Tsutsumi Takeya, Saito Makoto, Nagai Hiroyuki, Yamamoto Shinya, Ikeuchi Kazuhiko, Lim Lay Ahyoung, Adachi Eisuke, Koga Michiko, Okushin Kazuya, Akai Hiroyuki, Kunimatsu Akira, Yotsuyanagi Hiroshi
Division of Infectious Diseases, Advanced Clinical Research Center, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Department of Infectious Diseases and Applied Immunology, IMSUT Hospital, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Hepatol Res. 2021 Feb;51(2):227-232. doi: 10.1111/hepr.13577. Epub 2020 Oct 27.
Liver dysfunction is sometimes observed in patients with coronavirus disease 2019 (COVID-19), but most studies are from China, and the frequency in other countries is unclear. In addition, previous studies suggested several mechanisms of liver damage, but precise or additional mechanisms are not clearly elucidated. Therefore, we examined COVID-19 patients to explore the proportion of patients with liver dysfunction and also the factors associated with liver dysfunction.
We retrospectively examined 60 COVID-19 patients hospitalized at the Hospital affiliated with The Institute of Medical Science, The University of Tokyo (Tokyo, Japan). Patients who presented ≥40 U/L alanine aminotransferase (ALT) levels at least once during their hospitalization were defined as high-ALT patients, and the others as normal-ALT patients. The worst values of physical and laboratory findings during hospitalization for each patient were extracted for the analyses. Univariable and multivariable logistic regression models with bootstrap (for 1000 times) were carried out.
Among 60 patients, there were 31 (52%) high-ALT patients. The high-ALT patients were obese, and had significantly higher levels of D-dimer and fibrin/fibrinogen degradation products, as well as white blood cell count, and levels of C-reactive protein, ferritin, and fibrinogen. Multivariable analysis showed D-dimer and white blood cells as independent factors.
Considering that higher D-dimer level and white blood cell count were independently associated with ALT elevation, liver dysfunction in COVID-19 patients might be induced by microvascular thrombosis in addition to systemic inflammation.
2019冠状病毒病(COVID-19)患者有时会出现肝功能障碍,但大多数研究来自中国,其他国家的发生率尚不清楚。此外,以往研究提出了几种肝损伤机制,但确切或其他机制尚未明确阐明。因此,我们对COVID-19患者进行了检查,以探讨肝功能障碍患者的比例以及与肝功能障碍相关的因素。
我们回顾性研究了东京大学医学科学研究所附属东京医院收治的60例COVID-19患者。住院期间至少有一次丙氨酸氨基转移酶(ALT)水平≥40 U/L的患者被定义为高ALT患者,其他患者为正常ALT患者。提取每位患者住院期间身体和实验室检查结果的最差值进行分析。采用Bootstrap(1000次)进行单变量和多变量逻辑回归模型分析。
60例患者中,有31例(52%)为高ALT患者。高ALT患者肥胖,D-二聚体、纤维蛋白/纤维蛋白原降解产物水平以及白细胞计数、C反应蛋白、铁蛋白和纤维蛋白原水平显著更高。多变量分析显示D-二聚体和白细胞是独立因素。
鉴于较高的D-二聚体水平和白细胞计数与ALT升高独立相关,COVID-19患者的肝功能障碍可能除全身炎症外还由微血管血栓形成引起。