Steatosis, HBV‐related HCC, cirrhosis, and HBsAg seroclearance: A systematic review and meta‐analysis

医学 脂肪变性 内科学 胃肠病学 肝细胞癌 乙型肝炎表面抗原 肝硬化 优势比 乙型肝炎 荟萃分析 乙型肝炎病毒 免疫学 病毒
作者
Xianhua Mao,Ka Shing Cheung,Cheng-Zhi Peng,Lung‐Yi Mak,Ho Ming Cheng,James Fung,Noam Peleg,Howard Ho‐Wai Leung,Rajneesh Kumar,Jeong‐Hoon Lee,Amir Shlomai,Man‐Fung Yuen,Wai‐Kay Seto
出处
期刊:Hepatology [Wiley]
卷期号:77 (5): 1735-1745 被引量:35
标识
DOI:10.1002/hep.32792
摘要

Background and Aims: NAFLD and chronic hepatitis B (CHB) infection are common etiologies of HCC. The impact of hepatic steatosis on HCC in CHB, as well as its relationship with the development of cirrhosis, fibrosis, and HBsAg seroclearance, remains controversial. Approach and Results: Data from observational studies were collected through PubMed, EMBASE, and the Cochrane Library from inception to February 1, 2022. Outcomes of interest included the association of hepatic steatosis with HCC, cirrhosis, advanced fibrosis, and HBsAg seroclearance, expressed in terms of pooled ORs. Additional subgroup and sensitivity analyses were performed to validate the robustness of findings. A total of 34 studies with 68,268 patients with CHB were included. Hepatic steatosis was associated with higher odds of HCC (OR, 1.59; 95% CI, 1.12–2.26; I 2 = 72.5%), with the association remaining consistent in Asia (OR, 1.56; 95% CI, 1.08–2.25), studies with a median follow‐up duration of ≥5 years (OR, 2.82; 95% CI, 1.57–5.08), exclusion of alcohol use (OR, 1.71; 95% CI, 1.01–2.91), and biopsy‐proven steatosis (OR, 2.86; 95% CI, 1.61–5.06), although no significant association was noted among nucleos(t)ide analogue–treated patients (OR, 1.05; 95% CI, 0.62–1.77). Steatosis was associated with the development of cirrhosis (OR, 1.52; 95% CI, 1.07–2.16; I 2 = 0%) and HBsAg seroclearance (OR, 2.22; 95% CI, 1.58–3.10; I 2 = 49.0%). Conclusions: Hepatic steatosis was associated with an increased risk of HCC and cirrhosis among patients with CHB but with a higher chance of achieving a functional cure, highlighting the importance of identifying concomitant steatosis in CHB.
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