Ridgway G L, Mumtaz G, Robinson A J, Franchini M, Carder C, Burczak J, Lee H
Department of Clinical Microbiology, University College London Hospitals.
J Clin Pathol. 1996 Feb;49(2):116-9. doi: 10.1136/jcp.49.2.116.
To determine the sensitivity and specificity of ligase chain reaction (LCR) analysis of cervical and urine specimens from women compared with cell culture of cervical and urethral specimens for the diagnosis of genitourinary chlamydial infection.
Women (n = 624) attending the Genitourinary Medicine Clinic at University College London Hospitals, were enrolled. Patients who had received antibiotics within the previous two weeks were excluded. Specimens were obtained from the urethra and cervix for chlamydial culture, and from the cervix for LCR. A specimen of first void urine was also obtained for LCR. Discrepancies were resolved by direct immunofluorescence or a major outer membrane protein targeted LCR, or both.
The prevalence of Chlamydia trachomatis in 600 patients, using an expanded standard of a positive cell culture or two confirmed positive non-culture tests, was 13.2% (79/600). Cervical culture detected 68.4% and urethral culture 62% of all positive results compared with 81% detected by cervical LCR and 69% by urine LCR. Cervical and urethral culture combined detected 87.3% whereas cervical and urine LCR combined detected 91.1% of positive cases. Specificity of LCR was 100% in the cervix and 99.8% in urine.
This study demonstrates that LCR analysis of cervical and urine specimens is a reliable method for the diagnosis of chlamydial genital infection in women. However, the study also demonstrates that no single test will detect all chlamydial infections. Conventional non-culture tests and cell culture may grossly underestimate the prevalence of chlamydial infection. LCR analysis of a cervical specimen was superior to conventional cell culture without blind passage as a single test for diagnosing chlamydial infection in women, followed by LCR of a urine specimen.
确定与宫颈和尿道标本细胞培养相比,对女性宫颈和尿液标本进行连接酶链反应(LCR)分析在诊断泌尿生殖道衣原体感染中的敏感性和特异性。
招募了在伦敦大学学院医院泌尿生殖医学诊所就诊的624名女性。排除了在过去两周内接受过抗生素治疗的患者。从尿道和宫颈获取标本进行衣原体培养,从宫颈获取标本进行LCR检测。还获取了首次晨尿标本进行LCR检测。通过直接免疫荧光或靶向主要外膜蛋白的LCR或两者来解决差异。
采用阳性细胞培养扩大标准或两项确诊的非培养阳性检测,600名患者中沙眼衣原体的患病率为13.2%(79/600)。与宫颈LCR检测出的81%和尿液LCR检测出的69%相比,宫颈培养检测出所有阳性结果的68.4%,尿道培养检测出62%。宫颈和尿道培养联合检测出87.3%,而宫颈和尿液LCR联合检测出91.1%的阳性病例。LCR在宫颈中的特异性为100%,在尿液中的特异性为99.8%。
本研究表明,对宫颈和尿液标本进行LCR分析是诊断女性衣原体性生殖器感染的可靠方法。然而,该研究也表明,没有单一检测方法能检测出所有衣原体感染。传统的非培养检测和细胞培养可能会严重低估衣原体感染的患病率。作为诊断女性衣原体感染的单一检测方法,对宫颈标本进行LCR分析优于无盲传的传统细胞培养,其次是对尿液标本进行LCR检测。