Investigation of the Presence of Helicobacter Pylori and the cagA Gene in Nasal Polyp Tissues by PCR

dc.contributor.authorÜstündağ, Yasemin
dc.contributor.authorKavuk, Anil
dc.contributor.authorToraman, Zülal Aşçı
dc.contributor.authorTan, Mehmet
dc.contributor.authorKavuk, Yasemin
dc.contributor.authorKaradağ, Kadir Ziya
dc.contributor.authorÖner, Pınar
dc.date.accessioned2026-09-08T07:04:23Z
dc.date.issued2026
dc.departmentFırat Üniveristesi
dc.description.abstractPurpose : Nasal polyps are inflammatory lesions of the sinonasal mucosa and may be influenced by microbial factors. Helicobacter pylori and its cagA gene are of interest because of their possible association with mucosal inflammation. This study aimed to detect H. pylori DNA and the cagA gene in nasal polyp tissues by polymerase chain reaction (PCR). Materials and Methods : This cross-sectional study included 45 nasal polyp specimens from patients undergoing surgery. Genomic DNA was extracted using a commercial kit. PCR analysis targeted the glmM gene for H. pylori detection and the cagA gene for assessment of virulence-associated genetic material. Positive and negative controls were included. Demographic variables and PCR positivity rates were evaluated descriptively, and associations with age groups were assessed statistically. Results: All samples were successfully analyzed. The group included 26 men (57.78%) and 19 women (42.22%), aged 15-75 years. glmM-based H. pylori positivity was detected in 19 samples (42.22%), whereas 26 (57.78%) were negative. cagA positivity was found in 16 samples (35.55%), whereas 29 (64.45%) were negative. Although glmM and cagA positivity rates were numerically higher in the 50-59 and 60-75-year age groups, no significant association was found between age group and PCR positivity. Conclusion: PCR analysis demonstrated H. pylori DNA and the cagA gene in a subset of nasal polyp tissues, suggesting a possible association between microbial genetic material and the chronic inflammatory microenvironment. However, PCR positivity alone does not prove viable bacteria, active colonization, or causality. Larger controlled studies integrating molecular, microbiological, and clinical parameters are needed.
dc.identifier.dergipark1919535
dc.identifier.doi10.46332/aemj.1919535
dc.identifier.endpage274
dc.identifier.issn2619-9203
dc.identifier.issue2
dc.identifier.orcid0000-0003-3317-0279
dc.identifier.orcid0009-0005-0164-3141
dc.identifier.orcid0000-0001-5202-8564
dc.identifier.orcid0000-0001-8557-0886
dc.identifier.orcid0009-0000-7988-4889
dc.identifier.orcid0009-0009-2238-8839
dc.identifier.orcid0000-0001-9592-5986
dc.identifier.startpage265
dc.identifier.urihttps://doi.org/10.46332/aemj.1919535
dc.identifier.urihttps://hdl.handle.net/11508/64714
dc.identifier.volume10
dc.language.isoen
dc.publisherKırşehir Ahi Evran Üniversitesi
dc.relation.ispartofAhi Evran Medical Journal
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_DergiPark_20250903
dc.subjectbacterial proteins
dc.subjectglmM
dc.subjectinflammation
dc.subjectsinusitis
dc.subjectvirulence factors
dc.titleInvestigation of the Presence of Helicobacter Pylori and the cagA Gene in Nasal Polyp Tissues by PCR
dc.typeArticle

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