Research Article | Open Access
Maryam Monajemzadeh, Ata Abbasi, Parin Tanzifi, Sahar Taba Taba Vakili, Heshmat Irani, Leila Kashi, "The Relation between Helicobacter pylori Infection and Acute Bacterial Diarrhea in Children", International Journal of Pediatrics, vol. 2014, Article ID 191643, 5 pages, 2014. https://doi.org/10.1155/2014/191643
The Relation between Helicobacter pylori Infection and Acute Bacterial Diarrhea in Children
Background. H. pylori infection leads to chronic gastritis in both children and adults. But recently, there are arising theories of its protective effect in diarrheal diseases. Aim. To explore the prevalence of H. pylori infection in children with bacterial diarrhea and compare it with healthy controls. Patients and Methods. Two matched groups consisted of 122 consecutive children, aged 24–72 months old, with acute bacterial diarrhea, who had Shigellosis () and Salmonellosis () as patients group and 204 healthy asymptomatic children as control group enrolled in this study. Results. The prevalence of H. pylori infection in healthy control children was significantly higher than in patients group, (odds ratio = 3.6, 95% CI: 1.33–9.5, ). In our study, only 2/54 Salmonella infected patients and 3/68 of Shigellosis had evidence of H. pylori infection, while normal control children had 27/204 infected individuals. Conclusion. H. pylori infection may play a protective role against bacterial diarrhea in children. So it is important to consider all of the positive and negative aspects of H. pylori infection before its eradication.
Helicobacter pylori (H. pylori) is one of the most important factors in the gastroduodenal diseases. The infection is most commonly acquired in early childhood and leads to chronic gastritis in both children and adults and is the leading cause of peptic ulcer disease in humans [1–4]. It is a challenging matter for many physicians due to lack of knowledge about its life cycle and low rate of bacterial eradication. H. pylori has been shown to play a major role in the pathogenesis of gastric atrophy, chronic diarrhea, and growth retardation in children, intestinal metaplasia, dysplasia, and the development of gastric carcinoma and lymphoma subsequently [5–7]. Besides, some benefits are also noted such as reducing prevalence of esophageal adenocarcinoma by decreasing the periods of gastroesophageal reflux disease . Fecal-oral or oral-oral routes are the main candidate ways of its transmission, although much is unknown in this regard .
Gastroenteritis is another important disease in children caused by a variety of bacterial and viral agents and the exact responsible organisms are different from one area to another but generally, E. coli, Shigella, and Salmonella are the most common enteric bacterial pathogens [10, 11].
Recently, there are arising theories of protective effect of H. pylori infection on diarrheal diseases, showing the low prevalence of diarrhea in children infected by H. pylori [12–14], although there is still a living debate about it. On the other hand, it has been shown that H. pylori infection is associated with Vibrio cholerae and Salmonella infection possibly through hypochlorhydria resulting from acute or chronic H. pylori infection [9, 14].
As Salmonella and Shigella entritis and also H. pylori infection are common gastrointestinal problems in children, especially in developing and underdeveloped countries, we designed this study to investigate the association between H. pylori infection and this bacterial gastroenteritis in children.
2. Patients and Methods
The study is a case control study performed during 2009–2011 in the Children Medical Center Hospital, the major children’s hospital of Iran affiliated to Tehran University of Medical Sciences, Tehran, Iran.
Two matched groups were studied as follows: (1) group of children with acute bacterial gastroenteritis due to Salmonella or Shigella consisted of 122 consecutive children (55 females and 67 males), aged 24–72 months old, 68 with Shigellosis and 54 with Salmonellosis; (2) control group consisted of two hundred and four healthy children (100 males and 104 females) with no history of diarrhea and no bacterial growth in their stool cultures. Age parameter was matched between both genders ().
Healthy children with history of diarrhea within 2 weeks before sampling and any child in each group with history of antibiotic therapy within 4 weeks prior to stool collection were excluded from study. None of the participants were treated with a proton-pump inhibitor or bismuth preparations. No underlying medical disease or immunodeficiency was detected in enrolled groups.
Personal data including age (1–3 years and 3–6 years), gender, and address was also obtained from parents using a structured questionnaire. Cases were from urban area but parents defer to get information about the exact socioeconomic level but as the hospital is governmental and located in the middle part of the city and the admitted children were from nearby areas, one can conclude that cases belonged to medium socioeconomic level. The study was approved by the Tehran University of Medical Sciences Ethics Committee.
2.2. Determination of H. pylori Status
Stool samples were collected in the hospital and immediately frozen and stored at −70°C. Solid and semisolid stool specimens were tested for H. pylori antigen by the GA Generic Assays GmbH kit, H. pylori sandwich enzyme immunoassay (Germany), in accordance with the manufacturer’s instructions. In summary frozen specimens were immediately thawed and 100 mg (2-3 mm in diameter of a solid specimen) of feces was suspended thoroughly. Then the specimens were treated with anti-H. pylori antibody (antibiotin conjugate) and incubated at room temperature for 60 minutes. After washing, streptavidin-HRP conjugate (included in the kit) was added and the solution was incubated for 30 min at room temperature, then substrate F (included in the kit) was added, and after 15 min of incubation stop solution was added and finally the OD was read at 450 nm and interpreted according to the manufacturer’s guideline.
2.3. Media for the Isolation of Bacteria from Stools
Bacteria from stool samples were cultivated on eight different selective agar plates in order to isolate the microorganisms. MacConkey agar was used for the detection of E. coli, Salmonella, and Shigella species. Thiosulfate-citrate-bile salts-sucrose (TCBS) agar was used for the detection of Vibrio species, mannitol-malt agar (MSA) for Staphylococcus aureus, and SS and XLD for Shigella and Salmonella. The growth pattern of each organism on the specific agar including color and also biochemical tests were also used for organism detection.
2.4. Statistical Analysis
The results are expressed as mean ± SD. Statistical analyses were performed using SPSS version 16.0.1 (SPSS Inc., Chicago, IL, USA). The statistical differences between proportions were determined by analysis. Numerical data were evaluated using analysis of variance, followed by Tukey’s post hoc test. values less than 0.05 were considered to be statistically significant.
Among 112 patients enrolled in this study, 68 had Shigella infection and 54 had Salmonella infection. The prevalence of H. pylori infection in control group was significantly higher than in acute bacterial diarrhea group (), in which two of fifty-four cases of Samonella infection and three of sixty-eight cases of Shigellosis were infected by H. pylori while 27 out of 204 control children were infected. The risk of positive H. pylori infection in control group was 3.6 (odds ratio = 3.6, 95% CI: 1.33–9.5, ) times higher than bacterial infection group (Table 1). There was no statistical difference in prevalence of H. pylori infection in variable age groups in control versus patients groups (data not shown).
|HP: H. pylori.|
Diarrheal disease is recognized as a globally burdensome disease, associated with considerable children’s mortality and morbidity specifically in developing countries where most of the complications occur and can cause up to three million deaths per year [3, 15, 16].
The cause of diarrhea differs from one country to another and generally one can expect higher rates of bacterial infections in underdeveloped and developing countries in comparison with developed countries . Several pathogenic microorganisms are incriminated as the etiologic agents of acute diarrhea such as rotavirus, adenoviruses, caliciviruses, and astroviruses, Salmonella, Shigella, enteropathogenic and enterotoxigenic E. coli (EPEC and ETEC, resp.), Aeromonas, Plesiomonas spp. Campylobacter jejuni, Yersinia enterocolitica, Vibrio cholerae, protozoa, and helminthes [17, 18].
Gastroenteritis, especially bacterial gastroenteritis, mostly occurs in developing areas where H. pylori infection is more prevalent and it has been proposed that there may be a common rout for both H. pylori and Shigella transmission by houseflies . Previous studies have shown conflicting results on association of H. pylori infection with other gastrointestinal pathogens [3, 7, 9, 14].
In this study we evaluated the H. pylori status in children with gastroenteritis and compared it with normal controls. We focused on Shigella and Salmonella as they are the most frequent isolates from stool cultures of children in our area.
Our results revealed that the prevalence of H. pylori infection in healthy children was higher than in patients with bacterial diarrhea indicating that bacterial infected patients are less infected with H. pylori. These findings are in line with other studies showing protective role of H. pylori infection and reporting a reduced frequency of diarrheal illness in H. pylori infected children [12, 14]. It can be due to either increase in gastric acid production in individuals infected by H. pylori which leads to bacterial pathogens damage  or activation of immune system as a result of H. pylori infection and increased IgA production, which is fatal for enteric pathogens [20–23]. As a matter of fact, gastric acid and peptides are necessary for activation of some enteric pathogens especially that viruses and H. pylori infection can disrupt this process [24–27]. Previous studies have shown that children’s response to H. pylori infection is more severe than adults so this observation may be in part due to the natural response of immune system of children.
Contradictorily, some studies have shown H. pylori infection to be a risk factor of some bacterial gastroenteritis [28, 29]. According to the fact that the pathogenesis and etiology of H. pylori infection are not fully understood and there are very few studies considering the relation between H. pylori infection and other bacterial pathogens causing gastroenteritis, further investigations, considering different aspects including H. pylori life cycle, products, and cytotoxins are needed. Considering lack of correlation between prevalence of H. pylori infection and gender or age, it can be suggested that the difference in H. pylori prevalence in the two examined groups would be due to the organism itself. This hypothesis was previously noted by Perry et al. .
Our study has some limitations, such as having rather small number of enrolled patients in this study which may to some extent weaken our results. Another issue is about the method. Parenthetically, it should be mentioned that the specificity and sensitivity of the used kit were 100% and 91%, respectively, according to its manual. In the literature review, we found some conflicting data about this test but many of the articles indicated it as a good alternative in children [30–34].
There are different complications in H. pylori infection such as gastritis, gastric lymphoma, and carcinoma, but in contrast H. pylori infection decreases the risk of esophageal adenocarcinoma [6, 35, 36]. There are many studies showing association or protective role of H. pylori infection in different disease groups, for example, reducing Barrett’s esophagitis , decreasing risk of esophageal cancer , decreasing risk of gastric cardiac cancer , or decreasing the bleeding risk of esophageal varices in cirrhotic patients . According to our findings, H. pylori infection may be candidate agent which plays a protective role in gastroenteritis in children. So it is important to consider all of the positive and negative aspects of H. pylori infection before its eradication; however, because of the current debate and considering the fact that knowledge about H. pylori life cycle and its pathogenesis is not explicitly defined more comprehensive research is recommended. Searching for viral gastroenteritis and determining the Cag A status of H. pylori by means of PCR method are also suggested.
Conflict of Interests
The authors declare that there is no conflict of interests regarding the publication of this paper.
This study was supported by grants from Tehran University of Medical Sciences Research Fund.
- N. Gallo, C.-F. Zambon, F. Navaglia et al., “Helicobacter pylori infection in children and adults: a single pathogen but a different pathology,” Helicobacter, vol. 8, no. 1, pp. 21–28, 2003.
- A. E. Whitney, J. Guarner, L. Hutwagner, and B. D. Gold, “Helicobacter pylori gastritis in children and adults: comparative histopathologic study,” Annals of Diagnostic Pathology, vol. 4, no. 5, pp. 279–285, 2000.
- H. Shmuely, Z. Samra, S. Ashkenazi, G. Dinari, G. Chodick, and J. Yahav, “Association of Helicobacter pylori infection with Shigella gastroenteritis in young children,” American Journal of Gastroenterology, vol. 99, no. 10, pp. 2041–2045, 2004.
- F. Mansour-Ghanaei, N. Taefeh, F. Joukar, S. Besharati, M. Naghipour, and R. Nassiri, “Recurrence of Helicobacter pylori infection 1 year after successful eradication: a prospective study in Northern Iran,” Medical Science Monitor, vol. 16, no. 3, pp. CR144–CR148, 2010.
- P. M. Sherman, “Peptic ulcer disease in children—diagnosis, treatment, and the implication of Helicobacter pylori,” Gastroenterology Clinics of North America, vol. 23, no. 4, pp. 707–725, 1994.
- P. Correa, “Human gastric carcinogenesis: a multistep and multifactorial process—first American Cancer Society award lecture on cancer epidemiology and prevention,” Cancer Research, vol. 52, no. 24, pp. 6735–6740, 1992.
- D. J. Passaro, D. N. Taylor, R. Meza, L. Cabrera, R. H. Gilman, and J. Parsonnet, “Acute Helicobacter pylori infection is followed by an increase in diarrheal disease among Peruvian children,” Pediatrics, vol. 108, no. 5, article E87, 2001.
- J. Parsonnet, G. D. Friedman, D. P. Vandersteen et al., “Helicobacter pylori infection and the risk of gastric carcinoma,” The New England Journal of Medicine, vol. 325, no. 16, pp. 1127–1131, 1991.
- M. Monajemzadeh, M. T. H. Ashtiani, A. M. Ali et al., “Helicobacter pylori infection in children: association with giardiasis,” British Journal of Biomedical Science, vol. 67, no. 2, pp. 86–87, 2010.
- A. Raghunath, A. P. S. Hungin, D. Wooff, and S. Childs, “Prevalence of Helicobacter pylori in patients with gastro-oesophageal reflux disease: systematic review,” British Medical Journal, vol. 326, no. 7392, pp. 737–739, 2003.
- F. Jafari, M. Hamidian, M. Rezadehbashi et al., “Prevalence and antimicrobial resistance of diarrheagenic Escherichia coli and Shigella species associated with acute diarrhea in Tehran, Iran,” Canadian Journal of Infectious Diseases and Medical Microbiology, vol. 20, no. 3, pp. e56–e62, 2009.
- R. Ranjbar, M. M. Soltan Dallal, M. Talebi, and M. R. Pourshafie, “Increased isolation and characterization of Shigella sonnei obtained from hospitalized children in Tehran, Iran,” Journal of Health, Population and Nutrition, vol. 26, no. 4, pp. 426–430, 2008.
- S. Perry, L. Sanchez, S. Yang, T. D. Haggerty, P. Hurst, and J. Parsonnet, “Helicobacter pylori and risk of gastroenteritis,” The Journal of Infectious Diseases, vol. 190, no. 2, pp. 303–310, 2004.
- M. K. Bhan, R. Bahl, S. Sazawal et al., “Association between Helicobacter pylori infection and increased risk of typhoid fever,” The Journal of Infectious Diseases, vol. 186, no. 12, pp. 1857–1860, 2002.
- D. Antoš, J. Crone, N. Konstantopoulos, and S. Koletzko, “Evaluation of a novel rapid one-step immunochromatographic assay for detection of monoclonal Helicobacter pylori antigen in stool samples from children,” Journal of Clinical Microbiology, vol. 43, no. 6, pp. 2598–2601, 2005.
- F. Jafari, L. Shokrzadeh, M. Hamidian, S. Salmanzadeh-Ahrabi, and M. R. Zali, “Acute diarrhea due to enteropathogenic bacteria in patients at hospitals in Tehran,” Japanese Journal of Infectious Diseases, vol. 61, no. 4, pp. 269–273, 2008.
- S. M. El-Sheikh and S. M. El-Assouli, “Prevalence of viral, bacterial and parasitic enteropathogens among young children with acute diarrhoea in Jeddah, Saudi Arabia,” Journal of Health Population and Nutrition, vol. 19, no. 1, pp. 25–30, 2001.
- A. M. K. Al Jarousha, M. A. El Jarou, and I. A. El Qouqa, “Bacterial enteropathogens and risk factors associated with childhood diarrhea,” Indian Journal of Pediatrics, vol. 78, no. 2, pp. 165–170, 2011.
- M. F. Dixon, “Pathology of gastritis and peptic ulceration,” in Helicobacter Pylori: Physiology and Genetics, H. L. T. Mobley, G. L. Mendz, and S. L. Hazell, Eds., chapter 38, ASM Press, Washington, DC, USA, 2001.
- R. Goll, F. Gruber, T. Olsen et al., “Helicobacter pylori stimulates a mixed adaptive immune response with a strong T-regulatory component in human gastric mucosa,” Helicobacter, vol. 12, no. 3, pp. 185–192, 2007.
- H. A. Haeberle, M. Kubin, K. B. Bamford et al., “Differential stimulation of interleukin-12 (IL-12) and IL-10 by live and killed Helicobacter pylori in vitro and association of IL-12 production with gamma interferon-producing T cells in the human gastric mucosa,” Infection and Immunity, vol. 65, no. 10, pp. 4229–4235, 1997.
- R. Srivastava, A. Kashyap, M. Kumar, G. Nath, and A. K. Jain, “Mucosal IgA & IL-1β in Helicobacter pylori infection,” Indian Journal of Clinical Biochemistry, vol. 28, no. 1, pp. 19–23, 2013.
- A. Mattsson, A. Tinnert, A. Hamlet, H. Lönroth, I. Bölin, and A.-M. Svennerholm, “Specific antibodies in sera and gastric aspirates of symptomatic and asymptomatic Helicobacter pylori-infected subjects,” Clinical and Diagnostic Laboratory Immunology, vol. 5, no. 3, pp. 288–293, 1998.
- C. J. L. Murray and A. D. Lopez, “Mortality by cause for eight regions of the world: Global Burden of Disease study,” The Lancet, vol. 349, no. 9061, pp. 1269–1276, 1997.
- A. Mattsson, H. Lönroth, M. Quiding-Järbrink, and A.-M. Svennerholm, “Induction of B cell responses in the stomach of Helicobacter pylori—infected subjects after oral cholera vaccination,” Journal of Clinical Investigation, vol. 102, no. 1, pp. 51–56, 1998.
- J. E. Crabtree, “Immune and inflammatory responses to Helicobacter pylori infection,” Scandinavian Journal of Gastroenterology, vol. 31, no. 215, pp. 3–10, 1996.
- R. Ranjbar, M. M. Soltan-Dallal, M. R. Pourshafie, and C. Mammina, “Antibiotic resistance among Shigella serogroups isolated in Tehran, Iran (2002–2004),” Journal of Infection in Developing Countries, vol. 3, no. 8, pp. 647–648, 2009.
- M. Feldman, B. Cryer, K. E. McArthur, B. A. Huet, and E. Lee, “Effects of aging and gastritis on gastric acid and pepsin secretion in humans: a prospective study,” Gastroenterology, vol. 110, no. 4, pp. 1043–1052, 1996.
- J. Clemens, M. J. Albert, M. Rao et al., “Impact of infection by Helicobacter pylori on the risk and severity of endemic cholera,” The Journal of Infectious Diseases, vol. 171, no. 6, pp. 1653–1656, 1995.
- N. Konstantopoulos, H. Rüssmann, C. Tasch et al., “Evaluation of the Helicobacter pylori stool antigen test (HpSA) for detection of Helicobacter pylori infection in children,” American Journal of Gastroenterology, vol. 96, no. 3, pp. 677–683, 2001.
- S. Kato, K. Ozawa, M. Okuda et al., “Accuracy of the stool antigen test for the diagnosis of childhood Helicobacter pylori infection: a multicenter Japanese study,” American Journal of Gastroenterology, vol. 98, no. 2, pp. 296–300, 2003.
- M. P. Dore, R. Negrini, V. Tadeu et al., “Novel monoclonal antibody-based Helicobacter pylori stool antigen test,” Helicobacter, vol. 9, no. 3, pp. 228–232, 2004.
- S. Kato, K. Nakayama, T. Minoura et al., “Comparison between the 13C-urea breath test and stool antigen test for the diagnosis of childhood Helicobacter pylori infection,” Journal of Gastroenterology, vol. 39, no. 11, pp. 1045–1050, 2004.
- D. Rothenbacher, M. J. Blaser, G. Bode, and H. Brenner, “Inverse relationship between gastric colonization of Helicobacter pylori and diarrheal illnesses in children: results of a population-based cross-sectional study,” The Journal of Infectious Diseases, vol. 182, no. 5, pp. 1446–1449, 2000.
- A. Guarino, “Enterotoxic effect of the vacuolating toxin produced by Helicobacter pylori in caco-2 cells,” The Journal of Infectious Diseases, vol. 178, no. 5, pp. 1373–1378, 1998.
- Y. Abe, T. Koike, K. Iijima et al., “Esophageal adenocarcinoma developing after eradication of Helicobacter pylori,” Case Reports in Gastroenterology, vol. 5, no. 2, pp. 355–360, 2011.
- G. W. Falk, B. C. Jacobson, R. H. Riddell et al., “Barrett's esophagus: prevalence-incidence and etiology-origins,” Annals of the New York Academy of Sciences, vol. 1232, no. 1, pp. 1–17, 2011.
- F. J. Xie, Y. P. Zhang, Q. Q. Zheng et al., “Helicobacter pylori infection and esophageal cancer risk: an updated meta-analysis,” World Journal of Gastroenterology, vol. 19, no. 36, pp. 6098–6107, 2013.
- F. Kamangar, S. M. Dawsey, M. J. Blaser et al., “Opposing risks of gastric cardia and noncardia gastric adenocarcinomas associated with Helicobacter pylori seropositivity,” Journal of the National Cancer Institute, vol. 98, no. 20, pp. 1445–1452, 2006.
- Y. Sakamoto, K. Oho, A. Toyonaga, M. Kumamoto, T. Haruta, H. Inoue et al., “Effect of Helicobacter pylori infection on esophagogastric variceal bleeding in patients with liver cirrhosis and portal hypertension,” Journal of Gastroenterology and Hepatology, vol. 28, no. 9, pp. 1444–1449, 2013.
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