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[免疫印迹法检测幽门螺杆菌:一项多中心研究]

[Detection of Helicobacter pylori by immunoblot: a multiple-center study].

作者信息

Dong Xinhong, Hu Fulian, Gao Wen, Cheng Hong, Liu Xi, Xu Le, An Hejuan, Xie Yong, Lu Hong, Li Yan

机构信息

Department of Gastroenterology, Peking University First Hospital, Beijing 100034, China.

出版信息

Zhonghua Yi Xue Za Zhi. 2016 Jan 26;96(4):265-9. doi: 10.3760/cma.j.issn.0376-2491.2016.04.007.

Abstract

OBJECTIVE

To evaluate the accuracy and effectiveness of Helicobacter pylori(H.pylori)antibody detection kit (immunoblot) in typing H. pylori strains, and to investigate the relationship between characteristics of H. pylori strains and clinical outcomes.

METHODS

A total of 378 patients with upper gastrointestinal symptoms who had received gastroscopy and had pathological results within the period from March to August 2012 were collected from 6 centers in China.In all the patients, H. pylori antibody detection kit was used to detect and type serum H. pylori antibodies.The sensitivity, specificity, and accuracy of immunoblot in diagnosing H. pylori infection were evaluation in comparison to (13)C urea breath test (UBT) as the"gold standard". The results were also compared with those colloidal gold method.The relationship between H. pylori typing and clinical conditions was analyzed.

RESULTS

Totally 378 patients were enrolled, in which 257 had H. pylori-positive (13)C UBT results, and 121 were negative.With (13)C UBT as the"gold standard", the sensitivity, specificity, positive predictive value, negative predictive value, and concordance rate of H. pylori antibodies detection kit(immunoblot)were 97.7%, 86.8%, 94.0%, 94.6%, and 94.2%, respectively; the sensitivity, specificity, positive predictive value, negative predictive value, and concordance rate of colloidal gold method were 84.4%, 92.6%, 96.0%, 73.7%, and 87.0%, respectively.In patients diagnosed as H. pylori-positive by (13)C UBT and immunoblot, 93.0%(53/57) in H. pylori eradication failure patients and 93.8%(182/194)in untreated patients were infected with type Ⅰ H. pylori as detected by immunoblot, with no statistically significant difference (P=0.764). The type Ⅰ strains positive rate was 94.2%(65/69), 89.9%(62/69)and 98.2% (55/56) in non-atrophy gastritis, atrophy gastritis, and duodenal ulcer untreated patients, respectively, the positive rate of type Ⅰ strains higher in duodenal ulcer cases than in gastritis ones, but with no statistically significant difference(P=0.185).

CONCLUSIONS

Compared with the"gold standard"(13)C UBT, the accuracy of H. pylori antibody detection kit (immunoblot) and that of colloidal gold method are both fairly high.Different H. pylori strains may have significantly different potential in causing diseases, as typeⅠtrain appeared to be more virulent than type Ⅱ strain, especially in causing peptic ulcer.There was no obvious difference between eradication failure and untreated patients in terms of positive rate of type Ⅰ H. pylori strains, hence further study is needed to explore the relationship between type Ⅰ H. pylori and eradication rates.

摘要

目的

评估幽门螺杆菌(H.pylori)抗体检测试剂盒(免疫印迹法)对H.pylori菌株分型的准确性和有效性,并探讨H.pylori菌株特征与临床结局之间的关系。

方法

收集2012年3月至8月期间来自中国6个中心的378例有上消化道症状且接受过胃镜检查并获得病理结果的患者。所有患者均使用H.pylori抗体检测试剂盒检测血清H.pylori抗体并进行分型。以(13)C尿素呼气试验(UBT)作为“金标准”,评估免疫印迹法诊断H.pylori感染的敏感性、特异性和准确性。结果还与胶体金法进行比较。分析H.pylori分型与临床状况之间的关系。

结果

共纳入378例患者,其中(13)C UBT结果显示257例H.pylori阳性,121例阴性。以(13)C UBT作为“金标准”,H.pylori抗体检测试剂盒(免疫印迹法)的敏感性、特异性、阳性预测值、阴性预测值和符合率分别为97.7%、86.8%、94.0%、94.6%和94.2%;胶体金法的敏感性、特异性、阳性预测值、阴性预测值和符合率分别为84.4%、92.6%、96.0%、73.7%和87.0%。在经(13)C UBT和免疫印迹法诊断为H.pylori阳性的患者中,免疫印迹法检测显示,H.pylori根除失败患者中93.0%(53/57)、未治疗患者中93.8%(182/194)感染Ⅰ型H.pylori,差异无统计学意义(P = 0.764)。在未治疗的非萎缩性胃炎、萎缩性胃炎和十二指肠溃疡患者中,Ⅰ型菌株阳性率分别为94.2%(65/69)、89.9%(62/69)和98.2%(55/56),十二指肠溃疡患者中Ⅰ型菌株阳性率高于胃炎患者,但差异无统计学意义(P = 0.185)。

结论

与“金标准”(13)C UBT相比,H.pylori抗体检测试剂盒(免疫印迹法)和胶体金法的准确性均较高。不同的H.pylori菌株致病潜力可能存在显著差异,Ⅰ型菌株似乎比Ⅱ型菌株更具致病性,尤其是在导致消化性溃疡方面。H.pyloriⅠ型菌株阳性率在根除失败患者和未治疗患者之间无明显差异,因此需要进一步研究探索Ⅰ型H.pylori与根除率之间的关系。

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