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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.

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。

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