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

机译:p16INK4a和Ki-67检测可预测宫颈低度鳞状上皮内病变的进展

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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.
机译:目的:描述低度鳞状上皮内病变/宫颈上皮内瘤样变I级(LSIL / CIN1)的自然史,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,通过阴道镜辅助活检诊断出264例CIN1患者,并在北京大学人民医院进行了为期1年的随访。我们测量了生物标志物p16INK4a和Ki67的表达水平,以预测疾病的进展,持续或消退。我们使用卡方检验和逻辑回归分析来探讨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表达和患者年龄大于30岁与病情发展显着相关。单因素分析表明,年龄不是进展的危险因素(P> 0.05),但p16INK4a和Ki-67表达与进展显着相关(P <0.05)。多变量分析显示p16INK4a阳性和Ki-67蛋白的高表达与LSIL / CIN1的进展有关,优势比(OR)和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的高表达与LSIL / CIN1的进展有关。这些标志物可能是LSIL / CIN1进展的独立预测因子。

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