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口服铁剂治疗低铁蛋白正常范围不安腿综合征患者的疗效:一项随机、双盲、安慰剂对照研究。

Efficacy of oral iron in patients with restless legs syndrome and a low-normal ferritin: A randomized, double-blind, placebo-controlled study.

机构信息

Department of Medicine, Madigan Army Medical Center, Tacoma, WA 98431-1100, United States.

出版信息

Sleep Med. 2009 Oct;10(9):973-5. doi: 10.1016/j.sleep.2008.11.003. Epub 2009 Feb 18.

DOI:10.1016/j.sleep.2008.11.003
PMID:19230757
Abstract

BACKGROUND AND PURPOSE

Restless Legs Syndrome (RLS) is a primary disorder of sensation that affects sleep and has been associated with iron deficiency. The purpose of this study was to determine if symptomatic RLS patients with low-normal serum ferritin levels benefit from oral iron replacement.

PATIENTS AND METHODS

This was a randomized, placebo-controlled, double-blinded study. Eligible patients were randomized to oral iron therapy vs. appearance-matched placebo and followed over a 12 week period.

RESULTS

Baseline International Restless Leg Scale (IRLS) scores for the treatment (24.8+/-5.72) and placebo (23.0+/-5.03) groups were similar. Baseline ferritin levels for the treatment (40.6+/-15.3ng/ml) and placebo (36.7+/-20.8ng/ml) groups were also similar. After 12 weeks, IRLS scores decreased more in the treatment arm (10.3+/-7.40) than in the placebo arm (1.14+/-5.64), (p=0.01). Ferritin levels increased more in the treatment arm (25.1+/-20.3ng/ml) than in the placebo arm (7.5+/-13.7ng/ml), (p=0.04). We observed a nonsignificant trend toward improved quality of life in the treated patients, (p=0.07).

CONCLUSIONS

This is the first double-blinded, placebo-controlled study to demonstrate statistically significant improvement in RLS symptoms using oral iron therapy in patients with low-normal ferritin. The findings from this study suggest that additional larger randomized placebo-controlled trials of iron as treatment for patients with low-normal ferritin are warranted.

摘要

背景与目的

不宁腿综合征(RLS)是一种主要的感觉障碍,会影响睡眠,并与铁缺乏有关。本研究的目的是确定血清铁蛋白水平低正常的有症状 RLS 患者是否从口服铁补充中获益。

患者与方法

这是一项随机、安慰剂对照、双盲研究。符合条件的患者被随机分配接受口服铁治疗或外观匹配的安慰剂,并在 12 周的时间内进行随访。

结果

治疗组(24.8+/-5.72)和安慰剂组(23.0+/-5.03)的基线国际不宁腿量表(IRLS)评分相似。治疗组(40.6+/-15.3ng/ml)和安慰剂组(36.7+/-20.8ng/ml)的基线铁蛋白水平也相似。12 周后,治疗组的 IRLS 评分下降更明显(10.3+/-7.40),而安慰剂组仅下降 1.14+/-5.64),(p=0.01)。治疗组的铁蛋白水平升高更明显(25.1+/-20.3ng/ml),而安慰剂组仅升高 7.5+/-13.7ng/ml),(p=0.04)。我们观察到治疗患者的生活质量有改善的趋势,但无统计学意义(p=0.07)。

结论

这是第一项使用口服铁治疗低铁蛋白患者的双盲、安慰剂对照研究,表明 RLS 症状有统计学意义的改善。这项研究的结果表明,需要进行更大规模的随机安慰剂对照试验,以评估铁作为低铁蛋白患者的治疗方法。

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