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The evaluation of human papillomavirus genotyping in cervical liquid-based cytology specimens; Using the Roche Linear Array HPV genotyping assay

机译:宫颈液体基细胞标本中人乳头瘤病毒基因分型的评价; 使用Roche线性阵列HPV基因分型测定

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Objective: To ascertain the usefulness of the Roche Linear Array human papillomavirus (HPV) genotyping assay for assessing HPV genotypes in liquid-based cytology (LBC) samples and to evaluate this methodology within a cytopathology laboratory. These tests are of importance as persistent infection with high-risk HPV genotypes is considered a causal factor in the development of cervical cancer. Methods: A total of 175 cervical LBC samples were tested using the Roche Linear Array HPV genotyping test. The suitability of the assay use in routine cytopathology laboratory was considered. HPV genotypes were matched to the cervical cytology results, which included negative, borderline nuclear abnormalities, mild, moderate and severe dyskaryosis. Results: The assay could be applied to screening samples with the combined result available at the reporting stage. There were no test failures. All samples used after cytological analysis had sufficient DNA for testing. The results were reproducible and easily read and there was concordance of results between biomedical scientists. The results of the assay showed co-infection with multiple HPV genotypes was common in both high-grade and low-grade cytology samples. The percentage of HPV+ samples in the normal cytology samples (although in this grouping the number of samples was low) was 37%. In the cytology samples reported as severe dyskaryosis the HPV genotypes most commonly found were HPV16 and HPV51. Conclusion: The assay was able to detect multiple HPV infection with a wide range of genotypes in LBC samples sent for routine cytological analysis. It would be suitable for use in a cytopathology laboratory. The results of the assay show that the genotype profile has some variation from other geographical regions, and more work is needed to determine population prevalence, to ascertain the impact of the HPV vaccine, to evaluate test for cure and HPV triage management.
机译:目的:确定罗氏线性阵列人乳头瘤病毒(HPV)基因分型测定评估液体基细胞学(LBC)样品中HPV基因型的有用性,并在细胞病理学实验室中评估该方法。这些试验具有重要性,因为具有高风险HPV基因型的持续感染被认为是宫颈癌发育的因果因素。方法:使用Roche线性阵列HPV基因分型试验测试总共175个宫颈LBC样品。考虑了测定在常规细胞病变实验室的适用性。 HPV基因型与宫颈细胞学结果相匹配,其中包括阴性,边缘核异常,轻度,中度和严重的疑难关系。结果:该测定可应用于筛选样品,并在报告阶段提供的合并结果。没有测试失败。细胞学分析后使用的所有样品具有足够的DNA进行测试。结果是可重复的,易于阅读,生物医学科学家之间的结果一致。测定结果表明,在高档和低级细胞学样品中常见多种HPV基因型的共感染。正常细胞学样品中HPV +样品的百分比(尽管在该分组中,样品的数量低)为37%。在细胞学样本中报告为严重疑难关系,最常见的HPV基因型是HPV16和HPV51。结论:测定能够检测多种基因型在常规细胞学分析中的LBC样品中具有多种基因型的多种HPV感染。它适用于患细胞病变实验室。测定结果表明,基因型曲线具有与其他地理区域的一些变化,需要更多的作品来确定人口普遍性,以确定HPV疫苗的影响,评估治愈和HPV分类管理的测试。

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