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口腔幽门螺杆菌与胃部并发症的关联。

Association of oral Helicobacter pylori with gastric complications.

机构信息

Department of Oral Pathology, Dow Dental College, Dow University of Health Sciences, Karachi, Pakistan.

Department of Physiology, University of Karachi, Karachi, Pakistan.

出版信息

Life Sci. 2018 Jul 15;205:125-130. doi: 10.1016/j.lfs.2018.05.026. Epub 2018 May 12.

Abstract

AIM

This study was aimed to identify the presence of Helicobacter pylori (H. pylori) genes in oral mucosa and find out their relationship between oral H. pylori infection and gastric complications.

METHODS

This study is a case control study consists of 567 subjects with periodontal infection (278 gastric complication cases and 289 controls normal gastric intestinal mucosa) with age range of 20-80 years. Oral health status was recorded by calculating oral hygiene index (OHI), probing depths (PD) and clinical attachment loss (CAL). Each participant provided gastric biopsy and plaque samples which were subjected to H. pylori detection. Polymerase chain reaction (PCR) with different primers specifically β globulin, 16SrRNA, babA, cagA, ureA, ureC and vacA gene was performed which were then analyzed using gel electrophoresis.

RESULTS

No significant differences (χ = 11.873, p value > 0.05) were observed between oral H. pylori and gastric infections/complications. However, H. pylori increase the risk of developing gastro-esophageal reflux grade II (OR = 1.458, 95%CI = 0.659-3.226), normal upper GIT mucosa with lax esophageal sphincters (OR = 1.215, 95%CI = 0.285-5.181) and duodenal ulcer/duodenitis (OR = 2.187, 95%CI = 0.225-21.278). This study also showed a significant increased risk of gastritis with babA gene.

CONCLUSION

Oral pathogenic H. pylori genes may enhance the severity of the gastric infection.

摘要

目的

本研究旨在确定口腔黏膜中是否存在幽门螺杆菌(H. pylori)基因,并找出口腔 H. pylori 感染与胃部并发症之间的关系。

方法

本研究为病例对照研究,共纳入 567 例牙周感染患者(278 例有胃部并发症,289 例为胃-肠黏膜正常对照),年龄 20-80 岁。通过计算口腔卫生指数(OHI)、探诊深度(PD)和临床附着丧失(CAL)来记录口腔健康状况。每位参与者均提供胃活检和牙菌斑样本,用于检测 H. pylori。采用不同引物的聚合酶链反应(PCR)检测β球蛋白、16SrRNA、babA、cagA、ureA、ureC 和 vacA 基因,然后通过凝胶电泳进行分析。

结果

口腔 H. pylori 与胃部感染/并发症之间无显著差异(χ²=11.873,p 值>0.05)。然而,H. pylori 增加了发生 II 级胃食管反流的风险(OR=1.458,95%CI=0.659-3.226)、食管下括约肌松弛的正常上胃肠道黏膜(OR=1.215,95%CI=0.285-5.181)和十二指肠溃疡/十二指肠炎(OR=2.187,95%CI=0.225-21.278)的风险。本研究还显示 babA 基因与胃炎的发生风险显著增加有关。

结论

口腔致病性 H. pylori 基因可能会加重胃部感染的严重程度。

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