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通过寡核苷酸微阵列检测,自行采集的阴道样本与临床医生采集的宫颈样本中HPV DNA检测结果具有良好的相关性。

Good correlation of HPV DNA test between self-collected vaginal and clinician-collected cervical samples by the oligonucleotide microarray.

作者信息

Seo Sang-Soo, Song Yong-Sang, Kim Jae-Weon, Park Noh-Hyun, Kang Soon-Beom, Lee Hyo-Pyo

机构信息

Center for Uterine Cancer, National Cancer Center, 809 Madu1-dong, Goyang-si, Gyeonggi-do 411-351, Korea.

出版信息

Gynecol Oncol. 2006 Jul;102(1):67-73. doi: 10.1016/j.ygyno.2005.11.030. Epub 2006 Jan 10.

DOI:10.1016/j.ygyno.2005.11.030
PMID:16375952
Abstract

OBJECTIVES

To evaluate the efficacy of self-collected vaginal samples for high-risk HPV detection by the HPV oligonucleotide microarray method (HPVDNAChip).

METHODS

One hundred and eighteen patients with abnormal Pap smears were included. Self-collected vaginal and clinician-collected cervical samples for HPV testing were obtained. The result of the HPV DNA test was compared with the histopathological diagnosis or colposcopic finding.

RESULTS

Of the 118 patients, 42 (35.6%) had >or= cervical intraepithelial neoplasia (CIN) III lesions. Using the HPVDNAChip, high-risk types of HPV were detected in 38 of these 42 patients (90.5%) with the self-collected vaginal samples and in 37 of 42 (88.1%) with the clinician-collected cervical samples. The agreement of HPVDNAchip results between self- and clinician-collected samples was very good (kappa = 0.81) with a 93.2% concordance rate. Multiple HPV infections were found in 17 of 88 (19.3%) HPV-positive clinician-collected cervical samples. The rate of multiple HPV infection tended to decrease as the degree of pathologic classification increased.

CONCLUSION

Using the HPVDNAchip to assay for HPV infection, results from self-collected vaginal samples were compatible with those from clinician-collected cervical samples.

摘要

目的

通过人乳头瘤病毒寡核苷酸微阵列法(HPV DNA芯片)评估自行采集的阴道样本用于高危型HPV检测的效果。

方法

纳入118例巴氏涂片异常的患者。获取自行采集的阴道样本和临床医生采集的宫颈样本进行HPV检测。将HPV DNA检测结果与组织病理学诊断或阴道镜检查结果进行比较。

结果

118例患者中,42例(35.6%)患有≥宫颈上皮内瘤变(CIN)III级病变。使用HPV DNA芯片,在这42例患者中,38例(90.5%)通过自行采集的阴道样本检测到高危型HPV,42例中的37例(88.1%)通过临床医生采集的宫颈样本检测到高危型HPV。自行采集样本与临床医生采集样本的HPV DNA芯片检测结果一致性非常好(kappa = 0.81),一致率为93.2%。在88例HPV阳性的临床医生采集的宫颈样本中,17例(19.3%)发现多重HPV感染。随着病理分级程度增加,多重HPV感染率呈下降趋势。

结论

使用HPV DNA芯片检测HPV感染时,自行采集的阴道样本结果与临床医生采集的宫颈样本结果相符。

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