Fallone C A, Elizov M, Cleland P, Thompson J A, Wild G E, Lough J, Faria J, Barkun A N
Division of Gastroenterology, Montreal General Hospital, Québec, Canada.
Am J Gastroenterol. 1996 Jun;91(6):1145-9.
Most currently available tests for the detection of Helicobacter pylori are invasive, time consuming, or impractical. We examined the test performance of a simple and rapidly administered salivary IgG assay kit in the diagnosis of Helicobacter pylori infection.
Patients referred to a tertiary care setting for upper gastrointestinal endoscopy were included in a prospective evaluation of the test performance of the Helisal Kit which uses an ELISA technique to determine IgG antibodies in saliva. The results of the salivary IgG assay were compared to those of the Helisal Serum Kit, and to gastric histology. Two by two contingency table analyses were performed, and 95% confidence intervals (CI) were determined.
Upper gastrointestinal endoscopy was performed on 106 patients over a 3-month period. A statistically significant correlation was found between the blood and saliva IgG results (r = 0.60, p = 0.0001). When compared to serum IgG, the salivary assay test performance was: sensitivity 84% (CI: 70-93%), specificity 81% (CI: 69-90%), positive predictive value 76% (CI: 61-87%), negative predictive value 88% (CI: 76-95%), and diagnostic accuracy 88% (CI: 76-95%). Compared with gastric histology, the test performance of the salivary IgG assay decreased to: sensitivity 66% (CI: 52-79%), specificity 74% (CI: 60-85%), positive predictive value 71% (CI: 57-83%), negative predictive value 68% (CI: 55-80%), and diagnostic accuracy 70% (CI: 60-78%). More specifically, the salivary assay gave false-negative results in nine of 17 patients with duodenal ulcers. Results did not vary significantly when outcomes of the salivary and serum assays were combined. The incremental information obtained in the salivary test was greatest in the patient population exhibiting an intermediate pretest probability (30-70%) of being infected with Helicobacter.
The salivary IgG results correlated significantly with the serum IgG titers but exhibited only modest test performance, compared with the results of gastric histology. This salivary test may be most useful in certain patient subpopulations or in specific clinical contexts.
目前大多数用于检测幽门螺杆菌的检测方法具有侵入性、耗时或不实用。我们研究了一种简单且快速操作的唾液IgG检测试剂盒在诊断幽门螺杆菌感染中的检测性能。
被转诊至三级医疗机构进行上消化道内镜检查的患者被纳入对Helisal试剂盒检测性能的前瞻性评估,该试剂盒采用ELISA技术测定唾液中的IgG抗体。将唾液IgG检测结果与Helisal血清试剂盒的结果以及胃组织学结果进行比较。进行了两两列联表分析,并确定了95%置信区间(CI)。
在3个月内对106例患者进行了上消化道内镜检查。发现血液和唾液IgG结果之间存在统计学显著相关性(r = 0.60,p = 0.0001)。与血清IgG相比,唾液检测的性能为:敏感性84%(CI:70 - 93%),特异性81%(CI:69 - 90%),阳性预测值76%(CI:61 - 87%),阴性预测值88%(CI:76 - 95%),诊断准确性88%(CI:76 - 95%)。与胃组织学相比,唾液IgG检测的性能降至:敏感性66%(CI:52 - 79%),特异性74%(CI:60 - 85%),阳性预测值71%(CI:57 - 83%),阴性预测值68%(CI:55 - 80%),诊断准确性70%(CI:60 - 78%)。更具体地说,在17例十二指肠溃疡患者中,有9例唾液检测结果为假阴性。当将唾液和血清检测结果合并时,结果没有显著差异。在感染幽门螺杆菌的预测试概率为中等(30 - 70%)的患者群体中,唾液检测获得的增量信息最大。
唾液IgG结果与血清IgG滴度显著相关,但与胃组织学结果相比,检测性能仅适度。这种唾液检测在某些患者亚群体或特定临床背景下可能最有用。