The Role of Demographic Factors and IL-32 Levels in Helicobacter Pylori-Associated Diseases

Authors

  • Hussain Abdulhassan Owaid Department of Microbiology, College of Medicine, University of Thi-Qar, 64001, Iraq
  • Saad Abdulaziz Atyah Ali Department of Microbiology, College of Medicine, University of Thi-Qar, 64001, Iraq.
  • Faez Khalaf Abdulmuhsen Department of Microbiology, College of Medicine, University of Thi-Qar, 64001, Iraq

Keywords:

Gastric disorders, (Helicobacter pylori), IL-32(interlukin-32)

Abstract

Increased production of IL-32 proinflammatory cytokine, has been demonstrated in
Helicobacter pylori-associated gastric mucosal inflammation. IL-32, a newly characterized cytokine, is
thought to be a key mediator in host responses to bacterial infections.
Background: Helicobacter pylori (H.pylori) was discovered in 1983 and has been identified as the
main pathogenic factor for gastric and duodenal peptic ulcers and gastric cancer which is the third most
common cause of cancer-related death in the world The bacterium is a micro-aerophilic, curved, gram
negative bacteria, infection causes chronic gastritis. IL32, proinflammatory cytokine secreted by NK cell,
macrophage, endothelial cell and monocyte, the studies showed that increase expression of IL-32 is
elevated in human gastritis and gastric cancer tissues.
Aim of study: The study aimed to determined the relation of some demographic parameters to gastric
disorders due to H.pylori and assessment of IL-32 concentration.
Material and methods: The study design is a case - control . was performed in Thi-Qar Province,
Iraq, from Nov-2023 to Jan-2024. The diseases was diagnosed by physician and UBT. Serum samples
were taken from 180 participants in various age included (120 cases and 60 controls) . The ELISA
technique used to detects level IL-32 .
Results: The present study showed a significant difference at p. value <0.05, between patients and
control group according to sex, the highest percentage of infection in female were 69.17%, also, a
significant difference was recorded according to age groups, where the highest percent record in second
age group(16-30) 34.17%. With regard residency the study investigated a significant difference was urban
scored 70.83% of patients. IL-32 level was showed increased in the patients compared to control group,
at p.value <0.05.
Conclusion: H. Pylori infection generally associated with demographic data such as sex and age. High
increase in the level IL-32 indicated that the gastric H. pylori diseases induced strong systemic immune
response.

References

Peleteiro, B., et al., Prevalence of Helicobacter pylori infection worldwide: a systematic review of studies

with national coverage. Digestive diseases and sciences, 2014. 59: p. 1698-1709.

Takeshima, E., et al., Helicobacter pylori-induced interleukin-12 p40 expression. Infection and immunity,

77(4): p. 1337-1348.

Das, J.C. and N. Paul, Epidemiology and pathophysiology of Helicobacter pylori infection in children. The

Indian Journal of Pediatrics, 2007. 74(3): p. 287-290.

Ando, T., et al., Causal role of Helicobacter pylori infection in gastric cancer. World journal of

gastroenterology: WJG, 2006. 12(2): p. 181.

Koelman, L., et al., Cytokines for evaluation of chronic inflammatory status in ageing research: reliability

and phenotypic characterisation. Immunity & Ageing, 2019. 16: p. 1-12.

Romero-Adrián, T.B., et al., Helicobacter pylori: bacterial factors and the role of cytokines in the immune

response. Current microbiology, 2010. 60: p. 143-155.

Crabtree, J.E., The role of cytokine in Helicobacter pylori infection. Mucosal Immunology Update, 1994. 2: p. 5-7.

Sakitani, K., et al., Role of interleukin-32 in Helicobacter pylori-induced gastric inflammation. Infection

and immunity, 2012. 80(11): p. 3795-3803.

Mohammed, K.I.A., et al., Interleukin-32, interleukin-33 and acid phosphatase levels in patients with Helicobacter Pylori.

Metwally, M.A.E.A., et al., Relationship between Helicobacter Pylori Morphological Forms in Gastric

Biopsy and Helicobacter Pylori Stool Antigen. Benha Medical Journal, 2024. 41(2): p. 56-65.

Hong, W., et al., Prevalence of Helicobacter pylori infection in a third-tier Chinese city: relationship with

gender, age, birth-year and survey years. Microb Health Dis, 2019. 1: p. e150.

Akeel, M., et al., Prevalence and factors associated with H. pylori infection in Saudi patients with

dyspepsia. Electronic physician, 2018. 10(9): p. 7279.

Ashtari, S., et al., The prevalence of Helicobacter pylori is decreasing in Iranian patients. Gastroenterology

and hepatology from bed to bench, 2015. 8(Suppl1): p. S23.

Xia, H., et al., Demographic and endoscopic characteristics of patients with Helicobacter pylori positive

and negative peptic ulcer disease. Gastric Cancer, 2000. 2: p. 0.7.

Leung, K.K., N. Jawaid, and N. Bollegala, Gender differences in gastroenterology and hepatology

authorship and editorial boards. Gastrointestinal Endoscopy, 2021. 94(4): p. 713-723.

De Filippis, A., et al., Gastrointestinal disorders and metabolic syndrome: Dysbiosis as a key link and

common bioactive dietary components useful for their treatment. International Journal of Molecular Sciences, 2020.

(14): p. 4929.

Breckan, R.K., et al., The all‐age prevalence of helicobacter pylori infection and potential transmission

routes. a population‐based study. Helicobacter, 2016. 21(6): p. 586-595.

Zhang, M., et al., Dietary and lifestyle factors related to gastroesophageal reflux disease: a systematic

review. Therapeutics and Clinical Risk Management, 2021: p. 305-323.

Fitzenberger, J., et al., Urban–rural differences of age-and species-specific campylobacteriosis incidence,

Hesse, Germany, July 2005–June 2006. Eurosurveillance, 2010. 15(42): p. 19693.

Aguemon, B., et al., Prevalence and risk-factors for Helicobacter pylori infection in urban and rural

Beninese populations. Clinical microbiology and infection, 2005. 11(8): p. 611-617.

Brown, L.M., et al., Helicobacter pylori infection in rural China: demographic, lifestyle and environmental

factors. International journal of epidemiology, 2002. 31(3): p. 638-645.

Windsor, H.M., et al., Prevalence of Helicobacter pylori in Indigenous Western Australians: comparison

between urban and remote rural populations. Medical journal of Australia, 2005. 182(5): p. 210-213.

Johnson, C.H., et al., An evaluation of the epidemiology, management and outcomes for perforated peptic

ulcers across the North of England over 15 years: A retrospective cohort study. International Journal of Surgery,

64: p. 24-32.

Herbarth, O., et al., Helicobacter pylori prevalences and risk factors among school beginners in a German

urban center and its rural county. Environmental health perspectives, 2001. 109(6): p. 573-577.

Aguilar, G.R., G. Ayala, and G. Fierros-Zárate, Helicobacter pylori: recent advances in the study of its

pathogenicity and prevention. Salud publica de Mexico, 2001. 43: p. 237-247.

Alizadeh, A., et al., Seroprevalence of Helicobacter pylori in Nahavand: a population-based study. EMHJ

Eastern Mediterranean Health Journal, 15 (1), 129-135, 2009, 2009.

Zhou, X., J. Wu, and G. Zhang, Association between Helicobacter pylori and asthma: a meta-analysis.

European journal of gastroenterology & hepatology, 2013. 25(4): p. 460-468.

Xiong, X., et al., Helicobacter pylori infection and the prevalence of hypertension in Chinese adults: The

Dongfeng‐Tongji cohort. The Journal of Clinical Hypertension, 2020. 22(8): p. 1389-1395.

Huang, M., et al., Association between Helicobacter pylori infection and systemic arterial hypertension: a

meta-analysis. Arquivos Brasileiros de Cardiologia, 2021. 117: p. 626-636.

Makola, D., D.A. Peura, and S.E. Crowe, Helicobacter pylori infection and related gastrointestinal

diseases. Journal of clinical gastroenterology, 2007. 41(6): p. 548-558.

Griñó, S.P., J. Such, JA Casellas, M. Niveiro, M. Andreu, J. Sáez, E. Griñó, JM Palazón, F. Carnicer, M.

Pérez-Mateo, P, Comparison of diagnostic methods for Helicobacter pylori infection in patients with upper

gastrointestinal bleeding. Scandinavian journal of gastroenterology, 2001. 36(12): p. 1254-1258.

Pourakbari, B., et al., Diagnosis of Helicobacter pylori infection by invasive and noninvasive tests. Brazilian

Journal of Microbiology, 2013. 44: p. 795-798.

Monteiro, L., et al., Diagnosis ofHelicobacter PyloriInfection: Noninvasive Methods Compared To Invasive

Methods and Evaluation of Two New Tests. Official journal of the American College of Gastroenterology| ACG,

96(2): p. 353-358.

Cosgun, Y., et al., Evaluation of invasive and noninvasive methods for the diagnosis of Helicobacter pylori

infection. Asian Pacific journal of cancer prevention: APJCP, 2016. 17(12): p. 5265.

Peng, L.-s., et al., Elevated interleukin-32 expression is associated with Helicobacter pylori-related

gastritis. PLoS One, 2014. 9(3): p. e88270.

Song, X., et al., Association between interleukin gene polymorphisms and susceptibility to gastric cancer

in the Qinghai population. Journal of International Medical Research, 2021. 49(5): p. 03000605211004755.

Diakowska, D. and M. Krzystek-Korpacka, Local and Systemic Interleukin-32 in Esophageal, Gastric, and

Colorectal Cancers: Clinical and Diagnostic Significance. Diagnostics (Basel), 2020. 10(10).

Erturk, K., et al., Clinical significance of serum interleukin-29, interleukin-32, and tumor necrosis factor

alpha levels in patients with gastric cancer. Tumour Biol, 2016. 37(1): p. 405-12.

Liu, Q.-H., et al., Clinical implications of interleukins-31, 32, and 33 in gastric cancer. World Journal of

Gastrointestinal Oncology, 2022. 14(9): p. 1808.

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2024-11-12

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