Human cytomegalovirus reactivation in cirrhosis patients with acute decompensation.

IF 16.9 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Changze Hong, Zuxiong Huang, Yingli He, Rongqi Wang, Jiaying Lin, Yushan Liu, Baicheng Liu, Xiaoqin Lan, Qinjun He, Wenfan Luo, Qintao Lai, Ling Zhou, Tingting Qi, Yali Ji, Miaoxia Liu, Qiaoping Wu, Yichen Yao, Weihao Liang, Xianbo Wang, Guohong Deng, Yanhang Gao, Yan Huang, Feng Liu, Xiaobo Lu, Zhongji Meng, Yuemin Nan, Hai Li, Beiling Li, Rajiv Jalan, Jinjun Chen
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Abstract

Background/aims: The role of reactivation of Human cytomegalovirus (HCMV) in determining outcomes of cirrhotic patients with acute decompensation (AD) is unknown. We aimed to investigate HCMV incidence and potential correlation with hepatic outcomes in AD patients.

Methods: Two prospective multicentre cohorts with AD patients were investigated. Patients in cohort 1 were recruited from 4 centres, while patients in cohort 2 were randomly selected from a second multicentre cohort. HCMV reactivation was established with quantitative real-time polymerase chain reaction assay in seropositive patients.

Results: HCMV reactivation was found in 35 patients from cohort 1 (n=722) and 14 from cohort 2 (n=291), with both incidences at 4.8%. Bacterial infection and liver failure were independently correlated with HCMV reactivation. HCMV reactivation was an independent predictor of 90-day mortality. Among bacterial infection populations in these two cohorts, patients with HCMV reactivation had worse prognosis compared to those without. Incidence of ACLF was higher in patients with HCMV reactivation compared to those without and was also independently correlated with development of ACLF. In a total of 49 HCMV reactivation cases, 8 patients were treated with ganciclovir, in whom a significantly lower 90-day mortality compared with those not treated was observed. All 3 patients who underwent liver transplantation with reactivation of HCMV died.

Conclusions: In AD patients, HCMV reactivation was common, especially in those with bacterial infection or liver failure and were more prone to had ACLF and 90‑day mortality. The data proposes the need for active surveillance for HCMV infection in AD patients.

肝硬化急性代偿失代偿患者巨细胞病毒再激活的研究。
背景/目的:人巨细胞病毒(HCMV)再激活在肝硬化急性失代偿(AD)患者预后中的作用尚不清楚。我们的目的是研究阿尔茨海默病患者的HCMV发病率及其与肝脏预后的潜在相关性。方法:对两组AD患者进行前瞻性多中心队列研究。队列1的患者从4个中心招募,而队列2的患者从第二个多中心队列中随机选择。用实时定量聚合酶链反应法确定血清阳性患者的HCMV再激活。结果:队列1中有35例患者(n=722)和队列2中有14例患者(n=291)出现HCMV再激活,发生率均为4.8%。细菌感染和肝功能衰竭与HCMV再激活独立相关。HCMV再激活是90天死亡率的独立预测因子。在这两个队列的细菌感染人群中,HCMV再激活患者的预后比未激活患者差。与没有HCMV再激活的患者相比,HCMV再激活患者的ACLF发生率更高,并且与ACLF的发展也独立相关。在49例HCMV再激活病例中,有8例患者接受了更昔洛韦治疗,与未接受治疗的患者相比,这些患者的90天死亡率显著降低。3例HCMV再激活肝移植患者全部死亡。结论:在AD患者中,HCMV再激活是常见的,特别是那些有细菌感染或肝功能衰竭的患者,更容易发生ACLF和90天死亡率。这些数据表明,需要对阿尔茨海默病患者的HCMV感染进行主动监测。
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来源期刊
Clinical and Molecular Hepatology
Clinical and Molecular Hepatology Medicine-Hepatology
CiteScore
15.60
自引率
9.00%
发文量
89
审稿时长
10 weeks
期刊介绍: Clinical and Molecular Hepatology is an internationally recognized, peer-reviewed, open-access journal published quarterly in English. Its mission is to disseminate cutting-edge knowledge, trends, and insights into hepatobiliary diseases, fostering an inclusive academic platform for robust debate and discussion among clinical practitioners, translational researchers, and basic scientists. With a multidisciplinary approach, the journal strives to enhance public health, particularly in the resource-limited Asia-Pacific region, which faces significant challenges such as high prevalence of B viral infection and hepatocellular carcinoma. Furthermore, Clinical and Molecular Hepatology prioritizes epidemiological studies of hepatobiliary diseases across diverse regions including East Asia, North Asia, Southeast Asia, Central Asia, South Asia, Southwest Asia, Pacific, Africa, Central Europe, Eastern Europe, Central America, and South America. The journal publishes a wide range of content, including original research papers, meta-analyses, letters to the editor, case reports, reviews, guidelines, editorials, and liver images and pathology, encompassing all facets of hepatology.
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