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寄生虫学、免疫学、分子生物学和超声检查在诊断菲律宾流行地区野外工作者肠道血吸虫病中的诊断性能。

Diagnostic Performance of Parasitological, Immunological, Molecular, and Ultrasonographic Tests in Diagnosing Intestinal Schistosomiasis in Fieldworkers From Endemic Municipalities in the Philippines.

机构信息

Institute of Biology, College of Science, University of the Philippines Diliman, Quezon City, Philippines.

College of Medicine, University of the Philippines Manila, Manila, Philippines.

出版信息

Front Immunol. 2022 Jun 14;13:899311. doi: 10.3389/fimmu.2022.899311. eCollection 2022.

DOI:10.3389/fimmu.2022.899311
PMID:35774791
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9237846/
Abstract

Schistosomiasis remains to ha/ve a significant public health impact in the Philippines. The Kato-Katz (K-K) technique is the reference standard and most used technique for definitive diagnosis of intestinal schistosomiasis for control programs in endemic regions. However, this has a very low sensitivity when applied in areas of low endemicity and patients with light infection. Hence, this study determined the diagnostic performance of immunological, molecular, parasitological, and ultrasonographic tests in diagnosing intestinal schistosomiasis in endemic municipalities in the Philippines. We performed a community-based cross-sectional study to determine the positivity of schistosomiasis in Leyte, Philippines. The diagnostic performance of five different detection techniques: (1) three stool K-K with duplicate smears; (2) soluble egg antigen IgG ELISA; (3) urine point-of-care circulating cathodic antigen (POC-CCA) test; (4) detection of circulating DNA (SjcDNA) in serum and urine samples; (5) focused abdominal ultrasound (US), were also obtained in this study. Multiple stool examinations enhanced the sensitivity of K-K from 26.2% (95% CI [16.4, 38.8]) with single stool to 53.8% (95% CI [41.1, 66.1]) and 69.2% (95% CI [56.4, 80.0]) with two and three stools from consecutive days, respectively. Among the SjcDNA nucleic acid amplification test (NAAT)-based detection assays, loop-mediated isothermal amplification (LAMP) PCR using sera had the highest sensitivity at 92.3% (95% CI [82.2, 97.1]) with LAMP consistently identifying more positive cases in both serum and urine samples. This study showed that single stool K-K, which remains the only diagnostic test available in most endemic areas in the Philippines, had low sensitivity and failed to identify most patients with light infection. SjcDNA detection assay and POC-CCA urine test were more sensitive than stool microscopy in detecting schistosomiasis. On the other hand, US was less sensitive than the widely utilized K-K technique in diagnosing schistosomiasis. This study emphasizes the need to revisit the use of single stool K-K in the surveillance and case detection of schistosomiasis in endemic areas of the Philippines. The availability of advanced and more sensitive diagnostic tests will help better control, prevent, and eliminate schistosomiasis in the country.

摘要

在菲律宾,血吸虫病仍然对公共卫生有重大影响。加藤厚涂片(Kato-Katz,K-K)技术是流行地区控制项目中肠道血吸虫病的参考标准和最常用的确诊技术。然而,在低流行地区和轻度感染患者中,该方法的敏感性非常低。因此,本研究旨在确定在菲律宾血吸虫病流行市中,免疫、分子、寄生虫学和超声检测技术对肠道血吸虫病的诊断性能。我们进行了一项以社区为基础的横断面研究,以确定菲律宾莱特岛的血吸虫病阳性率。本研究还获得了五种不同检测技术的诊断性能:(1) 三份粪便加藤厚涂片(K-K),每份粪便做两次涂片;(2) 可溶性虫卵抗原 IgG 酶联免疫吸附试验(ELISA);(3) 尿液即时检测循环阴离子抗原(POC-CCA)检测;(4) 血清和尿液样本中循环 DNA(SjcDNA)的检测;(5) 腹部超声聚焦检查(US)。多次粪便检查提高了 K-K 的敏感性,从单次粪便的 26.2%(95%CI [16.4, 38.8])提高到连续 2 天 3 次粪便的 53.8%(95%CI [41.1, 66.1])和 69.2%(95%CI [56.4, 80.0])。在基于 SjcDNA 核酸扩增试验(NAAT)的检测方法中,使用血清的环介导等温扩增(LAMP)PCR 的敏感性最高,为 92.3%(95%CI [82.2, 97.1]),LAMP 始终能在血清和尿液样本中检测到更多的阳性病例。本研究表明,在菲律宾大多数流行地区仍然是唯一可用的诊断检测方法的单次粪便 K-K 具有低敏感性,无法识别大多数轻度感染的患者。SjcDNA 检测和 POC-CCA 尿液检测比粪便镜检更敏感,可用于检测血吸虫病。另一方面,US 在诊断血吸虫病方面的敏感性低于广泛使用的 K-K 技术。本研究强调需要重新考虑在菲律宾血吸虫病流行地区使用单次粪便 K-K 进行监测和病例检测。更先进和更敏感的诊断检测方法的可用性将有助于更好地控制、预防和消除该国的血吸虫病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5414/9237846/f9b757c1aa31/fimmu-13-899311-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5414/9237846/f1da8dc9e073/fimmu-13-899311-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5414/9237846/f1da8dc9e073/fimmu-13-899311-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5414/9237846/7951198d383e/fimmu-13-899311-g002.jpg
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