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本文引用的文献

1
The hepatocellular carcinoma risk in patients with HBV-related cirrhosis: a competing risk nomogram based on a 4-year retrospective cohort study.乙肝相关肝硬化患者的肝细胞癌风险:基于一项4年回顾性队列研究的竞争风险列线图
Front Oncol. 2024 May 16;14:1398968. doi: 10.3389/fonc.2024.1398968. eCollection 2024.
2
Global Burden and Trends of Primary Liver Cancer Attributable to Comorbid Type 2 Diabetes Mellitus Among People Living with Hepatitis B: An Observational Trend Study from 1990 to 2019.1990年至2019年乙型肝炎感染者中2型糖尿病合并症所致原发性肝癌的全球负担及趋势:一项观察性趋势研究
J Epidemiol Glob Health. 2024 Jun;14(2):398-410. doi: 10.1007/s44197-024-00237-1. Epub 2024 May 7.
3
Lifestyle factors, glycemic traits, and lipoprotein traits and risk of liver cancer: a Mendelian randomization analysis.生活方式因素、血糖特征、脂蛋白特征与肝癌风险:一项孟德尔随机化分析。
Sci Rep. 2024 Apr 12;14(1):8502. doi: 10.1038/s41598-024-59211-3.
4
Alcohol-associated liver disease.酒精相关性肝病。
J Clin Invest. 2024 Feb 1;134(3):e176345. doi: 10.1172/JCI176345.
5
Global trends in hepatocellular carcinoma epidemiology: implications for screening, prevention and therapy.全球肝细胞癌流行病学趋势:对筛查、预防和治疗的启示。
Nat Rev Clin Oncol. 2023 Dec;20(12):864-884. doi: 10.1038/s41571-023-00825-3. Epub 2023 Oct 26.
6
Associations of non-alcoholic fatty liver disease and cirrhosis with liver cancer in European and East Asian populations: A Mendelian randomization study.非酒精性脂肪性肝病和肝硬化与欧洲和东亚人群肝癌的关联:一项孟德尔随机研究。
Cancer Rep (Hoboken). 2024 Jan;7(1):e1913. doi: 10.1002/cnr2.1913. Epub 2023 Oct 16.
7
PAGE-B incorporating moderate HBV DNA levels predicts risk of HCC among patients entering into HBeAg-positive chronic hepatitis B.纳入中度乙肝病毒脱氧核糖核酸水平的PAGE-B可预测HBeAg阳性慢性乙型肝炎患者发生肝细胞癌的风险。
J Hepatol. 2024 Jan;80(1):20-30. doi: 10.1016/j.jhep.2023.09.011. Epub 2023 Sep 19.
8
Multiomics analyses reveal pathological mechanisms of HBV infection and integration in liver cancer.多组学分析揭示了乙型肝炎病毒感染和整合在肝癌中的病理机制。
J Med Virol. 2023 Aug;95(8):e28980. doi: 10.1002/jmv.28980.
9
Diabetes Mellitus Impacts on the Performance of Hepatocellular Carcinoma Risk Scores in Chronic Hepatitis B Patients.糖尿病对慢性乙型肝炎患者肝癌风险评分表现的影响。
Clin Gastroenterol Hepatol. 2023 Oct;21(11):2864-2875.e16. doi: 10.1016/j.cgh.2023.02.004. Epub 2023 Feb 22.
10
The flavonoid GL-V9 alleviates liver fibrosis by triggering senescence by regulating the transcription factor GATA4 in activated hepatic stellate cells.类黄酮GL-V9通过调节活化肝星状细胞中的转录因子GATA4触发衰老,从而减轻肝纤维化。
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乙肝患者并发原发性肝癌的影响因素分析及柱状图预测模型构建

Analysis of influencing factors of concurrent primary liver cancer in hepatitis B patients and construction of column chart prediction model.

作者信息

Cao Qunmei, Zhou Yilin, Wen Changlong, Li Qinglan

机构信息

Department of Infectious Disease, Ganzhou People's Hospital, Ganzhou, China.

出版信息

Epidemiol Infect. 2025 Sep 16;153:e111. doi: 10.1017/S0950268825100538.

DOI:10.1017/S0950268825100538
PMID:40955435
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12529427/
Abstract

A predictive column chart was developed to assess the risk of primary liver cancer (PLC) in hepatitis B patients. Data from 107 PLC patients and 107 controls were used as the training set, with 92 patients as the validation set. An additional 446 patients from other hospitals, including 15 with PLC, formed the external validation group. Multivariate logistic regression identified gender, BMI, alcohol consumption, diabetes, family history of liver cancer, cirrhosis, and HBV DNA load as independent risk factors. The model showed strong discrimination with AUCs of 0.882 and 0.859 in the training and validation sets, respectively, and good calibration (Hosmer-Lemeshow χ² = 2.648, P = 0.954; χ² = 4.117, P = 0.846). Decision curve analysis (DCA) confirmed clinical benefit within a risk threshold of 0.07-0.95. In the external validation group, the model maintained discrimination (AUC = 0.863) and calibration (Hosmer-Lemeshow χ² = 7.999, P = 0.434), with DCA showing net benefit across 0.14-0.95. These results indicate the column chart is a reliable tool for PLC risk prediction in hepatitis B patients.

摘要

开发了一种预测性柱状图来评估乙肝患者原发性肝癌(PLC)的风险。来自107例PLC患者和107例对照的数据用作训练集,92例患者作为验证集。来自其他医院的另外446例患者,包括15例PLC患者,组成了外部验证组。多变量逻辑回归确定性别、体重指数、饮酒、糖尿病、肝癌家族史、肝硬化和HBV DNA载量为独立危险因素。该模型在训练集和验证集中分别显示出较强的区分度,AUC分别为0.882和0.859,且校准良好(Hosmer-Lemeshow χ² = 2.648,P = 0.954;χ² = 4.117,P = 0.846)。决策曲线分析(DCA)证实在0.07-0.95的风险阈值内具有临床益处。在外部验证组中,该模型保持了区分度(AUC = 0.863)和校准(Hosmer-Lemeshow χ² = 7.999,P = 0.434),DCA显示在0.14-0.95范围内有净效益。这些结果表明,该柱状图是预测乙肝患者PLC风险的可靠工具。