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本文引用的文献

1
The Bethesda System for Reporting Cervical Cytology: A Historical Perspective.《贝塞斯达宫颈细胞学报告系统:历史视角》
Acta Cytol. 2017;61(4-5):359-372. doi: 10.1159/000477556. Epub 2017 Jul 11.
2
HPV L1 and P16 Expression in CIN1 to Predict Future CIN2.CIN1中HPV L1和P16的表达以预测未来的CIN2
Int J Gynecol Pathol. 2017 May;36(3):281-288. doi: 10.1097/PGP.0000000000000326.
3
Expression of the p16 and Ki67 in Cervical Squamous Intraepithelial Lesions and Cancer.p16和Ki67在宫颈鳞状上皮内病变及癌中的表达
Asian Pac J Cancer Prev. 2016;17(7):3201-6.
4
p16 staining has limited value in predicting the outcome of histological low-grade squamous intraepithelial lesions of the cervix.p16染色在预测宫颈组织学低级别鳞状上皮内病变的预后方面价值有限。
Mod Pathol. 2016 Jan;29(1):51-9. doi: 10.1038/modpathol.2015.126. Epub 2015 Nov 6.
5
The clinical impact of using p16(INK4a) immunochemistry in cervical histopathology and cytology: an update of recent developments.p16(INK4a)免疫化学在宫颈组织病理学和细胞学中的临床应用:近期进展更新
Int J Cancer. 2015 Jun 15;136(12):2741-51. doi: 10.1002/ijc.28900. Epub 2014 May 12.
6
Follow-up study of patients with cervical intraepithelial neoplasia grade 1 overexpressing p16Ink4a.p16Ink4a 过表达的宫颈上皮内瘤变 1 级患者的随访研究。
Int J Gynecol Cancer. 2013 Nov;23(9):1663-9. doi: 10.1097/IGC.0b013e3182a80b14.
7
p16INK4A immunohistochemical staining and predictive value for progression of cervical intraepithelial neoplasia grade 1: a prospective study in China.p16INK4A 免疫组化染色在预测宫颈上皮内瘤变 1 级进展中的价值:一项在中国的前瞻性研究。
Int J Cancer. 2014 Apr 1;134(7):1715-24. doi: 10.1002/ijc.28485. Epub 2013 Oct 12.
8
Prognostic value of p16-INK4A protein in women with negative or CIN1 histology result: a follow-up study.p16INK4A 蛋白在阴性或 CIN1 组织学结果的女性中的预后价值:一项随访研究。
Int J Cancer. 2014 Feb 15;134(4):897-904. doi: 10.1002/ijc.28407. Epub 2013 Aug 29.
9
p16(INK4a) immunohistochemistry is a promising biomarker to predict the outcome of low grade cervical intraepithelial neoplasia: comparison study with HPV genotyping.p16(INK4a)免疫组化是预测低级别宫颈上皮内瘤变结局的有前途的生物标志物:与 HPV 基因分型的对比研究。
J Gynecol Oncol. 2013 Jul;24(3):215-21. doi: 10.3802/jgo.2013.24.3.215. Epub 2013 Jul 4.
10
The Lower Anogenital Squamous Terminology Project and its implications for clinical care.下生殖器官鳞状上皮术语项目及其对临床护理的影响。
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p16INK4a和Ki-67检测可预测宫颈低度鳞状上皮内病变的进展。

p16INK4a and Ki-67 measurement predict progression of cervical low-grade squamous intraepithelial lesion.

作者信息

Zhang Xiaobo, Shen Danhua

机构信息

Department of Pathology, Peking University People's Hospital Beijing, China.

出版信息

Int J Clin Exp Pathol. 2018 Aug 1;11(8):4109-4116. eCollection 2018.

PMID:31949802
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6962782/
Abstract

OBJECTIVE

To describe the natural history of low-grade squamous intraepithelial lesion/cervical intraepithelial neoplasia grade I (LSIL/CIN1), and to analyze the predictive values of p16INK4a and Ki-67 for LSIL/CIN1 progression.

METHODS

From January 2013 to January 2016, 264 patients were diagnosed with CIN1 by colposcopy-assisted biopsy and were followed up at 1-year intervals at Peking University People's Hospital. We measured expression levels of biomarkers p16INK4a and Ki67 to predict progression, persistence, or regression of the disease. We used chi-square tests and logistic regression analysis to explore the relationships among LSIL/CIN1 progression, p16INK4a/Ki-67 expression, and patient age.

RESULTS

Among 264 patients with LSIL/CIN1, p16INK4a, Ki-67 expression and patient age > 30 years old were significantly associated with progression. Univariate analysis showed that age was not a risk factor for progression (P > 0.05) but that p16INK4a and Ki-67 expression were significantly associated with the progression (P < 0.05). Multivariate analysis showed that p16INK4a-positivity and high expression of Ki-67 protein were associated with LSIL/CIN1 progression, with odds ratios (OR) and 95% confidence intervals (CI) of 10.95 (3.04-39.53), and 9.7 (2.77-34.03), respectively.

CONCLUSION

p16INK4a-positivity and high expression of Ki-67correlated with LSIL/CIN1 progression. These markers may be independent predictors of LSIL/CIN1 progression.

摘要

目的

描述低度鳞状上皮内病变/宫颈上皮内瘤变1级(LSIL/CIN1)的自然病程,并分析p16INK4a和Ki-67对LSIL/CIN1进展的预测价值。

方法

2013年1月至2016年1月,264例患者经阴道镜辅助活检诊断为CIN1,并于北京大学人民医院进行每年1次的随访。我们检测生物标志物p16INK4a和Ki67的表达水平,以预测疾病的进展、持续或消退。我们采用卡方检验和逻辑回归分析,探讨LSIL/CIN1进展、p16INK4a/Ki-67表达与患者年龄之间的关系。

结果

在264例LSIL/CIN1患者中,p16INK4a、Ki-67表达及年龄>30岁与疾病进展显著相关。单因素分析显示,年龄不是进展的危险因素(P>0.05),但p16INK4a和Ki-67表达与进展显著相关(P<0.05)。多因素分析显示,p16INK4a阳性和Ki-67蛋白高表达与LSIL/CIN1进展相关,优势比(OR)及95%置信区间(CI)分别为10.95(3.04-39.53)和9.7(2.77-34.03)。

结论

p16INK4a阳性和Ki-67高表达与LSIL/CIN1进展相关。这些标志物可能是LSIL/CIN1进展的独立预测指标。