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Prevalence of helicobacter pylori infection among children living in a rural setting in Sub-Saharan Africa

  • Yaw Asante Awuku1Email author,
  • David Larbi Simpong2,
  • Ishmael Kunateh Alhassan2,
  • Derek Anamaale Tuoyire3,
  • Taiba Afaa4 and
  • Patrick Adu2
BMC Public HealthBMC series – open, inclusive and trusted201717:360

https://doi.org/10.1186/s12889-017-4274-z

Received: 12 July 2016

Accepted: 20 April 2017

Published: 24 April 2017

Abstract

Background

Helicobacter pylori infection affects more than half of the world’s population. It is generally acquired during childhood with no symptoms but has long- term clinical sequelae. This study estimated the prevalence of H. pylori infection amongst children in a rural environment in Africa.

Methods

We conducted a cross-sectional study over a four (4)-month period within two rural communities. 240 asymptomatic children were tested using lateral flow immunochromatographic assay for the qualitative detection of H. pylori antigen in a fecal specimen. Statistical analysis and processing was done using Stata version 11.

Results

The mean age of the participants was 10.5 ± 2.7 years with the predominant age range being 8–10 years (34.6%), and a mean household size of 7.1 ± 1.7. The study population showed a female preponderance of 57.1%. 88% of the H. pylori positive children lacked pipe and borehole drinking water. All of the positive H. pylori children practiced open-air defecation. The overall prevalence of H. pylori infection among children in this study was at least 14.2%.

Conclusion

Our study demonstrated a high prevalence of H. pylori infection among children in a rural setting. Educational status of parents did not affect H. pylori prevalence but increasing household numbers, female gender, source of drinking water other than pipe and borehole, open-air defecation and younger age were associated with a higher H. pylori prevalence.

Keywords

H.pylori infection Prevalence Immune chromatographic assay Children and Ghana

Background

Helicobacter pylori (H. pylori) is an important global infection with a worldwide prevalence of about 50 % [1, 2]. This infection is mostly acquired during childhood through the fecal-oral and oral-oral route [3, 4]. Initial infection with this organism is usually silent but symptoms and pathologic changes occur later in life. The clinical conditions and pathologic changes associated with H. pylori infection include gastritis, gastric and duodenal ulcers, gastric cancers, iron deficiency anaemia and idiopathic thrombocytopenic purpura (ITP) [58]. H. pylori infection exhibits a varied geographic distribution on both local and global scales. These variations are mostly socioeconomically driven; factors such as age, gender, genetic predisposition, ethnicity, educational level and sanitation determine the incidence and prevalence of this global infection [911].

The diagnosis of H. pylori infection is generally based on methods described as invasive or non-invasive approaches. The invasive methods are based on endoscopy and biopsy using modalities like culture, histology and rapid urease test. Non-invasive diagnostic methods include urea breath test (UBT), fecal antigen testing, serology and more recently polymerase chain reaction testing of feces. The sensitivities of the invasive and non-invasive tests are comparable and relevant in clinical practice [12, 13]. This study used the lateral flow monoclonal immune-chromatographic testing (ICT) technique to determine the prevalence of H. pylori among children.

The primary objective of this study was to determine the prevalence of H. pylori infection among the pediatric population in a rural West African setting.

Additionally, we evaluated the sociocultural and demographic factors influencing the prevalence of this infection in the communities.

Methods

Study population and design

This cross-sectional study was conducted from December 2014 to March 2015 within two rural communities in the Upper West region of Ghana. The Upper West is located at the North western corner of Ghana with latitude 9.8° - 11.0° north and longitude 1.6° - 3.0° west, bounded to Burkina Faso to the north. A total of 240 children (≤16 years) were recruited for the study. This was done by assigning the students’ numbers 1 and 2 with all those numbered 2 selected for this study. Informed consent was obtained through community leaders, teachers and parents of those who participated in the study.

Demographic details

The age, gender, type of toilet facility, source of drinking water, number of people in their household, number of siblings, and the educational level of the children as well as their parents were collected from all participants using a structured questionnaire.

Helicobacter pylori testing

Participants were given clean stool sample containers to provide fresh stool samples within 2 h in the sterilized containers provided.The children were asked to indicate the time and date of specimen collection. As an exclusion criteria, any specimen that lasted for more than 2 h before reaching us was discarded. All stool specimen were collected during their morning (7:00 am) assembly section and transported in a cold (−4 °C) specimen carrier to the laboratory. Specimen that we anticipated will stay more than 2 h before processing (from time indicated on the container and the time of testing) in the laboratory were refrigerated at (−20 °C). Eight samples in all were discarded with reference to the exclusion criteria defined in sample collection.

A lateral flow immunochromatographic assay for the qualitative detection of Helicobacter pylori antigen in human fecal specimen (OnSite H. pylori Ag Rapid Test, USA) was used.

Statistics

The data was captured using Microsoft excel, 2007 and exported to STATA version 11.0 for processing and analysis. Univariate and bivariate analysis were used to describe the results in the form of frequency and percentage distributions. Pearson’s chi squared and Fisher’s exact tests employed to test associations between various background characteristics of participants and the outcome of interest (H. pylori status) at p < 0.05 significance level.

Results

Characteristics of study population

The participant characteristics are as presented in Table 1. The mean age of the participants was 10.5 ± 2.7 years. The predominant age range was 8–10 years constituting 34.6%. However, the age group with the highest incidence of H. pylori infection was 5–7 years that had 19.5% positivity. The age group with the least H. pylori infection rate was 14–16 years with prevalence of 11.9%. The study population showed a female: male ratio of 1.3:1, with a higher proportion of females having H. pylori infection compared to males [16.8% (females) vs 10.7% (males)].
Table 1

Distribution of sample characteristics

 

H. Pylori Status

  
 

Negative

Positive

  

Characteristic

N (%)

N (%)

Total

95% CI

Participants

206 (85.8)

34 (14.2)

240

0.097, 0.186

AGE

 5–7

33 (80.5)

8 (19.5)

41

0.068, 0.321

 8–10

73 (87.9)

10 (12.1)

83

0.048, 0.191

 11–13

63 (85.1)

11 (14.9)

74

0.656, 0.231

 14–16

37 (88.1)

5 (11.9)

42

0.016, 0.221

 Pearson chi2(1) = 1.4762 Pr = 0.688

    

SEX

 Female

114 (83.2)

23 (16.8)

137

0.104, 0.231

 Male

92 (89.3)

11 (10.7)

103

0.461, 0167

 Pearson chi2(1) = 1.8044 Pr = 0.179

    
Table 2 stratifies the study participants with regards to H. pylori infection and its association with educational level of parents and household size. The educational level of either parent was not significantly associated with H. pylori infection rate. The mean household size of the study participants was 7.1 ± 1.7. Interestingly, participant household size was significantly associated with the prevalence of H. pylori infection (p = 0.000; Fisher’s exact test).
Table 2

Association of H. pylori infection with parent education and household size

 

H. Pylori Status

  
 

Negative

Positive

  

Characteristic

N (%)

N (%)

Total

95% CI

Mother’s Edu. Status

 No

170 (85.9)

28 (14.1)

198

0.092, 0.190

 Yes

36 (85.7)

6 (14.3)

42

0.032, 0.253

 Pearson chi2(1) = 0.0006 Pr = 0.981

    

Father’s Edu. Status

 No

140 (86.4)

22 (13.6)

162

0.824, 0.189

 Yes

66 (84.6)

12 (15.4)

78

0.071, 0.235

 Pearson chi2(1) = 0.1410 Pr = 0.707

    

No. of People in a Household

 4

11 (84.6)

2 (15.4)

13

0.073, 0.380

 5

20 (60.6)

13 (39.4)

33

0.217, 0.569

 6

22 (56.4)

17 (43.6)

39

0.273, 0.598

 7

51 (96.2)

2 (3.8)

53

0.015, 0.090

 8

43 (100)

0

43

-

 9

41 (100)

0

41

-

 10

18 (100)

0

18

-

 Fisher’s exact test: Pr = 0.000

    
Table 3 stratifies the H. pylori infection status of the participants with regards to number of siblings and lifestyle choices. Overall, 14.2% of the participants had H. pylori infection. About 48.3% of the participants had no access to pipe/borehole as a source of water. Whereas 25.9% (116/240) of those having no access to pipe/borehole were H. pylori positive, only 3.2% of those with pipe/borehole were H. pylori positive. This difference was statistically significant (p = 0.000; Fisher’s exact test). Overall, 88% (30/34) of the H. pylori stool antigen positive participants lacked pipe/borehole drinking water. In addition, 70.4% (169/240) of the participants practiced open air defaecation. Not surprisingly, 20.1% of those practicing open-air defaecation were H pylori positive, none of the participants using pit/wc was H. pylori positive.
Table 3

Association of H. pylori infection with lifestyle choices

 

H. Pylori Status

  
 

Negative

Positive

  

Characteristic

N (%)

N (%)

Total

95% CI

Number of siblings

 1–3

103 (75.2)

34 (24.8)

137

0.174, 0.321

 4+

103 (100%)

0

103

 Fischer’s exact test: p = 0.000

    

Pets/Livestock

 None

62(64.6)

34 (35.4)

96

0.256, 0.451

 Pet

49 (100)

0

49

 2 livestock

95 (100)

0

95

 Fischer’s exact test: p = 0.000

    

Source of drinking water

 Pipe/borehole

120 (96.8)

4 (3.2)

124

0.001, 0.063

 Other than pipe/borehole

86 (74.1)

30 (25.9)

116

0.177, 0.339

 Fisher’s exact test: Pr = 0.000

    

Type of laterine facility

 Open air

135 (79.9)

34 (20.1)

169

0.140, 2.262

 Pit/WC

71 (100)

0

71

Discussion

H. pylori infection affects more than half of the world’s population including children. Because of the fecal-oral mode of transmission it is more prevalent in poor socioeconomic environments. H. pylori is described in current medical literature as a group 1 carcinogen but the health implications of infection in children remains uncertain [2]. This may be problematic particularly in African children who may harbor more virulent strains. The long term sequelae of H. pylori infection was ignored because of what has been described as “African enigma” [6]. It has however been shown that all complications including carcinoma do occur in the African population [6, 14]. Our study used a noninvasive method to qualitatively detect H. pylori antigen in human fecal specimen. We acknowledge the limitation in testing as the H. pylori stool antigen testing was not compared with any gold standard diagnostic method. However, the ethical and feasibility challenges of upper gastrointestinal endoscopy as a screening tool in an asymptomatic pediatric population was strongly considered [15].

The global prevalence of H. pylori infection is generally higher in developing countries than the developed world [16, 17]. Transmission of H. pylori infection is rapidly decreasing in the developed countries predictably because of improvement in the sanitation [18, 19]. There is infrequent H. pylori infection during childhood in the developed countries with the United States reporting less than 5% in under five years and up to 10% by adolescent age. However in developing countries the story is different with about 50% of children under five infected and as high as 90% in some adult populations [20, 21]. We demonstrated a prevalence of at least 14.2% among asymptomatic children between the ages of 5–16 years living in a rural setting in sub-Saharan Africa (SSA). Our finding in terms of prevalence of H. pylori infection among children was not consistent with the developing countries data [2224]. This could be attributed to the differences in the study design, population dynamics, as well as the specificities of techniques employed in the studies. Antibody testing procedures for H. pylori detection are used in some studies but is unable to differentiate active infection from a previous in the early weeks of follow up after eradication therapy. Our study employed H. pylori stool antigen testing methods because of its non-invasive nature especially in a children population.

Our study had a female preponderance of 57.1% with higher H. pylori prevalence among females (16.8%) than males (10.7%). The gender effect on prevalence of H. pylori infection in many populations is varied. Woodward and colleagues reported a higher prevalence in men than women [20, 23] whiles others reported no difference. A meta-analysis reported a male predominance in adults but not in children [19, 25, 26]. Our study in children demonstrated a higher prevalence in females with no plausible explanation.

The age effect on prevalence is well documented in H. pylori epidemiology with a positive correlation between age and prevalence [27, 28]. Our study showed higher prevalence in the younger age group and decreasing prevalence with advancing age. This is a reverse of the pattern in most population studies. Educational status has been used as a proxy marker of socioeconomic status and an important determinant of H. pylori prevalence in developed and resource limited settings [2931]. The educational status of parents in our study did not affect the prevalence significantly. Crowding in households and increasing household contact have been linked as risk factors of H. pylori infection [32, 33]. As the number of people in a household increased the prevalence of H. pylori also increased [34]. Source of drinking water other than pipe and borehole increased the prevalence of H. pylori infection as well as open-air defecation. Water is an important source of H. pylori spread and many studies have actually confirmed it. Therefore, handling of water and poor sanitation will be a good milieu for the spread of this infection. Our study support this assertion as we also realized that source of water other than pipe and borehole and open air defecation were associated with higher prevalence of H. pylori infection [35, 36].

In our environment, poverty and poor socioeconomic status are associated with higher household numbers. It is therefore not surprising giving the mode of transmission that prevalence in our study increased with increasing household numbers. Proper hand washing and waste disposing systems will help control infection in households especially in crowded places.

Conclusion

Our study demonstrated a high prevalence of H. pylori infection among children in a rural setting. Educational status of parents did not affect H. pylori prevalence but increasing household numbers, female gender, younger age, open-air defecation and source of drinking water other than pipe and borehole were associated with a higher prevalence.

Abbreviations

ICT: 

Immune chromatographic testing

ITP: 

Idiopathic thrombocytopenic purpura

UBT: 

Urease Breath Test

Declarations

Acknowledgements

We acknowledge the parents,teachers and elders of the communities for their support during the data collection.

Funding

Self funded by authors.

Availability of data and materials

The datasets during and/or analysed during the current study is available from the corresponding author on reasonable request.

Authors' contributions

YAA concept, wrote and reviewed manuscript, DLS concept, data collection and reviewed manuscript, IKA data collection, DAT statistical analysis, TA reviewed manuscript, PA statistical display of results and reviewed manuscript. All authors read and approved the final manuscript.

Competing interests

The authors declare that they have no competing interests.

Consent for publication

Not applicable.

Ethics approval and consent to participate

Approval was obtained from the University of Cape Coast, Institutional Review Board for the conduct of this research work and publication. Informed consent was obtained from the parents and guardians of the study participants.

Publisher’s Note

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Authors’ Affiliations

(1)
Department of Medicine and Therapeutics, University of Cape Coast
(2)
Department of Medical Laboratory Technology, University of Cape Coast
(3)
Department of Community Medicine, Universty of Cape Coast
(4)
Department of Child Health, University of Ghana

References

  1. Go MF. Review article: natural history and epidemiology of Helicobacter pylori infection. Aliment Pharmacol Ther. 2002;16(Suppl 1):3–15.View ArticlePubMedGoogle Scholar
  2. Cancer, I.A.f.R.o, International Agency for Research on Cancer Working Group on the Evaluation of Carcinogenic Risks to Humans., in Helicobacter pylori. Schistosomes, Liver Flukes and Helicobacter pylori. Lyon, France: International Agency for Research; 1994. p. 177–240.Google Scholar
  3. Malaty HM, et al. Age at acquisition of Helicobacter pylori infection: a follow-up study from infancy to adulthood. Lancet. 2002;359(9310):931–5.View ArticlePubMedGoogle Scholar
  4. Parsonnet J, Shmuely H, Haggerty T. Fecal and oral shedding of Helicobacter pylori from healthy infected adults. JAMA. 1999;282(23):2240–5.View ArticlePubMedGoogle Scholar
  5. Bittencourt PF, et al. Gastroduodenal peptic ulcer and Helicobacter pylori infection in children and adolescents. J Pediatr. 2006;82(5):325–34.View ArticleGoogle Scholar
  6. Agha A, Graham DY. Evidence-based examination of the African enigma in relation to Helicobacter pylori infection. Scand J Gastroenterol. 2005;40(5):523–9.View ArticlePubMedGoogle Scholar
  7. Gasbarrini A, et al. Regression of autoimmune thrombocytopenia after eradication of Helicobacter pylori. Lancet. 1998;352(9131):878.View ArticlePubMedGoogle Scholar
  8. Franchini M, et al. Effect of Helicobacter pylori eradication on platelet count in idiopathic thrombocytopenic purpura: a systematic review and meta-analysis. J Antimicrob Chemother. 2007;60(2):237–46.View ArticlePubMedGoogle Scholar
  9. Malaty HM, et al. Natural history of Helicobacter pylori infection in childhood: 12-year follow-up cohort study in a biracial community. Clin Infect Dis. 1999;28(2):279–82.View ArticlePubMedGoogle Scholar
  10. Pounder RE, Ng D. The prevalence of Helicobacter pylori infection in different countries. Aliment Pharmacol Ther. 1995;9(Suppl 2):33–9.PubMedGoogle Scholar
  11. Archampong TN, Asmah RH, Wiredu E, Gyasi RK, Nkrumah KN, Rajakumar K. Epidemiology of Helicobacter pylori infection in dyspeptic Ghanaian patients. Pan Afr Med J. 2015;20:178.PubMedPubMed CentralGoogle Scholar
  12. Megraud F, European Paediatric Task Force on Helicobacter pylori. Comparison of non-invasive tests to detect Helicobacter pylori infection in children and adolescents: results of a multicenter European study. J Pediatr. 2005;146(2):198–203.View ArticlePubMedGoogle Scholar
  13. Gisbert JP, Pajares JM. Stool antigen test for the diagnosis of Helicobacter pylori infection: a systematic review. Helicobacter. 2004;9(4):347–68.View ArticlePubMedGoogle Scholar
  14. Segal I, Ally R, Mitchell H. Helicobacter pylori--an African perspective. QJM. 2001;94(10):561–5.View ArticlePubMedGoogle Scholar
  15. Bourke B, et al. Canadian Helicobacter Study Group Consensus Conference: Update on the approach to Helicobacter pylori infection in children and adolescents--an evidence-based evaluation. Can J Gastroenterol. 2005;19(7):399–408.View ArticlePubMedGoogle Scholar
  16. Perez-Perez GI, Rothenbacher D, Brenner H. Epidemiology of Helicobacter pylori infection. Helicobacter. 2004;9(Suppl 1):1–6.View ArticlePubMedGoogle Scholar
  17. Salih BA. Helicobacter pylori infection in developing countries: the burden for how long? Saudi J Gastroenterol. 2009;15(3):201–7.View ArticlePubMedPubMed CentralGoogle Scholar
  18. Brown LM. Helicobacter pylori: epidemiology and routes of transmission. Epidemiol Rev. 2000;22(2):283–97.View ArticlePubMedGoogle Scholar
  19. Khalifa MM, Sharaf RR, Aziz RK. Helicobacter pylori: a poor man's gut pathogen? Gut Pathog. 2010;2(1):2.View ArticlePubMedPubMed CentralGoogle Scholar
  20. Weaver LT. Royal Society of Tropical Medicine and Hygiene Meeting at Manson House, London, 16 February 1995. Aspects of Helicobacter pylori infection in the developing and developed world. Helicobacter pylori infection, nutrition and growth of West African infants. Trans R Soc Trop Med Hyg. 1995;89(4):347–50.View ArticlePubMedGoogle Scholar
  21. Rothenbacher D, Brenner H. Burden of Helicobacter pylori and H. pylori-related diseases in developed countries: recent developments and future implications. Microbes Infect. 2003;5(8):693–703.View ArticlePubMedGoogle Scholar
  22. Bassily S, et al. Seroprevalence of Helicobacter pylori among Egyptian newborns and their mothers: a preliminary report. AmJTrop Med Hyg. 1999;61(1):37–40.Google Scholar
  23. Frenck RW Jr, et al. Sensitivity and specificity of various tests for the diagnosis of Helicobacter pylori in Egyptian children. Pediatrics. 2006;118(4):e1195–202.View ArticlePubMedGoogle Scholar
  24. Abd El-Latif AM, Ali ASA, Abdel-Hady M, Borai MBM. Seroprevalence of Helicobacter Pylori in Secondary Immunocompromised Children. J Am Sci. 2011;7(9):592–5.Google Scholar
  25. de Martel C, Parsonnet J. Helicobacter pylori infection and gender: a meta-analysis of population-based prevalence surveys. Dig Dis Sci. 2006;51(12):2292–301.View ArticlePubMedGoogle Scholar
  26. Woodward M, Morrison C, McColl K. An investigation into factors associated with Helicobacter pylori infection. J Clin Epidemiol. 2000;53(2):175–81.View ArticlePubMedGoogle Scholar
  27. Breuer T, et al. Prevalence of and risk factors for Helicobacter pylori infection in the western part of Germany. Eur J Gastroenterol Hepatol. 1996;8(1):47–52.View ArticlePubMedGoogle Scholar
  28. Cherian S, et al. The epidemiology of Helicobacter pylori infection in African refugee children resettled in Australia. Med J Aust. 2008;189(8):438–41.PubMedGoogle Scholar
  29. Lopes AI, Vale FF, Oleastro M. Helicobacter pylori infection - recent developments in diagnosis. World J Gastroenterol. 2014;20(28):9299–313.PubMedPubMed CentralGoogle Scholar
  30. Darko R, et al. Changing Patterns of the Prevalence of Helicobacter Pylori Among Patients at a Corporate Hospital in Ghana. Ghana Med J. 2015;49(3):147–53.View ArticlePubMedPubMed CentralGoogle Scholar
  31. Campuzano-Maya G. Hematologic manifestations of Helicobacter pylori infection. World J Gastroenterol. 2014;20(36):12818–38.View ArticlePubMedPubMed CentralGoogle Scholar
  32. Rosenstock SJ, et al. Socioeconomic factors in Helicobacter pylori infection among Danish adults. Am J Public Health. 1996;86(11):1539–44.View ArticlePubMedPubMed CentralGoogle Scholar
  33. Mendall MA, et al. Childhood living conditions and Helicobacter pylori seropositivity in adult life. Lancet. 1992;339(8798):896–7.View ArticlePubMedGoogle Scholar
  34. McCallion WA, et al. Helicobacter pylori infection in children: relation with current household living conditions. Gut. 1996;39(1):18–21.View ArticlePubMedPubMed CentralGoogle Scholar
  35. Banda K, et al. Water handling, sanitation and defecation practices in rural southern India: a knowledge, attitudes and practices study. Trans R Soc Trop Med Hyg. 2007;101(11):1124–30.View ArticlePubMedGoogle Scholar
  36. Aziz RK, Khalifa MM, Sharaf RR. Contaminated water as a source of Helicobacter pylori infection: A review. J Adv Res. 2015;6(4):539–47.View ArticlePubMedGoogle Scholar

Copyright

© The Author(s). 2017

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