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首页> 外文期刊>Nutrition Journal >Placebo-controlled randomized clinical trial of fish oil’s impact on fatigue, quality of life, and disease activity in Systemic Lupus Erythematosus
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Placebo-controlled randomized clinical trial of fish oil’s impact on fatigue, quality of life, and disease activity in Systemic Lupus Erythematosus

机译:鱼油对系统性红斑狼疮疲劳,生活质量和疾病活动影响的安慰剂对照随机临床试验

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Introduction A recent metabolomic screen of sera from patients with Systemic Lupus Erythematosus (SLE) found reduction of antioxidants and substrates for energy generation. These metabolic alterations may underlie one of the most common features of SLE - fatigue. The metabolomic studies also noted reduced omega-3 fatty acids, which are powerful anti- oxidants. This deficiency may be causally related to oxidative stress, inflammation, disease activity, and fatigue in SLE. Supplementation of omega-3 fatty acids using fish oil in SLE has been shown to reduce oxidative stress in other studies. The objective of this study is to evaluate the effect of fish oil supplementation on clinical measures of fatigue, quality of life, and disease activity as part of a randomized clinical trial. Methods Fifty SLE patients recruited in outpatient clinics were randomized 1:1 to fish oil supplementation or olive oil placebo, and blinded to their treatment group. At baseline and after 6 months of treatment, RAND Short Form-36 (RAND SF-36), Fatigue Severity Scale (FSS), SLE Disease Activity Index (SLEDAI), and Physician Global Assessment (PGA) were completed; serum was also collected for soluble mediator analysis. Results Thirty-two patients completed the study. PGA improved significantly in the fish oil group compared with the placebo group (p?=?0.015). The RAND SF-36 Energy/fatigue and Emotional well-being scores demonstrated improvement trends (p?=?0.092 and 0.070). No clear difference was seen in FSS and SLEDAI (p?=?0.350 and p?=?0.417). Erythrocyte sedimentation rate and serum IL-12 were reduced (p?=?0.008 and p?=?0.058); while serum IL-13 was increased by fish oil supplementation (p?=?0.033). Conclusions In this randomized, placebo-controlled 6-month trial, SLE patients randomized to fish oil supplementation demonstrated improvement in their PGA, RAND SF-36, and some circulating inflammatory markers. Trial registration ClinicalTrials.gov Identifier: NCT02021513 (registered 13 December 2013).
机译:简介最近对系统性红斑狼疮(SLE)患者的血清进行了代谢组学筛选,发现减少了抗氧化剂和能量生成底物。这些代谢改变可能是SLE最常见的特征之一-疲劳。代谢组学研究还指出,ω-3脂肪酸含量降低,这是一种强大的抗氧化剂。此缺陷可能与SLE中的氧化应激,炎症,疾病活动和疲劳有关。在其他研究中,已证明在SLE中使用鱼油补充omega-3脂肪酸可减少氧化应激。这项研究的目的是评估鱼油补充剂对疲劳,生活质量和疾病活动性临床指标的影响,作为一项随机临床试验的一部分。方法将门诊招募的50例SLE患者按1:1的比例随机分配鱼油补充剂或橄榄油安慰剂,并使其治疗组不知情。在基线和治疗6个月后,完成了RAND短表格36(RAND SF-36),疲劳严重程度量表(FSS),SLE疾病活动指数(SLEDAI)和医师全球评估(PGA)。还收集血清用于可溶性介质分析。结果32名患者完成了研究。与安慰剂组相比,鱼油组中的PGA显着改善(p≥0.015)。 RAND SF-36的能量/疲劳和情绪健康分数显示出改善趋势(p?=?0.092和0.070)。在FSS和SLEDAI中没有观察到明显的差异(p≤0.350和p≤0.417)。红细胞沉降率和血清IL-12降低(p = 0.008和p = 0.058);补充鱼油可增加血清IL-13水平(p = 0.033)。结论在这项随机,安慰剂对照的为期6个月的试验中,随机分组补充鱼油的SLE患者表现出其PGA,RAND SF-36和某些循环炎症标记物的改善。试用注册ClinicalTrials.gov标识符:NCT02021513(2013年12月13日注册)。

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