AstraZeneca Gothenburg, Mölndal, Sweden.
Department of Clinical Sciences, Lund University, Malmö, Sweden.
J Clin Lipidol. 2018 Nov-Dec;12(6):1390-1403.e4. doi: 10.1016/j.jacl.2018.08.003. Epub 2018 Aug 10.
Treatment with omega-3 fatty acids and fenofibrates reduces serum triglyceride levels, but few studies have compared the effect of these agents on liver fat.
The aim of the EFFECT I trial (NCT02354976) was to determine the effects of free omega-3 carboxylic acids (OM-3CA) and fenofibrate on liver fat in overweight or obese individuals with non-alcoholic fatty liver disease and hypertriglyceridemia.
Seventy-eight patients were randomized to receive oral doses of 4 g OM-3CA (n = 25), 200 mg fenofibrate (n = 27), or placebo (n = 26) for 12 weeks in a double-blind, parallel-group study. Liver proton density fat fraction (PDFF) and volume, pancreas volume, and adipose tissue volumes were assessed by magnetic resonance imaging.
Changes in liver PDFF at 12 weeks were not significantly different across treatment groups (relative changes from baseline: placebo, +4%; OM-3CA, -2%; and fenofibrate, +17%). The common PNPLA3 genetic polymorphism (I148M) did not significantly influence the effects of OM-3CA or fenofibrate on liver PDFF. Fenofibrate treatment significantly increased liver and pancreas volumes vs placebo treatment, and the changes in liver and pancreas volumes were positively correlated (rho 0.45, P = .02). Total liver fat volume increased significantly in patients using fenofibrate vs OM-3CA (+23% vs -3%, P = .04). Compared with OM-3CA, fenofibrate increased total liver fat and liver volume. Serum triglycerides decreased with OM-3CA (-26%, P = .02) and fenofibrate (-38%, P < .001) vs placebo. In contrast to OM-3CA, fenofibrate reduced plasma docosahexaenoic acid levels and increased plasma acetylcarnitine and butyrylcarnitine levels, estimated delta-9 desaturase activity and the concentration of urine F2-isoprostanes.
OM-3CA and fenofibrate reduced serum triglycerides but did not reduce liver fat. Fenofibrate increased total liver volume and total liver fat volume vs OM-3CA, indicating a complex effect of fenofibrate on human hepatic lipid metabolism.
ω-3 脂肪酸和非诺贝特的治疗可降低血清甘油三酯水平,但很少有研究比较这些药物对肝脏脂肪的影响。
EFFECT I 试验(NCT02354976)的目的是确定游离 ω-3 羧酸(OM-3CA)和非诺贝特对超重或肥胖的非酒精性脂肪性肝病和高甘油三酯血症患者的肝脏脂肪的影响。
78 名患者被随机分为口服 4g OM-3CA(n=25)、200mg 非诺贝特(n=27)或安慰剂(n=26),在双盲、平行组研究中治疗 12 周。通过磁共振成像评估肝脏质子密度脂肪分数(PDFF)和体积、胰腺体积和脂肪组织体积。
12 周时,各组之间的肝 PDFF 变化无显著差异(与基线相比的相对变化:安慰剂,+4%;OM-3CA,-2%;非诺贝特,+17%)。常见的 PNPLA3 遗传多态性(I148M)并未显著影响 OM-3CA 或非诺贝特对肝 PDFF 的影响。与安慰剂相比,非诺贝特治疗显著增加了肝脏和胰腺的体积,并且肝脏和胰腺体积的变化呈正相关(rho 0.45,P=0.02)。与 OM-3CA 相比,使用非诺贝特治疗的患者总肝脂肪量显著增加(+23%比-3%,P=0.04)。与 OM-3CA 相比,非诺贝特增加了总肝脂肪和肝脏体积。血清甘油三酯降低与 OM-3CA(-26%,P=0.02)和非诺贝特(-38%,P<0.001)与安慰剂相比。与 OM-3CA 相比,非诺贝特降低了血浆二十二碳六烯酸水平,增加了血浆乙酰肉碱和丁酰肉碱水平,估计 delta-9 去饱和酶活性和尿液 F2-异前列烷浓度。
OM-3CA 和非诺贝特降低了血清甘油三酯,但并未降低肝脏脂肪。与 OM-3CA 相比,非诺贝特增加了总肝体积和总肝脂肪量,表明非诺贝特对人体肝脂质代谢有复杂的影响。