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既往肝脏疾病与 SARS-CoV-2 感染患者的不良结局相关;APCOLIS 研究(亚太肝脏研究学会 COVID-19 肝脏损伤谱研究)。

Pre-existing liver disease is associated with poor outcome in patients with SARS CoV2 infection; The APCOLIS Study (APASL COVID-19 Liver Injury Spectrum Study).

机构信息

Department of Hepatology and Liver Transplant, Institute of Liver and Biliary Sciences, New Delhi, 110070, India.

Humanity and Health Clinical Trial Center, Hong Kong SAR, China.

出版信息

Hepatol Int. 2020 Sep;14(5):690-700. doi: 10.1007/s12072-020-10072-8. Epub 2020 Jul 4.

Abstract

BACKGROUND AND AIMS

COVID-19 is a dominant pulmonary disease, with multisystem involvement, depending upon comorbidities. Its profile in patients with pre-existing chronic liver disease (CLD) is largely unknown. We studied the liver injury patterns of SARS-Cov-2 in CLD patients, with or without cirrhosis.

METHODS

Data was collected from 13 Asian countries on patients with CLD, known or newly diagnosed, with confirmed COVID-19.

RESULTS

Altogether, 228 patients [185 CLD without cirrhosis and 43 with cirrhosis] were enrolled, with comorbidities in nearly 80%. Metabolism associated fatty liver disease (113, 61%) and viral etiology (26, 60%) were common. In CLD without cirrhosis, diabetes [57.7% vs 39.7%, OR = 2.1 (1.1-3.7), p = 0.01] and in cirrhotics, obesity, [64.3% vs. 17.2%, OR = 8.1 (1.9-38.8), p = 0.002] predisposed more to liver injury than those without these. Forty three percent of CLD without cirrhosis presented as acute liver injury and 20% cirrhotics presented with either acute-on-chronic liver failure [5 (11.6%)] or acute decompensation [4 (9%)]. Liver related complications increased (p < 0.05) with stage of liver disease; a Child-Turcotte Pugh score of 9 or more at presentation predicted high mortality [AUROC 0.94, HR = 19.2 (95 CI 2.3-163.3), p < 0.001, sensitivity 85.7% and specificity 94.4%). In decompensated cirrhotics, the liver injury was progressive in 57% patients, with 43% mortality. Rising bilirubin and AST/ALT ratio predicted mortality among cirrhosis patients.

CONCLUSIONS

SARS-Cov-2 infection causes significant liver injury in CLD patients, decompensating one fifth of cirrhosis, and worsening the clinical status of the already decompensated. The CLD patients with diabetes and obesity are more vulnerable and should be closely monitored.

摘要

背景与目的

COVID-19 是一种主要的肺部疾病,其发病机制与多种系统有关,且与并存疾病密切相关。目前,人们对患有慢性肝病(CLD)的患者的 SARS-CoV-2 发病机制了解甚少。本研究旨在探讨是否存在与肝硬化相关的 COVID-19 患者的肝损伤模式。

方法

该研究从亚洲 13 个国家收集了患有已知或新发 CLD 并确诊 COVID-19 的患者的数据。

结果

共纳入 228 例患者[185 例无肝硬化的 CLD 和 43 例肝硬化的 CLD],其中近 80%的患者合并其他疾病。代谢相关脂肪性肝病(113 例,61%)和病毒性病因(26 例,60%)是常见的病因。在无肝硬化的 CLD 患者中,糖尿病[57.7%比 39.7%,比值比(OR)=2.1(1.13.7),p=0.01]和肝硬化患者中,肥胖[64.3%比 17.2%,OR=8.1(1.938.8),p=0.002]与肝损伤的发生更相关。43%的无肝硬化的 CLD 患者表现为急性肝损伤,20%的肝硬化患者表现为急性肝衰竭(5 例,11.6%)或慢性肝衰竭急性加重(4 例,9%)。随着肝病分期的增加,肝脏相关并发症增加(p<0.05);入院时的 Child-Turcotte Pugh 评分≥9 分预测死亡率较高[AUROC 0.94,HR=19.2(95%CI 2.3~163.3),p<0.001,敏感性 85.7%,特异性 94.4%]。在失代偿性肝硬化患者中,57%的患者肝损伤呈进行性发展,死亡率为 43%。胆红素和 AST/ALT 比值升高预示着肝硬化患者的死亡。

结论

SARS-CoV-2 感染可导致 CLD 患者发生严重的肝损伤,导致 1/5 的肝硬化患者病情恶化,并使已经失代偿的患者病情恶化。患有糖尿病和肥胖症的 CLD 患者更易受到影响,应密切监测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1007/7334898/ff685574fc84/12072_2020_10072_Fig1_HTML.jpg

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