Cardiometabolic and Lipid Clinic, Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA, USA.
Division of Translational Medicine and Human Genetics, Department of Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.
Lipids Health Dis. 2020 May 30;19(1):117. doi: 10.1186/s12944-020-01295-7.
Omega-3 fatty acids (OM3-FAs) are recommended with a low-fat diet for severe hypertriglyceridemia (SHTG), to reduce triglycerides and acute pancreatitis (AP) risk. A low-fat diet may reduce pancreatic lipase secretion, which is required to absorb OM3-ethyl esters (OM3-EEs), but not OM3-carboxylic acids (OM3-CAs).
In this exploratory, randomized, open-label, crossover study, 15 patients with SHTG and previous AP were instructed to take OM3-CA (2 g or 4 g) and OM3-EE 4 g once daily for 4 weeks, while adhering to a low-fat diet. On day 28 of each treatment phase, a single dose was administered in the clinic with a liquid low-fat meal, to assess 24-h plasma exposure. Geometric least-squares mean ratios were used for between-treatment comparisons of baseline (day 0)-adjusted area under the plasma concentration versus time curves (AUC) and maximum plasma concentrations (C) for eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA).
Before initiating OM3-FA treatment, mean baseline fasting plasma EPA + DHA concentrations (nmol/mL) were 723 for OM3-CA 2 g, 465 for OM3-CA 4 g and 522 for OM3-EE 4 g. At week 4, mean pre-dose fasting plasma EPA + DHA concentrations increased by similar amounts (+ 735 - + 768 nmol/mL) for each treatment. During the 24-h exposure assessment (day 28), mean plasma EPA + DHA increased from pre-dose to the maximum achieved concentration by + 32.7%, + 45.8% and + 3.1% with single doses of OM3-CA 2 g, OM3-CA 4 g and OM3-EE 4 g, respectively. Baseline-adjusted AUC was 60% higher for OM3-CA 4 g than for OM3-EE 4 g and baseline-adjusted C was 94% higher (both non-significant).
Greater 24-h exposure of OM3-CA versus OM3-EE was observed for some parameters when administered with a low-fat meal at the clinic on day 28. However, increases in pre-dose fasting plasma EPA + DHA over the preceding 4-week dosing period were similar between treatments, leading overall to non-significant differences in baseline (day 0)-adjusted AUC and C EPA + DHA values. It is not clear why the greater 24-h exposure of OM3-CA versus OM3-EE observed with a low-fat meal did not translate into significantly higher pre-dose fasting levels of DHA + EPA with longer-term use.
ClinicalTrials.gov, NCT02189252, Registered 23 June 2014.
ω-3 脂肪酸(OM3-FAs)与低脂肪饮食联合推荐用于严重高甘油三酯血症(SHTG),以降低甘油三酯和急性胰腺炎(AP)的风险。低脂肪饮食可能会减少胰腺脂肪酶的分泌,而这种酶是吸收 OM3-乙酯(OM3-EEs)所必需的,但不是 OM3-羧酸(OM3-CAs)。
在这项探索性、随机、开放标签、交叉研究中,15 名 SHTG 合并既往 AP 的患者被指示每天服用 OM3-CA(2g 或 4g)和 OM3-EE 4g,持续 4 周,同时坚持低脂肪饮食。在每个治疗阶段的第 28 天,在诊所给予单剂量低脂肪餐,以评估 24 小时血浆暴露情况。使用几何最小二乘均值比值比较基线(第 0 天)调整后的血浆浓度-时间曲线下面积(AUC)和最大血浆浓度(C)的 E 型多不饱和脂肪酸(EPA)和二十二碳六烯酸(DHA)的治疗间比值。
在开始 OM3-FA 治疗之前,OM3-CA 2g 的空腹基线 EPA+DHA 浓度(nmol/mL)为 723,OM3-CA 4g 为 465,OM3-EE 4g 为 522。在第 4 周时,每种治疗的空腹基线 EPA+DHA 浓度在前剂量增加了相似的量(+735-+768 nmol/mL)。在 24 小时暴露评估(第 28 天)期间,OM3-CA 2g、OM3-CA 4g 和 OM3-EE 4g 的单剂量分别使最大血浆 EPA+DHA 浓度从预剂量增加了+32.7%、+45.8%和+3.1%。OM3-CA 4g 的基线调整 AUC 比 OM3-EE 4g 高 60%,基线调整 C 高 94%(均无统计学意义)。
与 OM3-EE 相比,OM3-CA 在第 28 天在诊所给予低脂肪餐时观察到 24 小时的暴露更大。然而,在 4 周的给药期间,空腹基线 EPA+DHA 的增加在治疗之间相似,导致总体上 EPA+DHA 的基线(第 0 天)调整 AUC 和 C 值无统计学差异。OM3-CA 与 OM3-EE 相比,在 24 小时的暴露更大,为什么在长期使用中并未导致 DHA+EPA 的空腹水平显著升高,这一点尚不清楚。
ClinicalTrials.gov,NCT02189252,于 2014 年 6 月 23 日注册。