Impact of Diabetes, Drug-Induced Liver Injury, and Sepsis on Outcomes in Metabolic Dysfunction Associated Fatty Liver Disease–Related Acute-on-Chronic Liver Failure
The prevalence of metabolic dysfunction-associated fatty liver disease (MAFLD) and its complication, MAFLD-related acute-on-chronic liver failure (MAFLD-ACLF), is rising. Yet, factors determining patient outcomes in MAFLD-ACLF remain understudied.INTRODUCTIONThe prevalence of metabolic dysfunction-a...
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Published in | The American journal of gastroenterology |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
17.07.2024
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Abstract | The prevalence of metabolic dysfunction-associated fatty liver disease (MAFLD) and its complication, MAFLD-related acute-on-chronic liver failure (MAFLD-ACLF), is rising. Yet, factors determining patient outcomes in MAFLD-ACLF remain understudied.INTRODUCTIONThe prevalence of metabolic dysfunction-associated fatty liver disease (MAFLD) and its complication, MAFLD-related acute-on-chronic liver failure (MAFLD-ACLF), is rising. Yet, factors determining patient outcomes in MAFLD-ACLF remain understudied.Patients with MAFLD-ACLF were recruited from the Asian Pacific Association for the Study of the Liver-ACLF Research Consortium (AARC registry). The diagnosis of MAFLD-ACLF was made when the treating unit had identified the etiology of chronic liver disease as MAFLD (or previous nomenclature such as non-alcoholic fatty liver disease, non-alcoholic steatohepatitis, or non-alcoholic steatohepatitis-cirrhosis). Patients with coexisting other etiologies of chronic liver disease (such as alcohol, hepatitis B virus, hepatitis C virus, etc.) were excluded. Data were randomly split into derivation (n = 258) and validation (n = 111) cohorts at a 70:30 ratio. The primary outcome was 90-day mortality. Only the baseline clinical, laboratory features and severity scores were considered.METHODSPatients with MAFLD-ACLF were recruited from the Asian Pacific Association for the Study of the Liver-ACLF Research Consortium (AARC registry). The diagnosis of MAFLD-ACLF was made when the treating unit had identified the etiology of chronic liver disease as MAFLD (or previous nomenclature such as non-alcoholic fatty liver disease, non-alcoholic steatohepatitis, or non-alcoholic steatohepatitis-cirrhosis). Patients with coexisting other etiologies of chronic liver disease (such as alcohol, hepatitis B virus, hepatitis C virus, etc.) were excluded. Data were randomly split into derivation (n = 258) and validation (n = 111) cohorts at a 70:30 ratio. The primary outcome was 90-day mortality. Only the baseline clinical, laboratory features and severity scores were considered.The derivation group had 258 patients; 60% were male, with a mean age of 53. Diabetes was noted in 27% and hypertension in 29%. The dominant precipitants included viral hepatitis (hepatitis A virus and hepatitis E virus, 32%), drug-induced injury (drug-induced liver injury, 29%), and sepsis (23%). Model for End-Stage Liver Disease-Sodium (MELD-Na) and AARC scores on admission averaged 32 ± 6 and 10.4 ± 1.9. At 90 days, 51% survived. Nonviral precipitant, diabetes, bilirubin, international normalized ratio, and encephalopathy were independent factors influencing mortality. Adding diabetes and precipitant to MELD-Na and AARC scores, the novel MAFLD-MELD-Na score (+12 for diabetes, +12 for nonviral precipitant), and MAFLD-AARC score (+5 for each) were formed. These outperformed the standard scores in both cohorts.RESULTSThe derivation group had 258 patients; 60% were male, with a mean age of 53. Diabetes was noted in 27% and hypertension in 29%. The dominant precipitants included viral hepatitis (hepatitis A virus and hepatitis E virus, 32%), drug-induced injury (drug-induced liver injury, 29%), and sepsis (23%). Model for End-Stage Liver Disease-Sodium (MELD-Na) and AARC scores on admission averaged 32 ± 6 and 10.4 ± 1.9. At 90 days, 51% survived. Nonviral precipitant, diabetes, bilirubin, international normalized ratio, and encephalopathy were independent factors influencing mortality. Adding diabetes and precipitant to MELD-Na and AARC scores, the novel MAFLD-MELD-Na score (+12 for diabetes, +12 for nonviral precipitant), and MAFLD-AARC score (+5 for each) were formed. These outperformed the standard scores in both cohorts.Almost half of patients with MAFLD-ACLF die within 90 days. Diabetes and nonviral precipitants such as drug-induced liver injury and sepsis lead to adverse outcomes. The new MAFLD-MELD-Na and MAFLD-AARC scores provide reliable 90-day mortality predictions for patients with MAFLD-ACLF.DISCUSSIONAlmost half of patients with MAFLD-ACLF die within 90 days. Diabetes and nonviral precipitants such as drug-induced liver injury and sepsis lead to adverse outcomes. The new MAFLD-MELD-Na and MAFLD-AARC scores provide reliable 90-day mortality predictions for patients with MAFLD-ACLF. |
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AbstractList | The prevalence of metabolic dysfunction-associated fatty liver disease (MAFLD) and its complication, MAFLD-related acute-on-chronic liver failure (MAFLD-ACLF), is rising. Yet, factors determining patient outcomes in MAFLD-ACLF remain understudied.INTRODUCTIONThe prevalence of metabolic dysfunction-associated fatty liver disease (MAFLD) and its complication, MAFLD-related acute-on-chronic liver failure (MAFLD-ACLF), is rising. Yet, factors determining patient outcomes in MAFLD-ACLF remain understudied.Patients with MAFLD-ACLF were recruited from the Asian Pacific Association for the Study of the Liver-ACLF Research Consortium (AARC registry). The diagnosis of MAFLD-ACLF was made when the treating unit had identified the etiology of chronic liver disease as MAFLD (or previous nomenclature such as non-alcoholic fatty liver disease, non-alcoholic steatohepatitis, or non-alcoholic steatohepatitis-cirrhosis). Patients with coexisting other etiologies of chronic liver disease (such as alcohol, hepatitis B virus, hepatitis C virus, etc.) were excluded. Data were randomly split into derivation (n = 258) and validation (n = 111) cohorts at a 70:30 ratio. The primary outcome was 90-day mortality. Only the baseline clinical, laboratory features and severity scores were considered.METHODSPatients with MAFLD-ACLF were recruited from the Asian Pacific Association for the Study of the Liver-ACLF Research Consortium (AARC registry). The diagnosis of MAFLD-ACLF was made when the treating unit had identified the etiology of chronic liver disease as MAFLD (or previous nomenclature such as non-alcoholic fatty liver disease, non-alcoholic steatohepatitis, or non-alcoholic steatohepatitis-cirrhosis). Patients with coexisting other etiologies of chronic liver disease (such as alcohol, hepatitis B virus, hepatitis C virus, etc.) were excluded. Data were randomly split into derivation (n = 258) and validation (n = 111) cohorts at a 70:30 ratio. The primary outcome was 90-day mortality. Only the baseline clinical, laboratory features and severity scores were considered.The derivation group had 258 patients; 60% were male, with a mean age of 53. Diabetes was noted in 27% and hypertension in 29%. The dominant precipitants included viral hepatitis (hepatitis A virus and hepatitis E virus, 32%), drug-induced injury (drug-induced liver injury, 29%), and sepsis (23%). Model for End-Stage Liver Disease-Sodium (MELD-Na) and AARC scores on admission averaged 32 ± 6 and 10.4 ± 1.9. At 90 days, 51% survived. Nonviral precipitant, diabetes, bilirubin, international normalized ratio, and encephalopathy were independent factors influencing mortality. Adding diabetes and precipitant to MELD-Na and AARC scores, the novel MAFLD-MELD-Na score (+12 for diabetes, +12 for nonviral precipitant), and MAFLD-AARC score (+5 for each) were formed. These outperformed the standard scores in both cohorts.RESULTSThe derivation group had 258 patients; 60% were male, with a mean age of 53. Diabetes was noted in 27% and hypertension in 29%. The dominant precipitants included viral hepatitis (hepatitis A virus and hepatitis E virus, 32%), drug-induced injury (drug-induced liver injury, 29%), and sepsis (23%). Model for End-Stage Liver Disease-Sodium (MELD-Na) and AARC scores on admission averaged 32 ± 6 and 10.4 ± 1.9. At 90 days, 51% survived. Nonviral precipitant, diabetes, bilirubin, international normalized ratio, and encephalopathy were independent factors influencing mortality. Adding diabetes and precipitant to MELD-Na and AARC scores, the novel MAFLD-MELD-Na score (+12 for diabetes, +12 for nonviral precipitant), and MAFLD-AARC score (+5 for each) were formed. These outperformed the standard scores in both cohorts.Almost half of patients with MAFLD-ACLF die within 90 days. Diabetes and nonviral precipitants such as drug-induced liver injury and sepsis lead to adverse outcomes. The new MAFLD-MELD-Na and MAFLD-AARC scores provide reliable 90-day mortality predictions for patients with MAFLD-ACLF.DISCUSSIONAlmost half of patients with MAFLD-ACLF die within 90 days. Diabetes and nonviral precipitants such as drug-induced liver injury and sepsis lead to adverse outcomes. The new MAFLD-MELD-Na and MAFLD-AARC scores provide reliable 90-day mortality predictions for patients with MAFLD-ACLF. |
Author | Jha, Ashish K. Yaghi, Cesar Sargsyan, Violeta A. Maghade, Ravikiran Kim, Dong J. Chen, Tao Kedarisetty, Chandan K. Lesmana, Rinaldi C. Sollano, Jose D. Sarin, Shiv K. Jothimani, Dinesh Kumar Ning, Qin Ghazinyan, Hasmik Xin, Shaojie Verma, Nipun Karim, Fazal Mukewar, Saurabh S. Saithanyamurthi, Hemamala V. Lau, George K. Payawal, Diana A. Behera, Sanatan Goyal, Omesh Devarbhavi, Harshad Shrestha, Ananta Zhongping, Duan Eapen, Chundamanni E. Jafri, Wasim Alam, Shahinul Chowdhury, Debashis Singh, Virendra Mandot, Ameet Yuen, Man F. Goel, Ashish Arora, Anil Pati, Girish K. Sachdeva, Sanjeev Sood, Ajit Arora, Vinod Saraya, Anoop Shiha, Gamal E. Rathi, Pravin M. Patwa, Ajay K. Panackel, Charles Saigal, Sanjiv Butt, Amna S. Duseja, Ajay Dadhich, Sunil Tan, Seok S. Sharma, Praveen Kumar, Ajay Elbasiony, Mohamed Rajaram, Ruveena B. Kamani, Lubna Thanapirom, Kessarin Rao, Padaki N. Saraswat, Vivek A. Yattoo, Ghulam N. Jia, Jidong Kulkarni, Anand V. Kumar, Ashish Prasad, Babita Huang, Chien H. Rela, Mohamed Midha, Vandana Treeprasertsuk, Sombat Choudhury, Asho |
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PublicationTitle | The American journal of gastroenterology |
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References | Wong (R6-20240919) 2023; 79 Eslam (R1-20240919) 2020; 14 Kim (R19-20240919) 2016; 31 Powell (R2-20240919) 2021; 397 Sarin (R10-20240919) 2014; 8 Younossi (R4-20240919) 2023; 77 Sarin (R11-20240919) 2016; 13 Lazarus (R3-20240919) 2022; 19 Kumar (R15-20240919) 2013; 3 Sarin (R9-20240919) 2019; 13 Aggarwal (R14-20240919) 2021; 18 Younossi (R5-20240919) 2019; 70 Jindal (R13-20240919) 2022; 42 Sarin (R8-20240919) 2009; 3 Gawande (R16-20240919) 2019; 9 Bajaj (R20-20240919) 2022; 117 Younossi (R18-20240919) 2019; 114 Arroyo (R12-20240919) 2020; 382 Singal (R7-20240919) 2019; 4 Targher (R17-20240919) 2021; 18 |
References_xml | – volume: 117 start-page: 225 issue: 2 year: 2022 ident: R20-20240919 article-title: Acute-on-Chronic liver failure clinical guidelines publication-title: Am J Gastroenterol doi: 10.14309/ajg.0000000000001595 contributor: fullname: Bajaj – volume: 13 start-page: 131 issue: 3 year: 2016 ident: R11-20240919 article-title: Acute-on-chronic liver failure: Terminology, mechanisms and management publication-title: Nat Rev Gastroenterol Hepatol doi: 10.1038/nrgastro.2015.219 contributor: fullname: Sarin – volume: 3 start-page: 269 issue: 1 year: 2009 ident: R8-20240919 article-title: Acute-on-chronic liver failure: Consensus recommendations of the Asian Pacific Association for the Study of the Liver (APASL) publication-title: Hepatol Int doi: 10.1007/s12072-008-9106-x contributor: fullname: Sarin – volume: 18 start-page: 168 issue: 3 year: 2021 ident: R14-20240919 article-title: Hepatitis E: Current status in India publication-title: Clin Liver Dis doi: 10.1002/cld.1146 contributor: fullname: Aggarwal – volume: 77 start-page: 1335 issue: 4 year: 2023 ident: R4-20240919 article-title: The global epidemiology of nonalcoholic fatty liver disease (NAFLD) and nonalcoholic steatohepatitis (NASH): A systematic review publication-title: Hepatology doi: 10.1097/HEP.0000000000000004 contributor: fullname: Younossi – volume: 31 start-page: 427 issue: 2 year: 2016 ident: R19-20240919 article-title: Characterization of acute-on-chronic liver failure and prediction of mortality in Asian patients with active alcoholism publication-title: J Gastroenterol Hepatol doi: 10.1111/jgh.13084 contributor: fullname: Kim – volume: 19 start-page: 60 issue: 1 year: 2022 ident: R3-20240919 article-title: Advancing the global public health agenda for NAFLD: A consensus statement publication-title: Nat Rev Gastroenterol Hepatol doi: 10.1038/s41575-021-00523-4 contributor: fullname: Lazarus – volume: 8 start-page: 453 issue: 4 year: 2014 ident: R10-20240919 article-title: Acute-on-chronic liver failure: Consensus recommendations of the Asian Pacific Association for the Study of the Liver (APASL) 2014 publication-title: Hepatol Int doi: 10.1007/s12072-014-9580-2 contributor: fullname: Sarin – volume: 18 start-page: 599 issue: 9 year: 2021 ident: R17-20240919 article-title: The complex link between NAFLD and type 2 diabetes mellitus–mechanisms and treatments publication-title: Nat Rev Gastroenterol Hepatol doi: 10.1038/s41575-021-00448-y contributor: fullname: Targher – volume: 114 start-page: 1714 issue: 11 year: 2019 ident: R18-20240919 article-title: The impact of obesity and type 2 diabetes on chronic liver disease publication-title: Am J Gastroenterol doi: 10.14309/ajg.0000000000000433 contributor: fullname: Younossi – volume: 70 start-page: 531 issue: 3 year: 2019 ident: R5-20240919 article-title: Non-alcoholic fatty liver disease: A global public health perspective publication-title: J Hepatol doi: 10.1016/j.jhep.2018.10.033 contributor: fullname: Younossi – volume: 4 start-page: 74 year: 2019 ident: R7-20240919 article-title: Acute on chronic liver failure in non-alcoholic fatty liver and alcohol associated liver disease publication-title: Transl Gastroenterol Hepatol doi: 10.21037/tgh.2019.09.11 contributor: fullname: Singal – volume: 382 start-page: 2137 issue: 22 year: 2020 ident: R12-20240919 article-title: Acute-on-chronic liver failure publication-title: N Engl J Med doi: 10.1056/NEJMra1914900 contributor: fullname: Arroyo – volume: 397 start-page: 2212 issue: 10290 year: 2021 ident: R2-20240919 article-title: Non-alcoholic fatty liver disease publication-title: Lancet doi: 10.1016/S0140-6736(20)32511-3 contributor: fullname: Powell – volume: 3 start-page: 225 year: 2013 ident: R15-20240919 article-title: Hepatitis E and acute-on-chronic liver failure publication-title: J Clin Exp Hepatol doi: 10.1016/j.jceh.2013.08.013 contributor: fullname: Kumar – volume: 13 start-page: 353 issue: 4 year: 2019 ident: R9-20240919 article-title: Acute-on-chronic liver failure: Consensus recommendations of the Asian Pacific Association for the Study of the Liver (APASL): An update publication-title: Hepatol Int doi: 10.1007/s12072-019-09946-3 contributor: fullname: Sarin – volume: 79 start-page: 842 issue: 3 year: 2023 ident: R6-20240919 article-title: Changing epidemiology, global trends and implications for outcomes of NAFLD publication-title: J Hepatol doi: 10.1016/j.jhep.2023.04.036 contributor: fullname: Wong – volume: 14 start-page: 889 issue: 6 year: 2020 ident: R1-20240919 article-title: The Asian Pacific Association for the Study of the Liver clinical practice guidelines for the diagnosis and management of metabolic associated fatty liver disease publication-title: Hepatol Int doi: 10.1007/s12072-020-10094-2 contributor: fullname: Eslam – volume: 42 start-page: 2093 issue: 9 year: 2022 ident: R13-20240919 article-title: Epidemiology of liver failure in Asia-Pacific region publication-title: Liver Int doi: 10.1111/liv.15328 contributor: fullname: Jindal – volume: 9 start-page: 699 issue: 6 year: 2019 ident: R16-20240919 article-title: Acute-on-Chronic liver failure: Etiology of chronic and acute precipitating factors and their effect on mortality publication-title: J Clin Exp Hepatol doi: 10.1016/j.jceh.2019.04.050 contributor: fullname: Gawande |
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