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Article

A Retrospective Experience of Helicobacter pylori Histology in a Large Sample of Subjects in Northern Italy

by
Davide Giuseppe Ribaldone
1,*,
Carlo Zurlo
1,
Sharmila Fagoonee
2,
Chiara Rosso
1,
Angelo Armandi
1,
Gian Paolo Caviglia
1,*,
Giorgio Maria Saracco
1 and
Rinaldo Pellicano
3
1
Department of Medical Sciences, Division of Gastroenterology, University of Torino, 10124 Torino, Italy
2
Institute of Biostructure and Bioimaging (CNR), Molecular Biotechnology Center, 10126 Turin, Italy
3
Department of General and Specialist Medicine, Gastroenterologia-U, Città della Salute e della Scienza di Torino, C.so Bramante 88, 10126 Turin, Italy
*
Authors to whom correspondence should be addressed.
Life 2021, 11(7), 650; https://doi.org/10.3390/life11070650
Submission received: 18 June 2021 / Revised: 1 July 2021 / Accepted: 2 July 2021 / Published: 4 July 2021
(This article belongs to the Collection Bacterial Infections, Treatment and Antibiotic Resistance)

Abstract

:
Updated data about the prevalence of Helicobacter pylori (H. pylori) and its correlation with histological results are scarce. The aim of our study was to provide current data on the impact of H. pylori in a third-level endoscopy service. We performed a large, retrospective study analyzing the results of all histological samples of gastroscopy from the year 2019. In total, 1512 subjects were included. The prevalence of H. pylori was 16.8%. A significant difference between the prevalence in subjects born in Italy and those from eastern Europe, south America, or Africa was found (p < 0.0001, p = 0.006, and p = 0.0006, respectively). An association was found between H. pylori and active superficial gastritis (p < 0.0001). Current H. pylori and/or a previous finding of H. pylori was related to antral atrophy (p < 0.0001). Fifteen patients had low-grade dysplasia. There were no statistically significant associations with current or past H. pylori infection. One patient presented gastric cardia adenocarcinoma with regular gastric mucosa. One patient, H. pylori positive, was diagnosed with gastric signet ring cell adenocarcinoma in a setting of diffuse atrophy, without metaplasia.. Our study provides updated, solid (biopsy diagnosis and large population) data on the prevalence of H. pylori infection in a representative region of southern Europe.

1. Introduction

Helicobacter pylori (H. pylori) infection is the most common chronic bacterial infection in the world and is associated with numerous gastro-duodenal diseases such as duodenal ulcer, gastric ulcers, gastritis, gastric adenocarcinoma, and gastric MALT (mucosa-associated lymphoid tissue) lymphoma [1]. The prevalence of H. pylori shows large geographical variations: in developing countries, about 80% of the population is H. pylori-positive, even at a young age while, in industrialized countries, it generally remains below 40%, and is considerably lower in children and adolescents than in adults and the elderly [2,3,4].
H. pylori infection is the most frequent cause of metaplastic and dysplastic changes in the gastric mucosa and, for this reason, it is classified as a type I carcinogenic factor [5]. The search for H. pylori infection in gastric biopsies during a gastroscopy is also the most frequently made request [6].
European guidelines recommend using the “test-and-treat” strategy for H. pylori infection in countries where the prevalence of H. pylori is greater than 20% [5]. The data in the literature indicate that, in Italy, as in other southern European countries (e.g., Spain and Greece), the prevalence of H. pylori in adults appears to be around 50% [7,8]. Therefore, the “test-and-treat” strategy recommended in Italy.
Obtaining updated data on the prevalence of H. pylori in subjects belonging to a high-level specialist centre is important, both in terms of epidemiological data and to modify the clinical management of patients with gastric symptoms.
The main objective of this study is therefore a retrospective evaluation of Helicobacter pylori histology in a large sample of subjects who used the endoscopy service of the “A.O.U. Città della Salute e della Scienza di Torino”, Italy. The secondary objective is to evaluate and correlate the infection with pathological conditions based on the location, the activity of gastric inflammation, and the localization and extent of intestinal atrophy and metaplasia.

2. Materials and Methods

This retrospective study was based on the analysis of all gastric biopsies of patients referred to the endoscopy service in the period from 2 January 2019 to 31 December 2019.
The inclusion criteria were:
- At least two biopsy samples in the antrum to search for H. pylori infection;
- Age > 16 years.
The exclusion criterion were:
- A repeated examination in the same patient during the year.
H. pylori was searched for in all patients with gastric biopsies using the Giemsa stain. The sensitivity of the Giemsa stain for the detection of H. pylori is about 93%, while its specificity is about 100% [9]. Proton pump inhibitors (PPI) are stopped at least two weeks before gastroscopy (this is to improve the accuracy of H. pylori detection in patients undergoing biopsies in the antrum only [10])
Using the hospital’s centralized clinical reporting and archiving system, and the pathological anatomy service’s archiving and reporting system, all patients who underwent gastric biopsies during endoscopy in 2019 were selected.
The following clinical data were collected: age, sex, place of birth, previous gastroscopies, previous H. pylori infection, indication for gastroscopy, endoscopic result, localization of biopsies, and presence of H. pylori.
The study was conducted according to the guidelines of the Declaration of Helsinki. Ethical review, and approval was waived for this study due to the retrospective and anonymous data collection design. The hospital provided the form “CONSENT TO DATA PROCESSING FOR EXPERIMENTAL PURPOSES”. The shared database was collected anonymously. All the patients signed informed consent prior to examination (gastroscopy with biopsies). The STROBE guidelines were followed.
The primary outcome was the prevalence of H. pylori infection. The secondary outcomes were the correlation of the infection with histological conditions based on the location, the activity of gastric inflammation, and the localization and extent of intestinal atrophy and metaplasia.
Based on the presence or absence of inflammatory infiltrate, gastric atrophy, and intestinal metaplasia, as well as the localization of these alterations (only in the antrum, only in body/fund, or both sites), it was decided to associate the presence of atrophy only, i.e., without chronic inflammatory infiltrate, with the definition of atrophic gastritis, while considering the distinction regarding the nature of the inflammatory infiltrate (active or inactive).

Statistical Analysis

Continuous variables were reported as mean (standard deviation (SD)), geometric mean, or median (interquartile range (IQR), depending on data distribution. The normality of the data was evaluated by the D’Agostino–Pearson test. Categorical variables were summarized as frequency and percentage. The Chi-square, or Fisher’s exact test when appropriate, and the independent sample t-test or Mann–Whitney test were applied for categorical and continuous variables, respectively. Logistic regression (multivariate) analysis was performed, including all statistically significant parameters to the univariate analysis and using the “enter” method.
A p < 0.05 was considered statistically significant. The statistical analysis was performed with MedCalc Statistical Software version 18.9.1 (MedCalc Software bvba, Ostend, Belgium).

3. Results

During the inclusion period, 1540 patients who underwent gastroscopy with gastric biopsy were selected. Of these, 28 subjects were excluded due to inadequate histopathological examination results (ongoing PPI n = 23, one single biopsy specimens n = 4). In total, 1512 subjects were included in the final analysis. Table 1 shows the characteristics of the study population.
In total, 243 (16.1%) examinations showed normally endoscopic findings, 585 (38.7%) had antral hyperaemia or erosions in the stomach or the duodenum, 76 (5%) had single or multiple gastric and/or duodenal ulceration, and 544 (36%) showed atrophic gastric mucosa, while other conditions (64 patients, 4.2%) included single or multiple gastric polyps (37), congestive (2), oedematous (10), nodular (3), or gastropathy (or other, 12 patients).
In 1193 (78.9%) patients, multiple biopsies were performed in the antrum and in the body/fundus (staging according to Operative Link on Gastritis Assessment, OLGA Staging system). In 319 (21.1%) patients, random samples were collected in the antrum only. Histological results are reported in Table 2 and Table 3.
The prevalence of H. pylori infection in gastric biopsy was 254 out of 1512 (16.8%). The prevalence of H. pylori infection in patients at their first gastroscopy was 209 out of 890 (23.5%); in patients who had already undergone at least one gastroscopy, the prevalence of H. pylori infection was 45 out of 622 (7.2%) (p < 0.001). The prevalence of H. pylori infection in patients who had never undergone a gastroscopy, and with no known history of H. pylori infection, was 197 out of 804 (24.5%). The prevalence of H. pylori infection in patients with a previous diagnosis of infection was 30 out of 195 (15.4%). Table 4 summarizes the characteristics of the population and the prevalence of H. pylori infection.
There was no statistically significant correlation between the prevalence of H. pylori infection for patients born in southern, northern, or central Italy (there was a trend towards a higher prevalence for those born in southern Italy compared to those born in northern Italy, p = 0.067). There was a statistically significant difference (p < 0.0001) between the prevalence in subjects born in Italy and those born in eastern Europe. There was also a statistically significant difference between the prevalence in subjects born in Italy and those born in south America (p = 0.0061), as well as between subjects born in Italy and those born in Africa (p = 0.0006). Through multivariable regression analysis, geographical origin from south America or Africa remained statistically significant (p = 0.04 and p = 0.005, respectively). A significantly higher prevalence of H. pylori was found in follow-up gastroscopies for atrophic gastropathy or previous peptic ulcer (p < 0.0001), which was confirmed by multivariate analysis (p = 0.002).
The following prevalence of H. pylori infection was found in relation to endoscopic findings: normal 12.8% (31/243); atrophic gastropathy 14.5% (79/544); hyperaemia or erosions 19.5% (114/585) (p = 0.02 compared with normal or atrophic gastritis); and ulcers 31.6% (24/76) (p = 0.0002 compared with normal or atrophic gastritis).
The prevalence of H. pylori infection was 206 out of 1193 (17.2%) in the 1193 patients from whom antrum and body/fundus samples were taken. In the 319 patients who underwent antral-only biopsies, the prevalence of H. pylori infection was 46 out of 319 (15.7%). The histological results associated with H. pylori infection are reported in Table 5.
An association was found between H. pylori and active superficial gastritis of the antrum and body/fundus (p < 0.0001), which was confirmed by multivariate analysis (p = 0.003). By correlating the finding of current H. pylori and antral atrophy, the association was found to be at the limit of statistical significance (p = 0.068); considering a history of H. pylori (current H. pylori and/or previous finding of H. pylori), a significant correlation was observed (p < 0.0001), which was confirmed by multivariate analysis (p = 0.004). The presence of antral metaplasia was associated with antral atrophy in 99.3% (299/301) of the patients (p < 0.0001, p = 0.005 at multivariate analysis). Body/fundus localized metaplasia was associated with atrophy in 96% (98/102) of the patients (p < 0.0001). Fifteen patients had low-grade dysplasia—14 in the antrum and 1 in the body/fundus. One patient presented gastric cardia adenocarcinoma with regular gastric mucosa. One patient had gastric sign cell adenocarcinoma with diffuse atrophy, without the metaplasia associated with H. pylori positivity. There were no statistically significant associations with current or past H. pylori.

4. Discussion

In the population of our study, we found H. pylori infection in 16.8% of subjects. This retrospective experience of Helicobacter pylori histology reported an infection rate lower than the known Italian prevalence, although the studies present in the literature are small in number, are dated and, above all, have been conducted on serological data by measuring anti-H. pylori IgG antibodies that do not give reliable information on active infection [11]. The data of the association between H. pylori and age showed a different trend compared to that in the literature: among H. pylori-positive patients, median age was 58 years compared to 62 years in H. pylori-negative patients; although, it can be speculated that the elderly population was more likely to undergo an invasive/non-invasive search for H. pylori in their lifetime and thus to have eradicated the bacterium.
In line with the literature data, however, was the data of the association between H. pylori infection and geographical origin. In fact, the prevalence of H. pylori infection was higher in Africa (40%), in south America, in particular in Peru (34.6%), and in eastern Europe (32.5%). Differences were statistically significant, despite the lower population of the groups under examination compared to patients of Italian origin. This is explained by the different prevalence of infection that still exists between developing countries and western countries [12]. As for Italy, the highest prevalence of H. pylori infection was found in southern Italy (17.2%), with a difference very close to statistical significance (p = 0.067).
Among the endoscopic results, it was confirmed that hyperaemia or erosions and ulcers are those most associated with H. pylori infection (p = 0.02 and p = 0.0002, respectively).
In 2002, Rugge et al. defined the staging of gastric histological changes associated with H. pylori (OLGA), emphasizing the difficulty of detecting H. pylori infection in cases of extensive intestinal metaplasia or during acid-suppressive therapy with PPI. In such cases, H. pylori infection is suggested by the presence of an “active” infiltrate [13].
In our study, among the histological findings, those associated with H. pylori infection were the following: superficial antrum and body/fundus gastritis (48.5%), chronic atrophic antral gastritis with chronic superficial body/fundus gastritis (38.3%), atrophic pangastritis (11.7%), and superficial gastritis of the antrum with atrophic gastritis of the body/fundus (1.5%). It should be noted that, among all the histological results associated with H. pylori, none of them showed involvement of the antrum only or the body/fundus only. All of these histological pictures showed an activity, namely the presence of polymorphonuclear infiltrate in the context of the biopsied gastric mucosa (100%).
H. pylori infection is the leading cause of gastric atrophy, and antral atrophic gastritis has been observed to occur in approximately half of the population with H. pylori infection. It was confirmed that the pictures of gastric atrophy and metaplasia localized at the body/fundus are rare and, in any case, influenced by the age of the subject and by the greater permanence of the bacterium in the stomach. The percentage of H. pylori-positive patients with antral metaplasia was 22.5%. In a similar vein to antral atrophy, no statistically significant association was found between antral metaplasia and current H. pylori infection; however, when considering patients with active H. pylori infection together with patients with a history of pylori infection, this association was statistically significant (p < 0.001), confirming what is known from the literature. Antral metaplasia occurs in the Correa cascade in the context of atrophy [14] and, in our study, a statistically significant association was found between gastric atrophy, both antrum and body/fundus, and gastric metaplasia (p < 0.001). From an anatomopathological point of view, it was decided not to carry out the characterization of metaplasia (complete, incomplete), despite the fact that, in the literature, incomplete metaplasia is a risk factor for the progression and malignant transformation of the gastric mucosa. However, in the same guidelines for the management of precancerous lesions, the clinical utility of the characterization of metaplasia requires further study [15].
The main limitation of our study is the fact that the observational and retrospective design may be subject to selection bias and may result in missing data concerning additional risk factors for the study outcomes, which partially precluded the acquisition of pre-endoscopy data. However, all patients eligible for the study were carefully screened and the sample size of our study is large.

5. Conclusions

Despite the aforementioned limitations, this study, representing a retrospective experience of H. pylori histology in a large sample of subjects in northern Italy, is one of the few that reports updated data based on biopsy samples and correlated them with histological pictures. Prospective studies are mandatory to confirm whether the real prevalence of H. pylori in Italy has decreased under a threshold for which a “test-and-treat” strategy could be no longer valid.

Author Contributions

Conceptualization, R.P. and G.M.S.; methodology, D.G.R., C.R. and G.P.C.; software, G.P.C.; validation, A.A. and S.F.; formal analysis, C.Z.; investigation, C.Z.; resources, G.M.S.; data curation, A.A. and C.R.; writing—original draft preparation, C.Z.; writing—review and editing, D.G.R., R.P.; visualization, S.F.; supervision, G.M.S.; project administration, G.M.S. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki. Ethical review and approval were waived for this study, due to retrospective and anonymous data collection design. Hospital provided the form “CONSENT TO DATA PROCESSING FOR EXPERIMENTAL PURPOSES”.

Informed Consent Statement

Informed consent to gastroscopy with biopsies was obtained from all subjects involved in the study.

Data Availability Statement

The data were collected anonymously. Anonymous data can be requested in case of need.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Pellicano, R.; Ribaldone, D.G.; Fagoonee, S.; Astegiano, M.; Saracco, G.M.; Mégraud, F. A 2016 panorama of Helicobacter pylori infection: Key messages for clinicians. Panminerva Med. 2016, 58, 304–317. [Google Scholar] [PubMed]
  2. Nelson, A.; Bi, Y.; Harris, D. Helicobacter Pylori: A comprehensive review for primary care providers. Rom. J. Intern. Med. 2021, 59, 112–118. [Google Scholar] [PubMed]
  3. Hooi, J.K.Y.; Lai, W.Y.; Ng, W.K.; Suen, M.M.Y.; Underwood, F.E.; Tanyingoh, D.; Malfertheiner, P.; Graham, D.Y.; Wong, V.W.S.; Wu, J.C.Y.; et al. Global Prevalence of Helicobacter pylori Infection: Systematic Review and Meta-Analysis. Gastroenterology 2017, 153, 420–429. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Roberts, S.E.; Morrison-Rees, S.; Samuel, D.G.; Thorne, K.; Akbari, A.; Williams, J.G. Review article: The prevalence of Helicobacter pylori and the incidence of gastric cancer across Europe. Aliment. Pharmacol. Ther. 2016, 43, 334–345. [Google Scholar] [CrossRef] [PubMed]
  5. Malfertheiner, P.; Megraud, F.; O’Morain, C.; Gisbert, J.P.; Kuipers, E.J.; Axon, A.; Bazzoli, F.; Gasbarrini, A.; Atherton, J.; Graham, D.Y.; et al. Management of helicobacter pylori infection-the Maastricht V/Florence consensus report. Gut 2017, 66, 6–30. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. Rugge, M.; Savarino, E.; Sbaraglia, M.; Bricca, L.; Malfartheiner, P. Gastritis: The clinico-pathological spectrum. Dig. Liver Dis. 2021. In press. [Google Scholar] [CrossRef] [PubMed]
  7. Zagari, R.M.; Law, G.R.; Fuccio, L.; Cennamo, V.; Gilthorpe, M.S.; Forman, D.; Bazzoli, F. Epidemiology of Functional Dyspepsia and Subgroups in the Italian General Population: An Endoscopic Study. Gastroenterology 2010, 138, 1302–1311. [Google Scholar] [CrossRef] [PubMed]
  8. Eusebi, L.H.; Zagari, R.M.; Bazzoli, F. Epidemiology of Helicobacter pylori Infection. Helicobacter 2014, 19, 1–5. [Google Scholar] [CrossRef] [PubMed]
  9. Alkhamiss, A.S. Evaluation of better staining method among hematoxylin and eosin, giemsa and periodic acid schiff-alcian blue for the detection of helicobacter pylori in gastric biopsies. Malays. J. Med. Sci. 2020, 27, 53–61. [Google Scholar]
  10. Pichon, M.; Tran, C.T.; Motillon, G.; Debiais, C.; Gautier, S.; Aballea, M.; Cremniter, J.; Vasseur, P.; Tougeron, D.; Garcia, M.; et al. Where to Biopsy to Detect Helicobacter pylori and How Many Biopsies Are Needed to Detect Antibiotic Resistance in a Human Stomach. J. Clin. Med. 2020, 9, 2812. [Google Scholar] [CrossRef]
  11. Pellicano, R.; Ribaldone, D.G.; Astegiano, M.; Dughera, L.; Battaglia, E.; Morgando, A.; Arrigoni, A.; Spandre, M.; Grassini, M.; Saracco, G.M.; et al. Gastroenterology today: Between certainties and news. Minerva Gastroenterol. Dietol. 2018, 64, 323–332. [Google Scholar] [CrossRef] [PubMed]
  12. Kotilea, K.; Bontems, P.; Touati, E. Epidemiology, Diagnosis and Risk Factors of Helicobacter pylori Infection. In Advances in Experimental Medicine and Biology; Springer: New York, NY, USA, 2019; Volume 1149, pp. 17–33. [Google Scholar]
  13. Rugge, M.; Correa, P.; Dixon, M.F.; Fiocca, R.; Hattori, T.; Lechago, J.; Leandro, G.; Price, A.B.; Sipponen, P.; Solcia, E.; et al. Gastric mucosal atrophy: Interobserver consistency using new criteria for classification and grading. Aliment. Pharmacol. Ther. 2002, 16, 1249–1259. [Google Scholar] [CrossRef] [PubMed]
  14. Correa, P. Human Gastric Carcinogenesis: A Multistep and Multifactorial Process—First American Cancer Society Award Lecture on Cancer Epidemiology and Prevention. Cancer Res. 1992, 52, 6735–6740. [Google Scholar] [PubMed]
  15. Pimentel-Nunes, P.; Libânio, D.; Marcos-Pinto, R.; Areia, M.; Leja, M.; Esposito, G.; Garrido, M.; Kikuste, I.; Megraud, F.; Matysiak-Budnik, T.; et al. Management of epithelial precancerous conditions and lesions in the stomach (MAPS II): European Society of Gastrointestinal Endoscopy (ESGE), European Helicobacter and Microbiota Study Group (EHMSG), European Society of Pathology (ESP), and Sociedade Portuguesa de Endoscopia Digestiva (SPED) guideline update 2019. Endoscopy 2019, 51, 365–388. [Google Scholar]
Table 1. Baseline characteristics.
Table 1. Baseline characteristics.
Characteristics of the population (n = 1512)
Sex (n, %)
- Males597 (39.5%)
- Females 915 (60.5%)
AGE (years; median, IQR)62.0, 47–77
Geographical origin (n, %)
- Northern Italy804 (53.2%)
- Central Italy38 (2.5%)
- Southern Italy510 (33.7%)
- Central/Western Europe13 (0.9%)
- Eastern Europe77 (5.1%)
- Asia19 (1.2%)
- Africa25 (1.7%)
- South America26 (1.7%)
Previous H. pylori infection (n, %)195 (12.9%)
Gastroscopy (n, %)
- Naive890 (58.9%)
- Experienced622 (41.1%)
Gastroscopy indications (n, %)
- Dyspepsia 642 (42.5%)
- GERD 304 (20.1%)
- Surveillance of atrophic gastritis/previous peptic ulcer/gastric MALT lymphoma 193 (12.8%)
- Anaemia 105 (6.9%)
- Other (search for signs of portal hypertension, dysphagia, family history for gastric cancer, suspected celiac disease, pre-renal transplant evaluation, etc.)268 (17.7%)
IQR = interquartile range; H. pylori = Helicobacter pylori; GERD = gastro-esophageal reflux disease.
Table 2. A total 1193 patients on whom biopsies were performed in the antrum and body/fundus.
Table 2. A total 1193 patients on whom biopsies were performed in the antrum and body/fundus.
Resultn, %
Normal 159 (13.3%)
Chronic atrophic gastritis182 (15.3%) (antral only, 178, body/fundus only 4)
• active inflammatory infiltrate23
• inactive inflammatory infiltrate120
• no inflammatory infiltrate39
Chronic atrophic antral gastritis with chronic superficial body/fundus gastritis221 (18.5%)
• chronic inflammatory infiltrate without activity109
• chronic inflammatory infiltrate with activity112
Chronic atrophic body/fundus gastritis with chronic superficial gastritis in the antrum18 (1.4%)
• chronic inflammatory infiltrate without activity8
• chronic inflammatory infiltrate with activity8
• no inflammatory infiltrate2
Chronic atrophic gastritis of the antrum and body/fundus131 (11%)
• chronic inflammatory infiltrate without activity73
• chronic inflammatory infiltrate with activity50
• no inflammatory infiltrate8
Superficial antral or body/fundus gastritis187 (15.7%)
• chronic inflammatory infiltrate without activity167
• chronic inflammatory infiltrate with activity20
Chronic superficial gastritis of the antrum and body/fundus295 (24.7%)
• chronic inflammatory infiltrate without activity161
• chronic inflammatory infiltrate with activity134
n, number of patients.
Table 3. A total 319 patients on whom biopsies were performed only in the antrum.
Table 3. A total 319 patients on whom biopsies were performed only in the antrum.
Resultn, %
Normal 54 (16.9%)
Chronic superficial antral gastritis151 (47.3%)
• chronic inflammatory infiltrate without activity93
• chronic inflammatory infiltrate with activity 58
Indefinite chronic antral gastritis due to atrophy or metaplasia due to small sample size9 (2.8%)
• chronic inflammatory infiltrate without activity7
• chronic inflammatory infiltrate with activity2
Chronic atrophic antral gastritis94 (29.5%)
• chronic inflammatory infiltrate without activity55
• chronic inflammatory infiltrate with activity21
• no inflammatory infiltrate18
Insufficient material3 (0.9%)
n, number of patients.
Table 4. Characteristics of the population and Helicobacter pylori status (n = 1512).
Table 4. Characteristics of the population and Helicobacter pylori status (n = 1512).
Characteristics opulationn, % Median, IQRn, % in
H. pylori + (n = 254)
Median, IQR
n, % in
H. pylori − (n = 1258)
Median, IQR
p Value
Sex
Males597 (39.5)99 (39.0)498 (39.6)
Females915 (60.5)155 (61.0)760 (60.4)0.91
Age62, 47–7758, 42–7462, 46–780.06
Geographic origin
Northern Italy804 (53.2)109 (42.9)695 (55.2)0.061
Central Italy38 (2.5)6 (2.4)32 (2.5)0.89
Southern Italy510 (33.7)88 (34.6)422 (33.5)0.81
Central/Western Europe13 (0.9)2 (0.8)11 (0.9)0.79
Eastern Europe77 (5.1%)25 (9.8)52 (4.1)<0.0001
Asia19 (1.2%)5 (2.0)14 (1.1)0.057
Africa25 (1.7%)10 (3.9)15 (1.2)0.0003
South America26 (1.7%)9 (3.5)17 (1.4)0.005
Previous H. pylori infection195 (12.9)30 (11.8)165 (13.1)0.47
Gastroscopy
naïve890 (58.9%)209681
Experienced622 (41.1%)45577<0.001
Indication TO EGDS
Dyspepsia642 (42.5)129 (50.8)513 (40.8)0.061
GERD304 (20.1)54 (21.3)250 (19.9)0.56
Surveillance in atrophic gastritis or previous peptic ulcer 193 (12.8)71860.60
Anaemia105 (6.9)19 (7.5)86 (6.8)0.82
Other268 (17.7)45 (17.7)223 (17.7)0.99
n, number of patients; IQR, interquartile range; H. pylori, Helicobacter pylori; GERD, gastro-oesophageal reflux disease.
Table 5. Histological results and Helicobacter pylori status (n = 1512).
Table 5. Histological results and Helicobacter pylori status (n = 1512).
Histological Results
(Antrum and Corpus/Fundus)
n = 1193H. Pylori +H. Pylorip Values
n = 206n = 987
- Normal1590159p < 0.0001
- Superficial antral or body/fundus gastritis1870187p < 0.0001
- Superficial antral and body/fundus gastritis295100195p < 0.0001
- Chronic atrophic antral or body/fundus gastritis1820182p < 0.0001
- Chronic atrophic antral gastritis with chronic superficial body/fundus gastritis22179142p < 0.0001
- Chronic atrophic gastritis of antrum and body/fundus13124107p = 0.75
- Body/fundus atrophic gastritis with superficial antral gastritis18315p = 0.95
Histological results
(antrum)
n= 319H. pylori+H. pylori
n=48n= 271
- Normal57057p < 0.0015
- Chronic superficial antral gastritis15131120p = 0.06
- Small sample size918p = 0.74
- Chronic atrophic antral gastritis102086p = 0.0001
n, number of patients; H. pylori, Helicobacter pylori.
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MDPI and ACS Style

Ribaldone, D.G.; Zurlo, C.; Fagoonee, S.; Rosso, C.; Armandi, A.; Caviglia, G.P.; Saracco, G.M.; Pellicano, R. A Retrospective Experience of Helicobacter pylori Histology in a Large Sample of Subjects in Northern Italy. Life 2021, 11, 650. https://doi.org/10.3390/life11070650

AMA Style

Ribaldone DG, Zurlo C, Fagoonee S, Rosso C, Armandi A, Caviglia GP, Saracco GM, Pellicano R. A Retrospective Experience of Helicobacter pylori Histology in a Large Sample of Subjects in Northern Italy. Life. 2021; 11(7):650. https://doi.org/10.3390/life11070650

Chicago/Turabian Style

Ribaldone, Davide Giuseppe, Carlo Zurlo, Sharmila Fagoonee, Chiara Rosso, Angelo Armandi, Gian Paolo Caviglia, Giorgio Maria Saracco, and Rinaldo Pellicano. 2021. "A Retrospective Experience of Helicobacter pylori Histology in a Large Sample of Subjects in Northern Italy" Life 11, no. 7: 650. https://doi.org/10.3390/life11070650

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