Abdulrazaq Mozghan, Innes Jacqueline K, Calder Philip C
Human Development and Health Academic Unit, Faculty of Medicine, University of Southampton, Southampton, United Kingdom.
Human Development and Health Academic Unit, Faculty of Medicine, University of Southampton, Southampton, United Kingdom; National Institute for Health Research Southampton Biomedical Research Centre, University Hospital Southampton NHS Foundation Trust and University of Southampton, Southampton, United Kingdom.
Nutrition. 2017 Jul-Aug;39-40:57-66. doi: 10.1016/j.nut.2016.12.003. Epub 2016 Dec 21.
Pain is a significant problem in rheumatoid arthritis (RA) and is associated with prostaglandins derived from the ω-6 polyunsaturated fatty acid (PUFA) arachidonic acid. The ω-3 PUFAs eicosapentaenoic acid and docosahexaenoic acid have been shown to reduce inflammation, with some studies showing clinical improvements in RA. The aim of this systematic review was to investigate the effect of ω-3 PUFAs on arthritic pain.
A systematic literature review of ω-3 PUFAs and pain associated with RA was performed up to December 2015. Randomized controlled trials (RCTs) investigating the effect of ω-3 PUFAs (>2 g/d) on patient or physician assessment of pain, or assessment by both patient and physician, were included. The Cochrane Collaboration's tool for assessing risk for bias was employed. Data for outcomes of interest were extracted and collated for interpretation.
Eighteen RCTs published between 1985 and 2013 involving 1143 patients were included. Dosage of ω-3 PUFAs used was 2.1 to 9.1 g/d, with study durations of 12 to 52 wk. Ten studies supported the hypothesis that there is a reduction in patient or physician assessment of pain associated with RA after intake of ω-3 PUFAs. Eight studies found no statistically significant effect of ω-3 PUFAs on arthritic pain.
ω-3 PUFAs may have a therapeutic role in decreasing pain associated with RA, with doses of 3 to 6 g/d appearing to have a greater effect. Due to the limitations identified in the RCTs included in this review, more research is needed to investigate ω-3 PUFAs in larger populations and over extended periods of time.
疼痛是类风湿关节炎(RA)的一个重要问题,且与源自ω-6多不饱和脂肪酸(PUFA)花生四烯酸的前列腺素有关。ω-3多不饱和脂肪酸二十碳五烯酸和二十二碳六烯酸已被证明可减轻炎症,一些研究表明其对类风湿关节炎有临床改善作用。本系统评价的目的是研究ω-3多不饱和脂肪酸对关节炎疼痛的影响。
截至2015年12月,对ω-3多不饱和脂肪酸与类风湿关节炎相关疼痛进行了系统的文献综述。纳入了研究ω-3多不饱和脂肪酸(>2 g/d)对患者或医生疼痛评估或患者和医生双方评估影响的随机对照试验(RCT)。采用Cochrane协作网的偏倚风险评估工具。提取并整理感兴趣结局的数据以供解读。
纳入了1985年至2013年间发表的18项RCT,涉及1143例患者。使用的ω-3多不饱和脂肪酸剂量为2.1至9.1 g/d,研究持续时间为12至52周。十项研究支持以下假设:摄入ω-3多不饱和脂肪酸后,患者或医生对类风湿关节炎相关疼痛的评估有所减轻。八项研究发现ω-3多不饱和脂肪酸对关节炎疼痛无统计学显著影响。
ω-3多不饱和脂肪酸可能在减轻类风湿关节炎相关疼痛方面具有治疗作用,3至6 g/d的剂量似乎效果更佳。由于本综述纳入的RCT存在局限性,需要更多研究在更大规模人群和更长时间内研究ω-3多不饱和脂肪酸。