Predictors of advanced liver fibrosis and the performance of fibrosis scores: lean compared to non-lean metabolic dysfunction-associated steatotic liver disease (MASLD) patients.

IF 1.9 Q3 GASTROENTEROLOGY & HEPATOLOGY
Minerva gastroenterology Pub Date : 2024-09-01 Epub Date: 2023-10-27 DOI:10.23736/S2724-5985.23.03518-0
Shoham Dabbah, Gil Ben Yakov, Monika-Inda Kaufmann, Oranit Cohen-Ezra, Maria Likhter, Yana Davidov, Ziv Ben Ari
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Abstract

Background: Non-alcoholic fatty liver disease (NAFLD) in lean patients differs from that of NAFLD in non-lean patients. However, current data regarding predictors of advanced fibrosis and the performance of fibrosis-4 index (FIB-4) and NAFLD fibrosis score (NFS) in lean compared to non-lean metabolic dysfunction-associated steatotic liver disease (MASLD) patients is insufficient.

Methods: This was a cross-sectional study. Lean was defined as Body Mass Index <25 kg/m2. Advanced fibrosis (F3-F4) was detected by liver biopsy or two-dimension shear wave elastography (2D-SWE). Predictors of advanced fibrosis were identified using logistic regression and area under ROC curves (AUROC) were derived for FIB-4 and NFS.

Results: Lean patients (N.=153) comprised 19.2% of the MASLD cohort. Advanced fibrosis was associated with the number of cardiometabolic risk factors (CMRF) in lean (OR=2.06, P=0.011) and non-lean (OR=1.58, P<0.001) patients, however, hypertension and diabetes or impaired fasting glucose were significant only among non-lean. Age was associated with advanced fibrosis in both subgroups with age ≥65 showing higher odds in lean compared to non-lean patients (P=0.016). Non-lean patients had higher odds for advanced fibrosis relative to lean patients (OR=4.8, P=0.048). FIB-4 and NFS predicted advanced fibrosis among lean (AUROC=0.79 and AUROC=0.85, respectively) and non-lean (AUROC=0.79 and AUROC=0.76, respectively) patients. NFS ≥-1.445 showed higher specificity among lean compared to non-lean (P<0.001) and compared to that of FIB-4 ≥1.3 in lean patients (P<0.001).

Conclusions: The number of CMRF was predictive of advanced fibrosis in both subgroups while age ≥65 showed higher odds among lean patients. NFS ≥-1.445 is more specific than FIB-4 ≥1.3 for advanced fibrosis prediction in lean patients. These findings may help identify high-risk lean MASLD patients for further liver fibrosis stage assessment.

晚期肝纤维化的预测因素和纤维化评分的表现:瘦型与非瘦型代谢功能障碍相关脂肪变性肝病(MASLD)患者的比较。
背景:瘦型患者的非酒精性脂肪肝与非瘦型患者不同。然而,与非瘦代谢功能障碍相关的脂肪变性肝病(MASLD)患者相比,目前关于晚期纤维化的预测因素以及瘦型患者的纤维化-4指数(FIB-4)和NAFLD纤维化评分(NFS)的表现的数据不足。方法:这是一项横断面研究。瘦被定义为体重指数2。肝活检或二维剪切波弹性成像(2D-SWE)检测晚期纤维化(F3-F4)。使用逻辑回归确定晚期纤维化的预测因素,并推导FIB-4和NFS的ROC曲线下面积(AUROC)。结果:瘦型患者(N=153)占MASLD队列的19.2%。瘦型(OR=2.06,P=0.011)和非瘦型的晚期纤维化与心脏代谢危险因素(CMRF)的数量相关(OR=1.58,P结论:CMRF的数量在两个亚组中都可以预测晚期纤维化,而年龄≥65的瘦型患者的几率更高。NFS≥-1.445比FIB-4≥1.3对瘦型患者晚期纤维化的预测更具特异性。这些发现可能有助于识别高危瘦型MASLD患者,以进行进一步的肝纤维化分期评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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