慢性胃炎消化不良患者幽门螺杆菌oipA和dupA基因的检测

IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL Alexandria Journal of Medicine Pub Date : 2020-01-01 DOI:10.1080/20905068.2020.1780675
Marwa El-Sayed, N. Musa, M. Eltabbakh, D. Abdelhamid, S. M. Mostafa, M. Salah, H. Faheem, R. Hassan
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引用次数: 3

摘要

摘要幽门螺杆菌(H.pylori)是一种具有广泛遗传多样性的微生物,在发展中国家感染大多数人的胃,导致不同个体的多种临床结果,如胃炎、溃疡或癌症。外炎症蛋白A(oipA)和十二指肠溃疡促进基因(dupA)是决定患者预后的可能毒力因素。目的检测埃及消化不良患者幽门螺杆菌oipA和dupA基因,并探讨其和不同程度相关慢性胃炎的相关性。方法该研究招募了50名消化不良患者,他们于2019年6月至12月在艾因沙姆斯大学医院胃肠科和热带科的胃肠内窥镜科接受上消化道内窥镜检查。从每位患者身上取四个胃窦活检组织进行聚合酶链式反应测定,以检测毒力基因oipA、dupA和cagA,并进行组织病理学评估。结果40例患者经组织病理学及PCR检测均为幽门螺杆菌阳性。cagA、oipA和dupA分别在6例(15%)、13例(32.5%)和9例(22.5%)活检中被鉴定。cagA和oipA基因均与胃炎严重程度的增加高度相关。只有oipA毒力基因与胃十二指肠炎有高度显著的相关性。cagA和oipA基因之间存在高度显著的中度关联。结论oipA可能是一种毒力生物标志物,对预测慢性胃炎患者胃黏膜损伤的进展,以及针对这些患者进行抗菌治疗以预防严重的胃十二指肠疾病具有重要价值。
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Detection of Helicobacter pylori oipA and dupA genes among dyspeptic patients with chronic gastritis
ABSTRACT Helicobacter pylori (H. pylori) is a microbe with wide genetic diversity that infects the stomach of most people in developing countries, leading to several clinical outcomes among different individuals such as gastritis, ulcers, or gastric cancer. Outer inflammatory protein A (oipA) and duodenal ulcer promoting (dupA) genes are among the possible virulence factors which determine the patient outcome. Aim To detect oipA and dupA genes of H. pylori among dyspeptic Egyptian patients, and to investigate their correlation with the varying degrees of the associated chronic gastritis. Methods The study enrolled 50 patients with dyspepsia, attending the Gastrointestinal Endoscopy unit of the Gastroenterology and Tropical Departments at Ain Shams University Hospital for upper gastrointestinal endoscopy, in the period between, June and, December 2019. Four antral gastric biopsies were taken from each patient for polymerase chain reaction assay to detect the virulence genes oipA, dupA, and cagA and for histopathological assessment. Results Forty patients were H. pylori positive by histopathology and PCR. cagA, oipA, and dupA were identified in 6 (15%), 13 (32.5%), 9 (22.5%) of biopsies, respectively. Both cagA and oipA genes were highly significantly associated with increasing the severity of gastritis. Only oipA virulence gene showed a highly significant association with gastroduodenitis. There was a highly significant moderate association between cagA and oipA genes. Conclusion oipA could be a virulence biomarker that serves a great value in predicting the progress of gastric mucosal damage in patients with chronic gastritis, and targeting antimicrobial therapy in those patients to prevent severe gastroduodenal diseases.
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来源期刊
Alexandria Journal of Medicine
Alexandria Journal of Medicine MEDICINE, GENERAL & INTERNAL-
自引率
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发文量
15
审稿时长
10 weeks
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