Carvajal-Gonzalez Santos, Tuthill Theresa, Wai-Sun Wong Vincent, Ashworth Amy Lauren, Kayali Zeid, Fournier-Poizat Céline, Amin Neeta B
Pfizer Research and Development, Pfizer Inc, Cambridge, Massachusetts.
Medical Data Analytics Centre, Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong, China.
Gastro Hep Adv. 2025 Apr 8;4(7):100669. doi: 10.1016/j.gastha.2025.100669. eCollection 2025.
Magnetic resonance imaging-proton density fat fraction (MRI-PDFF) is an accurate, noninvasive tool for diagnosing metabolic dysfunction-associated steatotic liver disease, but its feasibility is limited in routine clinical practice. We aimed to assess the clinical utility of alternative, cost-efficient approaches for assessing liver fat changes and their relationship with MRI-PDFF changes.
This is a secondary analysis of a phase 2a study that included adults with metabolic dysfunction-associated steatotic liver disease who received clesacostat, a selective, reversible inhibitor of acetyl-CoA carboxylase. In this secondary analysis, responders were defined as those in whom a ≥30% decrease in liver fat by MRI-PDFF was observed with clesacostat or placebo. Other endpoints were evaluated for their ability to predict MRI-PDFF responder status, including controlled attenuation parameter (CAP), liver enzymes (alanine aminotransferase, aspartate aminotransferase, and gamma-glutamyl transferase), metabolic dysfunction-associated steatohepatitis-related biomarkers (liver stiffness measurement by vibration-controlled transient elastography, cytokeratin 18-M30, and cytokeratin 18-M65), and markers of hepatic steatosis (hepatic steatosis index and fatty liver index). These relationships were investigated through correlation, univariate, and multivariable regression analyses.
Of 260 participants with a baseline and on-treatment measure at week 12 or week 16, 143 were responders. Based on correlation analyses, a significant but weak positive correlation between MRI-PDFF and CAP measurements of relative percentage change from baseline in liver fat was observed. By combining the selected 6 parameters (CAP, hepatic steatosis index, fatty liver index, alanine aminotransferase, gamma-glutamyl transferase, and cytokeratin 18-M65) through multivariable regression modeling, responders can be predicted with a high level of sensitivity and specificity (mean area under the receiver operating characteristic curve = 0.831 from 10-fold cross-validation).
Modeling multiple noninvasive assessments of liver fat closely aligned with MRI-PDFF measurements. These data support further assessment of its suitability in real-world clinical practice.
磁共振成像质子密度脂肪分数(MRI-PDFF)是诊断代谢功能障碍相关脂肪性肝病的一种准确、无创的工具,但其在常规临床实践中的可行性有限。我们旨在评估用于评估肝脏脂肪变化及其与MRI-PDFF变化关系的替代的、具有成本效益的方法的临床实用性。
这是一项2a期研究的二次分析,该研究纳入了患有代谢功能障碍相关脂肪性肝病的成年人,他们接受了乙酰辅酶A羧化酶的选择性可逆抑制剂克利司他。在这项二次分析中,应答者被定义为在接受克利司他或安慰剂治疗后,通过MRI-PDFF观察到肝脏脂肪减少≥30%的患者。评估了其他终点预测MRI-PDFF应答者状态的能力,包括受控衰减参数(CAP)、肝酶(丙氨酸氨基转移酶、天冬氨酸氨基转移酶和γ-谷氨酰转移酶)、代谢功能障碍相关脂肪性肝炎相关生物标志物(通过振动控制瞬时弹性成像测量的肝脏硬度、细胞角蛋白18-M30和细胞角蛋白18-M65)以及肝脂肪变性标志物(肝脂肪变性指数和脂肪肝指数)。通过相关性、单变量和多变量回归分析研究了这些关系。
在260名在第12周或第16周有基线和治疗期测量值的参与者中,143名是应答者。基于相关性分析,观察到MRI-PDFF与肝脏脂肪相对于基线变化的相对百分比的CAP测量值之间存在显著但较弱的正相关。通过多变量回归建模结合所选的6个参数(CAP、肝脂肪变性指数、脂肪肝指数、丙氨酸氨基转移酶、γ-谷氨酰转移酶和细胞角蛋白18-M65),可以以较高的敏感性和特异性预测应答者(10倍交叉验证的受试者工作特征曲线下平均面积 = 0.831)。
对与MRI-PDFF测量密切相关的肝脏脂肪进行多种无创评估的建模。这些数据支持进一步评估其在实际临床实践中的适用性。