Choi Hyunseul, Kang Minhee, Yun Sun Ae, Yu Hui-Jin, Suh Eunsang, Kim Tae Yeul, Huh Hee Jae, Lee Nam Yong
Biomedical Engineering Research Center, Smart Healthcare Research Institute, Samsung Medical Center, Seoul, South Korea.
Center for Clinical Medicine, Samsung Biomedical Research Institute, Samsung Medical Center, Seoul, South Korea.
Microbiol Spectr. 2025 Jan 7;13(1):e0166224. doi: 10.1128/spectrum.01662-24. Epub 2024 Nov 29.
Current guidelines recommend a two-step algorithm rather than relying solely on a single test for diagnosing infection. This algorithm starts with enzyme immunoassay (EIA) for detecting glutamate dehydrogenase (GDH) and toxins A/B, followed by nucleic acid amplification test (NAAT) for GDH-positive but toxin-negative cases. This study compared the performance of three commercial NAATs: the STANDARD M10 , Xpert , and BD MAX Cdiff assays, utilized as confirmatory testing of the two-step algorithm. Two hundred archived stool specimens, previously tested GDH-positive but toxin-negative by EIA, were analyzed in parallel with these NAATs and toxigenic culture, which served as the reference standard. Sensitivity, specificity, positive predictive value, and negative predictive value were 89.1%, 92.6%, 94.6%, and 85.2%, respectively, for the M10 assay; 95.8%, 86.4%, 91.2%, and 93.3%, respectively, for the Xpert assay; and 89.8%, 91.4%, 93.8%, and 86.0%, respectively, for the BD MAX assay. The rates of invalid results were 1.0%, 0.5%, and 1.0% for the M10, Xpert, and BD MAX assays, respectively. In conclusion, the M10 assay is a reliable diagnostic tool, performing comparably to the Xpert and BD MAX assays when used as confirmatory testing in the two-step algorithm.IMPORTANCEWhile numerous studies have assessed nucleic acid amplification tests (NAATs) as stand-alone tests for diagnosing infection, limited research has compared their performance as confirmatory tests in a two-step algorithm. This study evaluated the performance of three commercial NAATs (M10, Xpert, and BD MAX assays) using 200 archived stool specimens initially tested as glutamate dehydrogenase (GDH)-positive but toxin-negative by GDH/toxin A/B enzyme immunoassay, the first step in the two-step algorithm. All three assays demonstrated high sensitivity (89.1% to 95.8%) and specificity (86.4% to 92.6%), with low rates of invalid results (≤1%). Our findings suggest that the M10 assay performs comparably to the Xpert and BD MAX assays when used as confirmatory testing in the two-step algorithm. Offering similar performance and turnaround time to these widely used assays at a slightly lower cost, the M10 assay serves as a practical alternative in this setting.
当前指南推荐采用两步算法,而非仅依靠单一检测来诊断感染。该算法首先通过酶免疫测定法(EIA)检测谷氨酸脱氢酶(GDH)和毒素A/B,然后对GDH阳性但毒素阴性的病例进行核酸扩增检测(NAAT)。本研究比较了三种商用NAAT的性能:STANDARD M10、Xpert和BD MAX艰难梭菌检测法,用作两步算法的确认性检测。对200份存档粪便标本进行分析,这些标本先前经EIA检测为GDH阳性但毒素阴性,并与这些NAAT和产毒培养法同时进行检测,产毒培养法作为参考标准。M10检测法的灵敏度、特异性、阳性预测值和阴性预测值分别为89.1%、92.6%、94.6%和85.2%;Xpert检测法分别为95.8%、86.4%、91.2%和93.3%;BD MAX检测法分别为89.8%、91.4%、93.8%和86.0%。M10、Xpert和BD MAX检测法的无效结果率分别为1.0%、0.5%和1.0%。总之,M10检测法是一种可靠的诊断工具,在两步算法中用作确认性检测时,其性能与Xpert和BD MAX检测法相当。
虽然有许多研究评估了核酸扩增检测(NAAT)作为诊断感染的独立检测方法,但将其作为两步算法中的确认性检测方法进行性能比较的研究有限。本研究使用200份存档粪便标本评估了三种商用NAAT(M10、Xpert和BD MAX检测法)的性能,这些标本最初经GDH/毒素A/B酶免疫测定法检测为谷氨酸脱氢酶(GDH)阳性但毒素阴性,这是两步算法的第一步。所有三种检测方法均显示出高灵敏度(89.1%至95.8%)和特异性(86.4%至92.6%),无效结果率较低(≤1%)。我们的研究结果表明,M10检测法在两步算法中用作确认性检测时,其性能与Xpert和BD MAX检测法相当。M10检测法在性能和周转时间上与这些广泛使用的检测方法相似,且成本略低,在这种情况下是一种实用的替代方法。