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宫颈上皮内瘤变中 HPV 基因型的年龄分布。

Age distribution of HPV genotypes in cervical intraepithelial neoplasia.

机构信息

Preventive Gynaecology Unit, European Institute of Oncology, via Ripamonti 435, Milan, Italy.

出版信息

Gynecol Oncol. 2011 Jun 1;121(3):510-3. doi: 10.1016/j.ygyno.2011.02.018. Epub 2011 Mar 11.

Abstract

OBJECTIVE

Recent data showed that HPV16 infections in young women can lead to CIN3 formation very quickly and questioned the common assumption that invasive cervical cancer develops through slowly progressing pre-cancer lesions, CIN1, CIN2 and CIN3. The aim of the study is to compare the age distribution of HPV 16/18 related and HPV16/18 not related CIN.

METHODS

We used the data generated from the clinical use of HPV genotyping (LINEAR ARRAY, Roche Diagnostics). Patients were grouped on the basis of histology, CIN1 vs. CIN2+ and on HR-HPV genotype status.

RESULTS

The probability to develop a CIN2+ seemed to decrease with age in patients infected with HR-HPV genotype 16/18 while the inverse effect was observed in CIN2+ patients who were HR-HPV positive but HPV16/18 negative (Chi-square test, p(trend)=0.01). Only in HR-HPV positive but HPV 16/18 negative patients, a relative reduction of CIN1 vs. CIN2+ was observed with increasing age (Cochran-Armitage test, p(trend)=0.01); finally, in HR-HPV non-16/18 infected patients only a statistically significant difference in mean age between CIN1 and CIN2+ patients below age 35 was observed.

CONCLUSIONS

Besides the limitations of the present cross-sectional analysis, these data suggest a genotype specific natural history of cervical cancer precursors development: one type, more frequent, HPV16/18 related, which develops quick and early in life; another one, non-16/18 HR-HPV related, which develops later, slowly, through low- to high-grade lesions. If confirmed, this hypothesis could influence screening policies, especially in the vaccinated population.

摘要

目的

最近的数据表明,年轻女性中的 HPV16 感染可迅速导致 CIN3 的形成,并对宫颈癌是通过缓慢进展的癌前病变(CIN1、CIN2 和 CIN3)发展而来的常见假设提出质疑。本研究旨在比较 HPV16/18 相关和 HPV16/18 不相关的 CIN 的年龄分布。

方法

我们使用 HPV 基因分型(线性阵列,罗氏诊断)的临床应用产生的数据。根据组织学、CIN1 与 CIN2+以及 HR-HPV 基因型状态对患者进行分组。

结果

在感染 HR-HPV 基因型 16/18 的患者中,发展为 CIN2+的可能性似乎随着年龄的增长而降低,而在 HR-HPV 阳性但 HPV16/18 阴性的 CIN2+患者中则观察到相反的效果(卡方检验,p(趋势)=0.01)。仅在 HR-HPV 阳性但 HPV16/18 阴性的患者中,随着年龄的增长,观察到 CIN1 与 CIN2+的相对减少(Cochran-Armitage 检验,p(趋势)=0.01);最后,在 HR-HPV 非 16/18 感染的患者中,仅观察到年龄小于 35 岁的 CIN1 和 CIN2+患者之间的平均年龄存在统计学差异。

结论

除了本横断面分析的局限性外,这些数据还表明宫颈癌前病变发展存在特定的基因型自然史:一种类型,更常见,HPV16/18 相关,在生命早期迅速发展;另一种类型,非 16/18 HR-HPV 相关,通过低级别到高级别病变缓慢发展。如果得到证实,这一假设可能会影响筛查策略,尤其是在接种疫苗的人群中。

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