Cho Yongin, Rhee Hyungjin, Kim Young-Eun, Lee Minyoung, Lee Byung-Wan, Kang Eun Seok, Cha Bong-Soo, Choi Jin-Young, Lee Yong-Ho
Department of Endocrinology and Metabolism, Inha University School of Medicine, Incheon, Republic of Korea.
Graduate School, Yonsei University College of Medicine, Seoul, Republic of Korea.
BMC Med. 2022 Mar 21;20(1):93. doi: 10.1186/s12916-022-02288-2.
The effect of ezetimibe, Niemann-Pick C1-like 1 inhibitor, on liver fat is not clearly elucidated. Our primary objective was to evaluate the efficacy of ezetimibe plus rosuvastatin versus rosuvastatin monotherapy to reduce liver fat using magnetic resonance imaging-derived proton density fat fraction (MRI-PDFF) in patients with non-alcoholic fatty liver disease (NAFLD).
A randomized controlled, open-label trial of 70 participants with NAFLD confirmed by ultrasound who were assigned to receive either ezetimibe 10 mg plus rosuvastatin 5 mg daily or rosuvastatin 5 mg for up to 24 weeks. The liver fat change was measured as average values in each of nine liver segments by MRI-PDFF. Magnetic resonance elastography (MRE) was used to measure liver fibrosis change.
Combination therapy significantly reduced liver fat compared with monotherapy by MRI-PDFF (mean difference: 3.2%; p = 0.020). There were significant reductions from baseline to study completion by MRI-PDFF for both the combination and monotherapy groups, respectively (18.1 to 12.3%; p < 0.001 and 15.0 to 12.4%; p = 0.003). Individuals with higher body mass index, type 2 diabetes, insulin resistance, and severe liver fibrosis were likely to be good responders to treatment with ezetimibe. MRE-derived change in liver fibrosis was not significantly different (both groups, p > 0.05). Controlled attenuation parameter (CAP) by transient elastography was significantly reduced in the combination group (321 to 287 dB/m; p = 0.018), but not in the monotherapy group (323 to 311 dB/m; p = 0.104).
Ezetimibe and rosuvastatin were found to be safe to treat participants with NAFLD. Furthermore, ezetimibe combined with rosuvastatin significantly reduced liver fat in this population.
The trial was registered at ClinicalTrials.gov (registration number: NCT03434613 ).
尼曼-匹克C1样1抑制剂依折麦布对肝脏脂肪的影响尚未明确阐明。我们的主要目标是在非酒精性脂肪性肝病(NAFLD)患者中,使用磁共振成像衍生的质子密度脂肪分数(MRI-PDFF)评估依折麦布联合瑞舒伐他汀与瑞舒伐他汀单药治疗降低肝脏脂肪的疗效。
一项随机对照、开放标签试验,纳入70例经超声确诊的NAFLD参与者,他们被分配接受每日10 mg依折麦布加5 mg瑞舒伐他汀或5 mg瑞舒伐他汀治疗,为期24周。通过MRI-PDFF测量肝脏九个节段中每个节段的肝脏脂肪变化平均值。使用磁共振弹性成像(MRE)测量肝脏纤维化变化。
与单药治疗相比,联合治疗通过MRI-PDFF显著降低了肝脏脂肪(平均差异:3.2%;p = 0.020)。联合治疗组和单药治疗组从基线到研究完成时,MRI-PDFF均有显著降低(分别从18.1%降至12.3%;p < 0.001和从15.0%降至12.4%;p = 0.003)。体重指数较高、患有2型糖尿病、胰岛素抵抗和严重肝纤维化的个体可能对依折麦布治疗反应良好。MRE得出的肝脏纤维化变化无显著差异(两组,p > 0.05)。联合治疗组经瞬时弹性成像得出的控制衰减参数(CAP)显著降低(从321 dB/m降至287 dB/m;p = 0.018),而单药治疗组未降低(从323 dB/m降至311 dB/m;p = 0.104)。
发现依折麦布和瑞舒伐他汀治疗NAFLD参与者是安全的。此外,依折麦布联合瑞舒伐他汀在该人群中显著降低了肝脏脂肪。
该试验在ClinicalTrials.gov注册(注册号:NCT03434613)。