{"title":"Clinical Utility of <i>Helicobacter pylori</i> Stool Antigen Testing with a Bioluminescent Enzyme Immunoassay Using a Fecal Occult Blood Test Container.","authors":"Atsushi Imagawa, Sho Takahashi, Katsuhiro Mabe","doi":"10.2169/internalmedicine.3480-24","DOIUrl":null,"url":null,"abstract":"<p><p>Objective A dedicated stool container is required for Helicobacter pylori stool antigen testing. If H. pylori fecal antigen can be measured from a fecal occult blood test container (S fecal collection container or S container), which is widely used for colorectal cancer screening, screening of the upper and lower gastrointestinal tract can be performed with a single stool sample. We investigated the clinical usefulness of an H. pylori stool antigen assay using an S container. Materials A total of 347 patients who underwent esophagogastroduodenoscopy (EGD) were included. After the procedure, H. pylori stool antigen was measured using the S container and collection container recommended for H. pylori stool antigen (BL-stool collection container or BL container), and the qualitative outcomes of each were compared. A bioluminescent enzyme immunoassay (BLEIA) was used to measure H. pylori stool antigen. Results The overall agreement between S containers and BL containers was 100% (347/347), indicating that the qualitative outcomes were equivalent. As a secondary analysis, the results of the S container samples were evaluated according to the diagnosis made by physicians, and the overall agreement rate was 99.7% (345/346), indicating a high correlation. Conclusion The detection of H. pylori stool antigen using the S container is clinically useful because the results are equivalent to those obtained by the usual method. Screening of the upper and lower gastrointestinal tract is expected to be possible with a single stool sample in the future.</p>","PeriodicalId":13719,"journal":{"name":"Internal Medicine","volume":" ","pages":"3271-3275"},"PeriodicalIF":1.0000,"publicationDate":"2024-12-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Internal Medicine","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.2169/internalmedicine.3480-24","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/5/9 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0
Abstract
Objective A dedicated stool container is required for Helicobacter pylori stool antigen testing. If H. pylori fecal antigen can be measured from a fecal occult blood test container (S fecal collection container or S container), which is widely used for colorectal cancer screening, screening of the upper and lower gastrointestinal tract can be performed with a single stool sample. We investigated the clinical usefulness of an H. pylori stool antigen assay using an S container. Materials A total of 347 patients who underwent esophagogastroduodenoscopy (EGD) were included. After the procedure, H. pylori stool antigen was measured using the S container and collection container recommended for H. pylori stool antigen (BL-stool collection container or BL container), and the qualitative outcomes of each were compared. A bioluminescent enzyme immunoassay (BLEIA) was used to measure H. pylori stool antigen. Results The overall agreement between S containers and BL containers was 100% (347/347), indicating that the qualitative outcomes were equivalent. As a secondary analysis, the results of the S container samples were evaluated according to the diagnosis made by physicians, and the overall agreement rate was 99.7% (345/346), indicating a high correlation. Conclusion The detection of H. pylori stool antigen using the S container is clinically useful because the results are equivalent to those obtained by the usual method. Screening of the upper and lower gastrointestinal tract is expected to be possible with a single stool sample in the future.
背景幽门螺旋杆菌粪便抗原检测需要专用的粪便容器。如果幽门螺杆菌粪便抗原能从广泛用于大肠癌筛查的粪便隐血试验容器(S 型粪便收集容器或 S 型容器)中检测出来,那么只需一份粪便样本就能对上下消化道进行筛查。我们研究了使用 S 型容器进行幽门螺杆菌粪便抗原检测的临床实用性。患者和材料 共纳入 347 名接受食管胃十二指肠镜检查(EGD)的患者。术后,使用 S 型容器和推荐的幽门螺杆菌粪便抗原收集容器(BL-凳子收集容器或 BL 容器)对幽门螺杆菌粪便抗原进行检测,并比较两种容器的定性结果。使用生物发光酶免疫测定(BLEIA)测量幽门螺杆菌粪便抗原。结果 S容器和BL容器之间的总体一致性为100%(347/347),表明定性结果相同。作为辅助分析,根据医生的诊断对 S 型容器样本的结果进行了评估,总体一致率为 99.7%(345/346),表明两者具有高度相关性。结论 使用 S 型容器检测幽门螺杆菌粪便抗原在临床上是有用的,因为其结果与常规方法的结果相当。预计今后只需一份粪便样本就能筛查上下消化道。
期刊介绍:
Internal Medicine is an open-access online only journal published monthly by the Japanese Society of Internal Medicine.
Articles must be prepared in accordance with "The Uniform Requirements for Manuscripts Submitted to Biomedical Journals (see Annals of Internal Medicine 108: 258-265, 1988), must be contributed solely to the Internal Medicine, and become the property of the Japanese Society of Internal Medicine. Statements contained therein are the responsibility of the author(s). The Society reserves copyright and renewal on all published material and such material may not be reproduced in any form without the written permission of the Society.