首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Detection and Genotyping of Human Papillomavirus in Self-Obtained Cervicovaginal Samples by Using the FTA Cartridge: New Possibilities for Cervical Cancer Screening
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Detection and Genotyping of Human Papillomavirus in Self-Obtained Cervicovaginal Samples by Using the FTA Cartridge: New Possibilities for Cervical Cancer Screening

机译:使用FTA弹药筒检测和自测宫颈阴道样本中人乳头瘤病毒的基因分型:宫颈癌筛查的新可能性

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摘要

This study assesses human papillomavirus (HPV) detection and genotyping in self-sampled genital smears applied to an indicating FTA elute cartridge (FTA cartridge). The study group consisted of 96 women, divided into two sample sets. All samples were analyzed by the HPV SPF10-Line Blot 25. Set 1 consisted of 45 women attending the gynecologist; all obtained a self-sampled cervicovaginal smear, which was applied to an FTA cartridge. HPV results were compared to a cervical smear (liquid based) taken by a trained physician. Set 2 consisted of 51 women who obtained a self-sampled cervicovaginal smear at home, which was applied to an FTA cartridge and to a liquid-based medium. DNA was obtained from the FTA cartridges by simple elution as well as extraction. Of all self-obtained samples of set 1, 62.2% tested HPV positive. The overall agreement between self- and physician-obtained samples was 93.3%, in favor of the self-obtained samples. In sample set 2, 25.5% tested HPV positive. The overall agreement for high-risk HPV presence between the FTA cartridge and liquid-based medium and between DNA elution and extraction was 100%. This study shows that HPV detection and genotyping in self-obtained cervicovaginal samples applied to an FTA cartridge is highly reliable. It shows a high level of overall agreement with HPV detection and genotyping in physician-obtained cervical smears and liquid-based self-samples. DNA can be obtained by simple elution and is therefore easy, cheap, and fast. Furthermore, the FTA cartridge is a convenient medium for collection and safe transport at ambient temperatures. Therefore, this method may contribute to a new way of cervical cancer screening.
机译:这项研究评估了适用于指示性FTA洗脱弹药筒(FTA弹药筒)的自取样生殖器涂片中的人类乳头瘤病毒(HPV)检测和基因分型。该研究小组由96名妇女组成,分为两组。所有样本均通过HPV SPF10-Line Blot 25进行分析。第一组包括45位就诊妇科医生的妇女;所有人都获得了自体宫颈阴道涂片,并将其应用于FTA弹药筒。将HPV结果与经过培训的医师进行的宫颈涂片检查(液基)进行比较。第2组由51名妇女组成,她们在家中进行了宫颈宫颈阴道涂片的自我取样,将其涂在FTA药筒和液体培养基上。通过简单的洗脱和提取从FTA药筒中获得DNA。在一组1的所有自获取样本中,有62.2%的HPV阳性。自我获取和医生获取的样本之间的总体一致性为93.3%,支持自我获取的样本。在样品组2中,有25.5%的HPV阳性。 FTA药筒和液体培养基之间以及DNA洗脱和提取之间存在高风险HPV的总体协议是100%。这项研究表明,将自体宫颈阴道样本中的HPV检测和基因分型应用于FTA药盒是高度可靠的。它显示了在医生获得的宫颈涂片和基于液体的自我样品中,HPV检测和基因分型的总体水平很高。 DNA可以通过简单的洗脱获得,因此简单,便宜和快速。此外,FTA滤芯是在环境温度下收集和安全运输的便捷介质。因此,该方法可能有助于宫颈癌筛查的新方法。

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