肝脏 ›› 2025, Vol. 30 ›› Issue (12): 1687-1690.

• 肝纤维化与肝硬化 • 上一篇    下一篇

肝脏硬度值联合门静脉血流动力学指标对慢性乙型肝炎肝纤维化的评估作用

刘静, 龚丽, 江圆满   

  1. 621100 绵阳 三台县人民医院(川北医学院附属三台医院超声科)
  • 收稿日期:2025-02-20 发布日期:2026-02-10
  • 基金资助:
    四川省绵阳市卫生健康委员会科研课题(202322)

Evaluation of liver fibrosis in chronic hepatitis B by liver stiffness measurement combined with portal vein hemodynamics

LIU Jing, GONG Li, JIANG Yuan-man   

  1. Department of Ultrasound, Santai County People's Hospital (affiliated with Chuanbei Medical College Santai Hospital), Mianyang 621100, China
  • Received:2025-02-20 Published:2026-02-10

摘要: 目的 探究肝脏硬度值(LSM)联合门静脉血流动力学指标评估CHB肝纤维化状态的作用。方法 纳入2020年2月至2024年6月三台县人民医院诊治的CHB患者145例,其中轻、重度肝纤维化分别为49例、96例。比较轻、重度肝纤维化以及重度肝纤维化中非肝硬化与肝硬化LSM、门静脉血流动力学指标的差异,分析LSM、门静脉血流动力学指标对重度肝纤维化、肝硬化的评估效能。结果 轻度肝纤维化LSM、PVD、PVVmean、PVQ及CI分别为(6.3±1.1)kPa、(1.0±0.2)cm、(16.9±0.6)cm/s、1 030.0(895.6,1 233.5)mL/min及(0.05±0.01),重度肝纤维化患者分别为(13.0±1.8)kPa、(1.4±0.4)cm、(14.8±0.5)cm/s、1 570.2(1 382.4,1 687.5)mL/min及(0.09±0.02),差异有统计学意义(P<0.05)。LSM、PVD、PVVmean、PVQ、CI联合诊断重度肝纤维化的AUC、灵敏度及特异度均高于单一定量指标检测。重度肝纤维化中肝硬化37例,非肝硬化患者LSM、PVD、PVVmean、PVQ及CI为(11.0±1.4)kPa、(1.2±0.3)cm、(16.7±1.0)cm/s、1 530.2(1 382.4,1 577.2)mL/min及(0.08±0.02),肝硬化患者分别为(16.1±2.1)kPa、(1.7±0.4)cm、(11.8±0.4)cm/s、1 611.4(1 424.3,1 687.5)mL/min及(0.11±0.02),差异有统计学意义(P<0.05)。LSM、PVD、PVVmean、PVQ、CI联合诊断肝硬化的AUC、灵敏度及特异度均高于单一定量指标检测。结论 LSM联合门静脉血流动力学指标可以有效鉴别CHB肝纤维化程度。

关键词: 慢性乙型肝炎, 瞬时弹性成像, 肝脏硬度值, 门静脉血流动力学指标

Abstract: Objective The role of liver stiffness measurement combined with portal venous hemodynamic parameters in evaluting hepatic fibrosis states in patients with CHB. Methods 145 patients with CHB who were diagnosed and treated in Santai County People's Hospital between February 2020 and June 2024 were collected. According to the degree of liver fibrosis, patients with CHB were divided into a mild fibrosis group and a severe fibrosis group, and the differences in LSM and portal vein hemodynamics indexes between the two groups were compared, and the evaluation efficiency of LSM and portal vein hemodynamic indexes for severe liver fibrosis and cirrhosis was analyzed. Results Among 145 patients with CHB, 49 cases were mild and 96 cases were severe liver fibrosis. The values of LSM, PVD, PVVmean, PVQ, and CI in mild hepatic fibrosis were (6.3±1.1) kPa, (1.0±0.2) cm, (16.9±0.6) cm/s, 1 030.0 (895.6~1 233.5) mL/min, and (0.05±0.01), respectively. These parameters showed statistically significant differences compared to those in severe hepatic fibrosis [(13.0±1.8) kPa, (1.4±0.4) cm, (14.8±0.5) cm/s, 1 570.2 (1 382.4~1 687.5) mL/min, and (0.09±0.02), P<0.05]. Taking the above indexes as test variables and the severity of liver fibrosis as state variables, the evaluation efficiency of LSM and portal hemodynamics indexes in patients with severe liver fibrosis in CHB was analyzed. The results showed that the AUC, sensitivity and specificity of combined diagnosis of LSM, PVD, PVVmean, PVQ and CI were higher than those of single diagnosis (P<0.05). Thirty-seven patients with severe liver fibrosis can be diagnosed as cirrhosis. In non-cirrhotic patients, the values of LSM, PVD, PVVmean, PVQ, and CI were (11.0±1.4) kPa, (1.2±0.3) cm, (16.7±1.0) cm/s, 1 530.2 (1 382.4~1 577.2) mL/min, and (0.08±0.02), respectively. These parameters demonstrated statistically significant differences when compared to cirrhotic patients [(16.1±2.1) kPa, (1.7±0.4) cm, (11.8±0.4) cm/s, 1 611.4 (1 424.3~1 687.5) mL/min, and (0.11±0.02), P<0.05]. Taking the above indexes as test variables and cirrhosis status as the state variable, the evaluation efficiency of LSM and portal hemodynamics in patients with CHB was analyzed. The results showed that the AUC, sensitivity and specificity of combined diagnosis of LSM, PVD, PVVmean, PVQ and CI were higher than those of single diagnosis (P<0.05). Conclusion LSM combined with portal hemodynamics can effectively differentiate hepatic fibrosis state in CHB patients, which can be popularized in clinical practice.

Key words: Chronic hepatitis B, Transient elastography, Liver stiffness measurement, Portal vein hemodynamic index