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挪威北特伦德拉格大学医院:对宫颈微小病变女性进行 HPV mRNA 检测的经验。

HPV mRNA test in women with minor cervical lesions: experience of the University Hospital of North Norway.

机构信息

Department of Clinical Pathology, The University Hospital of North Norway, Postboks 16, 9038 Tromso, Norway.

出版信息

J Virol Methods. 2010 Oct;169(1):219-22. doi: 10.1016/j.jviromet.2010.07.011. Epub 2010 Jul 16.

Abstract

In the Norwegian Cervical Cancer Screening Programme tests for detection of human papillomavirus (HPV) are used to triage women with minor cytological cervical lesions. The material in this study comprises samples from 1798 women in the period 2006-2008. The HPV test was performed according to the guidelines of the Norwegian Cancer Registry. The HPV mRNA test (PreTect HPV-Proofer) detects and types 5 high-risk genotypes (16, 18, 31, 33 and 45). The HPV mRNA results were compared to cytology and then biopsy up to December 2009. Women with minor cytological cervical lesions and negative HPV test were followed with a new PAP smear after 12 months. A total of 327 women (18%) were HPV mRNA positive. Of the 1798 women with minor cytological lesions, 232 women (13%) had moderate dysplasia, severe dysplasia or cancer and 144 women (8%) had severe dysplasia or cancer in biopsy. 57% of the women with a positive HPV mRNA test had moderate dysplasia, severe dysplasia or cancer. 37% had severe dysplasia or cancer. The sensitivity of the HPV mRNA test to detect moderate dysplasia, severe dysplasia or cancer was 81%. The specificity for moderate dysplasia, severe dysplasia or cancer was 91%. The negative predictive value (NPV) of the HPV mRNA test for moderate dysplasia, severe dysplasia or cancer was 97%. Of 11 women with cervical cancer, 10 were positive for HPV type 16 or 18. The HPV mRNA test seems more suitable than HPV DNA tests to triage women with minor cytological cervical lesions due to its higher specificity.

摘要

在挪威的宫颈癌筛查计划中,使用人乳头瘤病毒(HPV)检测来对细胞学宫颈病变程度较轻的女性进行分类。本研究的材料包括 2006-2008 年期间 1798 名女性的样本。HPV 检测按照挪威癌症登记处的指南进行。HPV mRNA 检测(PreTect HPV-Proofer)可检测和分型 5 种高危基因型(16、18、31、33 和 45)。HPV mRNA 检测结果与细胞学结果进行了比较,然后在 2009 年 12 月前进行了活检。细胞学宫颈病变程度较轻且 HPV 检测结果为阴性的女性,在 12 个月后进行新的巴氏涂片检查。共有 327 名女性(18%)HPV mRNA 阳性。在 1798 名细胞学宫颈病变程度较轻的女性中,232 名(13%)女性有中度不典型增生、重度不典型增生或癌症,144 名(8%)女性活检中发现重度不典型增生或癌症。HPV mRNA 检测阳性的女性中,57%有中度不典型增生、重度不典型增生或癌症,37%有重度不典型增生或癌症。HPV mRNA 检测对中度不典型增生、重度不典型增生或癌症的敏感性为 81%。对中度不典型增生、重度不典型增生或癌症的特异性为 91%。HPV mRNA 检测对中度不典型增生、重度不典型增生或癌症的阴性预测值(NPV)为 97%。11 名宫颈癌患者中,有 10 名 HPV 类型 16 或 18 阳性。HPV mRNA 检测似乎比 HPV DNA 检测更适合对细胞学宫颈病变程度较轻的女性进行分类,因为其特异性更高。

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