Wang Fengjiao, Zhu Lingxiao, Chen Yanfei, Li Lanjuan
Shandong First Medical University, Jinan City, 250022, China.
Jinan Microecological Biomedicine Shandong Laboratory, Jinan City, 250022, China.
BMC Infect Dis. 2025 Apr 29;25(1):630. doi: 10.1186/s12879-025-11040-z.
BACKGROUND & AIM: The impact of Omicron variants on cirrhosis was largely unknown. Herein, we aimed to evaluate the impact of SARS-CoV-2 omicron variants infection on the clinical course and mortality of patients with liver cirrhosis.
Between 26 December 2022, and 27 January 2023, eighty-two hospitalized patients with cirrhosis and confirmed SARS-CoV-2 infection were enrolled. The clinical and pulmonary CT imaging features were retrospectively collected. A gender and age-matched cohort of 51 non-cirrhotic patients with COVID-19 were also included.
Our results indicated the symptom heterogeneity in patients with cirrhosis infected with omicron variants. Patients with more severe liver disease tended to have less severe respiratory symptoms and less pulmonary lesions. SARS-CoV-2 omicron did not cause obvious perturbation of liver function or cirrhosis decompensation. In comparison with hospitalized COVID-19 patients without liver cirrhosis, cirrhotic patients showed more severe pulmonary lesions and higher levels of inflammatory cytokine IL-6, but no significant increase in mortality. Multivariate analysis identified lung lesions proportion, MELD ≥ 15 score, and APTT as independent predictors for 28-day-mortality in these patients.
SARS-CoV-2 omicron variants caused a more severe inflammatory response in cirrhotic patients than in non-cirrhotic patients, but no further deterioration of liver function. Instead, patients with advanced stage of liver cirrhosis showed milder respiratory symptoms and pulmonary lesions. These results underscore the intricate relationship between Omicron infection and cirrhosis, highlighting the necessity for personalized clinical approaches in managing this specific patient group.
奥密克戎变异株对肝硬化的影响在很大程度上尚不清楚。在此,我们旨在评估感染严重急性呼吸综合征冠状病毒2(SARS-CoV-2)奥密克戎变异株对肝硬化患者临床病程及死亡率的影响。
2022年12月26日至2023年1月27日期间,纳入82例住院的确诊感染SARS-CoV-2的肝硬化患者。回顾性收集其临床和肺部CT影像特征。还纳入了51例年龄和性别匹配的非肝硬化COVID-19患者作为对照队列。
我们的结果表明,感染奥密克戎变异株的肝硬化患者症状存在异质性。肝病较严重的患者往往呼吸道症状较轻,肺部病变较少。SARS-CoV-2奥密克戎变异株未引起肝功能明显紊乱或肝硬化失代偿。与无肝硬化的住院COVID-19患者相比,肝硬化患者肺部病变更严重,炎症细胞因子白细胞介素-6水平更高,但死亡率无显著增加。多因素分析确定肺部病变比例、终末期肝病模型(MELD)评分≥15分和活化部分凝血活酶时间(APTT)是这些患者28天死亡率的独立预测因素。
SARS-CoV-2奥密克戎变异株在肝硬化患者中引起的炎症反应比非肝硬化患者更严重,但肝功能没有进一步恶化。相反,晚期肝硬化患者的呼吸道症状和肺部病变较轻。这些结果强调了奥密克戎感染与肝硬化之间的复杂关系,突出了针对这一特定患者群体采取个性化临床治疗方法的必要性。