Omatsu Takashi, Koseki Masahiro, Ito Kaori, Saga Ayami, Sawabe Hiroshi, Tanaka Katsunao, Inui Hiroyasu, Okada Takeshi, Nishida Makoto, Takahashi Hirokazu, Aishima Shinichi, Kamada Yoshihiro, Yoshida Hiroshi, Sakata Yasushi
Department of Cardiovascular Medicine, The University of Osaka Graduate School of Medicine.
Advanced Medicine Development Dept., BML, Inc.
J Atheroscler Thromb. 2025 Jul 16. doi: 10.5551/jat.65748.
Desmosterol, a cholesterol precursor, is converted by Δ24-dehydrocholesterol reductase. Hence, desmosterol levels are considered to reflect cholesterol metabolism. This study aimed to evaluate sterols as novel biomarkers of liver condition in Asian moderate obese patients with metabolic dysfunction-associated steatotic liver disease (MASLD).
In total, 218 patients with MASLD who underwent liver biopsy were prospectively enrolled. Liver biopsy samples were evaluated by a well-versed pathologist according to the criteria. The serum sterols of biopsy-proven patients', such as desmosterol, sitosterol, and campesterol, of the patients with biopsy-proven MASLD were analyzed using liquid chromatography-mass spectrometry.
Inflammation grade 0/1/2/3 was observed in 8/107/90/12 patients, and fibrosis stage 0/1/2/3/4 was observed in 25/48/64/63/17 patients, respectively. Serum desmosterol levels were significantly different by inflammation grade 0-3 (one-way analysis of variance [ANOVA], p = 0.004), with a beta coefficient of 0.219 (95% confidence interval [CI]: 0.088-0.350, p<0.01). Ordinal logistic regression analysis data on inflammation grade, adjusted for other parameters, showed that desmosterol had an odds ratio of 3.727 (95% CI 1.422-9.901, p<0.005). Although desmosterol levels are influenced by statin treatment, in non-statin-treated patients, serum desmosterol levels remained significantly different by inflammation grade (one-way ANOVA, p = 0.041), and the beta coefficient was 0.233 (95% CI: 0.066-0.400, p<0.01).
Serum desmosterol levels indicated the degree of hepatic inflammatory activity in patients with MASLD. Since desmosterol, a ligand of nuclear receptor LXR, reflects hepatic cholesterol metabolism, we hope that our findings will contribute to establishing a novel biomarker to screen the high-risk patients for cardiovascular diseases in MASLD.
胆固醇前体——羊毛甾醇可由Δ24 - 脱氢胆固醇还原酶转化而来。因此,羊毛甾醇水平被认为可反映胆固醇代谢情况。本研究旨在评估甾醇作为亚洲中度肥胖且患有代谢功能障碍相关脂肪性肝病(MASLD)患者肝脏状况的新型生物标志物。
前瞻性纳入了总共218例接受肝脏活检的MASLD患者。由经验丰富的病理学家根据标准对肝脏活检样本进行评估。采用液相色谱 - 质谱法分析经活检证实患有MASLD患者的血清甾醇,如羊毛甾醇、豆甾醇和菜油甾醇。
分别有8/107/90/12例患者观察到炎症分级为0/1/2/3,25/48/64/63/17例患者观察到纤维化分期为0/1/2/3/4。血清羊毛甾醇水平在炎症分级0 - 3之间存在显著差异(单因素方差分析[ANOVA],p = 0.004),β系数为0.219(95%置信区间[CI]:0.088 - 0.350,p<0.01)。对炎症分级进行序贯逻辑回归分析,并对其他参数进行校正,结果显示羊毛甾醇的比值比为3.727(95% CI 1.422 - 9.901,p<0.005)。尽管羊毛甾醇水平受他汀类药物治疗影响,但在未接受他汀类药物治疗的患者中,血清羊毛甾醇水平在炎症分级之间仍存在显著差异(单因素方差分析,p = 0.041),β系数为0.233(95% CI:0.066 - 0.400,p<0.01)。
血清羊毛甾醇水平可表明MASLD患者肝脏炎症活动程度。由于羊毛甾醇作为核受体LXR的配体,反映肝脏胆固醇代谢情况,我们希望我们的研究结果将有助于建立一种新型生物标志物,用于筛查MASLD中患心血管疾病的高危患者。