Insulin resistance is associated with the inactivation of lipoprotein lipase and elevated levels of remnant lipoproteins, including remnant cholesterol (Rem-C). On the other hand, insulin resistance is the risk factor for progression of MASLD, and might induces cirrhosis, hepatocellular caricinoma, and liver-related death. Additionally, DM, high Rem-C level, and MASLD are risk factors for cardiovascular disease (CVD), and these three pathologies may be closely related. However, the correlation between REM-C levels and the pathophysiology of MASLD remains unclear. The present study aimed to elucidate the relationship between serum REM-C levels and the histological finding of MAFLD. We assessed 222 patients (94 men and 128 women; age 20-80 years) who were diagnosed with NAFLD by liver biopsy with available medical history, physical examination, and biochemical measurement data. Serum ester-type cholesterol and free cholesterol contents in the remnant lipoproteins were measured using an enzymatic method. The relationship between serum Rem-C levels and histological findings was analyzed. Serum Rem-C levels were significantly higher in patients with NAFLD activity score (NAS) 5-8,>66% steatosis grade, lobular inflammation with ≥ 5 foci, and many cells/prominent ballooning cells than in patients with NAS 1-4, < 33% steatosis grade, lobular inflammation with < 2 foci, and few ballooning cells. While univariate analysis revealed no significant association between Rem-C levels and advanced fibrosis, a significant association between Rem-C levels and NAS was evident. The relationship remained significant in multivariate analysis adjusted for confounders.
In conclusion, high serum Rem-C levels were associated with high NAS but not with fibrosis stage. Controlling serum Rem-C level may help alleviate NAFLD.
T. Miyake: None. S. Furukawa: Speaker's Bureau; Lilly Diabetes, Novo Nordisk, Mitsubishi Tanabe Pharma Corporation. B. Matsuura: None. O. Yoshida: None. A. Kanamoto: None. M. Miyazaki: None. A. Shiomi: None. H. Nakaguchi: None. M. Hirooka: None. M. Abe: None. Y. Hiasa: None.