Background
Helicobacter pylori (H. pylori) and gastritis with atrophy are both risk factors for gastric cancer [
1]. Around one-third of infected patients are estimated to have gastritis with atrophy [
2] and the regression of these pre-neoplasm lesions may occur after successful eradication [
3‐
5]. As such,
H. pylori eradication in patients with gastritis with atrophy is recommended by current guidelines [
1,
6,
7].
Although eradication is essential for this group of patients, the accurate identification of
H. pylori against a background of gastritis with atrophy remains difficult [
8]. False negative results occur even under more reliable
H. pylori diagnostic tests like histology Giemsa stain [
9]. False negative status, or the so-called sampling error, may result from patchy bacterial colonization through the stomach and altered distribution because of gastritis with atrophy and intestinal metaplasia. Thus, it is important to set a recommended biopsy site.
The updated Sydney Classification had set the gold standard for gastric biopsy more than 10 years ago [
10]. According to this Classification, five biopsy sites should be collected: one specimen each should be obtained from the lesser and the greater curvature of the antrum, both within 2–3 cm form the pylorus; from the lesser curvature of the corpus about 4 cm proximal to the angulus; from the middle portion of the greater curvature of the corpus, approximately 8 cm from the cardia; and one from incisura angularis. However, for the consideration of patient’s comfort and operator’s convenience, this kind of extensive approach is uncommon in our daily practice. Studies on the most practical biopsy site for diagnosing
H. pylori infection have conflicting results. Antrum biopsy is recommended by Genta et al. [
11] while others recommend at least one corpus biopsy [
12,
13]. Hazell et al. and Woo et al. found it necessary to take both antral and corpus biopsies [
14,
15]. According to current guidelines, there is no optimal site when performing a biopsy-based test in a general condition, much less in those with gastritis with atrophy [
16].
It is suggested that as gastritis with atrophy progresses, the mid corpus is the last area involved and is the last “lodgeable” mucosa for
H. pylori in the stomach [
17,
18]. Additional corpus biopsy is suggested in these situations [
12] but the exact additional benefit is not well known.
This prospectively designed study used the combination method as gold standard to investigate the correlation among sensitivity of biopsy-based test, biopsy location, degree of gastritis with atrophy, and H. pylori prevalence rate.
Methods
Patient population
Dyspeptic patients scheduled for upper gastrointestinal endoscopy were recruited. Patients with any of the following conditions were excluded: (1) ulcer complications (e.g., bleeding, stenosis, or perforation); (2) previous stomach surgery; (3) gastric neoplasms; (4) use of any substituted benzimidazoles and bismuth-containing preparations within the last 7 days prior to the start of the study; (5) past or current treatment with anti-H. pylori therapy; or (6) severe systemic diseases. All patients provided prior informed consent and received invasive and non-invasive tests for H. pylori. The local Ethics Committee on Human Test approved the study.
Endoscopy and biopsy sampling
According to the updated Sydney system, the biopsy sampling protocol required that more than five biopsy samples were obtained: two from the antral mucosa; one from the mucosa of the angularis incisura; two from the oxyntic area. For the consideration of patients’ comfort and operator’s convenience, we modified this recommendation. Two biopsy sites with multiple biopsies were applied to our endoscopy biopsy protocol. Three sets of biopsy specimens each from the greater curvature of the mid-body and lesser curvature of the antrum near the incisura were obtained during endoscopy for urease, histologic, and culture tests.
Rapid urease test
One biopsy from the greater curvature of the mid-body and one from the lesser curvature near the incisura were obtained for the urease test (CLO test; Delta West, Bentley, Australia). Antral and body biopsy specimens were evaluated separately, and the test was considered positive when the color changed from orange to pink within 24 hours.
Histologic evaluation of the biopsy samples
Biopsy specimens from the antrum and the body were fixed in formalin and assessed for the presence of
H. pylori by a modified Giemsa stain, and for the degree of inflammatory cell infiltration, atrophy, and intestinal metaplasia by hematoxylin and eosin staining. The antrum and body histologic features of gastric mucosa were graded according to the updated Sydney System (0, none; 1, mild; 2, moderate; and 3, severe) [
10]. In addition, the degree of gastritis activity was evaluated in Giemsa-negative patients with positive for either rapid urease test or serology. Also, the activity of gastritis was recorded according to the updated Sydney System. (1–4 points with 1 representing “normal”, 2 to 4 representing “mildly, moderately and markedly active gastritis”, respectively). Those who got two or more points on the pathological review were regarded as active gastritis which is an indirect sign of
H. pylori infection. An experienced pathologist (Anna Fen-Yau Li) who was blinded to the results of other tests for
H. pylori evaluated all histologic sections.
Culture
In culture, the biopsy sample was homogenized with 0.3 mL broth, plated on chocolate agar, and incubated at 37°C in a micro-aerobic (15% CO2 and 5% O2) incubator until the colony appeared, which was usually 3 days. The negative plates were kept for 7 days. The growth of H. pylori was confirmed by the characteristic morphology (Gram-negative and curved) and positive catalase, oxidase, and urease reactions observed.
Serologic evaluation
Serum specimens were tested for the presence of IgG antibodies against H. pylori using a quantitative ELISA test (HEL-pTEST II; AMRAD, Kew, Australia) according to the manufacturer’s instructions. A specimen was considered positive if it contained >50 units/mL and negative if it contained ≤50 units/mL.
Serum pepsinogen levels
For serology studies, blood was drawn immediately after endoscopy and collected and stored at −70°C until assay. Fasting serum Pepsinogen I was measured in all patients by radioimmunoassay (Pepsik; Sorin Biomedica, Saluggia, Italy) according to the manufacturer’s instructions, while basal Pepsinogen II levels were determined using a specific enzyme immunoassay (BIOHIT Plc, Helsinki, Finland).
Gold standard definition
To define the gold standard of active
H. pylori infection, we modified the approach used by Shin et al. before [
8]. A patient was classified as current
H. pylori infection based on either a positive culture or, in the case of a negative culture, both positive histology and positive urease test (Group A). A patient was classified as
H. pylori-negative when the culture, histologic examination, urease test, and serology were all negative (Group E). When either the histologic examination (Giemsa stain or presence of active gastritis) or urease test was positive, the results were classified based on the results of serology test. When IgG antibodies to
H. pylori were detected, the results were considered “probably positive” (Group B). When IgG antibodies were not detected, the results were regarded as being “probably negative” (Group C). When a patient was serologically positive but negative on all biopsy-based tests, this was interpreted as either a past
H. pylori infection or a false-positive result and the patient was classified as negative for current
H. pylori infection (Group D). Groups A and B were defined as gold standard positive while Groups C, D, and E were gold standard negative.
Statistical analysis
Standard methods were used to calculate the sensitivity, specificity, and positive and negative predictive values, their 95% confidence intervals, and their test validity. Chi-square tests were used to compare variables (i.e., number of cases who had moderate-to-marked gastritis with atrophy at the antrum and corpus). To examine the decreasing trend in the prevalence of histology, as influenced by the severity of glandular atrophy, chi-square test for trend was applied. All statistical analyses and database collection were performed using the Statistical Package for Social Sciences (SPSS 17.0 for Windows, SPSS. Inc., Chicago, IL, USA).
Discussion
Biopsy-based tests are important diagnostic tools for
H. pylori. However, the optimal biopsy site is still unknown, especially in cases of gastritis with atrophy. Current guidelines only recommend combining antrum and body biopsies for rapid urease test in the circumstance of antibiotics or proton pump inhibitors exposure. Sampling from the angularis, corpus, and antrum for histology was ever suggested in the same situation [
16]. Reviewing recent studies, there is little practical information about the adequate biopsy numbers and suitable biopsy sites. Single and multiple specimens at the antrum alone, at the body alone, or in combination of antrum and body had been described and applied (Table
4). These diagnostic approaches seem largely arbitrarily [
8,
16,
19‐
28]. In order to clarify the exact benefit of these biopsy sites, a gold standard is necessary.
Table 4
Studies on the diagnostic tests of
H. pylori
and the respective biopsy sites chosen, published between November 2005 and February 2011
| Korea, health check-up examinees | *1LA1LB | 1LA | Mean 47.8 | 515 | 53.2 |
| Taiwan, dyspepsia | - | 1LA vs. 1LA1GB | Mean 55.0-57.8 | 355 | 33.5 |
| Italy, dyspepsia | 2A | 2A | Median 52 | 1000 | 45.3 |
| Malaysia, dyspepsia | 1A1B | 1A1B | Mean 50.7 | 206 | 53.9 |
| Korea, gastritis with atrophy | 2A2B | 1A1B | Mean 57.7 | 651 | 41.2 |
| Kuwait, endoscopy evaluation | - | 1A vs. 2A vs. 3A vs. 4A | Mean 36.1 | 100 | - |
| Korea, dyspepsia | 2A2B | 1LA1LB | Mean 56.8 | 430 | - |
| Pakistan, dyspepsia | 2A | 2A | Mean 43 | 109 | 57.0 |
| Korea, gastric cancer | 2LA2LB2GB | 1GB | Median 61 | 194 | 84.0 |
| Taiwan, bleeding | 2B2U | 2A | Mean 63.5 | 324 | 53.7 |
Roma-Giannikou et al. [ 30] | Greece | 1A | 1A | Mean 10.4 | 254 | - |
| Guideline | 1GA1GB1Ag | 1AgB1GA | - | - | - |
In 2009, Shin et al. modified
H. pylori diagnostic methods and set a validated gold standard according to combination tests results [
8]. Since the combination method is the preferred approach in patients with gastritis with atrophy, the defined gold standard may best correlate with active
H. pylori infection. Our study follows this approach to determine the best biopsy site with highest sensitivity against a background of gastritis with atrophy.
The present study has several findings. First, making a biopsy at the antrum increases the risk of obtaining atrophic gastric mucosa, which is associated higher frequency of false negative results. Second, when body gastritis with atrophy develops, antrum atrophy exists already. Third, antrum biopsy alone has decreased sensitivity when there is moderate-to-severe antrum gastritis with atrophy (CLOtest up to 16% and histology up to 12%) and moderate-to-severe body gastritis with atrophy (CLOtest up to 16.67% and histology up to 8.34%).
First, the frequency of antrum gastritis with atrophy is higher than that of the body. This is consistent with previous studies [
22,
29]. It is believed that gastritis with atrophy progresses from the antrum initially and extends to the body in the advanced stage [
12,
17,
18]. Thus, the prevalence rate of antrum gastritis with atrophy is significantly higher than that of the body. As such, taking a biopsy at the antrum may yield higher chances of atrophic gastric mucosa than taking one from the body.
Regardless of biopsy site, if the degree of gastritis with atrophy in each specimen is considered, sensitivity decreases as the severity of gastritis with atrophy progresses (Figure
3). This is similar to the findings of Kim et al. [
22]. These false negative subjects could be proven to be
H. pylori infected after combining with other diagnostic methods. Such phenomenon is explained by the increasing rate of sampling error as gastritis with atrophy progresses [
29]. Thus, biopsy at antrum increases the risk of getting atrophic gastric mucosa that is associated with higher frequency of false negatives.
Second, applying the aforementioned conclusion on biopsy site and on the degree of gastritis with atrophy, it is interesting to find an opposite results between antrum atrophy and body atrophy. Theoretically, biopsy site at the atrophic area yields poorer sensitivity so single antrum biopsy done in antrum atrophy subjects results in less sensitivity. However, this principle does not apply in single body biopsy performed in body atrophy cases. Instead, the present study reveals a general rule that antrum biopsy results in lower sensitivity in either antrum or body atrophy. This is because when body gastritis with atrophy occurs, antrum atrophy exists already [
17,
18,
29]. In fact, most of the patients here with moderate-to-severe body atrophy (n=23) also have moderate-to-severe antrum atrophy (20/23).
Third, single body biopsy discloses an increased sensitivity as compared with single antrum biopsy in a background of moderate-to-severe antrum gastritis with atrophy (CLOtest up to 16% and histology up to 12%). Similar finding is founded when corpus biopsy is taken in moderate-to-severe body gastritis with atrophy (with a increased sensitivity in CLOtest up to 16.67% and histology up to 8.34%). In contrast, single antrum and single corpus has comparable sensitivity when gastritis with atrophy is normal-to-mild (CLOtest 97.47–95.66 and histology 96.74–98.73). Poor colonization of
H. pylori in the atrophic mucosa and intestinal metaplasia have been well discussed [
9,
12]. When performing biopsy-based test in a background of gastritis with atrophy, sampling errors, insufficient bacterial load [
9], bacterial migration, bacterial clearance [
12], bacterial patchy distribution, and poor mucosal colonization in areas of intestinal metaplasia are common causes of false negative results. Furthermore, as the gastritis with atrophy progresses, the prevalence of
H. pylori infection decreases. Single specimen sampling at the antrum may miss this relative small but risky patients. And this approach may miss those who could get benefit from eradication. Therefore, the present study recommends additional corpus biopsy to avoid false negative results in moderate-to-severe gastritis with atrophy.
This study has several potential limitations. First, it was conducted in a
H. pylori endemic area, such that the interpretation and application of the study results should consider the local
H. pylori prevalence rate. Second, in evaluating gastritis with atrophy by histology, the sampling method used was based on the modified Updated Sydney Classification. The latest approach method to evaluate gastritis with atrophy is OLGA staging, which is composed of multiple antrum and body biopsy specimens [
30]. The average grade of antrum and body gastritis with atrophy in these specimens was evaluated while staging was based on the degree and extent of gastritis with atrophy. In this study, only one piece at the antrum and one at the body was used to represent the whole antrum and body mucosal condition. This may be inadequate. However, compared to histology, non-invasive methods like Pepsinogen I/II ratio also disclosed lower values in moderate-to-severe gastritis with atrophy (mean Pepsinogen I/II ratio, 1.96 in moderate-to-severe antrum gastritis with atrophy and 1.79 in moderate-to-severe body gastritis with atrophy). This may eliminate the concern of inadequate sampling in the present study. Third, though we used visual analogue scale to score the gastritis with atrophy, grading of antrum atrophy is most difficult for pathologists since kappa values are very low and this wound be our limitation [
10].
Competing interests
The authors have no potential conflicts (financial, professional, or personal).
Authors’ contributions
HC Lin, TS Chen and HC Lan designed the project. TS Chen, FY Chang and AFY Lee performed the experiments. HC Lan wrote the manuscript. TS Chen and HC Lan contributed to the discussion of the data and the revision of the manuscript. All readers read and approved the final manuscript.