Tan You-Wen, Wang Jia-Min, Zhou Xing-Bei
Department of Hepatology, The Third Hospital of Zhenjiang Affiliated Jiangsu University, Zhenjiang 212003, Jiangsu Province, China.
World J Hepatol. 2023 Feb 27;15(2):237-254. doi: 10.4254/wjh.v15.i2.237.
Although many studies have investigated the impact of chronic hepatitis B virus (HBV) infection and nonalcoholic fatty liver disease (NAFLD) on liver disease, few have investigated the relationship between nonalcoholic steatohepatitis (NASH) defined by liver pathology and the prognosis of chronic HBV infection. Most patients were followed up for a short time. This study aimed to further explore the impact of NAFLD and the pathological changes confirmed by liver pathology in patients with chronic HBV infection.
To study the effect of NAFLD confirmed using liver pathology on the outcomes of long-term serious adverse events [cirrhosis, hepatocellular carcinoma (HCC), and death] in patients with chronic hepatitis B (CHB) virus infection.
We enrolled patients with chronic hepatitis B virus (HBV) infection who underwent liver biopsy at the Third People's Hospital of Zhenjaing Affiliated Jiangsu University between January 2005 and September 2020. Baseline clinical and pathological data on liver pathology and clinical data at the end of follow-up were collected. Propensity score matching (PSM) was used to balance baseline parameters, Kaplan-Meier (K-M) survival analysis was used to evaluate the risk of clinical events, and Cox regression was used to analyze the risk factors of events.
Overall, 456 patients with chronic HBV infection were included in the study, of whom 152 (33.3%) had histologically confirmed NAFLD. The median follow-up time of the entire cohort was 70.5 mo. Thirty-four patients developed cirrhosis, which was diagnosed using ultrasound during the follow-up period. K-M survival analysis showed that NAFLD was not significantly associated with the risk of cirrhosis (log-rank test, > 0.05). Patients with CHB with fibrosis at baseline were more prone to cirrhosis (log-rank test, = 0.046). After PSM, multivariate analysis showed that diabetes mellitus, ballooning deformation (BD), and platelet (PLT) were independent risk factors for cirrhosis diagnosed using ultrasound ( < 0.05). A total of 10 patients (2.2%) developed HCC, and six of these patients were in the combined NAFLD group. K-M survival analysis showed that the cumulative risk of HCC in the NAFLD group was significantly higher (log-rank test, < 0.05). Hepatocyte ballooning, and severe liver fibrosis were also associated with an increased risk of HCC (log-rank test, all < 0.05). Cox multivariate analysis revealed that hepatocyte ballooning, liver fibrosis, and diabetes mellitus were independent risk factors for HCC.
There was no significant correlation between chronic HBV infection and the risk of cirrhosis in patients with NAFLD. Diabetes mellitus, BD, and PLT were independent risk factors for liver cirrhosis. Patients with chronic HBV infection and NASH have an increased risk of HCC. BD, liver fibrosis, and diabetes mellitus are independent risk factors for HCC.
尽管许多研究调查了慢性乙型肝炎病毒(HBV)感染和非酒精性脂肪性肝病(NAFLD)对肝脏疾病的影响,但很少有研究调查肝脏病理学定义的非酒精性脂肪性肝炎(NASH)与慢性HBV感染预后之间的关系。大多数患者随访时间较短。本研究旨在进一步探讨NAFLD及肝脏病理学证实的病理变化对慢性HBV感染患者的影响。
研究经肝脏病理学证实的NAFLD对慢性乙型肝炎(CHB)病毒感染患者长期严重不良事件[肝硬化、肝细胞癌(HCC)和死亡]结局的影响。
我们纳入了2005年1月至2020年9月在江苏大学附属镇江第三人民医院接受肝脏活检的慢性乙型肝炎病毒(HBV)感染患者。收集肝脏病理学的基线临床和病理数据以及随访结束时的临床数据。采用倾向评分匹配(PSM)来平衡基线参数,采用Kaplan-Meier(K-M)生存分析评估临床事件风险,采用Cox回归分析事件的危险因素。
总体而言,456例慢性HBV感染患者纳入研究,其中152例(33.3%)经组织学证实为NAFLD。整个队列的中位随访时间为70.5个月。34例患者发生肝硬化,在随访期间通过超声诊断。K-M生存分析显示,NAFLD与肝硬化风险无显著相关性(对数秩检验,P>0.05)。基线时有纤维化的CHB患者更容易发生肝硬化(对数秩检验,P=0.046)。PSM后,多因素分析显示,糖尿病、气球样变(BD)和血小板(PLT)是超声诊断肝硬化的独立危险因素(P<0.05)。共有10例患者(2.2%)发生HCC,其中6例患者在合并NAFLD组。K-M生存分析显示,NAFLD组HCC的累积风险显著更高(对数秩检验,P<0.05)。肝细胞气球样变和严重肝纤维化也与HCC风险增加相关(对数秩检验,均P<0.05)。Cox多因素分析显示,肝细胞气球样变、肝纤维化和糖尿病是HCC的独立危险因素。
慢性HBV感染与NAFLD患者的肝硬化风险无显著相关性。糖尿病、BD和PLT是肝硬化的独立危险因素。慢性HBV感染合并NASH的患者HCC风险增加。BD、肝纤维化和糖尿病是HCC的独立危险因素。