Peralta L, Durako S J, Ma Y
Department of Pediatrics, University of Maryland School of Medicine, Baltimore, Maryland 21201, USA.
J Adolesc Health. 2001 Sep;29(3 Suppl):87-92. doi: 10.1016/s1054-139x(01)00283-x.
(a) To examine the concordance between ligase chain reaction (LCR) results from urine and cervical samples for Chlamydia trachomatis and Neisseria gonorrhoeae in HIV infected and uninfected adolescent women, and (b) to examine factors that may influence the concordance of LCR results in this population.
Baseline specimens from 269 of 334 female subjects enrolled in a longitudinal study of HIV infection in adolescents were analyzed for C. trachomatis and N. gonorrhoeae using ligase chain reaction (LCR) assays in a central laboratory. Concordance was measured using kappa coefficient with permutation analyses to calculate the difference between HIV status groups. Discordant LCR results were examined for the co-infection with the other microorganism, bacterial vaginosis, or Trichomonas vaginalis.
The prevalence of C. trachomatis detected by LCR in the HIV infected and uninfected groups was 19.3% and 12.2%, respectively (p = .16); the prevalence of N. gonorrhoeae was 7.0% and 2.4%, respectively (p = .16). Urine LCR assay sensitivity to detect cervical C. trachomatis infection was 86% (95% CI: 68%-96%) in the HIV infected group and 100% (95% CI: 69%-100%) in the HIV uninfected group. Urine LCR assay sensitivity to detect cervical N. gonorrhoeae infection was 92% (95% CI: 62%-100%) in the HIV infected group. There were only 2 N. gonorrhoeae infections in the HIV uninfected group, and both were urine LCR positive. Differences in sensitivity between HIV infected and HIV uninfected subjects were not statistically significant. Coinfection with N. gonorrhoeae, bacterial vaginosis or Trichomonas vaginalis was not associated with the concordance of urine and cervical LCR results.
The relatively high sensitivity of urine LCR testing overall suggests that urine screening may be reasonable for sexually active adolescent females with or without HIV infection in situations in which urine screening may be more acceptable than pelvic examinations.
(a) 检测感染和未感染人类免疫缺陷病毒(HIV)的青春期女性尿液和宫颈样本中沙眼衣原体及淋病奈瑟菌的连接酶链反应(LCR)结果的一致性;(b) 检测可能影响该人群LCR结果一致性的因素。
在一个中心实验室,对参与青少年HIV感染纵向研究的334名女性受试者中的269名的基线样本,采用连接酶链反应(LCR)检测法分析沙眼衣原体和淋病奈瑟菌。使用kappa系数和排列分析测量一致性,以计算HIV状态组之间的差异。对不一致的LCR结果检测是否合并感染其他微生物、细菌性阴道病或阴道毛滴虫。
LCR检测出的HIV感染组和未感染组沙眼衣原体患病率分别为19.3%和12.2%(p = 0.16);淋病奈瑟菌患病率分别为7.0%和2.4%(p = 0.16)。HIV感染组尿液LCR检测法检测宫颈沙眼衣原体感染的敏感性为86%(95%可信区间:68%-96%),HIV未感染组为100%(95%可信区间:69%-100%)。HIV感染组尿液LCR检测法检测宫颈淋病奈瑟菌感染的敏感性为92%(95%可信区间:62%-100%)。HIV未感染组仅2例淋病奈瑟菌感染,且均为尿液LCR阳性。HIV感染和未感染受试者之间的敏感性差异无统计学意义。合并感染淋病奈瑟菌、细菌性阴道病或阴道毛滴虫与尿液和宫颈LCR结果的一致性无关。
尿液LCR检测总体敏感性较高,这表明在尿液筛查可能比盆腔检查更易接受的情况下,对有或无HIV感染的性活跃青春期女性进行尿液筛查可能是合理的。