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      "Fast, faster, and fastest: science on the run during COVID-19 drama"—"do not forget the liver"

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      Hepatology International
      Springer India

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          Abstract

          Who did ever think that the twenty-first century with the best of scientific innovations and health care system would witness a historic pandemic of a novel Corona virus, SARS-CoV-2, which is crumbling humanity globally. Each day we are confronted with rising statistics and at the time of this writing, the global watch has registered more than 1249107 confirmed cases of Coronavirus disease or COVID-19. On a positive side, 256,059 (20%) have fully recovered and on a darker side 67,999 (5.4%) precious lives have been lost according to the Johns Hopkins University Coronavirus Resource Center until April 5 [1]. Much of the scientific data have come from China and together with the emerging data from the West where old age has been unequivocally identified as the major risk factor with increased mortality due to COVID-19. The origin of the novel coronavirus can be traced to Hubei Province, in China, which first reported to WHO, on Dec 30, 2019, several cases of pneumonia with an unknown infectious agent. The bronchoalveolar lavage collected from patient in Wuhan hospital tested positive for pan-betacoronavirus by real-time PCR. The Chinese agencies were quick in getting the full-length genomic sequence of the virus which had about 80% similarity to bat SARS-like coronavirus strain BatCov RaTG13. On 7 Jan 2020, the novel human coronavirus was first named as 2019-nCoV(human) and later it was renamed as severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). On February 11, 2020, the WHO announced the outbreak of coronavirus-associated disease and in a short span of 2 months, the virus spread globally and on 11 March, WHO declared it a pandemic [2]. While COVID-19 is predominantly a respiratory disease, subjects with underlying chronic disease such as diabetes and cardiovascular disorders are at higher risk of getting severe disease which can be lethal as well [3]. The published reports have not underscored the importance of liver disorder as a major risk factor; however, few papers have indicated “2–11% of patients with COVID-19 had liver comorbidities” and these mostly included patients with severe case of COVID-19 [4]. However, a common clinical finding in COVID-19 is raised levels of alanine aminotransferase (ALT) and reduced albumin level indicating liver injury. The angiotensin-converting enzyme 2 is a key receptor for the SARS-CoV-2 viral entry which is also expressed by cholangiocytes in liver and enterocytes in intestine (besides the type II lung epithelial cells). This indicates the possibility of extrapulmonary sites as reservoir for viral replication. In support of this, a recent study has shown that half of the SARS-CoV-2-infected subjects who have completely cleared the infection from the respiratory tract show virus shedding in their fecal samples up to 11 days after respiratory samples became negative [5]. This raises a serious concern of fecal–oral route of transmission, which in turn poses risk of pathogen transfer through FMT procedure [6]. Asia, in particular China, has high incidence of HBV; however, data are scant with respect to its influence on COVID-19. One report suggests that about 2.0% of severe cases had HBV infection compared to those with mild disease (0.06%) [7]. With respect to COVID-19, the other vulnerable groups with liver disease include patients who have undergone liver transplant and currently on immunosuppressants, liver cirrhosis/ACLF with immune dysfunction and those with hepatocellular carcinoma with immune exhaustion status. Patients with NASH have associated comorbidities of diabetes and cardiovascular disorder and they too are at high risk of being infected and may progress to severe form of COVID-19. As for the liver pathology in COVID-19, one report indicates mild steatosis which is mostly attributable to drug-induced liver injury rather than the virus [8]. With liver being a major organ for drug detoxification, the current proposed treatments with hydroxychloroquine, antibiotics, and antiviral drugs may further aggravate liver injury. Thus, a causal relation between underlying liver disease, effect of hepatotoxic drugs, and COVID-19 will await further investigations. Several liver societies have come up with management guidance for COVID-19 developing in liver disease patients, including one on liver transplant and COVID-19 from Liver Transplant Society of India (online in Hepatology International) and the EASL management plan care of COVID-19 patients with liver disease [9] Tobias Boettler, J Hep Reports). The patients who have fully recovered from COVID-19 and those who are asymptomatic but show viral shedding in feces pose a new challenge to hepatologists and gastroenterologists in the coming days. Will there be a second outbreak, reactivation, and new wave of SARS-CoV-2 infection via a fecal–oral route? The need of the hour is to initiate well-planned clinical studies in symptomatic and also recovered patients to generate more scientific evidences about not only the course of the disease but also to develop effective clinical management strategies. COVID-19 has brought in a sea of change in all sectors of life especially the clinical and scientific world. There is fast pace of clinical and scientific research, with fast-breaking published reports and those on preprint servers even under lockdown. We commend the heroic clinical trials which could be designed even under immense COVID-19 pressure. The brave new world in era of Covid-19 has seen emergence of heroic breed of clinicians, nurses, scientific, technical, governance staff, and community workers a.k.a “Covidwarriors” fighting and chasing the rogue virus. Dr. Gayatri Ramakrishna and her team have prepared a snapshot of COVID-19, by collecting the latest information on COVID-19 infection and have presented it in a lucid, poetic manner. It is hoped that this virus scan will find a place on your desk or wall for ready reference. We invite rapid contributions from colleagues across the globe to use Hepatology International for educating the world and help in overcoming the devastating crisis. The global pandemic has to be fought locally by collective sharing and open access of scientific data and technology at a global level. Every small step taken for preventing the spread of SARS-CoV-2 is a big leap for protecting mankind. We at Hepatology International are dedicated towards the cause of fighting the virus and preventing COVID-19. Science and Humanity will surely win this battle too!

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          Most cited references7

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          Clinical course and risk factors for mortality of adult inpatients with COVID-19 in Wuhan, China: a retrospective cohort study

          Summary Background Since December, 2019, Wuhan, China, has experienced an outbreak of coronavirus disease 2019 (COVID-19), caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Epidemiological and clinical characteristics of patients with COVID-19 have been reported but risk factors for mortality and a detailed clinical course of illness, including viral shedding, have not been well described. Methods In this retrospective, multicentre cohort study, we included all adult inpatients (≥18 years old) with laboratory-confirmed COVID-19 from Jinyintan Hospital and Wuhan Pulmonary Hospital (Wuhan, China) who had been discharged or had died by Jan 31, 2020. Demographic, clinical, treatment, and laboratory data, including serial samples for viral RNA detection, were extracted from electronic medical records and compared between survivors and non-survivors. We used univariable and multivariable logistic regression methods to explore the risk factors associated with in-hospital death. Findings 191 patients (135 from Jinyintan Hospital and 56 from Wuhan Pulmonary Hospital) were included in this study, of whom 137 were discharged and 54 died in hospital. 91 (48%) patients had a comorbidity, with hypertension being the most common (58 [30%] patients), followed by diabetes (36 [19%] patients) and coronary heart disease (15 [8%] patients). Multivariable regression showed increasing odds of in-hospital death associated with older age (odds ratio 1·10, 95% CI 1·03–1·17, per year increase; p=0·0043), higher Sequential Organ Failure Assessment (SOFA) score (5·65, 2·61–12·23; p<0·0001), and d-dimer greater than 1 μg/mL (18·42, 2·64–128·55; p=0·0033) on admission. Median duration of viral shedding was 20·0 days (IQR 17·0–24·0) in survivors, but SARS-CoV-2 was detectable until death in non-survivors. The longest observed duration of viral shedding in survivors was 37 days. Interpretation The potential risk factors of older age, high SOFA score, and d-dimer greater than 1 μg/mL could help clinicians to identify patients with poor prognosis at an early stage. Prolonged viral shedding provides the rationale for a strategy of isolation of infected patients and optimal antiviral interventions in the future. Funding Chinese Academy of Medical Sciences Innovation Fund for Medical Sciences; National Science Grant for Distinguished Young Scholars; National Key Research and Development Program of China; The Beijing Science and Technology Project; and Major Projects of National Science and Technology on New Drug Creation and Development.
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            Pathological findings of COVID-19 associated with acute respiratory distress syndrome

            Since late December, 2019, an outbreak of a novel coronavirus disease (COVID-19; previously known as 2019-nCoV)1, 2 was reported in Wuhan, China, 2 which has subsequently affected 26 countries worldwide. In general, COVID-19 is an acute resolved disease but it can also be deadly, with a 2% case fatality rate. Severe disease onset might result in death due to massive alveolar damage and progressive respiratory failure.2, 3 As of Feb 15, about 66 580 cases have been confirmed and over 1524 deaths. However, no pathology has been reported due to barely accessible autopsy or biopsy.2, 3 Here, we investigated the pathological characteristics of a patient who died from severe infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) by postmortem biopsies. This study is in accordance with regulations issued by the National Health Commission of China and the Helsinki Declaration. Our findings will facilitate understanding of the pathogenesis of COVID-19 and improve clinical strategies against the disease. A 50-year-old man was admitted to a fever clinic on Jan 21, 2020, with symptoms of fever, chills, cough, fatigue and shortness of breath. He reported a travel history to Wuhan Jan 8–12, and that he had initial symptoms of mild chills and dry cough on Jan 14 (day 1 of illness) but did not see a doctor and kept working until Jan 21 (figure 1 ). Chest x-ray showed multiple patchy shadows in both lungs (appendix p 2), and a throat swab sample was taken. On Jan 22 (day 9 of illness), the Beijing Centers for Disease Control (CDC) confirmed by reverse real-time PCR assay that the patient had COVID-19. Figure 1 Timeline of disease course according to days from initial presentation of illness and days from hospital admission, from Jan 8–27, 2020 SARS-CoV-2=severe acute respiratory syndrome coronavirus 2. He was immediately admitted to the isolation ward and received supplemental oxygen through a face mask. He was given interferon alfa-2b (5 million units twice daily, atomisation inhalation) and lopinavir plus ritonavir (500 mg twice daily, orally) as antiviral therapy, and moxifloxacin (0·4 g once daily, intravenously) to prevent secondary infection. Given the serious shortness of breath and hypoxaemia, methylprednisolone (80 mg twice daily, intravenously) was administered to attenuate lung inflammation. Laboratory tests results are listed in the appendix (p 4). After receiving medication, his body temperature reduced from 39·0 to 36·4 °C. However, his cough, dyspnoea, and fatigue did not improve. On day 12 of illness, after initial presentation, chest x-ray showed progressive infiltrate and diffuse gridding shadow in both lungs. He refused ventilator support in the intensive care unit repeatedly because he suffered from claustrophobia; therefore, he received high-flow nasal cannula (HFNC) oxygen therapy (60% concentration, flow rate 40 L/min). On day 13 of illness, the patient's symptoms had still not improved, but oxygen saturation remained above 95%. In the afternoon of day 14 of illness, his hypoxaemia and shortness of breath worsened. Despite receiving HFNC oxygen therapy (100% concentration, flow rate 40 L/min), oxygen saturation values decreased to 60%, and the patient had sudden cardiac arrest. He was immediately given invasive ventilation, chest compression, and adrenaline injection. Unfortunately, the rescue was not successful, and he died at 18:31 (Beijing time). Biopsy samples were taken from lung, liver, and heart tissue of the patient. Histological examination showed bilateral diffuse alveolar damage with cellular fibromyxoid exudates (figure 2A, B ). The right lung showed evident desquamation of pneumocytes and hyaline membrane formation, indicating acute respiratory distress syndrome (ARDS; figure 2A). The left lung tissue displayed pulmonary oedema with hyaline membrane formation, suggestive of early-phase ARDS (figure 2B). Interstitial mononuclear inflammatory infiltrates, dominated by lymphocytes, were seen in both lungs. Multinucleated syncytial cells with atypical enlarged pneumocytes characterised by large nuclei, amphophilic granular cytoplasm, and prominent nucleoli were identified in the intra-alveolar spaces, showing viral cytopathic-like changes. No obvious intranuclear or intracytoplasmic viral inclusions were identified. Figure 2 Pathological manifestations of right (A) and left (B) lung tissue, liver tissue (C), and heart tissue (D) in a patient with severe pneumonia caused by SARS-CoV-2 SARS-CoV-2=severe acute respiratory syndrome coronavirus 2. The pathological features of COVID-19 greatly resemble those seen in SARS and Middle Eastern respiratory syndrome (MERS) coronavirus infection.4, 5 In addition, the liver biopsy specimens of the patient with COVID-19 showed moderate microvesicular steatosis and mild lobular and portal activity (figure 2C), indicating the injury could have been caused by either SARS-CoV-2 infection or drug-induced liver injury. There were a few interstitial mononuclear inflammatory infiltrates, but no other substantial damage in the heart tissue (figure 2D). Peripheral blood was prepared for flow cytometric analysis. We found that the counts of peripheral CD4 and CD8 T cells were substantially reduced, while their status was hyperactivated, as evidenced by the high proportions of HLA-DR (CD4 3·47%) and CD38 (CD8 39·4%) double-positive fractions (appendix p 3). Moreover, there was an increased concentration of highly proinflammatory CCR6+ Th17 in CD4 T cells (appendix p 3). Additionally, CD8 T cells were found to harbour high concentrations of cytotoxic granules, in which 31·6% cells were perforin positive, 64·2% cells were granulysin positive, and 30·5% cells were granulysin and perforin double-positive (appendix p 3). Our results imply that overactivation of T cells, manifested by increase of Th17 and high cytotoxicity of CD8 T cells, accounts for, in part, the severe immune injury in this patient. X-ray images showed rapid progression of pneumonia and some differences between the left and right lung. In addition, the liver tissue showed moderate microvesicular steatosis and mild lobular activity, but there was no conclusive evidence to support SARS-CoV-2 infection or drug-induced liver injury as the cause. There were no obvious histological changes seen in heart tissue, suggesting that SARS-CoV-2 infection might not directly impair the heart. Although corticosteroid treatment is not routinely recommended to be used for SARS-CoV-2 pneumonia, 1 according to our pathological findings of pulmonary oedema and hyaline membrane formation, timely and appropriate use of corticosteroids together with ventilator support should be considered for the severe patients to prevent ARDS development. Lymphopenia is a common feature in the patients with COVID-19 and might be a critical factor associated with disease severity and mortality. 3 Our clinical and pathological findings in this severe case of COVID-19 can not only help to identify a cause of death, but also provide new insights into the pathogenesis of SARS-CoV-2-related pneumonia, which might help physicians to formulate a timely therapeutic strategy for similar severe patients and reduce mortality. This online publication has been corrected. The corrected version first appeared at thelancet.com/respiratory on February 25, 2020
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              Liver injury in COVID-19: management and challenges

              In December, 2019, an outbreak of a novel coronavirus (severe acute respiratory syndrome coronavirus 2 [SARS-CoV-2], previously 2019-nCoV) started in Wuhan, China, and has since become a global threat to human health. The number of confirmed cases of 2019 coronavirus disease (COVID-19) has reached 87 137 worldwide as of March 1, 2020, according to WHO COVID-19 situation report 41; most of these patients are in Wuhan, China. Many cases of COVID-19 are acute and resolve quickly, but the disease can also be fatal, with a mortality rate of around 3%. 1 Onset of severe disease can result in death due to massive alveolar damage and progressive respiratory failure. 2 SARS-CoV-2 shares 82% genome sequence similarity to SARS-CoV and 50% genome sequence homology to Middle East respiratory syndrome coronavirus (MERS-CoV)—all three coronaviruses are known to cause severe respiratory symptoms. Liver impairment has been reported in up to 60% of patients with SARS 3 and has also been reported in patients infected with MERS-CoV. 4 At least seven relatively large-scale case studies have reported the clinical features of patients with COVID-19.1, 5, 6, 7, 8, 9, 10 In this Comment, we assess how the liver is affected using the available case studies and data from The Fifth Medical Center of PLS General Hospital, Beijing, China. These data indicate that 2–11% of patients with COVID-19 had liver comorbidities and 14–53% cases reported abnormal levels of alanine aminotransferase and aspartate aminotransferase (AST) during disease progression (table ). Patients with severe COVID-19 seem to have higher rates of liver dysfunction. In a study in The Lancet by Huang and colleagues, 5 elevation of AST was observed in eight (62%) of 13 patients in the intensive care unit (ICU) compared with seven (25%) of 28 patients who did not require care in the ICU. Moreover, in a large cohort including 1099 patients from 552 hospitals in 31 provinces or provincial municipalities, more severe patients with disease had abnormal liver aminotransferase levels than did non-severe patients with disease. 1 Furthermore, in another study, 8 patients who had a diagnosis of COVID-19 confirmed by CT scan while in the subclinical phase (ie, before symptom onset) had significantly lower incidence of AST abnormality than did patients diagnosed after the onset of symptoms. Therefore, liver injury is more prevalent in severe cases than in mild cases of COVID-19. Table Comorbidity with liver disease and liver dysfunction in patients with SARS-CoV-2 infection Patients with SARS-CoV-2 infection Patients with pre-existing liver conditions Patients with abnormal liver function Notes Guan et al 1 1099 23 (2·3%) AST abnormal (22·2%), ALT abnormal (21·3%) Elevated levels of AST were observed in 112 (18·2%) of 615 patients with non-severe disease and 56 (39·4%) of 142 patients with severe disease. Elevated levels of ALT were observed in 120 (19·8%) of patients with non-severe disease and 38 (28·1%) of 135 patients with severe disease. Huang et al 5 41 1 (2·0%) 15 (31·0%) Patients with severe disease had increased incidence of abnormal liver function. Elevation of AST level was observed in eight (62%) of 13 patients in the ICU compared with seven (25%) 25 patients who did not require care in the ICU. Chen et al 6 99 NA 43 (43·0%) One patient with severe liver function damage. Wang et al 7 138 4 (2·9%) NA .. Shi et al 8 81 7 (8·6%) 43 (53·1%) Patients who had a diagnosis of COVID-19 confirmed by CT scan while in the subclinical phase had significantly lower incidence of AST abnormality than did patients diagnosed after the onset of symptoms. Xu et al 9 62 7 (11·0%) 10 (16·1%) .. Yang et al 10 52 NA 15 (29·0%) No difference for the incidences of abnormal liver function between survivors (30%) and non-survivors (28%). Our data (unpublished) 56 2 (3·6%) 16 (28·6%) One fatal case, with evaluated liver injury. 13 AST= aspartate aminotransferase. ALT= alanine aminotransferase. ICU=intensive care unit. Liver damage in patients with coronavirus infections might be directly caused by the viral infection of liver cells. Approximately 2–10% of patients with COVID-19 present with diarrhoea, and SARS-CoV-2 RNA has been detected in stool and blood samples. 11 This evidence implicates the possibility of viral exposure in the liver. Both SARS-CoV-2 and SARS-CoV bind to the angiotensin-converting enzyme 2 (ACE2) receptor to enter the target cell, 7 where the virus replicates and subsequently infects other cells in the upper respiratory tract and lung tissue; patients then begin to have clinical symptoms and manifestations. Pathological studies in patients with SARS confirmed the presence of the virus in liver tissue, although the viral titre was relatively low because viral inclusions were not observed. 3 In patients with MERS, viral particles were not detectable in liver tissue. 4 Gamma-glutamyl transferase (GGT), a diagnostic biomarker for cholangiocyte injury, has not been reported in the existing COVID-19 case studies; we found that it was elevated in 30 (54%) of 56 patients with COVID-19 during hospitalisation in our centre (unpublished). We also found that elevated alkaline phosphatase levels were observed in one (1·8%) of 56 patients with COVID-19 during hospitalisation. A preliminary study (albeit not peer-reviewed) suggested that ACE2 receptor expression is enriched in cholangiocytes, 12 indicating that SARS-CoV-2 might directly bind to ACE2-positive cholangiocytes to dysregulate liver function. Nevertheless, pathological analysis of liver tissue from a patient who died from COVID-19 showed that viral inclusions were not observed in the liver. 13 It is also possible that the liver impairment is due to drug hepatotoxicity, which might explain the large variation observed across the different cohorts. In addition, immune-mediated inflammation, such as cytokine storm and pneumonia-associated hypoxia, might also contribute to liver injury or even develop into liver failure in patients with COVID-19 who are critically ill. Liver damage in mild cases of COVID-19 is often transient and can return to normal without any special treatment. However, when severe liver damage occurs, liver protective drugs have usually been given to such patients in our unit. Chronic liver disease represents a major disease burden globally. Liver diseases including chronic viral hepatitis, non-alcoholic fatty liver disease, and alcohol-related liver disease affect approximately 300 million people in China. Given this high burden, how different underlying liver conditions influence liver injury in patients with COVID-19 needs to be meticulously evaluated. However, the exact cause of pre-existing liver conditions has not been outlined in the case studies of COVID-19 and the interaction between existing liver disease and COVID-19 has not been studied. Immune dysfunction—including lymphopenia, decreases of CD4+ T-cell levels, and abnormal cytokine levels (including cytokine storm)—is a common feature in cases of COVID-19 and might be a critical factor associated with disease severity and mortality. For patients with chronic hepatitis B in immunotolerant phases or with viral suppression under long-term treatment with nucleos(t)ide analogues, evidence of persistent liver injury and active viral replication after co-infection with SARS-CoV-2 need to be further investigated. In patients with COVID-19 with autoimmune hepatitis, the effects of administration of glucocorticoids on disease prognosis is unclear. Given the expression of the ACE2 receptor in cholangiocytes, whether infection with SARS-CoV-2 aggravates cholestasis in patients with primary biliary cholangitis, or leads to an increase in alkaline phosphatase and GGT, also needs to be monitored. Moreover, patients with COVID-19 with liver cirrhosis or liver cancer might be more susceptible to SARS-CoV-2 infection because of their systemic immunocompromised status. The severity, mortality, and incidence of complications in these patients, including secondary infection, hepatic encephalopathy, upper gastrointestinal bleeding, and liver failure, need to be examined in large-cohort clinical studies. Considering their immunocompromised status, more intensive surveillance or individually tailored therapeutic approaches is needed for severe patients with COVID-19 with pre-existing conditions such as advanced liver disease, especially in older patients with other comorbidities. Further research should focus on the causes of liver injury in COVID-19 and the effect of existing liver-related comorbidities on treatment and outcome of COVID-19.
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                Author and article information

                Contributors
                shivsarin@gmail.com
                Journal
                Hepatol Int
                Hepatol Int
                Hepatology International
                Springer India (New Delhi )
                1936-0533
                1936-0541
                10 April 2020
                : 1-2
                Affiliations
                GRID grid.418784.6, ISNI 0000 0004 1804 4108, Department of Hepatology, , Institute of Liver and Biliary Sciences, ; New Delhi, 110023 India
                Article
                10042
                10.1007/s12072-020-10042-0
                7145935
                32277386
                00a50643-7787-4383-a98e-d1f00ba8195a
                © Asian Pacific Association for the Study of the Liver 2020

                This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.

                History
                : 7 April 2020
                : 7 April 2020
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                Gastroenterology & Hepatology
                Gastroenterology & Hepatology

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