Muldoon M F, Laderian B, Kuan D C H, Sereika S M, Marsland A L, Manuck S B
Heart and Vascular Institute, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Department of Medicine, Jackson Memorial Hospital, Miami, FL, USA.
J Intern Med. 2016 Jan;279(1):98-109. doi: 10.1111/joim.12442. Epub 2015 Oct 26.
The n-3 polyunsaturated fatty acids eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) may prevent a range of chronic conditions through anti-inflammatory actions. However, as clinical trials using these fatty acids for primary prevention are yet unavailable, their putative role in disease prevention rests, in part, on evidence of anti-inflammatory actions in healthy individuals.
To investigate in a double-blind, placebo-controlled clinical trial whether supplementation with a moderate dose of EPA+DHA reduces common biomarkers of chronic, systemic inflammation in healthy individuals.
A total of 261 healthy individuals aged 30-54 years who were free of inflammatory conditions and consumed ≤ 300 mg per day EPA+DHA were included in the study. Participants were randomly assigned to 18 weeks of either fish oil supplementation providing 1400 mg per day EPA+DHA or matching placebo. Outcome measures were serum levels of C-reactive protein (CRP) and interleukin (IL)-6. In a substudy, ex vivo cytokine production was measured. Missing data for CRP and IL-6 were estimated using regression imputation. Data analyses conformed to intention-to-treat principles.
Participant blinding was verified. Red blood cell EPA+DHA increased by 64% in the active treatment group, but serum CRP and IL-6 were not affected by supplementation (P ≥ 0.20). Findings were consistent with and without imputed values and across subgroups. Similarly, EPA+DHA supplementation did not alter ex vivo production of four pro-inflammatory cytokines (P ≥ 0.20).
Supplementation with 1400 mg EPA+DHA did not reduce common markers of systemic inflammation in healthy adults. Whether this or a higher dose affects other measures of inflammation, oxidative stress or immune function warrants examination.
n-3多不饱和脂肪酸二十碳五烯酸(EPA)和二十二碳六烯酸(DHA)可能通过抗炎作用预防一系列慢性疾病。然而,由于目前尚无使用这些脂肪酸进行一级预防的临床试验,它们在疾病预防中的假定作用部分基于健康个体的抗炎作用证据。
在一项双盲、安慰剂对照的临床试验中,研究补充中等剂量的EPA+DHA是否能降低健康个体慢性全身性炎症的常见生物标志物。
共有261名年龄在30至54岁之间、无炎症疾病且每天摄入EPA+DHA≤300毫克的健康个体纳入研究。参与者被随机分配接受为期18周的鱼油补充剂(每天提供1400毫克EPA+DHA)或匹配的安慰剂。观察指标为血清C反应蛋白(CRP)和白细胞介素(IL)-6水平。在一项子研究中,测量了体外细胞因子的产生。使用回归插补法估计CRP和IL-6的缺失数据。数据分析符合意向性分析原则。
验证了参与者的盲法。活性治疗组红细胞EPA+DHA增加了64%,但补充剂对血清CRP和IL-6没有影响(P≥0.20)。有无插补值以及各亚组的结果均一致。同样,补充EPA+DHA并未改变四种促炎细胞因子的体外产生(P≥0.20)。
补充1400毫克EPA+DHA并不能降低健康成年人全身性炎症的常见标志物。这一剂量或更高剂量是否会影响炎症、氧化应激或免疫功能的其他指标,值得进一步研究。