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在台湾,二甲双胍可降低糖尿病合并慢性丙型肝炎患者抗病毒治疗成功后的肝细胞癌发病率。

Metformin reduces hepatocellular carcinoma incidence after successful antiviral therapy in patients with diabetes and chronic hepatitis C in Taiwan.

作者信息

Tsai Pei-Chien, Kuo Hsing-Tao, Hung Chao-Hung, Tseng Kuo-Chih, Lai Hsueh-Chou, Peng Cheng-Yuan, Wang Jing-Houng, Chen Jyh-Jou, Lee Pei-Lun, Chien Rong-Nan, Yang Chi-Chieh, Lo Gin-Ho, Kao Jia-Horng, Liu Chun-Jen, Liu Chen-Hua, Yan Sheng-Lei, Bair Ming-Jong, Lin Chun-Yen, Su Wei-Wen, Chu Cheng-Hsin, Chen Chih-Jen, Tung Shui-Yi, Tai Chi-Ming, Lin Chih-Wen, Lo Ching-Chu, Cheng Pin-Nan, Chiu Yen-Cheng, Wang Chia-Chi, Cheng Jin-Shiung, Tsai Wei-Lun, Lin Han-Chieh, Huang Yi-Hsiang, Yeh Ming-Lun, Huang Chung-Feng, Hsieh Meng-Hsuan, Huang Jee-Fu, Dai Chia-Yen, Chung Wan-Long, Chen Chi-Yi, Yu Ming-Lung

机构信息

Hepatobiliary Section, Department of Internal Medicine, and Hepatitis Center, Kaohsiung Medical University Hospital; Hepatitis Research Center, School of Medicine and Center for Liquid Biopsy and Cohort Research, Kaohsiung Medical University, Kaohsiung, Taiwan; Health Management Center, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.

Division of Hepatogastroenterology, Department of Internal Medicine, Chi Mei Medical Center, Tainan, Taiwan; School of Medicine, College of Medicine, National Sun Yat-sen University, Kaohsiung, Taiwan.

出版信息

J Hepatol. 2023 Feb;78(2):281-292. doi: 10.1016/j.jhep.2022.09.019. Epub 2022 Oct 5.

Abstract

BACKGROUND & AIMS: Diabetes mellitus (DM) is known to increase the risk of hepatocellular carcinoma (HCC) among individuals with chronic hepatitis C (CHC). We aimed to evaluate whether metformin reduces HCC risk among individuals with DM and CHC after successful antiviral therapy.

METHODS

Individuals with CHC who achieved a sustained virological response (SVR) after interferon-based therapy were enrolled in a large-scale, multicenter cohort in Taiwan (T-COACH). Cases of HCC at least 1 year after SVR were identified through linkage to the catastrophic illness and cancer registry databases.

RESULTS

Of 7,249 individuals with CHC enrolled in the study, 781 (10.8%) had diabetes and 647 (82.8%) were metformin users. During a median follow-up of 4.4 years, 227 patients developed new-onset HCC. The 5-year cumulative HCC incidence was 10.9% in non-metformin users and 2.6% in metformin users, compared to 3.0% in individuals without DM (adjusted hazard ratio [aHR] 2.83; 95% CI 1.57-5.08 and aHR 1.46; 95% CI 0.98-2.19, respectively). Cirrhosis was the most important factor significantly associated with higher HCC risk in Cox regression analysis, followed by DM non-metformin use, older age, male sex, and obesity; whereas hyperlipidemia with statin use was associated with a lower HCC risk. Using the two most crucial risk factors, cirrhosis and DM non-metformin use, we constructed a simple risk model that could predict HCC risk among individuals with CHC after SVR. Metformin use was shown to reduce the risk of all liver-related complications.

CONCLUSIONS

Metformin use greatly reduced HCC risk after successful antiviral therapy in individuals with diabetes and CHC. A simple risk stratification model comprising cirrhosis and DM non-metformin use could predict long-term outcomes in individuals with CHC after SVR.

IMPACT AND IMPLICATIONS

The current study provides evidence that metformin could reduce hepatocellular carcinoma (HCC) incidence after successful antiviral therapy among those with diabetes and chronic hepatitis C in a large-scale nationwide cohort study. Although successful antiviral therapy greatly reduces HCC risk in individuals with chronic hepatitis C, those with cirrhosis, diabetes, obesity, and the elderly remain at high risk of HCC development. We demonstrated that a simple risk model composed of two crucial unfavorable factors, cirrhosis and diabetes without metformin use, predicts the risk of HCC and major liver-related complications after successful antiviral therapy in individuals with chronic hepatitis C. Metformin use is highly recommended for individuals with diabetes and chronic hepatitis C after viral eradication to reduce the risk of HCC.

摘要

背景与目的

已知糖尿病(DM)会增加慢性丙型肝炎(CHC)患者患肝细胞癌(HCC)的风险。我们旨在评估二甲双胍是否能降低成功抗病毒治疗后的糖尿病合并CHC患者的HCC风险。

方法

在台湾的一项大规模多中心队列研究(T-COACH)中,纳入了接受基于干扰素治疗后获得持续病毒学应答(SVR)的CHC患者。通过与重大疾病和癌症登记数据库进行关联,确定SVR后至少1年发生HCC的病例。

结果

在该研究纳入的7249例CHC患者中,781例(10.8%)患有糖尿病,647例(82.8%)使用二甲双胍。在中位随访4.4年期间,227例患者发生了新发HCC。未使用二甲双胍患者的5年累积HCC发病率为10.9%,使用二甲双胍患者为2.6%,而无糖尿病患者为3.0%(调整后风险比[aHR]分别为2.83;95%CI 1.57 - 5.08和aHR 1.46;95%CI 0.98 - 2.19)。在Cox回归分析中,肝硬化是与较高HCC风险显著相关的最重要因素,其次是糖尿病且未使用二甲双胍、年龄较大、男性和肥胖;而使用他汀类药物治疗的高脂血症与较低的HCC风险相关。利用两个最关键的风险因素,即肝硬化和糖尿病且未使用二甲双胍,我们构建了一个简单的风险模型,该模型可以预测SVR后CHC患者的HCC风险。结果显示,使用二甲双胍可降低所有肝脏相关并发症的风险。

结论

在糖尿病合并CHC患者中,成功抗病毒治疗后使用二甲双胍可大大降低HCC风险。一个包含肝硬化和糖尿病且未使用二甲双胍的简单风险分层模型可以预测SVR后CHC患者的长期预后。

影响与意义

本研究提供的证据表明,在一项全国性大规模队列研究中,二甲双胍可降低糖尿病合并慢性丙型肝炎患者成功抗病毒治疗后的肝细胞癌(HCC)发病率。尽管成功的抗病毒治疗可大大降低慢性丙型肝炎患者的HCC风险,但肝硬化、糖尿病、肥胖和老年人仍有较高的HCC发生风险。我们证明,一个由两个关键不利因素,即肝硬化和未使用二甲双胍的糖尿病组成的简单风险模型,可以预测慢性丙型肝炎患者成功抗病毒治疗后的HCC风险和主要肝脏相关并发症。强烈建议糖尿病合并慢性丙型肝炎患者在病毒清除后使用二甲双胍以降低HCC风险。

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