School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Department of Internal Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Hemodial Int. 2022 Jul;26(3):408-414. doi: 10.1111/hdi.13007. Epub 2022 Feb 3.
Chronic kidney disease-associated pruritus is a common complication in patients with end-stage renal disease. In this study, we have explored the outcome of omega-3 supplementary intake for the treatment of this symptom.
This double-blinded, randomized, crossover study was conducted in two dialysis centers in which 40 hemodialysis patients suffering from pruritus were randomly assigned into two groups (Group A and Group B). Patients in Group A consumed omega-3 capsules for 4 weeks and after a washout period (6 weeks), they took placebo for another 4 weeks. The same was performed in Group B but in the reverse order. Pruritus score was determined at the baseline, Week 4, 10, and 14. Serum levels of prostaglandin E2 were also recorded at the baseline and Week 4.
There was a statistically significant reduction of pruritus score in patients who took the omega-3 fatty acid supplement. The mean pruritus score decreased significantly in both first (-3.41 ± 2.62, p < 0.001) and second (-1.00 ± 1.84, p = 0.04) treatment period after omega-3 treatment; but no significant mean pruritus score difference in placebo group after both intervention periods was observed. The decrease in prostaglandin E2 amount was not statistically significant in the intervention (omega-3) group compared to the placebo group (p = 0.204).
Our observations indicate that omega-3 fatty acids (3 grams per day) have decreasing effects on pruritus. Also, reduction in prostaglandin E2 levels in the omega-3 group did not differ from the changes in the placebo group.
慢性肾脏病相关瘙痒是终末期肾病患者的常见并发症。在这项研究中,我们探讨了ω-3 补充剂治疗该症状的效果。
这是一项在两家透析中心进行的双盲、随机、交叉研究,40 名患有瘙痒的血液透析患者被随机分为两组(A 组和 B 组)。A 组患者连续 4 周服用 ω-3 胶囊,洗脱期(6 周)后再服用 4 周安慰剂。B 组患者则以相反的顺序服用。在基线、第 4、10 和 14 周时测定瘙痒评分。在基线和第 4 周时还记录了前列腺素 E2 的血清水平。
服用 ω-3 脂肪酸补充剂的患者瘙痒评分有显著降低。两组患者的瘙痒评分在首次(-3.41±2.62,p<0.001)和第二次(-1.00±1.84,p=0.04)治疗期均有显著降低;但在安慰剂组,两个干预期后瘙痒评分的平均值均无显著差异。与安慰剂组相比,干预(ω-3)组前列腺素 E2 量的减少无统计学意义(p=0.204)。
我们的观察结果表明,ω-3 脂肪酸(每天 3 克)对瘙痒有减轻作用。此外,ω-3 组前列腺素 E2 水平的降低与安慰剂组的变化无差异。