To the editor, We read the article "Head-to-head comparison of magnetic resonance elastography-based liver stiffness, fat fraction, and T1 relaxation time in identifying at-risk NASH" by Li et al [1] with interest. This is a pivotal clinical research area that paves the way for the potential elimination of invasive biopsies in treating patients with NAFLD. This study compared several imaging-derived techniques and concluded that liver stiffness measurement from magnetic resonance elastography (MRE) was the superior test for identifying those with NASH and fibrosis. We believe there are some key study methodological elements that need to be highlighted before the stated conclusion can be firmly established.Liver stiffness measurement from MRE has been shown to perform very well in identifying those with fibrosis, [2] yet seldom has been the sole standout in predicting fibrotic NASH. This has led to proposed combinations like MEFIB (MRE and fibrosis-4) [3] and MAST (MRE, proton density fat fraction, and AST). [4] In original head-to-head comparisons of imaging-derived biomarkers, [5] liver stiffness measurement was superior for fibrosis but considerably inferior to tests more sensitive to disease activity, such as proton density fat fraction and iron-corrected T1 (cT1). While the statistical methods in Li et al are appropriate, it appears the groupings were not; discriminating levels of fibrosis within a NASH population is not the same as diagnosing NASH with fibrosis from an NAFLD population. This is a slight but important difference that should be communicated to ensure the correct interpretation of the findings.The authors introduced the MRI biomarker cT1, [6] yet T1-mapping as the measurement under investigation. cT1 is based on T1-mapping from a specific MRI acquisition that is then adjusted for iron and standardized across different field strengths and manufacturers. cT1 is not the same as T1-mapping reported directly from the MRI scanner, and cT1 thresholds recommended for changing clinical management may not apply to the T1 reported in this article.Existing studies underscore that liver stiffness tests should not stand alone in NASH evaluation. The field needs to be more diligent when reporting on the various biomarkers for their utility in NASH to avoid adding yet more confusion to a very dynamic field of medical research.