cancer: follow-up endoscopy for all gastric ulcers? Dig Dis Sci 1993;38:284–288.

61. Podolsky I, Storms PR, Richardson CT, Peterson WL, Fordtran JS. Gastric adenocarcinoma masquerading endoscopically as benign gastric ulcer: a five-year experience. Dig Dis Sci 1988;33:1057–1063.

62. Saini SD, Eisen G, Mattek N, Schoenfeld P. Utilization of upper endoscopy for surveillance of gastric ulcers in the United States. Am J Gastroenterol 2008;103:1920–1925.

63. Breslin NP, Sutherland LR. Survey of current practices among members of CAG in the follow-up of patients diagnosed with gastric ulcer. Can J Gastroenterol 1999;13:489–493.

64. Kaltenbach T, Sano Y, Friedland S, Soetikno R, ; American Gastroenterological Association. American Gastroenterological Association (AGA) Institute technology assessment on image-enhanced endoscopy. Gastroenterology 2008;134:327–340.

65. Goh KL. Prevalence of and risk factors for Helicobacter pylori infection in a multi-racial dyspeptic Malaysian population undergoing endoscopy. J Gastroenterol Hepatol 1997;12:S29–S35.

66. Niv Y, Boltin D, Halpern M, et al. Membrane-bound mucins and mucin terminal glycans expression in idiopathic or Helicobacter pylori, NSAID associated peptic ulcers. World J Gastroenterol 2014;20:14913–14920.

67. Niv Y, Boltin D. Secreted and membrane-bound mucins and idiopathic peptic ulcer disease. Digestion 2012;86:258–263.

68. Azuma T, Konishi J, Ito Y, et al. Genetic differences between duodenal ulcer patients who were positive or negative for Helicobacter pylori. J Clin Gastroenterol 1995;21 Suppl 1:S151–S154.

69. Xia HH, Wong BC, Wong KW, et al. Clinical and endoscopic characteristics of non-Helicobacter pylori, nonNSAID duodenal ulcers: a long-term prospective study. Aliment Pharmacol Ther 2001;15:1875–1882.

70. Cryer B, Redfern JS, Goldschmiedt M, Lee E, Feldman M. Effect of aging on gastric and duodenal mucosal prostaglandin concentrations in humans. Gastroenterology 1992;102(4 Pt 1):1118–1123.

71. Lee YC, Yen AM, Tai JJ, et al. The effect of metabolic risk factors on the natural course of gastro-oesophageal reflux disease. Gut 2009;58:174–181.

72. Ma L, Chow JY, Cho CH. Effects of cigarette smoking on gastric ulcer formation and healing: possible mechanisms of action. J Clin Gastroenterol 1998;27 Suppl 1:S80–S86.

73. Luo JC, Leu HB, Hou MC, et al. Cirrhotic patients at increased risk of peptic ulcer bleeding: a nationwide population-based cohort study. Aliment Pharmacol Ther 2012;36:542–550.

74. Kanno T, Iijima K, Abe Y, et al. Hemorrhagic ulcers after Great East Japan Earthquake and Tsunami: features of post-disaster hemorrhagic ulcers. Digestion 2013;87:40–46.

75. Kanno T, Iijima K, Abe Y, et al. Peptic ulcers after the Great East Japan earthquake and tsunami: possible existence of psychosocial stress ulcers in humans. J Gastroenterol 2013;48:483–490.

76. Levenstein S, Rosenstock S, Jacobsen RK, Jorgensen T. Psychological stress increases risk for peptic ulcer, regardless of Helicobacter pylori infection or use of nonsteroidal anti-inflammatory drugs. Clin Gastroenterol Hepatol 2015;13:498.e1–506.e1.

77. Freston JW. Review article: role of proton pump inhibitors in non-H. pylori-related ulcers. Aliment Pharmacol Ther 2001;15 Suppl 2:2–5.

78. Freston JW. Helicobacter pylori-negative peptic ulcers: frequency and implications for management. J Gastroenterol 2000;35 Suppl 12:29–32.

79. Howden CW, Leontiadis GI. Current indications for acid suppressants in Helicobacter pylori-negative ulcer disease. Best Pract Res Clin Gastroenterol 2001;15:401–412.

80. McColl KE. Helicobacter pylori-negative ulcer disease. J Gastroenterol 2000;35 Suppl 12:47–50.

81. Bytzer P, Teglbjaerg PS PS, ; Danish Ulcer Study Group. Helicobacter pylori-negative duodenal ulcers: prevalence, clinical characteristics, and prognosis: results from a randomized trial with 2-year follow-up. Am J Gastroenterol 2001;96:1409–1416.

82. Hyvarinen H, Salmenkyla S, Sipponen P. Helicobacter pylori-negative duodenal and pyloric ulcer: role of NSAIDs. Digestion 1996;57:305–309.

83. McColl KE, el-Nujumi AM, Chittajallu RS, et al. A study of the pathogenesis of Helicobacter pylori negative chronic duodenal ulceration. Gut 1993;34:762–768.

84. Wong GL, Wong VW, Chan Y, et al. High incidence of mortality and recurrent bleeding in patients with Helicobacter pylori-negative idiopathic bleeding ulcers. Gastroenterology 2009;137:525–531.

85. Gillen D, Wirz AA, Neithercut WD, Ardill JE, McColl KE. Helicobacter pylori infection potentiates the inhibition of gastric acid secretion by omeprazole. Gut 1999;44:468–475.

Article information Continued

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.