Comparison of NAFLD, MAFLD and MASLD characteristics and mortality outcomes in United States adults

被引:14
|
作者
Song, Rui [1 ]
Li, Zhao [2 ]
Zhang, Yingzhi [1 ]
Tan, Jiahe [3 ]
Chen, Zhiwei [1 ,4 ]
机构
[1] Chongqing Med Univ, Inst Viral Hepatitis, Dept Infect Dis, Key Lab Mol Biol Infect Dis,Affiliated Hosp 2,Mini, Chongqing, Peoples R China
[2] Seventh Peoples Hosp Chongqing, Dept Gastroenterol, Chongqing, Peoples R China
[3] Chongqing Med Univ, Dept Neurosurg, Affiliated Hosp 1, Chongqing, Peoples R China
[4] Chongqing Med Univ, Inst Viral Hepatitis, Dept Infect Dis, Key Lab Mol Biol Infect Dis,Affiliated Hosp 2,Mini, 74 Linjiang Rd, Chongqing 400010, Peoples R China
关键词
MAFLD; MASLD; mortality; NAFLD; NHANES III;
D O I
10.1111/liv.15856
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: Following the classification of metabolic dysfunction-associated fatty liver disease (MAFLD), non-alcoholic fatty liver disease (NAFLD) has recently been redefined again as metabolic dysfunction-associated steatotic liver disease (MASLD). However, the distinctions in characteristics and mortality outcomes between NAFLD, MAFLD and MASLD remain unclear. Methods: We analysed data from 7519 participants in the third National Health and Nutrition Examination Surveys of United States (US) and their linked mortality until 2019. Survey weight-adjusted multivariable Cox proportional model was used to study the mortality over three terms. Results: The prevalence of NAFLD, MAFLD and MASLD was 18.5%, 19.3% and 20.8%, respectively. Most individuals with NAFLD (94.5%) or MAFLD (100%) can be classified as MASLD, while a relatively low percentage of those with MASLD were also diagnosed with either NAFLD (84.1%) or MAFLD (92.7%). During a median follow-up of 26.9 years, both MAFLD and MASLD were associated with increased risk of all-cause mortality (adjusted hazard ratio [aHR] 1.18, 95% CI 1.04-1.33 and 1.19, 1.06-1.34, respectively), this association was mainly observed in NAFLD-/MASLD+ subgroups. NAFLD was not associated with all-cause mortality. However, all three terms were associated with an increased risk of all-cause mortality in individuals with advanced fibrosis (aHR: 1.71-1.81). Subgroup analyses showed that higher risk of all-cause mortality for both MAFLD and MASLD were observed among older adults (>= 65 year), non-Hispanic whites and those without diabetes. Conclusions: Both MASLD and MALFD were linked to higher all-cause mortality risk, but MASLD identified a greater number of individuals compared to MAFLD.
引用
收藏
页码:1051 / 1060
页数:10
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