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β乳头瘤病毒感染的持续存在是光化性角化病(皮肤鳞状细胞癌的前驱病变)的一个风险因素。

Persistence of betapapillomavirus infections as a risk factor for actinic keratoses, precursor to cutaneous squamous cell carcinoma.

作者信息

Plasmeijer Elsemieke I, Neale Rachel E, de Koning Maurits N C, Quint Wim G V, McBride Penelope, Feltkamp Mariet C W, Green Adele C

机构信息

Department of Medical Microbiology, Leiden University Medical Center, Leiden, The Netherlands.

出版信息

Cancer Res. 2009 Dec 1;69(23):8926-31. doi: 10.1158/0008-5472.CAN-09-1186. Epub 2009 Nov 10.

Abstract

Human papillomaviruses from the beta genus (betaPV) are a possible cause of cutaneous squamous cell carcinoma (SCC). We assessed the extent to which betaPV infections persisted long-term in a subtropical Australian community and whether betaPV persistence is positively associated with actinic keratoses, precursor for SCC. Eyebrow hairs were collected from 171 participants of the community-based Nambour Skin Cancer Study in 1996 and 2003. Hair samples were tested for the presence of DNA from 25 different betaPV types and assessed in relation to actinic keratosis presence in 2007. In 1996, a total of 413 betaPV infections were found in 73% of participants, increasing to 490 infections among 85% in 2003. Of the total betaPV infections detected, 211 (30%) were found to persist. Age was significantly associated with betaPV persistence: those ages >60 years had 1.5-fold (95% confidence interval, 1.1-1.9) increased risk of type-specific viral persistence than those ages <40 years. After accounting for actinic keratoses at baseline, persistence of betaPV DNA resulted in a 1.4-fold (95% confidence interval, 1.0-1.9) increase in risk of having actinic keratoses on the face in 2007. In conclusion, persistent betaPV infections in this population were associated with an increased occurrence of actinic keratosis. Additional studies are needed to determine the possible association of betaPV persistence with SCC.

摘要

β属人乳头瘤病毒(βPV)可能是皮肤鳞状细胞癌(SCC)的一个病因。我们评估了βPV感染在澳大利亚一个亚热带社区中长期持续存在的程度,以及βPV持续感染是否与SCC的前体光化性角化病呈正相关。1996年和2003年,从基于社区的楠伯皮肤癌研究的171名参与者中收集了眉毛毛发。对毛发样本进行检测,以确定是否存在来自25种不同βPV类型的DNA,并于2007年评估其与光化性角化病的存在情况的关系。1996年,在73%的参与者中总共发现了413例βPV感染,到2003年,85%的参与者中感染增加到490例。在检测到的所有βPV感染中,发现211例(30%)持续存在。年龄与βPV持续感染显著相关:年龄>60岁的人比年龄<40岁的人发生特定类型病毒持续感染的风险增加1.5倍(95%置信区间,1.1 - 1.9)。在考虑了基线时的光化性角化病后,βPV DNA的持续存在导致2007年面部出现光化性角化病的风险增加1.4倍(95%置信区间,1.0 - 1.9)。总之,该人群中持续的βPV感染与光化性角化病的发生率增加有关。需要进一步的研究来确定βPV持续感染与SCC之间可能的关联。

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