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通过尿液连接酶链反应检测法诊断女性沙眼衣原体泌尿生殖道感染

Diagnosis of Chlamydia trachomatis genitourinary infection in women by ligase chain reaction assay of urine.

作者信息

Lee H H, Chernesky M A, Schachter J, Burczak J D, Andrews W W, Muldoon S, Leckie G, Stamm W E

机构信息

Abbott Laboratories, Abbott Park, Illinois 60064.

出版信息

Lancet. 1995 Jan 28;345(8944):213-6. doi: 10.1016/s0140-6736(95)90221-x.

DOI:10.1016/s0140-6736(95)90221-x
PMID:7823713
Abstract

Genitourinary infection with Chlamydia trachomatis is a common and potentially serious sexually transmitted disease. Diagnosis of C trachomatis infection in women typically relies on culture of endocervical swabs, an invasive and expensive procedure. The ligase chain reaction (LCR) is an in-vitro nucleic acid amplification technique that exponentially amplifies selected DNA sequences. We have compared an LCR-based assay to detect C trachomatis plasmid DNA in first void urine with culture of endocervical swabs for matched specimens from 1937 women from four geographic regions. Discordant specimen pairs were further tested by direct fluorescent antibody staining for elementary bodies and an alternative LCR assay based on the chlamydial outer membrane protein gene. An "expanded gold standard" was defined to include all culture-positive as well as culture-negative, confirmed LCR-positive women. The sensitivity and specificity of the LCR assay with first void urine samples compared with the expanded gold standard were 93.8% and 99.9%, respectively; the corresponding values for culture were 65.0% and 100%, respectively. Thus, an automated LCR assay of readily obtained urine samples showed a detection rate for infected women almost 30% greater than that of endocervical swab culture. The LCR assay was highly effective for the detection of C trachomatis in urine from women with or without signs or symptoms of chlamydial genitourinary tract infection.

摘要

沙眼衣原体引起的泌尿生殖系统感染是一种常见且可能严重的性传播疾病。女性沙眼衣原体感染的诊断通常依赖于宫颈拭子培养,这是一种侵入性且昂贵的方法。连接酶链反应(LCR)是一种体外核酸扩增技术,可指数级扩增选定的DNA序列。我们将基于LCR的检测方法与宫颈拭子培养法进行了比较,以检测来自四个地理区域的1937名女性的配对标本首次晨尿中的沙眼衣原体质粒DNA。对不一致的标本对进一步通过直接荧光抗体染色检测原体,并基于衣原体外膜蛋白基因进行另一种LCR检测。定义了一个“扩展金标准”,包括所有培养阳性以及培养阴性但经确认LCR阳性的女性。与扩展金标准相比,首次晨尿样本LCR检测的敏感性和特异性分别为93.8%和99.9%;培养法的相应值分别为65.0%和100%。因此,对易于获取的尿液样本进行自动化LCR检测显示,感染女性的检出率比宫颈拭子培养法高出近30%。LCR检测对于检测有或无沙眼衣原体泌尿生殖道感染体征或症状的女性尿液中的沙眼衣原体非常有效。

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