TY - JOUR
T1 - Impact of Diabetes, Drug-Induced Liver Injury, and Sepsis on Outcomes in Metabolic Dysfunction Associated Fatty Liver Disease-Related Acute-on-Chronic Liver Failure
AU - the APASL ACLF Research Consortium (AARC) for APASL ACLF Working Party
AU - Kumar, Ashish
AU - Arora, Anil
AU - Choudhury, Ashok
AU - Arora, Vinod
AU - Rela, Mohamed
AU - Jothimani, Dinesh Kumar
AU - Mahtab, Mamun A.
AU - Devarbhavi, Harshad
AU - Eapen, Chundamanni E.
AU - Goel, Ashish
AU - Yaghi, Cesar
AU - Ning, Qin
AU - Chen, Tao
AU - Jia, Jidong
AU - Zhongping, Duan
AU - Hamid, Saeed S.
AU - Butt, Amna S.
AU - Jafri, Wasim
AU - Shukla, Akash
AU - Tan, Seok S.
AU - Kim, Dong J.
AU - Saraya, Anoop
AU - Hu, Jinhua
AU - Sood, Ajit
AU - Goyal, Omesh
AU - Midha, Vandana
AU - Pati, Girish K.
AU - Singh, Ayaskant
AU - Lee, Guan H.
AU - Treeprasertsuk, Sombat
AU - Thanapirom, Kessarin
AU - Mandot, Ameet
AU - Maghade, Ravikiran
AU - Lesmana, Rinaldi C.
AU - Ghazinyan, Hasmik
AU - Mohan Prasad, Virukalpatti G.
AU - Dokmeci, Abdul K.
AU - Sollano, Jose D.
AU - Abbas, Zaigham
AU - Shrestha, Ananta
AU - Lau, George K.
AU - Payawal, Diana A.
AU - Shiha, Gamal E.
AU - Duseja, Ajay
AU - Taneja, Sunil
AU - Verma, Nipun
AU - Rao, Padaki N.
AU - Kulkarni, Anand V.
AU - Karim, Fazal
AU - Saraswat, Vivek A.
N1 - Publisher Copyright:
© 2024 by The American College of Gastroenterology.
PY - 2024
Y1 - 2024
N2 - INTRODUCTION: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.
AB - INTRODUCTION: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.
KW - AARC score
KW - ACLF
KW - DILI
KW - MELD
KW - liver failure
KW - metabolic dysfunction-associated steatotic liver disease (MASLD)
KW - sepsis
UR - http://www.scopus.com/inward/record.url?scp=85206525097&partnerID=8YFLogxK
U2 - 10.14309/ajg.0000000000002951
DO - 10.14309/ajg.0000000000002951
M3 - Article
C2 - 39016385
AN - SCOPUS:85206525097
SN - 0002-9270
JO - American Journal of Gastroenterology
JF - American Journal of Gastroenterology
M1 - e02951
ER -