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Article: Impact of Diabetes, Drug-Induced Liver Injury, and Sepsis on Outcomes in Metabolic Dysfunction Associated Fatty Liver Disease-Related Acute-on-Chronic Liver Failure

TitleImpact of Diabetes, Drug-Induced Liver Injury, and Sepsis on Outcomes in Metabolic Dysfunction Associated Fatty Liver Disease-Related Acute-on-Chronic Liver Failure
Authors
KeywordsAARC score
ACLF
DILI
liver failure
MELD
metabolic dysfunction-associated steatotic liver disease (MASLD)
sepsis
Issue Date1-Apr-2025
PublisherLippincott, Williams & Wilkins
Citation
The American Journal of Gastroenterology, 2024, v. 120, n. 4, p. 816-826 How to Cite?
AbstractINTRODUCTION: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.METHODS: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.RESULTS: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.DISCUSSION: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.
Persistent Identifierhttp://hdl.handle.net/10722/362646
ISSN
2023 Impact Factor: 8.0
2023 SCImago Journal Rankings: 2.391

 

DC FieldValueLanguage
dc.contributor.authorKumar, Ashish-
dc.contributor.authorArora, Anil-
dc.contributor.authorChoudhury, Ashok-
dc.contributor.authorArora, Vinod-
dc.contributor.authorRela, Mohamed-
dc.contributor.authorJothimani, Dinesh Kumar-
dc.contributor.authorMahtab, Mamun A.-
dc.contributor.authorDevarbhavi, Harshad-
dc.contributor.authorEapen, Chundamanni E.-
dc.contributor.authorGoel, Ashish-
dc.contributor.authorYaghi, Cesar-
dc.contributor.authorNing, Qin-
dc.contributor.authorChen, Tao-
dc.contributor.authorJia, Jidong-
dc.contributor.authorZhongping, Duan-
dc.contributor.authorHamid, Saeed S.-
dc.contributor.authorButt, Amna S.-
dc.contributor.authorJafri, Wasim-
dc.contributor.authorShukla, Akash-
dc.contributor.authorTan, Seok S.-
dc.contributor.authorKim, Dong J.-
dc.contributor.authorSaraya, Anoop-
dc.contributor.authorHu, Jinhua-
dc.contributor.authorSood, Ajit-
dc.contributor.authorGoyal, Omesh-
dc.contributor.authorMidha, Vandana-
dc.contributor.authorPati, Girish K.-
dc.contributor.authorSingh, Ayaskant-
dc.contributor.authorLee, Guan H.-
dc.contributor.authorTreeprasertsuk, Sombat-
dc.contributor.authorThanapirom, Kessarin-
dc.contributor.authorMandot, Ameet-
dc.contributor.authorMaghade, Ravikiran-
dc.contributor.authorLesmana, Rinaldi C.-
dc.contributor.authorGhazinyan, Hasmik-
dc.contributor.authorMohan Prasad, Virukalpatti G.-
dc.contributor.authorDokmeci, Abdul K.-
dc.contributor.authorSollano, Jose D.-
dc.contributor.authorAbbas, Zaigham-
dc.contributor.authorShrestha, Ananta-
dc.contributor.authorLau, George K.-
dc.contributor.authorPayawal, Diana A.-
dc.contributor.authorShiha, Gamal E.-
dc.contributor.authorDuseja, Ajay-
dc.contributor.authorTaneja, Sunil-
dc.contributor.authorVerma, Nipun-
dc.contributor.authorRao, Padaki N.-
dc.contributor.authorKulkarni, Anand V.-
dc.contributor.authorKarim, Fazal-
dc.contributor.authorSaraswat, Vivek A.-
dc.contributor.authorAlam, Shahinul-
dc.contributor.authorChowdhury, Debashis-
dc.contributor.authorKedarisetty, Chandan K.-
dc.contributor.authorSaigal, Sanjiv-
dc.contributor.authorSharma, Praveen-
dc.contributor.authorYattoo, Ghulam N.-
dc.contributor.authorKoshy, Abraham-
dc.contributor.authorPatwa, Ajay K.-
dc.contributor.authorElbasiony, Mohamed-
dc.contributor.authorRathi, Pravin M.-
dc.contributor.authorMaharshi, Sudhir-
dc.contributor.authorDayal, Vishwa M.-
dc.contributor.authorJha, Ashish K.-
dc.contributor.authorKalista, Kemal F.-
dc.contributor.authorGani, Rino A.-
dc.contributor.authorYuen, Man F.-
dc.contributor.authorSingh, Virendra-
dc.contributor.authorSargsyan, Violeta A.-
dc.contributor.authorHuang, Chien H.-
dc.contributor.authorMukewar, Saurabh S.-
dc.contributor.authorXin, Shaojie-
dc.contributor.authorRajaram, Ruveena B.-
dc.contributor.authorPanackel, Charles-
dc.contributor.authorDadhich, Sunil-
dc.contributor.authorSachdeva, Sanjeev-
dc.contributor.authorKumar, Ajay-
dc.contributor.authorBehera, Sanatan-
dc.contributor.authorKamani, Lubna-
dc.contributor.authorSaithanyamurthi, Hemamala V.-
dc.contributor.authorPrasad, Babita-
dc.contributor.authorSarin, Shiv K.-
dc.date.accessioned2025-09-26T00:36:42Z-
dc.date.available2025-09-26T00:36:42Z-
dc.date.issued2025-04-01-
dc.identifier.citationThe American Journal of Gastroenterology, 2024, v. 120, n. 4, p. 816-826-
dc.identifier.issn0002-9270-
dc.identifier.urihttp://hdl.handle.net/10722/362646-
dc.description.abstractINTRODUCTION: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.METHODS: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.RESULTS: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.DISCUSSION: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.-
dc.languageeng-
dc.publisherLippincott, Williams & Wilkins-
dc.relation.ispartofThe American Journal of Gastroenterology-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectAARC score-
dc.subjectACLF-
dc.subjectDILI-
dc.subjectliver failure-
dc.subjectMELD-
dc.subjectmetabolic dysfunction-associated steatotic liver disease (MASLD)-
dc.subjectsepsis-
dc.titleImpact of Diabetes, Drug-Induced Liver Injury, and Sepsis on Outcomes in Metabolic Dysfunction Associated Fatty Liver Disease-Related Acute-on-Chronic Liver Failure-
dc.typeArticle-
dc.identifier.doi10.14309/ajg.0000000000002951-
dc.identifier.pmid39016385-
dc.identifier.scopuseid_2-s2.0-85206525097-
dc.identifier.volume120-
dc.identifier.issue4-
dc.identifier.spage816-
dc.identifier.epage826-
dc.identifier.eissn1572-0241-
dc.identifier.issnl0002-9270-

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