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

IF 8 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
American Journal of Gastroenterology Pub Date : 2025-04-01 Epub Date: 2024-07-17 DOI:10.14309/ajg.0000000000002951
Ashish Kumar, Anil Arora, Ashok Choudhury, Vinod Arora, Mohamed Rela, Dinesh Kumar Jothimani, Mamun A Mahtab, Harshad Devarbhavi, Chundamanni E Eapen, Ashish Goel, Cesar Yaghi, Qin Ning, Tao Chen, Jidong Jia, Duan Zhongping, Saeed S Hamid, Amna S Butt, Wasim Jafri, Akash Shukla, Seok S Tan, Dong J Kim, Anoop Saraya, Jinhua Hu, Ajit Sood, Omesh Goyal, Vandana Midha, Girish K Pati, Ayaskant Singh, Guan H Lee, Sombat Treeprasertsuk, Kessarin Thanapirom, Ameet Mandot, Ravikiran Maghade, Rinaldi C Lesmana, Hasmik Ghazinyan, Virukalpatti G Mohan Prasad, Abdul K Dokmeci, Jose D Sollano, Zaigham Abbas, Ananta Shrestha, George K Lau, Diana A Payawal, Gamal E Shiha, Ajay Duseja, Sunil Taneja, Nipun Verma, Padaki N Rao, Anand V Kulkarni, Fazal Karim, Vivek A Saraswat, Shahinul Alam, Debashis Chowdhury, Chandan K Kedarisetty, Sanjiv Saigal, Praveen Sharma, Ghulam N Yattoo, Abraham Koshy, Ajay K Patwa, Mohamed Elbasiony, Pravin M Rathi, Sudhir Maharshi, Vishwa M Dayal, Ashish K Jha, Kemal F Kalista, Rino A Gani, Man F Yuen, Virendra Singh, Violeta A Sargsyan, Chien H Huang, Saurabh S Mukewar, Shaojie Xin, Ruveena B Rajaram, Charles Panackel, Sunil Dadhich, Sanjeev Sachdeva, Ajay Kumar, Sanatan Behera, Lubna Kamani, Hemamala V Saithanyamurthi, Babita Prasad, Shiv K Sarin
{"title":"Impact of Diabetes, Drug-Induced Liver Injury, and Sepsis on Outcomes in Metabolic Dysfunction Associated Fatty Liver Disease-Related Acute-on-Chronic Liver Failure.","authors":"Ashish Kumar, Anil Arora, Ashok Choudhury, Vinod Arora, Mohamed Rela, Dinesh Kumar Jothimani, Mamun A Mahtab, Harshad Devarbhavi, Chundamanni E Eapen, Ashish Goel, Cesar Yaghi, Qin Ning, Tao Chen, Jidong Jia, Duan Zhongping, Saeed S Hamid, Amna S Butt, Wasim Jafri, Akash Shukla, Seok S Tan, Dong J Kim, Anoop Saraya, Jinhua Hu, Ajit Sood, Omesh Goyal, Vandana Midha, Girish K Pati, Ayaskant Singh, Guan H Lee, Sombat Treeprasertsuk, Kessarin Thanapirom, Ameet Mandot, Ravikiran Maghade, Rinaldi C Lesmana, Hasmik Ghazinyan, Virukalpatti G Mohan Prasad, Abdul K Dokmeci, Jose D Sollano, Zaigham Abbas, Ananta Shrestha, George K Lau, Diana A Payawal, Gamal E Shiha, Ajay Duseja, Sunil Taneja, Nipun Verma, Padaki N Rao, Anand V Kulkarni, Fazal Karim, Vivek A Saraswat, Shahinul Alam, Debashis Chowdhury, Chandan K Kedarisetty, Sanjiv Saigal, Praveen Sharma, Ghulam N Yattoo, Abraham Koshy, Ajay K Patwa, Mohamed Elbasiony, Pravin M Rathi, Sudhir Maharshi, Vishwa M Dayal, Ashish K Jha, Kemal F Kalista, Rino A Gani, Man F Yuen, Virendra Singh, Violeta A Sargsyan, Chien H Huang, Saurabh S Mukewar, Shaojie Xin, Ruveena B Rajaram, Charles Panackel, Sunil Dadhich, Sanjeev Sachdeva, Ajay Kumar, Sanatan Behera, Lubna Kamani, Hemamala V Saithanyamurthi, Babita Prasad, Shiv K Sarin","doi":"10.14309/ajg.0000000000002951","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>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.</p><p><strong>Methods: </strong>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.</p><p><strong>Results: </strong>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.</p><p><strong>Discussion: </strong>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.</p>","PeriodicalId":7608,"journal":{"name":"American Journal of Gastroenterology","volume":" ","pages":"816-826"},"PeriodicalIF":8.0000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of Gastroenterology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.14309/ajg.0000000000002951","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/7/17 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"GASTROENTEROLOGY & HEPATOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

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.

糖尿病、药物性肝损伤和败血症对 MAFLD 相关急性慢性肝衰竭预后的影响
背景:代谢功能障碍相关性脂肪肝(MAFLD)及其并发症--MAFLD相关性急性和慢性肝衰竭(MAFLD-ACLF)的发病率正在上升。然而,决定 MAFLD-ACLF 患者预后的因素仍未得到充分研究:方法:从AARC登记处招募MAFLD-ACLF患者。当治疗单位确定慢性肝病(CLD)的病因为MAFLD(或以前的命名,如NAFLD、NASH或NASH-肝硬化)时,即可诊断为MAFLD-ACLF。同时合并其他病因(如酒精、HBV、HCV 等)的 CLD 患者除外。数据按 70:30 的比例随机分为衍生组(n=258)和验证组(n=111)。主要结果是 90 天死亡率。只考虑基线临床、实验室特征和严重程度评分:衍生组有 258 名患者;60% 为男性,平均年龄为 53 岁。糖尿病患者占 27%,高血压患者占 29%。主要诱因包括病毒性肝炎(HAV 和 HEV,32%)、药物性损伤(DILI,29%)和败血症(23%)。入院时的 MELD-Na 和 AARC 评分平均为 32±6 和 10.4±1.9。90 天后,51% 的患者存活。非病毒性诱发因素、糖尿病、胆红素、INR和脑病是影响死亡率的独立因素。在MELD-Na和AARC评分的基础上加上糖尿病和诱因,形成了新的MAFLD-MELD-Na评分(糖尿病+12,非病毒诱因+12)和MAFLD-AARC评分(各+5)。这些评分在两个队列中的表现均优于标准评分:结论:近一半的 MAFLD-ACLF 患者在 90 天内死亡。结论:近一半的 MAFLD-ACLF 患者在 90 天内死亡,糖尿病和非病毒性诱因(如 DILI 和败血症)导致了不良后果。新的MAFLD-MMELD-Na和MAFLD-AARC评分能可靠地预测MAFLD-ACLF患者的90天死亡率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
American Journal of Gastroenterology
American Journal of Gastroenterology 医学-胃肠肝病学
CiteScore
11.40
自引率
5.10%
发文量
458
审稿时长
12 months
期刊介绍: Published on behalf of the American College of Gastroenterology (ACG), The American Journal of Gastroenterology (AJG) stands as the foremost clinical journal in the fields of gastroenterology and hepatology. AJG offers practical and professional support to clinicians addressing the most prevalent gastroenterological disorders in patients.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信