Nuovo Gerard J, Bartholomew Deborah, Jung Woon-Won, Han In-Kwon, Um Taeyoung, Grabarz Donald F, Lee Duck-Joo, McCabe R Tyler
Department of Pathology, Ohio State University Medical Center, OH, USA.
Diagn Mol Pathol. 2008 Jun;17(2):107-11. doi: 10.1097/PDM.0b013e318161e4dd.
A human papillomavirus (HPV) microarray system allows the determination of HPV type in clinical samples. The purpose of this study was to determine the presence of HPV in liquid-based Pap smears with the MyGene MyHPV Chip Kit HPV genotyping microarray test (MyGene Assay), and to correlate this with the cytology and biopsy diagnoses, clinical follow-up, HPV Hybrid Capture data, and HPV sequence analyses. Four hundred and two Pap smears (93 ThinPrep, 309 SurePath) were available for study. Correlation of HPV DNA detection by the MyGene Assay with the Pap smear diagnosis showed a detection rate of 19/97 (19%) for normal Pap smears, 181/242 (74%) for atypical squamous cells of undetermined significance (ASCUS), and 61/63 (97%) for squamous intraepithelial lesions (SILs). Biopsy data on 248 women were available. HPV was noted by the MyGene Assay in the Pap smear in 98/100 (98%) of the cases, for which the corresponding biopsy had been diagnosed as SIL, compared with 103/148 (69%) of the cases for which the biopsy had been negative for SIL. Clinical follow-ups were available for 200 women with ASCUS Pap smears. A significant increase was observed in the rate of biopsy-proven SILs in women with ASCUS Pap smears that were HPV-positive (63/66=95%) as compared with those that were HPV-negative (96/134=71%, P<0.05). The MyGene Assay and Hybrid Capture system gave equivalent results for all the categories studied, except for the presence of multiple infections, as determined by viral sequence analysis. Specifically, the Hybrid Capture system overestimated the presence of dual infection (low-risk and high-risk positive) by 48% and missed many cases of multiple infections, especially when 2 or more high-risk types were present. It is concluded that the MyGene Assay allows for the routine typing of HPV in liquid-based Pap smears, and that the presence of HPV DNA in ASCUS Pap smears is strongly correlated with a biopsy-proven SIL.
人乳头瘤病毒(HPV)微阵列系统可用于确定临床样本中的HPV类型。本研究的目的是通过MyGene MyHPV芯片试剂盒HPV基因分型微阵列检测(MyGene检测法)来确定液基巴氏涂片样本中HPV的存在情况,并将其与细胞学和活检诊断、临床随访、HPV杂交捕获数据以及HPV序列分析结果进行关联。共有402份巴氏涂片样本(93份ThinPrep样本,309份SurePath样本)可供研究。MyGene检测法检测到的HPV DNA与巴氏涂片诊断结果的相关性显示,正常巴氏涂片的检测率为19/97(19%),意义不明确的非典型鳞状细胞(ASCUS)的检测率为181/242(74%),鳞状上皮内病变(SIL)的检测率为61/63(97%)。有248名女性的活检数据可供分析。在巴氏涂片中,MyGene检测法检测到HPV的病例中,有98/100(98%)的病例对应的活检诊断为SIL,而活检结果为SIL阴性的病例中,这一比例为103/148(69%)。对200名ASCUS巴氏涂片的女性进行了临床随访。结果发现,HPV阳性的ASCUS巴氏涂片女性中,活检证实为SIL的比例显著高于HPV阴性者(63/66 = 95% 对比 96/134 = 71%,P<0.05)。除了通过病毒序列分析确定的多重感染情况外,MyGene检测法和杂交捕获系统在所有研究类别中给出了等效结果。具体而言,杂交捕获系统将双重感染(低风险和高风险均为阳性)的存在情况高估了48%,并且遗漏了许多多重感染病例,尤其是当存在两种或更多高风险类型时。结论是,MyGene检测法可用于液基巴氏涂片中HPV的常规分型,并且ASCUS巴氏涂片中HPV DNA的存在与活检证实的SIL密切相关。