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Front. Physiol., 17 March 2021
Sec. Gastrointestinal Sciences

A High Percentage of Patients Recovered From COVID-19 but Discharged With Abnormal Liver Function Tests

\r\nQinyi Gan&#x;Qinyi Gan1†Beilei Gong,&#x;Beilei Gong2,3†Manli Sun&#x;Manli Sun4†Zhujun CaoZhujun Cao1Yuyan ZhengYuyan Zheng5Yajie ZhangYajie Zhang5Pengfei WenPengfei Wen6Yuanbing Shen,Yuanbing Shen2,3Lei Hong,Lei Hong2,3Tingting Hou,Tingting Hou2,3Yuqin Jia*&#x;Yuqin Jia7*‡Wei Li,*&#x;Wei Li2,3*‡Hecheng Li*&#x;Hecheng Li5*‡Qing Xie*&#x;Qing Xie1*‡
  • 1Department of Infectious Diseases, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China
  • 2The First Affiliated Hospital of Bengbu Medical College, Bengbu, China
  • 3Clinical Research Center for Respiratory Disease in Anhui Province, Bengbu, China
  • 4Department of Medicine and Education, Bengbu Infectious Disease Hospital, Bengbu, China
  • 5Department of Thoracic Surgery, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China
  • 6Bengbu Institute of Medical Sciences, Bengbu, China
  • 7Bengbu City Center for Disease Control and Prevention, Bengbu, China

Background: Coronavirus disease 2019 (COVID-19) pandemic has become the most severe global health issue. Abnormal liver functions are frequently reported in these patients. However, liver function abnormality was often overlooked during COVID-19 treatment, and data regarding liver functions after cure of COVID-19 is limited. This study aimed to reveal the changes of liver function tests (LFTs) during hospitalization, and its clinical significance in patients with COVID-19.

Methods: In this retrospective, bi-center study, a total of 158 hospitalized patients diagnosed with COVID-19 in China were included from January 22nd, 2020 to February 20th, 2020. Clinical features, laboratory parameters including LFTs, and treatment data were collected and analyzed. LFTs included alanine transaminase, aspartate aminotransferase, alkaline phosphatase, gamma-glutamyl transferase, and total bilirubin. Patients were considered with abnormal LFTs when any value of these tests was higher than upper limit of normal.

Results: Of 158 patients with COVID-19, 67 (42.41%) patients had abnormal LFTs on admission and another 50 (31.65%) patients developed abnormal LFTs during hospitalization. The incidence of LFTs abnormality in severe COVID-19 cases was significantly higher than non-severe cases. All LFTs in COVID-19 patients were correlated with oxygenation index. There was no statistical difference in treatment between the patients with or without liver test abnormalities. By the time of discharge, there were still 64 (40.50%) patients with abnormal LFTs. Logistic regression analysis identified younger age, hypertension and low lymphocyte counts as independent risk factors for persistent abnormal LFTs during hospitalization.

Conclusion: Liver function tests abnormality was common in COVID-19 patients and was more prevalent in severe cases than in non-severe cases. A substantial percentage of patients still had abnormal LFTs by the time of discharge.


The coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has posed a serious threat to the global public health (Zhu et al., 2020). The main manifestations of COVID-19 include fever, dry cough, fatigue, vomit, and respiratory distress. Despite atypical pneumonia as the primary symptom, liver impairment has been observed in many clinical cases (Wang et al., 2020; Chen et al., 2020a). In patients with SARS-CoV infection, liver dysfunction has also been reported as a common clinical manifestation (Humar et al., 2004), but is most often mild. Previous studies suggested that patients with abnormal liver tests had significantly higher odds of developing severe pneumonia, and medication such as lopinavir/ritonavir may increase the risks of liver injury (Bloom et al., 2020; Cai et al., 2020).Hence, a surveillance of liver function change and outcome of COVID-19 patients is necessary. However, the clinical significance, underlying mechanisms and changes of liver function abnormality during hospitalization and its risk factors in COVID-19 patients are still unclear.

The current study aimed to investigate the clinical characteristics and changes of liver function tests (LFTs) during hospitalization in patients with COVID-19.


Study Design

This was a retrospective study performed in two government-designated COVID-19 treatment units from Anhui province, China (the Bengbu Infectious Disease Hospital and the First Affiliated Hospital of Bengbu Medical College). The study protocol was reviewed and approved by the Ethics Committee of Bengbu Infectious Disease Hospital and the First Affiliated Hospital of Bengbu Medical College. Patient informed consent was waived by the Committee considering the retrospective design.


Chart review was performed in all patients who admitted to the two hospitals from January 22, to February 20, 2020. Inclusion criteria were as following: in-patients with positive SARS-CoV-2 as confirmed by the RT-PCR test of the nasopharynx swab samples. Exclusion criteria: (1) age below 18 years old; (2) with established chronic liver disease; and (3) with cancer or other end-stage disease status. Laboratory tests were performed to rule out chronic liver disease, such as viral hepatitis. Abdominal ultrasound was performed on the basis of laboratory tests and patients reported medical history, if necessary.

Main Variables

Demographic and clinical data were collected as follows: age, gender, comorbidity, symptoms, the first recorded vital signs on admission, laboratory findings on admission, and medications before and during hospitalization and length of stay. In addition to admission value, peak and value at discharge for liver biochemistry parameters were also collected, including alanine transaminase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), gamma-glutamyl transferase (GGT), and total bilirubin (TB). The ratio of the partial pressure of arterial oxygen to the fraction of inspired oxygen (PaO2: FiO2) at admission was estimated for each patient with the use of methods developed by Brown and colleagues (Rice et al., 2007; Brown et al., 2017). Clinical outcome of each patient was classified into death and alive according to the vital status at discharge.


Severity of COVID-19 was defined according to the sixth edition of the Chinese national guideline on the diagnosis and treatment of COVID-19. Patients were defined as severe COVID-19 with the presence of any of the following conditions: (1) respiration rate ≥30 times/min; (2) oxygen saturation (resting state) ≤93%; (3) PaO2: FiO2 ≤ 300 mmHg (1 mm Hg = 0.133 kPa); or (4) the occurrence of respiratory or other organ failure that requires intensive care unit (ICU) monitoring and treatment, or shock. Otherwise, patients were diagnosed as non-severe COVID-19. LFTs, including ALT, AST, GGT, ALP, and TB, was considered abnormal when any of these markers was higher than upper normal limit.

Statistical Analysis

Categorical variables were described as count (percentages). Continuous variables with normal distribution were presented as mean ± standard deviation, otherwise as median (Inter Quartile Range). Means for continuous variables were compared using independent group t-tests when the data were normally distributed; otherwise, the Mann–Whitney test was used. Categorical variables were compared using the χ2 test or the Fisher’s exact test as appropriate. Clinical characteristics and baseline laboratory findings were compared between patients with and without liver test abnormality. Pearson’s correlation analysis was performed to determine the association of calculated PaO2/FiO2 with ALT, AST, GGT, ALP, or TB. Univariate logistic regression was performed to identify the risk factors of persistently abnormal LFTs during hospitalization, followed by multivariate logistic regression to adjust potential confounding effects. All statistical analyses were performed using Graphpad Prism 7.0 or STATA 15.1. A 2-sided α of less than 0.05 was considered statistically significant.


Clinical Characteristics and Laboratory Results of Patients With COVID-19 on Admission

A total of 160 patients with COVID-19 were identified. Of them, 1 patient under 18 years of age and 1 patient with chronic Hepatitis B were excluded. 158 were finally included for analysis. The median age was 53 (IQR 44.5–60) years, and 76 (48.1%) were male. The most common symptoms were fever (97.5%) followed by fatigue (45.6%), cough (41.8%), and chest distress (32.9%). Among all the patients, 65 (41.1%) had one or more coexisting chronic medical conditions, of which 48 (30.4%) had hypertension and 23 (14.6%) had diabetes mellitus. A total of 121 (76.6%) patients were non-severe COVID-19 and 37 (23.4%) were severe. Laboratory findings at admission were enumerated in Table 1. Of note, 22 and 44 patients were receiving antiviral and antibiotics before admission, respectively. 5 (3.16%) patients died during hospitalization because of COVID-19 induced respiratory failure or multiple organ dysfunction syndrome.


Table 1. Baseline characteristics of patients with COVID-19.

All these 158 patients were classified into patients with (N = 67) and without (N = 91) abnormal LFTs based on variables at admission. In patients with abnormal LFTs, 30 (33.0%), 45 (49.5%), 8 (8.8%), 4 (4.4%), or 40 (44.0%) patients had elevated ALT, AST, TB, ALP, or GGT, respectively. Besides, they were more likely to be male, with lower calculated PaO2/FiO2 and lymphocyte count, higher lactic dehydrogenase and C-reactive protein (Table 1).

Association of LFTs Abnormality With Disease Severity, PaO2: FiO2 and Medications

During hospitalization, additional 50 patients had abnormal LFTs, adding to 117 (74.05%) patients with abnormal LFTs. The proportion of patients with abnormal LFTs was significantly higher in severe group than in non-severe group (89.2% vs 69.4%, p = 0.018; Figure 1). Moreover, the value of calculated PaO2/FiO2 was negatively correlated with ALT (r = −0.44, p < 0.0001), AST (r = −0.43, p < 0.0001), TB (r = −0.33, p < 0.0001), ALP (r = −0.3, p = 0.0001), and GGT (r = −0.28, p = 0.0003; Table 2). There was no difference in the percentages of patients with abnormal LFTs between patients with and without antivirals, antibiotics, NSAIDs, or herbals (Table 3).


Figure 1. Distribution of normal and abnormal LFTs* according to severity of COVID-19. LFTs, Liver function tests. *Patients with any value of ALT/AST/ALP/GGT/TB higher than upper limit of normal range during hospitalization was considered with abnormal LFTs, otherwise with normal LFTs.


Table 2. Pearson’s correlation coefficients between calculated PaO2/FiO2 and LFTs.


Table 3. Treatments in patients with COVID-19 according to the presence or absence of abnormal LFTs during entire hospitalization.

Persistence of LFTs Abnormality During Hospitalization and Risk Factors

Among 117 patients with abnormal LFTs, 52 patients with abnormal LFTs on admission had at least one additional LFTs before discharge. Among them, 23 (44.2%), 35 (67.3%), 7 (13.5%), 4 (7.7%), or 33 (63.5%) patients had elevated ALT, AST, TB, ALP, or GGT, respectively (Table 4). Patients with abnormal LFTs tended to recover from elevated AST (71.4%) or ALP (100%) but not elevated ALT (39.1%), TB (42.9%), and GGT (18.2%). Overall, 38 (73.1%) patients had persistently abnormal LFTs at last assessment. Univariate logistic regression analysis showed that age, hypertension and lymphocyte counts were significantly associated with persistently abnormal LFTs during hospitalization. Among these risk factors, age and lymphocyte counts were independently associated with persistently abnormal LFTs after adjusting use of antibiotics and herbals in multivariate logistic regression (Table 5).


Table 4. Dynamic changes of LFTs between admission and discharge.


Table 5. Logistic regression analyses of clinical factors associated with persistently abnormal LFTs during hospitalization.


Increasing evidences support that patients with COVID-19 could develop liver injury mainly manifested as abnormal ALT or AST levels accompanied by slightly elevated bilirubin levels (Wang et al., 2020; Chen et al., 2020a; Xu et al., 2020a). Despite the publication of several papers regarding the liver impairment during COVID-19, few has focused on the changes of LFTs and associated risk factors. Consistent with previous studies, our current study demonstrated a high percentage of patients with abnormal LFTs and these patients developed more severe COVID-19 than those without abnormal LFTs. The values of LFTs reversely correlated with the value of calculated PaO2/FiO2, suggesting a linkage between progression of COVID-19 and impairment of liver function. Unexpectedly, a substantial rate of patients discharged with alleviated respiratory symptoms and negative SARS-COV-2 but with abnormal LFTs, suggesting an asynchronous recovery of lung and liver dysfunction in patients with COVID-19. Patients at younger age, with hypertension or low lymphocyte counts were associated with persistent abnormal LFTs during hospitalization in multivariate regression analyses.

The exact pathogenesis of liver injury in SARS-COV-2 infection remains unclear. Possible mechanism includes direct virus-induced cytopathic effects, exacerbation of preexisting liver disease, hypoxemia, drug induced, and overshooting inflammatory responses. Though patients with diagnosed chronic liver disease have been ruled out in this study, there could be a few patients with underlying liver disease that were not captured due to limited access to more advanced imaging technique, such as MRI during the pandemic. Same as SARS-CoV, SARS-CoV-2 uses ACE2 as its entry receptor (Bourgonje et al., 2020). ACE2 expression has been found in bile duct cell, which are crucial in liver regeneration and immune response (Banales et al., 2019). The compensatory regeneration of parenchymal cells from bile duct cells may upregulate ACE2 expression in liver cells that lead to liver impairment. In the current study, AST was most commonly elevated followed by GGT, ALT and ALP. AST is normally present in liver and cardiac cells and has been associated with disease severity (Lei et al., 2020; Qin et al., 2020; Chen et al., 2020b). Previous studies also revealed that AST was more frequently increased than ALT in severe patients upon admission (Guan et al., 2020; Wang et al., 2020). GGT and ALP were both considered indexes of cholangiocytes injury and ALP is more sensitive than GGT for detecting bile duct injury. Our results showed a slight elevation of variables reflecting bile duct injury, suggesting that the duct epithelium injury by SARS-CoV-2 itself is very limited.

Patients with abnormal LFTs were more likely to be male, with poorer oxygenation, lower lymphocyte count, higher neutrophil count, LDH, and CRP comparing to patients with normal LFTs. It was reported that male patients were susceptible to SARS-COV-2 infection and progression of COVID-19 (Li et al., 2020; Zheng et al., 2020) and were therefore at higher risk of having liver impairment. Elevated LDH and CRP, as well as decreased oxygenation index and lymphocyte count were reported to be associated with severe disease progression in patients with COVID-19 (Wynants et al., 2020). The elevated level of LDH in COVID-19 patients is expected because ACE2 is highly expressed in cardiac blood vessels. CRP is a well-known biochemical marker of acute inflammation and is produced primarily in the liver (Ballantyne and Nambi, 2005). Neutrophils elevation manifests as common immune response to infection. The proportion of liver test abnormality in severe patients was significantly higher than in non-severe patients (p = 0.018) in our study, which was similar with previous studies (Cai et al., 2020; Huang et al., 2020; Zhang et al., 2020). This could be explained that the inflammatory cytokine storm observed in severe COVID-19 cases may result in multi organ dysfunction, including the liver. Moreover, liver damage may be associated with organ-specific immune response to SARS-CoV-2 or secondary to hypoxemia and systemic inflammation response. Hypoxic hepatitis, also called ischemic hepatitis, is frequently encountered in critically ill patients because of passive congestion or diminished perfusion of the liver. It usually rapidly progresses with a severe elevation of transaminase levels (20 ULN) accompanied by LDH level elevation (Yang et al., 2020). Though our data did not conform with the typical biochemical behavior of hypoxic hepatitis, we found that all liver function indexes, including ALT, AST, TB, ALP, and GGT, were significantly correlated with the oxygenation index. Therefore, liver damage in COVID-19 patients could be related to hypoxia and/or ischemia of hepatocytes, while the specific mechanism requires further study.

Postmortem and liver biopsies of SARS-associated coronavirus showed ballooning of hepatocytes and mild to moderate lobular lymphocytic infiltration, indicating the injury could be caused by either SARS-CoV-2 infection or drug-induced liver injury (Chau et al., 2004; Xu et al., 2020b). Medications of COVID-19 patients in the current study before and after admission included antiviral agents, antibiotics, herbal, NSAIDs and supportive therapies. Antiviral agents included interferon, lopinavir/ritonavir, arbidol, oseltamivir, darunavir, and ribavirin. Antibiotics mainly included quinolone, β-lactam, carbapenem, and oxazolidinone. Herbal medicine mainly refers to Lianhuaqingwen capsule, a manufactured product of the traditional Chinese medicine formula, reported as to ameliorate clinical symptoms of COVID-19 without known side effects on liver function (Hu et al., 2020). 88.6% of patients used lopinavir/ritonavir, a potential therapy for COVID-19 that is also associated with liver injury (Cai et al., 2020; Fan et al., 2020). However, the rate of patients with abnormal LFTs was similar between lopinavir/ritonavir recipients and non-recipients, probably due to the relatively short time of usage or limited sample size. In addition, no significant increase of abnormal LFTs was observed in patients receiving other antiviral agents, antibiotics, herbal or NSAIDs in our study. Therefore, drug-induced liver injury may not be the main reason of liver impairment in COVID-19 patients based on our results.

The high rate of patients discharged with abnormal liver tests in our study could be partly explained by the management strategy of COVID-19 during the pandemic. That is to discharge patients once their SARS-COV-2 being negative to allow more infected patients to be admitted. Therefore, liver dysfunction could be overlooked under such circumstance. Our current data further identified younger age, hypertension and low lymphocyte counts as independent risk factors for persistent liver dysfunction during hospitalization. Whether these patients could benefit from more active treatment on liver dysfunction remains to be investigated. Further studies with longer follow-up are required to investigate the long term outcome of liver function.

The current study has some limitations. It is a retrospective study, which only demonstrates association, not causation. Besides, we are unable to assess the association of liver function abnormalities and mortality, as only 5 patients died in our cohort. Moreover, the duration of abnormal LFTs persistence after COVID-19 recovery remains unknown in our study due to lack of long term follow up. Future study with larger population and longer follow-up period are needed to investigate the mechanism and outcome of liver function abnormalities.


In this bi-center retrospective study, LFTs abnormality was common in COVID-19 patients and was more prevalent in severe cases than in non-severe cases. A high percentage of patients recovered from COVID-19 but discharged with abnormal LFTs. Younger age, hypertension and low lymphocyte counts were identified as independent risk factors for persistent liver dysfunction during hospitalization. Long-term outcomes of these patients who discharged with abnormal LFTs are needed in follow-up studies.

Data Availability Statement

The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author/s.

Ethics Statement

The studies involving human participants were reviewed and approved by the Ethics Committee of Bengbu Infectious Disease Hospital and the First Affiliated Hospital of Bengbu Medical College. Written informed consent for participation was not required for this study in accordance with the national legislation and the institutional requirements.

Author Contributions

QX, HL, WL, and YJ: study concept and design. BG, MS, PW, YS, LH, and TH: data collection. QG and YuZ: data analysis and visualization. QG, ZC, and QX: data interpretation. QG: manuscript drafting. QG, ZC, and QX: critical revision. All authors have approved the final draft submitted.


This work was funded by The Emergency Project of COVID-19 for Ministry of Science and Technology (2020YFC0846800); Construction of Scientific and Technological Innovation Base-Clinical Medical Research Center (2020b07030008); Key Projects in the National Science & Technology Pillar Program during the Thirteenth Five-Year Plan Period (2017ZX10203201-008, 2018ZX09201016-003-001, and 2017ZX10202202-005-004); the Shanghai Three-Year Plan of the Clinical Skills and Innovations (16CR1002A); and the Shanghai Municipal Key Clinical Specialty (shslczdzk01103).

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.


Ballantyne, C. M., and Nambi, V. (2005). Markers of inflammation and their clinical significance. Atheroscler. Suppl. 6, 21–29. doi: 10.1016/j.atherosclerosissup.2005.02.005

PubMed Abstract | CrossRef Full Text | Google Scholar

Banales, J. M., Huebert, R. C., Karlsen, T., Strazzabosco, M., LaRusso, N. F., and Gores, G. J. (2019). Cholangiocyte pathobiology. Nat. Rev. Gastroenterol. Hepatol. 16, 269–281. doi: 10.1038/s41575-019-0125-y

PubMed Abstract | CrossRef Full Text | Google Scholar

Bloom, P. P., Meyerowitz, E. A., Reinus, Z., Daidone, M., Gustafson, J., Kim, A. Y., et al. (2020). Liver biochemistries in hospitalized patients with COVID-19. Hepatology doi: 10.1002/hep.31326 [Epub ahead of print].

CrossRef Full Text | PubMed Abstract | Google Scholar

Bourgonje, A. R., Abdulle, A. E., Timens, W., Hillebrands, J. L., Navis, G. J., Gordijn, S. J., et al. (2020). Angiotensin-converting enzyme 2 (ACE2), SARS-CoV-2 and the pathophysiology of coronavirus disease 2019 (COVID-19). J. Pathol. 251, 228–248. doi: 10.1002/path.5471

PubMed Abstract | CrossRef Full Text | Google Scholar

Brown, S. M., Duggal, A., Hou, P. C., Tidswell, M., Khan, A., Exline, M., et al. (2017). Nonlinear imputation of PaO2/FIO2 from SpO2/FIO2 among mechanically ventilated patients in the ICU: a prospective, observational study. Crit. Care Med. 45, 1317–1324. doi: 10.1097/CCM.0000000000002514

PubMed Abstract | CrossRef Full Text | Google Scholar

Cai, Q., Huang, D., Yu, H., Zhu, Z., Xia, Z., Su, Y., et al. (2020). COVID-19: abnormal liver function tests. J. Hepatol. 73, 566–574. doi: 10.1016/j.jhep.2020.04.006

PubMed Abstract | CrossRef Full Text | Google Scholar

Chau, T. N., Lee, K. C., Yao, H., Tsang, T. Y., Chow, T. C., Yeung, Y. C., et al. (2004). SARS-associated viral hepatitis caused by a novel coronavirus: report of three cases. Hepatology 39, 302–310. doi: 10.1002/hep.20111

PubMed Abstract | CrossRef Full Text | Google Scholar

Chen, G., Wu, D., Guo, W., Cao, Y., Huang, D., Wang, H., et al. (2020a). Clinical and immunological features of severe and moderate coronavirus disease 2019. J. Clin. Invest. 130, 2620–2629. doi: 10.1172/JCI137244

CrossRef Full Text | Google Scholar

Chen, N., Zhou, M., Dong, X., Qu, J., Gong, F., Han, Y., et al. (2020b). Epidemiological and clinical characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan, China: a descriptive study. Lancet 395, 507–513. doi: 10.1016/S0140-6736(20)30211-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Fan, Z., Chen, L., Li, J., Cheng, X., Yang, J., Tian, C., et al. (2020). Clinical features of COVID-19-related liver functional abnormality. Clin. Gastroenterol. Hepatol. 18, 1561–1566. doi: 10.1016/j.cgh.2020.04.002

PubMed Abstract | CrossRef Full Text | Google Scholar

Guan, W. J., Ni, Z. Y., Hu, Y., Liang, W. H., Ou, C. Q., He, J. X., et al. (2020). Clinical characteristics of coronavirus disease 2019 in China. N. Engl. J. Med. 382, 1708–1720. doi: 10.1056/NEJMoa2002032

PubMed Abstract | CrossRef Full Text | Google Scholar

Hu, K., Guan, W. J., Bi, Y., Zhang, W., Li, L., Zhang, B., et al. (2020). Efficacy and safety of Lianhuaqingwen capsules, a repurposed Chinese herb, in patients with coronavirus disease 2019: a multicenter, prospective, randomized controlled trial. Phytomedicine doi: 10.1016/j.phymed.2020.153242 [Epub ahead of print].

CrossRef Full Text | PubMed Abstract | Google Scholar

Huang, C., Wang, Y., Li, X., Ren, L., Zhao, J., Hu, Y., et al. (2020). Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China. Lancet 395, 497–506. doi: 10.1016/S0140-6736(20)30183-5

PubMed Abstract | CrossRef Full Text | Google Scholar

Humar, A., McGilvray, I., Phillips, M. J., and Levy, G. A. (2004). Severe acute respiratory syndrome and the liver. Hepatology 39, 291–294. doi: 10.1002/hep.20069

PubMed Abstract | CrossRef Full Text | Google Scholar

Lei, F., Liu, Y. M., Zhou, F., Qin, J. J., Zhang, P., Zhu, L., et al. (2020). Longitudinal association between markers of liver injury and mortality in COVID-19 in China. Hepatology 72, 389–398. doi: 10.1002/hep.31301

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, L. Q., Huang, T., Wang, Y. Q., Wang, Z. P., Liang, Y., Huang, T. B., et al. (2020). COVID-19 patients’ clinical characteristics, discharge rate, and fatality rate of meta-analysis. J. Med. Virol. 92, 577–583. doi: 10.1002/jmv.25757

PubMed Abstract | CrossRef Full Text | Google Scholar

Qin, C., Zhou, L., Hu, Z., Zhang, S., Yang, S., Tao, Y., et al. (2020). Dysregulation of immune response in patients with COVID-19 in Wuhan, China. Clin. Infect. Dis. 71, 762–768. doi: 10.1093/cid/ciaa248

CrossRef Full Text | Google Scholar

Rice, T. W., Wheeler, A. P., Bernard, G. R., Hayden, D. L., Schoenfeld, D. A., and Ware, L. B. (2007). Comparison of the SpO2/FIO2 ratio and the PaO2/FIO2 ratio in patients with acute lung injury or ARDS. Chest 132, 410–417. doi: 10.1378/chest.07-0617

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, D., Hu, B., Hu, C., Zhu, F., Liu, X., Zhang, J., et al. (2020). Clinical characteristics of 138 hospitalized patients with 2019 novel coronavirus-infected Pneumonia in Wuhan, China. JAMA 323, 1061–1069. doi: 10.1001/jama.2020.1585

PubMed Abstract | CrossRef Full Text | Google Scholar

Wynants, L., Van Calster, B., Collins, G. S., Riley, R. D., Heinze, G., Schuit, E., et al. (2020). Prediction models for diagnosis and prognosis of covid-19 infection: systematic review and critical appraisal. BMJ 369:m1328. doi: 10.1136/bmj.m1328

CrossRef Full Text | Google Scholar

Xu, X. W., Wu, X. X., Jiang, X. G., Xu, K. J., Ying, L. J., Ma, C. L., et al. (2020a). Clinical findings in a group of patients infected with the 2019 novel coronavirus (SARS-Cov-2) outside of Wuhan, China: retrospective case series. BMJ 368:m606. doi: 10.1136/bmj.m606

PubMed Abstract | CrossRef Full Text | Google Scholar

Xu, Z., Shi, L., Wang, Y., Zhang, J., Huang, L., Zhang, C., et al. (2020b). Pathological findings of COVID-19 associated with acute respiratory distress syndrome. Lancet Respir. Med. 8, 420–422. doi: 10.1016/S2213-2600(20)30076-X

CrossRef Full Text | Google Scholar

Yang, R. X., Zheng, R. D., and Fan, J. G. (2020). Etiology and management of liver injury in patients with COVID-19. World J. Gastroenterol. 26, 4753–4762. doi: 10.3748/wjg.v26.i32.4753

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, Y., Zheng, L., Liu, L., Zhao, M., Xiao, J., and Zhao, Q. (2020). Liver impairment in COVID-19 patients: a retrospective analysis of 115 cases from a single centre in Wuhan city. China. Liver Int. 40, 2095–2103. doi: 10.1111/liv.14455

CrossRef Full Text | Google Scholar

Zheng, Z., Peng, F., Xu, B., Zhao, J., Liu, H., Peng, J., et al. (2020). Risk factors of critical & mortal COVID-19 cases: a systematic literature review and meta-analysis. J. Infect. 81, e16–e25. doi: 10.1016/j.jinf.2020.04.021

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhu, N., Zhang, D., Wang, W., Li, X., Yang, B., Song, J., et al. (2020). A novel coronavirus from patients with Pneumonia in China, 2019. N. Engl. J. Med. 382, 727–733. doi: 10.1056/NEJMoa2001017

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: SARS-CoV-2, COVID-19, coronavirus, liver function tests, risk factor

Citation: Gan Q, Gong B, Sun M, Cao Z, Zheng Y, Zhang Y, Wen P, Shen Y, Hong L, Hou T, Jia Y, Li W, Li H and Xie Q (2021) A High Percentage of Patients Recovered From COVID-19 but Discharged With Abnormal Liver Function Tests. Front. Physiol. 12:642922. doi: 10.3389/fphys.2021.642922

Received: 17 December 2020; Accepted: 24 February 2021;
Published: 17 March 2021.

Edited by:

Kusum K. Kharbanda, University of Nebraska Medical Center, United States

Reviewed by:

Marco A. Olivera-Martinez, University of Nebraska Medical Center, United States
Govind K. Makharia, All India Institute of Medical Sciences, India

Copyright © 2021 Gan, Gong, Sun, Cao, Zheng, Zhang, Wen, Shen, Hong, Hou, Jia, Li, Li and Xie. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Qing Xie,; Hecheng Li,; Wei Li,; Yuqin Jia,

These authors share first authorship

These authors share last authorship

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