Demirtürk L, Ozel A M, Yazgan Y, Solmazgül E, Yildirim S, Gültepe M, Gürbüz A K
Department of Gastroenterology, Gülhane Military Medical Academy Haydarpaşa Training Hospital, Istanbul, Turkey.
Helicobacter. 2001 Jun;6(2):163-8. doi: 10.1046/j.1523-5378.2001.00024.x.
CagA seropositivity is closely associated with that of vacuolating cytotoxin (VacA). Helicobacter pylori strains positive for both VacA and CagA were reported to be strongly associated with peptic ulcer disease. Different results reporting that cagA gene is not associated with more serious diseases, lowers the importance of CagA protein as a marker. In this study, CagA seropositivity is examined in Turkish peptic ulcer and nonulcer dyspepsia patients; histopathologic scores of CagA (+) and CagA (-) groups were compared.
Sixty consecutive patients (one gastric ulcer, 13 duodenal ulcer and 46 nonulcer dyspepsia) (mean age 40.9 +/- 14.7; 33 women, 27 men) with dyspeptic complaints who underwent upper gastrointestinal (GI) endoscopy were included. Biopsies from the antrum and corpus were used for histopathologic examination and for rapid urease test. H. pylori-negative patients comprised the control group. Histopathologic findings were graded using a previously described grading system (for inflammation, activity, atrophy, intestinal metaplasia and H. pylori, grades from 0 to 3 were used to quantify the findings). In H. pylori-positive patients, antibodies against CagA protein were determined using an ELISA METHOD:
H. pylori was (+) in 46 patients. One duodenal ulcer and 13 nonulcer dyspepsia patients were negative for H. pylori. CagA positivity is significantly higher in peptic ulcer patients [12/12] than in nonulcer dyspepsia patients [25/33]. While inflammation, activity and atrophy scores were significantly higher in CagA positive patients, intestinal metaplasia and H. pylori load scores were not. Although the histopathologic scores in controls were lower than CagA (-) group, statistical significance was observed only in inflammation and intestinal metaplasia scores.
Development of more prominent gastritis and severe atrophy in CagA (+) patients is an indicator of the importance of CagA rather than H. pylori load. Therefore, we suggest that nonulcer dyspepsia patients should also be tested for CagA status along with the tests for H. pylori status; and a positive CagA testing should be considered as an indication for eradication treatment. If CagA is negative, further assesment should be performed to decide whether or not to treat the patient.
细胞毒素相关基因A(CagA)血清阳性与空泡毒素(VacA)血清阳性密切相关。据报道,VacA和CagA均呈阳性的幽门螺杆菌菌株与消化性溃疡病密切相关。不同的研究结果表明cagA基因与更严重的疾病无关,这降低了CagA蛋白作为一种标志物的重要性。在本研究中,我们检测了土耳其消化性溃疡和非溃疡性消化不良患者的CagA血清阳性情况,并比较了CagA(+)组和CagA(-)组的组织病理学评分。
纳入60例因消化不良症状接受上消化道内镜检查的连续患者(1例胃溃疡、13例十二指肠溃疡和46例非溃疡性消化不良)(平均年龄40.9±14.7岁;女性33例,男性27例)。取自胃窦和胃体的活检组织用于组织病理学检查和快速尿素酶试验。幽门螺杆菌阴性患者作为对照组。组织病理学结果采用先前描述的分级系统进行分级(对于炎症、活动性、萎缩、肠化生和幽门螺杆菌,采用0至3级来量化结果)。在幽门螺杆菌阳性患者中,采用酶联免疫吸附测定法检测抗CagA蛋白抗体。
46例患者幽门螺杆菌呈阳性。1例十二指肠溃疡和13例非溃疡性消化不良患者幽门螺杆菌呈阴性。消化性溃疡患者[12/12]的CagA阳性率显著高于非溃疡性消化不良患者[25/33]。虽然CagA阳性患者的炎症、活动性和萎缩评分显著更高,但肠化生和幽门螺杆菌载量评分则不然。虽然对照组的组织病理学评分低于CagA(-)组,但仅在炎症和肠化生评分中观察到统计学意义。
CagA(+)患者中更显著的胃炎和严重萎缩的发生是CagA重要性的一个指标,而非幽门螺杆菌载量。因此,我们建议非溃疡性消化不良患者除了进行幽门螺杆菌检测外,还应检测CagA状态;CagA检测呈阳性应被视为根除治疗的指征。如果CagA为阴性,则应进一步评估以决定是否对患者进行治疗。