Department of Microbiology and Center of Infectious Diseases, School of Basic Medical Sciences, Peking University Health Science Center, 38 Xueyuan Road, Haidian District, Beijing, 100191, China.
The Clinical Laboratory of Tianjin Chest Hospital, Tianjin, China.
BMC Infect Dis. 2024 Jul 23;24(1):723. doi: 10.1186/s12879-024-09617-1.
Numerous HBeAg-positive chronic hepatitis B (CHB) patients with persistently normal ALT have significant liver histopathology. It is imperative to identify true "immune tolerant" patients. We aimed to evaluate the liver histopathology features of HBeAg-positive CHB patients with normal ALT and the incidence of liver cirrhosis and HCC in CHB patients during follow-up.
179 HBeAg-positive CHB patients with normal ALT who performed liver biopsy from 2009 to 2018 were retrospectively analyzed. Liver necroinflammation ≥ G2 and/or liver fibrosis ≥ S2 was defined as significant liver histopathological change.
57.5% patients were in the indeterminate phase with significant liver histological changes. The proportion of the patients with evident liver necroinflammation was higher in the high-normal ALT group (21-40U/L) when compared with the low-normal ALT group (≤ 20 U/L) (51.3% vs. 30.0%, p < 0.05), and patients aged ≥ 40 years had a higher proportion of significant fibrosis than those aged < 40 years (64.5% vs. 39.9%, p < 0.05). The percentages of patients with ≥ S2 and ≥ G2/S2 in the HBV DNA < 10 IU/mL group were higher than those in the HBV DNA ≥ 10 IU/mL group (72.7% vs. 40.1%, p < 0.01; 81.8% vs. 54.1%, p < 0.05). During follow-up, two of immune tolerant patients and four of indeterminate patients developed into cirrhosis, and one of immune tolerant patients and one of indeterminate patients developed into HCC, respectively.
HBeAg-positive CHB patients with high-normal ALT or HBV DNA < 10 IU/mL were tend to be indeterminate. Liver biopsy or noninvasive approaches are recommended to evaluate liver histopathology, and antiviral therapy is recommended for patients with significant liver histopathology.
许多 HBeAg 阳性慢性乙型肝炎(CHB)患者的丙氨酸氨基转移酶(ALT)持续正常,但存在显著的肝脏组织病理学改变。因此,识别真正的“免疫耐受”患者至关重要。本研究旨在评估 HBeAg 阳性 CHB 患者 ALT 正常时的肝脏组织病理学特征,并分析这些患者在随访期间发生肝硬化和肝细胞癌(HCC)的发生率。
回顾性分析了 2009 年至 2018 年间进行肝活检的 179 例 HBeAg 阳性 CHB 患者,这些患者的 ALT 持续正常。将肝坏死性炎症≥G2 和/或肝纤维化≥S2 定义为显著的肝脏组织病理学改变。
57.5%的患者处于不确定期,存在显著的肝脏组织学改变。高正常 ALT 组(21-40U/L)的患者明显肝坏死性炎症的比例明显高于低正常 ALT 组(≤20U/L)(51.3%比 30.0%,p<0.05),年龄≥40 岁的患者显著纤维化的比例明显高于年龄<40 岁的患者(64.5%比 39.9%,p<0.05)。HBV DNA<10IU/mL 组的患者≥S2 和≥G2/S2 的比例明显高于 HBV DNA≥10IU/mL 组(72.7%比 40.1%,p<0.01;81.8%比 54.1%,p<0.05)。在随访期间,2 例免疫耐受患者和 4 例不确定患者发展为肝硬化,1 例免疫耐受患者和 1 例不确定患者发展为 HCC。
高正常 ALT 或 HBV DNA<10IU/mL 的 HBeAg 阳性 CHB 患者倾向于处于不确定状态。建议进行肝活检或非侵入性方法来评估肝脏组织病理学,并建议对存在显著肝脏组织病理学改变的患者进行抗病毒治疗。