Tanggal: 1 April 2020
Oleh: Dr. John W Ward, The Coalition for Global Hepatitis Elimination
Diterjemahkan oleh: Caroline Thomas (14 Juni 2020)
In December 2019, a novel coronavirus was identified as the cause of severe pneumonia, respiratory failure and mortality in Wuhan China (1).
The virus was found to have 82% genetic homology with SARS-CoV, a virus identified in 2002 as the cause of Severe Acute Respiratory Syndrome and 50% homology with MERS-CoV identified in 2012 as the cause of Middle Eastern Respiratory Syndrome. In February 2020, WHO named the virus SARS-CoV-2 and the related disease Coronavirus Disease 2019 (COVID-19)[*]
Epidemiologic studies revealed SARS- CoV-2 readily transmitted through exposures to respiratory droplets of infected persons (2,3). SARS-CoV-2 spread rapidly in China and progressively and quickly to other countries globally. On March 11, 2020, WHO declared COVID-19 a pandemic. As of March 28, 2020, a total of 571,678 confirmed COVID-19 cases and 26,494 deaths have been reported worldwide (4)
In the absence of a vaccine or licensed therapies, countries are implementing public health measures to prevent transmission and marshalling clinical care capacity for those with severe COVID-19 disease.
The emergence of SARS-CoV-2 as a major pathogen raises the question of the interrelationship between this infection and liver disease (13,14). Reports from China identified older age, immunocompromised states, and underlying health conditions as risks for severe COVID-19 disease (2,3,5-11).
Chronic liver disease (CLD) is considered an underlying disease placing COVID-19 patients at risk (4). In case series published to date, only a small proportion (3-11%) of COVID-19 patients had CLD at diagnosis (4, 8,10). A recent CDC study found persons with underlying health conditions were more likely to be hospitalized (27-%-30%) and to require intensive care (13%-14%) than others with COVD-19, (7%–8%) and (2%), respectively. Diabetes mellitus (11%), chronic lung disease (9%), and cardiovascular disease (9%) were the most frequently reported conditions. CLD was reported for less than 1% of the study population. Additional case series can add experience to the management of COVID-19 patients with CLD.
Liver injury is relatively common during the course of COVID-19 disease. Available data suggest ~15% – 45% of patients with COVID-19 have some evidence of liver injury during the course of disease. Alanine aminotransferase (ALT) levels are typically mildly elevated and often accompanied by elevations of enzymes on other liver function tests (LFTs) including alkaline phosphatase, aspartate aminotransferase (AST), and lactate dehydrogenase. Some studies find increases in LFTs (ALT, AST) correlate with severity of disease requiring longer hospitalizations and intensive care (5, 8, 10). A study of the clinical course of deceased COVID-19 patients found elevations in ALT and AST associated with shorter survival after hospitalization; however, liver failure was not listed as a cause of death for any patient (9)
A study of 52 COVID-19 patients requiring intensive care found 15 (29%) with liver dysfunction; there was no difference in hepatitis impairment among survivors versus non-survivors (11). In the United States, the first patient reported with COVID-19 had progressive increases in ALT exceeding four times the upper limit of normal (ULN) by the 9th hospital day. However, by that time, the patient’s clinical course was improving and was soon discharged (12). Evidence regarding SARS-CoV-2/ HBV and SARS-CoV-2/HCV coinfections is needed.
The observations in previous years regarding liver impairment among persons with SARS is instructive (12-16). Elevations in LFTs are common (22%-56%). Increases in ALT tend to be modest with a median ALT levels on admission and during hospitalization of 0.55 and 1.53 times the ULN, respectively (15). For most patients, LFT elevations are transient; in one study of SARS patients with abnormal ALT, ~70% had normal values by hospital discharge. Large increases (>5 X ULN) in ALT are associated with poor outcomes from SARS. However, in this series, HBV co-infection was not associated with high peak ALT level, ICU admission, or mortality. Another study of SARS patients revealed chronic HBV infection as a significant risk for acute respiratory distress and intensive care; however liver damage was not greater for these severely ill patients (17).
The liver damage observed among patients with COVID-19 is probably related to several factors. Viral infection of liver cells could play a role. SARS-CoV has been isolated from liver tissue although not in large quantities; isolation of SARS- CoV-2 has yet to be reported. For cell entry, both SARS-CoV and SARS-CoV-2 bind to the receptor angiotensin converting enzyme 2 (ACE2); ACE2 is found on hepatocytes and in greater quantities cholangiocytes providing a site for direct viral binding and impairment of hepatitis function (18). Interestingly, cholestatic liver disease is not a common feature of COVID-19 disease (13). Other etiologies can have a role. Certain medications cause hepatotoxicity. One study found the elevation in LFTs in COVID-19 patients significantly associated with administration of lopinavir/ritonavir (5). Postmortem biopsies of patients with COVID‐19 show findings- moderate microvascular steatosis, mild lobular and portal activity- indicative of injuries from either SARS‐CoV‐2 infection or medications (7,19). Clinical trials can look for hepatotoxicity among promising therapeutic agents for COVID-19 (20). Liver damage can also result from immune mediated inflammation. (9,10). This is observed for other viral infections. Elevation in ALT can be accompanied by increases in LDH and creatinine kinase suggesting extra-hepatic origins of these enzyme elevations.
In summary, SARS-CoV-2 infection is the cause of an ongoing and growing pandemic. The understanding of the relationship between this infection, COVID-19 disease and liver disease continues to evolve. The cause of liver injury among patients with COVID-19 appears multifactorial. The liver injury is often mild with but can be severe for patients with advanced COVID-19 disease. There is scant evidence regarding SARS-CoV-2 infection among persons with current HBV or HCV infection. Based on current evidence, persons with viral hepatitis and chronic liver disease should continue to be regarded as populations at increased risk for co-morbid complications during the course of COVID-19 disease.
Coalition for Global Hepatitis Elimination (CGHE) will update this resource as data become available from trusted sources and local investigators (21-24). CGHE encourages partners to submit reports for inclusion in the series.
- Khan S, Siddique R, Shereen MA, et al. The emergence of a novel coronavirus (SARS-CoV-2), their biology and therapeutic options. J Clin Microbiol. 2020 Mar 11. pii: JCM.00187-20. doi: 10.1128/JCM.00187-20. [Epub ahead of print]. Accessed March 28, 2020.
- Chen N, Zhou M, Dong X, et al. Epidemiological and clinical characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan, China: a descriptive study. Lancet 2020; 395: 507–13. https://www.thelancet.com/journals/lancet/article/PIIS0140-6736(20)30211-7/fulltext
- Guan W, Ni Z, Hu Y, et al. Clinical Characteristics of Coronavirus Disease 2019 in China. N Engl J Med. published on February 28, 2020, and last updated on March 6, 2020, NEJM.org. https://www.nejm.org/doi/full/10.1056/NEJMoa2002032
- CDC. Preliminary estimates of the prevalence of selected underlying health conditions among patients with coronavirus disease 2019 — United States, February 12–March 28, 2020. MMWR Morb Mortal Wkly Rep. ePub: 31 March 2020. DOI: http://dx.doi.org/10.15585/mmwr.mm6913e2 .
- Fan Z, Chen L, Li J , et al. Clinical features of COVID-19 -related liver damage. medRxiv preprint doi: https://doi.org/10.1101/2020.02.26.20026971.
- Shi H, Han X, Jiang N, et al. Radiological findings from 81 patients with COVID‐19 pneumonia in Wuhan, China: a descriptive study. Lancet Infect Dis, 2020. https://www.thelancet.com/journals/laninf/article/PIIS1473-3099(20)30086-4/fulltext
- Xu L, Liu J, Lu M, Yang M, Zheng X. Liver injury during highly pathogenic human coronavirus infections. Liver Int. 2020 Mar 14. doi: 10.1111/liv.14435. [Epub ahead of print] accessed March 28, 2020. https://onlinelibrary.wiley.com/doi/full/10.1111/liv.14435
- Xu X‐W, Wu X‐X, Jiang X‐G, et al. Clinical findings in a group of patients infected with the 2019 novel coronavirus (SARS‐Cov‐2) outside of Wuhan, China: retrospective case series. BMJ. 2020;m606. https://www.bmj.com/content/368/bmj.m606.long
- Zhang B, Zhou X, Qiu Y, et al. Clinical characteristics of 82 death cases with COVID‐19. medRxiv. 2020; in press. https://doi.org/10.1101/2020.02.26.20028191.
- Wang D, Hu B, Hu C, et al. Clinical characteristics of 138 hospitalised patients with 2019 novel coronavirus-infected pneumonia in Wuhan, China. JAMA 2020; published online Feb 7. DOI:10.1001/jama.2020.1585. https://jamanetwork.com/journals/jama/fullarticle/2761044https://jamanetwork.com/journals/jama/fullarticle/2761044.
- Yang X, Yu Y, Xu J, et al. Clinical course and outcomes of critically ill patients with SARS-CoV-2 pneumonia in Wuhan, China: a single-centered, retrospective, observational study. Lancet Respir Med 2020; published online Feb 24. DOI:10.1016/S2213-2600(20)30079-5. https://www.thelancet.com/action/showPdf?pii=S2213-2600%2820%2930079-5
- Holshue, M. L. et al. First case of 2019 novel coronavirus in the United States. N. Engl. J. Med. https://doi.org/10.1056/NEJMoa2001191 (2020) .
- Ong J, Young B, Ong S, COVID-19 in gastroenterology: a clinical perspective. Gut Epub ahead of print: accessed March 28, 2020. doi:10.1136/gutjnl-2020-321051.
- Bangash MN, Patel J, Parekh D. COVID-19 and the liver: little cause for concern. Lancet Gastroenterol Hepatol 2020. Published Online March 20, 2020 https://doi.org/10.1016/S2468-1253(20)30084-4.
- Chan H, Kwan A, To K-F, et al. Clinical significance of hepatic derangement in severe acute respiratory syndrome. World J Gastroenterol 2005;11(14):2148-2153.
- Farcas G, Poutanen S, Mazzulli T, et al. Fatal severe acute respiratory syndrome is associated with multiorgan involvement by coronavirus. J Infect Dis. 2005;191(2):193‐197.
- Peiris JSM, Chu CM, Cheng, VCC, et al. Clinical progression and viral load in a community outbreak of coronavirus-associated SARS pneumonia: a prospective study. Lancet. 2003 May 24;361(9371):1767-72.
- Li W, Moore MJ, Vasilieva N, et al. Angiotensin‐converting enzyme 2 is a functional receptor for the SARS coronavirus. Nature. 2003;426(6965):450‐454.
- Xu Z, Shi L, Wang Y et al. Pathological findings of COVID‐19 associated with acute respiratory distress syndrome. Lancet Respir Med, 2020. https://doi.org/10.1016/S2213‐2600(20)30076‐X
- Li G, DeClercq E. Therapeutic options for the 2019 novel coronavirus (2019-nCoV). Nature Reviews | Drug Discovery 2020; 19: 149-150. https://www.nature.com/articles/d41573-020-00016-0
- AASLD. https://www.aasld.org/about-aasld/covid-19-resources
- EASL. https://easl.eu/covid-19-and-the-liver/
- ECDC. https://www.ecdc.europa.eu/en/covid-19-pandemic
- CDC. https://www.cdc.gov/coronavirus/2019-ncov/index.html
Original article: CGHE Synthesis: COVID-19 and Liver Disease