Department of Intensive Care Unit, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, 310000, Zhejiang, China.
Department of Hepatology, The Affiliated Hospital of Hangzhou Normal University, No. 126 Wenzhou Road, Gongshu District, Hangzhou, 310015, Zhejiang, China.
Sci Rep. 2023 Jan 25;13(1):1388. doi: 10.1038/s41598-023-28351-3.
This case-control study aimed to identify the clinical characteristics and explore the risk factors for liver fibrosis in metabolic associated fatty liver disease (MAFLD) patients with hepatitis B virus (HBV) infection. The patients were grouped into MAFLD + HBV and MAFLD (without HBV infection). Propensity score matching (PSM) was used to match baseline features between the groups. We included 401 patients with biopsy-proven MAFLD, 179 of whom had HBV infection. A total of 83 pairs were successfully matched via PSM, and steatosis scores and ballooning in the MAFLD + HBV group were lower than those in the MAFLD group, while the inflammation scores and liver fibrosis stages were higher. After adjusted for confounding factors, HBV infection was associated with a higher risk of significant liver fibrosis in patients with MAFLD [odds ratio (OR): 3.140, P = 0.003]. Overall, 43.58% (78/179) of patients in the MAFLD + HBV group had significant liver fibrosis. Further multivariate regression analysis, hypertension (OR: 2.640; P = 0.031), type 2 diabetes (OR: 4.939; P = 0.035), and elevated glutamyl-transferase levels (OR: 3.980; P = 0.001) were risk factors for liver fibrosis in the MAFLD + HBV group. This suggests metabolic rather than viral factors are more closely associated with liver fibrosis in MAFLD patients with HBV infection.
本病例对照研究旨在确定代谢相关脂肪性肝病(MAFLD)合并乙型肝炎病毒(HBV)感染患者的临床特征,并探讨其肝纤维化的危险因素。将患者分为 MAFLD+HBV 和 MAFLD(无 HBV 感染)两组。采用倾向评分匹配(PSM)对两组患者的基线特征进行匹配。共纳入 401 例经肝活检证实的 MAFLD 患者,其中 179 例有 HBV 感染。通过 PSM 共成功匹配 83 对,MAFLD+HBV 组的脂肪变性评分和气球样变评分低于 MAFLD 组,而炎症评分和肝纤维化分期则更高。校正混杂因素后,HBV 感染与 MAFLD 患者发生显著肝纤维化的风险增加相关[比值比(OR):3.140,P=0.003]。总体而言,MAFLD+HBV 组中 43.58%(78/179)的患者存在显著肝纤维化。进一步的多变量回归分析显示,高血压(OR:2.640;P=0.031)、2 型糖尿病(OR:4.939;P=0.035)和谷氨酰转肽酶水平升高(OR:3.980;P=0.001)是 MAFLD+HBV 组发生肝纤维化的危险因素。这表明代谢因素而非病毒因素与 MAFLD 合并 HBV 感染患者的肝纤维化更为密切相关。