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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)
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 cir...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer India
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7334898/ https://www.ncbi.nlm.nih.gov/pubmed/32623632 http://dx.doi.org/10.1007/s12072-020-10072-8 |
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author | Sarin, Shiv Kumar Choudhury, Ashok Lau, George K. Zheng, Ming-Hua Ji, Dong Abd-Elsalam, Sherief Hwang, Jaeseok Qi, Xiaolong Cua, Ian Homer Suh, Jeong Ill Park, Jun Gi Putcharoen, Opass Kaewdech, Apichat Piratvisuth, Teerha Treeprasertsuk, Sombat Park, Sooyoung Wejnaruemarn, Salisa Payawal, Diana A. Baatarkhuu, Oidov Ahn, Sang Hoon Yeo, Chang Dong Alonzo, Uzziel Romar Chinbayar, Tserendorj Loho, Imelda M. Yokosuka, Osamu Jafri, Wasim Tan, Soeksiam Soo, Lau Ing Tanwandee, Tawesak Gani, Rino Anand, Lovkesh Esmail, Eslam Saber Khalaf, Mai Alam, Shahinul Lin, Chun-Yu Chuang, Wan-Long Soin, A. S. Garg, Hitendra K. Kalista, Kemal Batsukh, Badamnachin Purnomo, Hery Djagat Dara, Vijay Pal Rathi, Pravin Al Mahtab, Mamun Shukla, Akash Sharma, Manoj K. Omata, Masao |
author_facet | Sarin, Shiv Kumar Choudhury, Ashok Lau, George K. Zheng, Ming-Hua Ji, Dong Abd-Elsalam, Sherief Hwang, Jaeseok Qi, Xiaolong Cua, Ian Homer Suh, Jeong Ill Park, Jun Gi Putcharoen, Opass Kaewdech, Apichat Piratvisuth, Teerha Treeprasertsuk, Sombat Park, Sooyoung Wejnaruemarn, Salisa Payawal, Diana A. Baatarkhuu, Oidov Ahn, Sang Hoon Yeo, Chang Dong Alonzo, Uzziel Romar Chinbayar, Tserendorj Loho, Imelda M. Yokosuka, Osamu Jafri, Wasim Tan, Soeksiam Soo, Lau Ing Tanwandee, Tawesak Gani, Rino Anand, Lovkesh Esmail, Eslam Saber Khalaf, Mai Alam, Shahinul Lin, Chun-Yu Chuang, Wan-Long Soin, A. S. Garg, Hitendra K. Kalista, Kemal Batsukh, Badamnachin Purnomo, Hery Djagat Dara, Vijay Pal Rathi, Pravin Al Mahtab, Mamun Shukla, Akash Sharma, Manoj K. Omata, Masao |
author_sort | Sarin, Shiv Kumar |
collection | PubMed |
description | 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. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12072-020-10072-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7334898 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer India |
record_format | MEDLINE/PubMed |
spelling | pubmed-73348982020-07-06 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) Sarin, Shiv Kumar Choudhury, Ashok Lau, George K. Zheng, Ming-Hua Ji, Dong Abd-Elsalam, Sherief Hwang, Jaeseok Qi, Xiaolong Cua, Ian Homer Suh, Jeong Ill Park, Jun Gi Putcharoen, Opass Kaewdech, Apichat Piratvisuth, Teerha Treeprasertsuk, Sombat Park, Sooyoung Wejnaruemarn, Salisa Payawal, Diana A. Baatarkhuu, Oidov Ahn, Sang Hoon Yeo, Chang Dong Alonzo, Uzziel Romar Chinbayar, Tserendorj Loho, Imelda M. Yokosuka, Osamu Jafri, Wasim Tan, Soeksiam Soo, Lau Ing Tanwandee, Tawesak Gani, Rino Anand, Lovkesh Esmail, Eslam Saber Khalaf, Mai Alam, Shahinul Lin, Chun-Yu Chuang, Wan-Long Soin, A. S. Garg, Hitendra K. Kalista, Kemal Batsukh, Badamnachin Purnomo, Hery Djagat Dara, Vijay Pal Rathi, Pravin Al Mahtab, Mamun Shukla, Akash Sharma, Manoj K. Omata, Masao Hepatol Int Original Article 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. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12072-020-10072-8) contains supplementary material, which is available to authorized users. Springer India 2020-07-04 /pmc/articles/PMC7334898/ /pubmed/32623632 http://dx.doi.org/10.1007/s12072-020-10072-8 Text en © 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. |
spellingShingle | Original Article Sarin, Shiv Kumar Choudhury, Ashok Lau, George K. Zheng, Ming-Hua Ji, Dong Abd-Elsalam, Sherief Hwang, Jaeseok Qi, Xiaolong Cua, Ian Homer Suh, Jeong Ill Park, Jun Gi Putcharoen, Opass Kaewdech, Apichat Piratvisuth, Teerha Treeprasertsuk, Sombat Park, Sooyoung Wejnaruemarn, Salisa Payawal, Diana A. Baatarkhuu, Oidov Ahn, Sang Hoon Yeo, Chang Dong Alonzo, Uzziel Romar Chinbayar, Tserendorj Loho, Imelda M. Yokosuka, Osamu Jafri, Wasim Tan, Soeksiam Soo, Lau Ing Tanwandee, Tawesak Gani, Rino Anand, Lovkesh Esmail, Eslam Saber Khalaf, Mai Alam, Shahinul Lin, Chun-Yu Chuang, Wan-Long Soin, A. S. Garg, Hitendra K. Kalista, Kemal Batsukh, Badamnachin Purnomo, Hery Djagat Dara, Vijay Pal Rathi, Pravin Al Mahtab, Mamun Shukla, Akash Sharma, Manoj K. Omata, Masao 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) |
title | 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) |
title_full | 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) |
title_fullStr | 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) |
title_full_unstemmed | 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) |
title_short | 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) |
title_sort | 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) |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7334898/ https://www.ncbi.nlm.nih.gov/pubmed/32623632 http://dx.doi.org/10.1007/s12072-020-10072-8 |
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