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类风湿性关节炎患者的膳食补充ω-3脂肪酸与萘普生治疗

Dietary omega-3 fatty acid supplementation and naproxen treatment in patients with rheumatoid arthritis.

作者信息

Kjeldsen-Kragh J, Lund J A, Riise T, Finnanger B, Haaland K, Finstad R, Mikkelsen K, Førre O

机构信息

Department of General Practice, University of Oslo, Norway.

出版信息

J Rheumatol. 1992 Oct;19(10):1531-6.

PMID:1464864
Abstract

In a controlled, double blind, clinical trial we tested the effect of dietary omega-3 fatty acid supplementation with and without naproxen and placebo, respectively, in 67 patients with active rheumatoid arthritis. The patients were randomized into 3 groups that received the following treatment: Group 1, corn oil ("placebo omega-3 fatty acids"), 7 g/day for 16 weeks, and naproxen, 750 mg/day for 10 weeks followed by a stepwise reduction to 0 mg/day during the following 3 weeks; Group 2, omega-3 fatty acids, 3.8 g of eicosapentaenoic acid plus 2.0 g of docosahexaenoic acid, and naproxen, 750 mg/day for 16 weeks; and Group 3, omega-3 fatty acids as Group 2 and naproxen as Group 1. At the end of the trial, patients in Group 2 had improved with respect to duration of morning stiffness and global assessment by physician and patient. In Groups 1 and 3 there was a significant deterioration for most of the variables measured. However, for duration of morning stiffness the deterioration was significantly less pronounced in Group 3 compared with Group 1. These effects might be ascribed to the dietary omega-3 fatty acid supplementation.

摘要

在一项对照、双盲临床试验中,我们分别对67例活动性类风湿关节炎患者进行了膳食补充ω-3脂肪酸(同时或不同时服用萘普生及安慰剂)的效果测试。患者被随机分为3组,接受以下治疗:第1组,玉米油(“安慰剂ω-3脂肪酸”),每日7克,共16周,以及萘普生,每日750毫克,共10周,随后在接下来的3周内逐步减至每日0毫克;第2组,ω-3脂肪酸,3.8克二十碳五烯酸加2.0克二十二碳六烯酸,以及萘普生,每日750毫克,共16周;第3组,ω-3脂肪酸同第2组,萘普生同第1组。试验结束时,第2组患者在晨僵持续时间以及医生和患者的整体评估方面均有改善。第1组和第3组中,大多数测量变量均出现显著恶化。然而,对于晨僵持续时间,第3组的恶化程度与第1组相比明显较轻。这些效果可能归因于膳食补充ω-3脂肪酸。

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