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慢性胃炎患者口腔与胃内幽门螺杆菌的检测分析 被引量:17

Detection and analysis of Helicobacter pylori in oral cavity and stomach from chronic gastritis patients
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摘要 目的 研究胃炎患者口腔内是否存在幽门螺杆菌 (Hp) ,并分析口腔内Hp与胃内Hp的基因型的异同。方法 依据Hp特异的尿素酶C和cagA基因设计引物 ,建立PCR方法。检测和鉴定32例慢性胃炎患者不同牙齿的龈上和龈下菌斑 (每人检查 6个牙 12份菌斑 )中的Hp ,并用单链构象多态性 (SSCP)分析菌斑和胃内Hp的基因型异同。结果  32例患者中有 2 7例口腔内至少一份牙菌斑中检出Hp ,共计 384份菌斑有 113份 (2 9 4% )检测出Hp ,龈下菌斑中Hp检出率 (37% ) ,显著高于龈上菌斑 (2 1 9% ) (P <0 0 1)。同一家庭 4例患者中有 3例菌斑与胃内Hp的SSCP带型相同 ,4例患者菌斑中至少有一种相同SSCP带型的Hp。 Objective To investigate the prevalence of Helicobacter pylori (Hp) in the oral cavity of gastritis patients and analyze the genotype similarity of Hp in the oral cavity with that in the stomach. Methods A total of 384 plaque samples were collected from 32 patients with chronic gastritis and chronic periodontitis, one supragingival plaque sample and one subgingival plaque sample from one tooth, totally 6 teeth having been examined for one patient. Gastric biopsy specimens were collected by gastroscopy, four pieces of specimen for one patient, to undergo rapid urease test, histopathology, and Warthin-Starry silver staining. PCR assay was conducted on each specimen with primers based on the sequences of urease C gene and cag A gene specific to Hp to amplify the 294-bp and 400-bp DNA fragments. The identity of amplified products was confirmed by restriction endonuclease digestion. Two PCR positive products (Hp urease C gene 294 bp fragments) from the dental plaque samples and one gastric biopsy specimen from one of the four patients in the same family, totalling 12 specimens, were further examined by single-strand conformation polymorphism (SSCP). Results Twenty-seven patients (84.4%) had at least one Hp positive dental plaque sample. In total, 113 (29.4%) of the 384 tested samples were urease C gene positive and 9 (2.3%) were positive for both urease C gene and cag A gene. The Hp positive rate was significantly higher in subgingival plaque (71/192, 37%) than in supragingival plaque (42/192, 21.9%) (P<0.01). The Hp positive rate in dental plaque was 57.1% (48/84) at the gingiva with the probing depth (PD)≥4 mm, significantly higher than that at the gingiva with the PD <4 mm (34.3%, 37/108, P<0.05). The Hp positive rate in the specimens of gastric mucosa was 96.7% (31/32). The Hp in the 12 dental plaque specimens and gastric biopsy specimens from the 4 patients in the same family had 3 banding patterns all together. One of the patients had at least one identical banding pattern in both the plaque specimens and gastric biopsy specimens. One specific banding patern was found in the Hp from the dental plaques of all 4 patients. In one patient, the SSCP banding pattern in the Hp from dental plaque was inconsistent with that from gastric biopsy specimens. Conclusion Hp exists in the oral cavity of gastritis patients. Oral Hp infection may be an important source of gastric Hp infection. Familial clustering and oral-oral transmission of Hp infection exist.
出处 《中华医学杂志》 CAS CSCD 北大核心 2002年第15期1037-1041,共5页 National Medical Journal of China
基金 国家自然科学基金资助项目 ( 30 0 0 0 192 )
关键词 幽门螺杆菌 菌斑 胃炎 聚合酶链反应 基因型 Helicobacter pylori Dental plaque Gastritis PCR Genotype
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  • 1Li C,J Clin Pathol,1995年,48卷,662页
  • 2王蔚虹,中华消化杂志,1995年,15卷,增刊,9页
  • 3宋敏,中华流行病学杂志,1993年,14卷,237页

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