Castle Philip E, Sadorra Mark, Garcia Francisco, Holladay E Blair, Kornegay Janet
Division of Cancer Epidemiology, National Cancer Institute, NIH, DHHS, Bethesda, MD 20892-7234, USA.
J Clin Microbiol. 2006 Nov;44(11):3915-7. doi: 10.1128/JCM.01305-06. Epub 2006 Sep 13.
We evaluated a commercialized PCR assay, Linear Array, that detects 37 human papillomavirus (HPV) genotypes, using a sample of liquid cytology specimens (n = 534). We found a strong association of an increasing level of HPV risk (HPV type 16 [HPV16] > HPV18 > other carcinogenic types > noncarcinogenic types > negative specimens) with increasing severities of cytologic interpretations (P(Trend) < 0.0005) and histologic diagnoses (P(Trend) < 0.0005).
我们使用一份液基细胞学标本样本(n = 534),对一种商业化的聚合酶链反应(PCR)检测方法——线性阵列法进行了评估,该方法可检测37种人乳头瘤病毒(HPV)基因型。我们发现,HPV风险水平升高(HPV 16型[HPV16] > HPV18型 > 其他致癌型 > 非致癌型 > 阴性标本)与细胞学判读严重程度增加(P(趋势)< 0.0005)及组织学诊断严重程度增加(P(趋势)< 0.0005)之间存在强烈关联。