Peng Hong-Ye, Lu Chun-Li, Zhao Mo, Huang Xiao-Qiang, Huang Shu-Xia, Zhuo Zi-Wen, Liu Jing, Lu Yan-Ping, Lv Wen-Liang
Department of Infection, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, 100053, China.
Graduate School, Beijing University of Chinese Medicine, Beijing, 100029, China.
BMC Gastroenterol. 2025 May 14;25(1):372. doi: 10.1186/s12876-025-03912-0.
Our objective was to compare the clinical features of Metabolic dysfunction-associated steatotic liver disease (MASLD) /metabolic alcohol-related liver disease (MetALD)/metabolic associated fatty liver disease (MAFLD)/nonalcoholic fatty liver disease (NAFLD) and the relative risk analysis of metabolic disorders.
The National Health and Nutrition Examination Survey for the 2017-2018 cycle was used to screen the participants. Multivariate-adjusted logistic regression models were applied to explore the difference in relative risk analysis between NAFLD/MAFLD/MASLD/MetALD and metabolic disorders.
Among the 1,862 eligible individuals, 358(44.84%) had MASLD, 213(11.44%) had MetALD, 841(45.17%) had MAFLD, and 1,125(60.42%) had NAFLD. Positive associations with the risk of hypertension were discovered for MASLD (OR = 2.892, 95%CI = 2.226-3.756), MetALD (OR = 1.802, 95% CI = 1.355-2.398), MAFLD (OR = 3.455, 95%CI = 2.741-4.354) and NAFLD (OR = 1.983, 95%CI = 1.584-2.484). Positive associations with the risk of T2DM were discovered for MASLD (OR = 6.360, 95%CI = 4.440-9.109), MAFLD (OR = 7.026, 95%CI = 4.893-10.090) and NAFLD (OR = 3.372, 95%CI = 2.511-4.528). We discovered similar results for hyperlipidemia. Compared to mild steatosis, moderate to severe steatosis in patients with MASLD (OR = 3.924, 95%CI = 2.399-6.419), MAFLD (OR = 3.814, 95%CI = 2.367-6.144), NAFLD (OR = 4.910, 95%CI = 2.983-8.080) has a higher risk for T2DM.
The proposed definitions of MASLD and MetALD are valuable and deserve further exploration. Our findings suggest that MAFLD is a more effective indicator for identifying patients at increased risk for metabolic disorders.
我们的目的是比较代谢功能障碍相关脂肪性肝病(MASLD)/代谢性酒精性肝病(MetALD)/代谢相关脂肪性肝病(MAFLD)/非酒精性脂肪性肝病(NAFLD)的临床特征以及代谢紊乱的相对风险分析。
使用2017 - 2018周期的国家健康与营养检查调查来筛选参与者。应用多变量调整逻辑回归模型来探讨NAFLD/MAFLD/MASLD/MetALD与代谢紊乱在相对风险分析方面的差异。
在1862名符合条件的个体中,358人(44.84%)患有MASLD,213人(11.44%)患有MetALD,841人(45.17%)患有MAFLD,1125人(60.42%)患有NAFLD。发现MASLD(OR = 2.892,95%CI = 2.226 - 3.756)、MetALD(OR = 1.802,95%CI = 1.355 - 2.398)、MAFLD(OR = 3.455,95%CI = 2.741 - 4.354)和NAFLD(OR = 1.983,95%CI = 1.584 - 2.484)与高血压风险呈正相关。发现MASLD(OR = 6.360,95%CI = 4.440 - 9.109)、MAFLD(OR = 7.026,95%CI = 4.893 - 10.090)和NAFLD(OR = 3.372,95%CI = 2.511 - 4.528)与2型糖尿病风险呈正相关。对于高脂血症,我们发现了类似的结果。与轻度脂肪变性相比,MASLD(OR = 3.924,95%CI = 2.399 - 6.419)、MAFLD(OR = 3.814,95%CI = 2.367 - 6.144)、NAFLD(OR = 4.910,95%CI = 2.983 - 8.080)患者的中度至重度脂肪变性患2型糖尿病的风险更高。
所提出的MASLD和MetALD定义是有价值的,值得进一步探索。我们的研究结果表明,MAFLD是识别代谢紊乱风险增加患者的更有效指标。