Long-term outcomes and risk modifiers of metabolic dysfunction-associated steatotic liver disease between lean and non-lean populations

被引:6
|
作者
Danpanichkul, Pojsakorn [1 ]
Suparan, Kanokphong [2 ]
Prasitsumrit, Vitchapong [3 ]
Ahmed, Aijaz [4 ]
Wijarnpreecha, Karn [5 ,6 ,7 ]
Kim, Donghee [4 ]
机构
[1] Texas Tech Univ, Hlth Sci Ctr, Dept Internal Med, Lubbock, TX USA
[2] Chiang Mai Univ, Fac Med, Dept Microbiol, Immunol Unit, Chiang Mai, Thailand
[3] Mahidol Univ, Fac Med, Siriraj Hosp, Bangkok, Thailand
[4] Stanford Univ, Sch Med, Div Gastroenterol & Hepatol, 300 Pasteur Dr, Stanford, CA 94304 USA
[5] Univ Arizona, Coll Med, Dept Med, Div Gastroenterol & Hepatol, 475 N 5th St, Phoenix, AZ 85004 USA
[6] Banner Univ, Med Ctr, Dept Internal Med, Div Gastroenterol & Hepatol, Phoenix, AZ USA
[7] Univ Arizona, BIO5 Inst, Coll Med Phoenix, Phoenix, AZ USA
关键词
NAFLD; Nonobese; SLD; Liver disease; Mortality; MASLD; BODY-MASS INDEX; CLINICAL-OUTCOMES; DIABETES-MELLITUS; OVERWEIGHT; NAFLD; OBESITY; METAANALYSIS; INDIVIDUALS; SEVERITY; INCIDENT;
D O I
10.3350/cmh.2024.0631
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
One-third of adults across the globe exhibit metabolic dysfunction-associated steatotic liver disease (MASLD)& horbar;formerly known as nonalcoholic fatty liver disease (NAFLD). To date, MASLD is the fastest-growing etiology of chronic liver disease and hepatocellular carcinoma (HCC). Besides the population with obesity, MASLD can also be found in lean populations, accounting for 13% of the global population, especially Asians. Notably, individuals with lean MASLD face equal or higher overall mortality rates compared to their non-lean counterparts. Risk modifiers encompass advanced age, hepatic fibrosis, and type 2 diabetes mellitus (T2DM). Moreover, the population with lean MASLD is associated with an increased risk of HCC, while their non-lean counterparts are more prone to cardiovascular outcomes and T2DM. Existing evidence indicates a similar risk of liver-related events and extrahepatic cancer between the two groups. However, MASLD-related genetic variants, such as PNPLA3 and TM6SF2, did not significantly affect mortality between the two populations. Still, underreporting alcohol consumption and regional representation limits the study's comprehensiveness. Longitudinal studies and mechanistic explorations are needed to understand differences in lean versus non-lean MASLD populations. This review highlights the need for awareness and tailored interventions in managing MASLD, considering lean individuals' unique risks. (Clin Mol Hepatol 2025;31:74-89)
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页数:17
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