Toye B, Peeling R W, Jessamine P, Claman P, Gemmill I
Department of Pathology and Laboratory Medicine, Ottawa General Hospital, Ontario, Canada.
J Clin Microbiol. 1996 Jun;34(6):1396-400. doi: 10.1128/jcm.34.6.1396-1400.1996.
A PCR assay was evaluated for its ability to detect genital chlamydial infection in asymptomatic men and women. Urethral swab specimens were collected from 472 men for culture and PCR assay, and first-void urine (FVU) specimens were collected from 379 of these men for enzyme immunoassay (EIA) and PCR assay. Cervical swab specimens were collected from 242 women for culture, EIA, and PCR assay. Patients were considered infected if they were culture positive or positive by PCR with both plasmid- and major outer membrane protein-based primers. By using this extended "gold standard," the prevalence of infection in this population was 7.6% for men and 7.9% for women. For men, the sensitivities of urethral swab specimen culture and PCR and FVU specimen EIA and PCR were 61, 72, 55, and 91%, respectively. All assays had specificities of > or = 99.8%. The positive and negative predictive values for PCR testing of FVU specimens were 100 and 99.4%, respectively, compared with values of 96.3 and 97.8%, respectively, for PCR of urethral swab specimens. The sensitivities of cervical swab specimen culture and PCR testing were 42 and 90%, respectively, with corresponding specificities of 100 and 99.3%. All cervical swabs were negative by EIA. Molecular techniques such as PCR assays are valuable tools for the detection of symptomatic genital chlamydial infection. In particular, PCR assays of FVU specimens from men offer a highly sensitive, noninvasive screening tool that will likely improve patient compliance for diagnostic testing.
对一种聚合酶链反应(PCR)检测方法检测无症状男性和女性生殖道衣原体感染的能力进行了评估。从472名男性中采集尿道拭子标本进行培养和PCR检测,从其中379名男性中采集首次晨尿(FVU)标本进行酶免疫测定(EIA)和PCR检测。从242名女性中采集宫颈拭子标本进行培养、EIA和PCR检测。如果患者培养阳性或使用基于质粒和主要外膜蛋白的引物进行PCR检测呈阳性,则被视为感染。通过使用这种扩展的“金标准”,该人群中男性的感染率为7.6%,女性为7.9%。对于男性,尿道拭子标本培养、PCR以及FVU标本EIA和PCR的敏感性分别为61%、72%、55%和91%。所有检测方法的特异性均≥99.8%。FVU标本PCR检测的阳性预测值和阴性预测值分别为100%和99.4%,而尿道拭子标本PCR检测的阳性预测值和阴性预测值分别为96.3%和97.8%。宫颈拭子标本培养和PCR检测的敏感性分别为42%和90%,相应的特异性分别为100%和99.3%。所有宫颈拭子EIA检测均为阴性。PCR检测等分子技术是检测有症状生殖道衣原体感染的宝贵工具。特别是,对男性FVU标本进行PCR检测提供了一种高度敏感、非侵入性的筛查工具,可以提高患者对诊断检测的依从性。