Comparative application of MAFLD and MASLD diagnostic criteria on NAFLD patients: insights from a single-center cohort.

IF 3.2 4区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Maha Elsabaawy, Madiha Naguib, Ahmed Abuamer, Ahmed Shaban
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引用次数: 0

Abstract

The diagnostic criteria for Metabolic Dysfunction-Associated Fatty Liver Disease (MAFLD) and Metabolic Associated Steatotic Liver Disease (MASLD) aim to refine the classification of fatty liver diseases previously grouped under Non-Alcoholic Fatty Liver Disease (NAFLD). This study evaluates the applicability of the MAFLD and MASLD frameworks in NAFLD patients, exploring their clinical utility in identifying high-risk patients. A total of 369 NAFLD patients were assessed using MAFLD and MASLD diagnostic criteria. Baseline characteristics, metabolic profiles, hepatic fibrosis, and cardiovascular risks were compared across the groups. Among NAFLD patients, 97.55% (n = 359) met MASLD criteria, and 97.01% (n = 357) fulfilled MAFLD criteria. Both frameworks MAFLD and MASLD captured overlapping populations, with MASLD encompassing slightly more cases. No significant differences were observed in metabolic risk factors, fibrosis indices (APRI, FIB-4, NAFLD fibrosis score), or cardiovascular risk (10-year ASCVD score). A small subset of lean NAFLD patients (10 cases) with distinct profiles remained uncategorized by either framework. Pure NAFLD cases (n = 10) were with mild insulin resistance (HOMA-IR: 3.07 ± 0.33) and slightly elevated LDL (102.5 ± 42.87 mg/dL), while fibrosis indices indicated low fibrosis risk. Steatosis indices supported the diagnosis of early-stage NAFLD with preserved liver function. These patients do not meet the criteria for inclusion in the MAFLD or MASLD frameworks, highlighting a gap in the current diagnostic systems. MAFLD and MASLD criteria align closely with NAFLD in capturing patients with metabolic risk with MASLD-enhanced inclusivity. Further refinement is required to address heterogeneity, particularly in lean NAFLD patients. Hypertension prevalence was comparable (17.4% in NAFLD, 18.2% in MAFLD, 17.8% in MASLD; p = 0.960), as was diabetes mellitus (36.7%, 37.8%, and 37.6%, respectively; p = 0.945). Body mass index was also similar across groups, with medians of 33.25, 33.6, and 33.4 kg/m2 (p = 0.731). Non-invasive markers of hepatic fibrosis, including APRI, FIB-4, and NAFLD fibrosis scores, did not differ significantly, with median FIB-4 scores around 1.05 (p = 0.953). Similarly, were the results of hepatic steatosis index and ASCVD score.

MAFLD和MASLD诊断标准在NAFLD患者中的比较应用:来自单中心队列的见解。
代谢功能障碍相关脂肪性肝病(MAFLD)和代谢相关脂肪性肝病(MASLD)的诊断标准旨在细化先前归为非酒精性脂肪性肝病(NAFLD)的脂肪性肝病的分类。本研究评估了MAFLD和MASLD框架在NAFLD患者中的适用性,探讨了它们在识别高危患者中的临床应用。采用MAFLD和MASLD诊断标准对369例NAFLD患者进行评估。比较各组的基线特征、代谢谱、肝纤维化和心血管风险。在NAFLD患者中,97.55% (n = 359)符合MASLD标准,97.01% (n = 357)符合MAFLD标准。框架MAFLD和MASLD都捕获了重叠的人群,MASLD包含的案例稍微多一些。代谢危险因素、纤维化指数(APRI、FIB-4、NAFLD纤维化评分)或心血管风险(10年ASCVD评分)均无显著差异。一小部分具有不同特征的瘦型NAFLD患者(10例)仍未被任何一种框架分类。纯NAFLD患者(n = 10)有轻度胰岛素抵抗(HOMA-IR: 3.07±0.33),低密度脂蛋白(LDL)轻度升高(102.5±42.87 mg/dL),纤维化指标显示低纤维化风险。脂肪变性指标支持早期NAFLD的诊断并保留肝功能。这些患者不符合纳入mald或MASLD框架的标准,突出了当前诊断系统中的差距。MAFLD和MASLD的标准与NAFLD在捕获代谢风险患者方面密切一致,具有MASLD增强的包容性。需要进一步细化以解决异质性,特别是在瘦型NAFLD患者中。高血压患病率相当(NAFLD为17.4%,MAFLD为18.2%,MASLD为17.8%;P = 0.960),糖尿病患者分别为36.7%、37.8%和37.6%;p = 0.945)。各组的体重指数也相似,中位数分别为33.25、33.6和33.4 kg/m2 (p = 0.731)。非侵入性肝纤维化标志物,包括APRI、FIB-4和NAFLD纤维化评分,差异无统计学意义,FIB-4评分中位数约为1.05 (p = 0.953)。同样,肝脂肪变性指数和ASCVD评分的结果也是如此。
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来源期刊
Clinical and Experimental Medicine
Clinical and Experimental Medicine 医学-医学:研究与实验
CiteScore
4.80
自引率
2.20%
发文量
159
审稿时长
2.5 months
期刊介绍: Clinical and Experimental Medicine (CEM) is a multidisciplinary journal that aims to be a forum of scientific excellence and information exchange in relation to the basic and clinical features of the following fields: hematology, onco-hematology, oncology, virology, immunology, and rheumatology. The journal publishes reviews and editorials, experimental and preclinical studies, translational research, prospectively designed clinical trials, and epidemiological studies. Papers containing new clinical or experimental data that are likely to contribute to changes in clinical practice or the way in which a disease is thought about will be given priority due to their immediate importance. Case reports will be accepted on an exceptional basis only, and their submission is discouraged. The major criteria for publication are clarity, scientific soundness, and advances in knowledge. In compliance with the overwhelmingly prevailing request by the international scientific community, and with respect for eco-compatibility issues, CEM is now published exclusively online.
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