Bianchi A, Scieux C, Brunat N, Vexiau D, Kermanach M, Pezin P, Janier M, Morel P, Lagrange P H
Laboratoire de Microbiologie, Hôpital St-Louis, Paris, France.
Sex Transm Dis. 1994 Jul-Aug;21(4):196-200. doi: 10.1097/00007435-199407000-00003.
The new commercially available polymerase chain reaction (PCR)-based assay, Amplicor C. trachomatis, was compared with cell culture of C. trachomatis, for the detection of chlamydial urogenital infections.
To evaluate whether the Amplicor C. trachomatis PCR could improve the diagnosis of chlamydial urogenital infections, compared with cell culture of C. trachomatis considered as the reference method.
A total of 466 men and 290 women attending a sexually transmitted disease (STD) clinic were tested by the Amplicor test in urine in men, and in the cervix and urethra in women, and by cell culture in the urethra of both men and women and in the cervix of the women.
The prevalence of C. trachomatis was 13.7% by cell culture and 14.4% by the Amplicor test in men, and 3.5% by cell culture and 4.5% by the Amplicor test in women. After resolution of the discrepant results, the sensitivity of culture was 91.4% in male urethral specimens and 83.3% in endocervical and female urethral specimens. The resolved sensitivity of the PCR assay was 92.7% in male urine, 91.7% in endocervical samples, and reached 100% in testing both endocervical and female urethral specimens.
This rapid PCR-based assay showed an improvement in quality for diagnosing C. trachomatis infections.
将新上市的基于聚合酶链反应(PCR)的检测方法——Amplicor沙眼衣原体检测法,与沙眼衣原体细胞培养法进行比较,以检测衣原体性泌尿生殖系统感染。
评估与被视为参考方法的沙眼衣原体细胞培养法相比,Amplicor沙眼衣原体PCR检测法能否改善衣原体性泌尿生殖系统感染的诊断。
对466名男性和290名女性性传播疾病(STD)门诊患者进行检测,男性采用Amplicor检测法检测尿液,女性采用该检测法检测宫颈和尿道;同时采用细胞培养法检测男性和女性的尿道以及女性的宫颈。
男性中,沙眼衣原体细胞培养法的患病率为13.7%,Amplicor检测法为14.4%;女性中,细胞培养法的患病率为3.5%,Amplicor检测法为4.5%。在解决不一致结果后,培养法在男性尿道标本中的敏感性为91.4%,在宫颈和女性尿道标本中的敏感性为83.3%。PCR检测法在男性尿液中的敏感性为92.7%,在宫颈标本中的敏感性为91.7%,在检测宫颈和女性尿道标本时敏感性达到100%。
这种基于PCR的快速检测法在诊断沙眼衣原体感染方面显示出质量上的提升。