Ghadersoltani Paria, Shoraka Shahrzad, Sadjadi Alireza, Saniee Parastoo
Department of Microbiology and Microbial Biotechnology, Faculty of Life Science and Biotechnology, Shahid Beheshti University, Tehran, Iran.
Digestive Oncology Research Center, Digestive Diseases Research Institute, Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran.
BMC Gastroenterol. 2024 Dec 19;24(1):466. doi: 10.1186/s12876-024-03516-0.
Helicobacter pylori exhibit considerable genetic diversity, especially in the cagA gene, which is prone to rearrangement, affecting gastric pathology. This study aims to identify changes in the cagA EPIYA motif patterns and gastric pathology during long-term colonization and to explore how factors such as smoking, alcohol consumption, gender, and age influence these changes.
Paired formalin-fixed paraffin-embedded (FFPE) gastric biopsies from 100 H. pylori-positive patients with digestive disorders obtained 10 years apart. After DNA extraction, the presence of H. pylori was detected by PCR amplification of the 16 S rRNA gene, and the cagA gene and its EPIYA motif patterns were identified by PCR using specific primers.
Our results showed that 90% and 91% of primary and secondary samples were cagA positive respectively. The most frequent patterns were AB and ABC, and in 52% of patients, notable changes occurred in the motif pattern of cagA. The most frequent gastric pathology was chronic inflammation in both sets of samplings and in 45% of patients, changes in pathology outcomes were reported. A significant association was found between changes in pathology outcomes and gender (P = 0.01), with alterations observed in 24 male patients and 21 female patients, and between changes in pathology outcomes and smoking (P = 0.00). Among those with changes in pathology outcomes, only 18 patients had smoking habits, indicating a potential inverse correlation between smoking and the observed changes. A logistic regression analysis was performed to examine the association between smoking, gender, changes in cagA and alterations in gastric pathology. The finding revealed no significant relationship with smoking (P = 0.978 OR = 1.012) and gender (P = 0.901, OR = 0.950), but identified a significant association with changes in the cagA gene (p = 0.001, OR = 0.296), CONCLUSION: he study highlights substantial heterogeneity in the cagA EPIYA motif patterns in long-term H. pylori colonization and notes an inverse relationship between pathology outcomes and smoking, warranting further investigation.
幽门螺杆菌表现出相当大的遗传多样性,尤其是在cagA基因中,该基因容易发生重排,影响胃部病理。本研究旨在确定长期定植期间cagA EPIYA基序模式和胃部病理的变化,并探讨吸烟、饮酒、性别和年龄等因素如何影响这些变化。
从100例幽门螺杆菌阳性的消化系统疾病患者中获取间隔10年的成对福尔马林固定石蜡包埋(FFPE)胃活检组织。提取DNA后,通过16S rRNA基因的PCR扩增检测幽门螺杆菌的存在,并使用特异性引物通过PCR鉴定cagA基因及其EPIYA基序模式。
我们的结果显示,初次和二次样本中分别有90%和91%的cagA呈阳性。最常见的模式是AB和ABC,52%的患者cagA基序模式发生了显著变化。两组样本中最常见的胃部病理是慢性炎症,45%的患者报告了病理结果的变化。病理结果变化与性别之间存在显著关联(P = 0.01),24名男性患者和21名女性患者出现了变化,病理结果变化与吸烟之间也存在显著关联(P = 0.00)。在病理结果有变化的患者中,只有18名有吸烟习惯,表明吸烟与观察到的变化之间可能存在负相关。进行逻辑回归分析以检验吸烟、性别、cagA变化与胃部病理改变之间的关联。结果显示与吸烟(P = 0.978,OR = 1.012)和性别(P = 0.901,OR = 0.950)无显著关系,但与cagA基因变化存在显著关联(p = 0.001,OR = 0.296)。
该研究突出了长期幽门螺杆菌定植中cagA EPIYA基序模式的显著异质性,并指出病理结果与吸烟之间存在负相关关系,值得进一步研究。