Liver Cirrhosis, Not Antiviral Therapy, Predicts Clinical Outcome in Cohorts with Heterogeneous Hepatitis B Viral Status

被引:14
作者
Kim, Mi Na [1 ]
Hwang, Seong Gyu [1 ]
Kim, Beom Kyung [2 ]
Park, Jun Yong [2 ]
Kim, Do Young [2 ]
Han, Kwang-Hyub [2 ]
Kim, Seung Up [2 ]
Ahn, Sang Hoon [2 ]
机构
[1] CHA Univ, Sch Med, CHA Bundang Med Ctr, Dept Internal Med, Seongnam, South Korea
[2] Yonsei Univ, Coll Med, Dept Internal Med, 50 Yonsei Ro, Seoul 03722, South Korea
基金
新加坡国家研究基金会;
关键词
Liver cirrhosis; Fibrosis; Antiviral therapy; Hepatitis B; Clinical outcome; HEPATOCELLULAR-CARCINOMA INCIDENCE; TERM LAMIVUDINE THERAPY; RISK-ASSESSMENT; ENTECAVIR; FIBROSIS; HEPATOCARCINOGENESIS; LEVEL;
D O I
10.5009/gnl18204
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: Antiviral therapy (AVT) reduces the risk of hepatocellular carcinoma (HCC) development in patients with chronic hepatitis B (CHB). This multicenter retrospective study investigated the effects of AVT and hepatitis B virus (HBV)-related factors on the risk of HCC development in a cohort with heterogeneous HBV status. Methods: A total of 1,843 patients with CHB from two institutions were included in this study. Ultrasound and laboratory tests, including the a-fetoprotein test, were conducted regularly to detect HCC development. Results: The mean age of our study population (1,063 men and 780 women) was 49.4 years. Cirrhosis was identified in 617 patients (33.5%). During follow-up (median, 42.5 months), 81 patients developed HCC (1.39% per person-year). A total of 645 patients (35.0%) received ongoing AVT at enrollment. Ongoing AVT was not significantly associated with the risk of HCC development (all p>0.05). HBV-related variables (HBV DNA level, hepatitis B e antigen status, and alanine aminotransferase level) were also not significantly associated with the risk of HCC development (all p>0.05). In contrast, cirrhosis was significantly associated with the risk of HCC development, regardless of adjustment (adjusted hazard ratio=4.098 to 7.020; all p<0.05). Cirrhosis significantly predicted the risk of HCC development in subgroups with and without ongoing AVT at enrollment, regardless of adjustment. Conclusions: Our study showed that cirrhosis, not AVT and HBV-related variables, was associated with HCC development in a cohort of patients with heterogeneous HBV status. Our results may help clinicians apply individualized surveillance strategies according to fibrotic status in patients with CHB.
引用
收藏
页码:197 / +
页数:15
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