The effect of acclydine in chronic fatigue syndrome: a randomized controlled trial.

Gerard K H The, Gijs Bleijenberg, Jos W M van der Meer
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引用次数: 21

Abstract

Objectives: It is unclear whether insulin-like growth factor (IGF) function is involved in the pathophysiology of chronic fatigue syndrome (CFS). Unpublished data and reports in patient organization newsletters suggest that Acclydine, a food supplement, could be effective in the treatment of CFS by increasing biologically active IGF1 levels. Here we aimed to measure the IGF1 and IGF binding protein (IGFBP) 3 status of CFS patients compared to age- and gender-matched neighborhood controls, and to assess the effect of Acclydine on fatigue severity, functional impairment, and biologically active IGF1 level (IGFBP3/IGF1 ratio).

Design: A randomized, placebo-controlled, double-blind clinical trial.

Setting: Radboud University Nijmegen Medical Centre, The Netherlands.

Participants: Fifty-seven adult patients who fulfilled the US Centers for Disease Control and Prevention criteria for CFS. IGF status of 22 CFS patients was compared to that of 22 healthy age- and gender-matched neighborhood control individuals.

Intervention: Acclydine or placebo for 14 wk.

Outcome measures: Outcomes were fatigue severity (Checklist Individual Strength, subscale fatigue severity [CIS-fatigue]), functional impairment (Sickness Impact Profile-8 [SIP-8]), and biologically active IGF1 serum concentrations. Analyses were on an intention-to-treat basis.

Results: There was no difference in IGF status in 22 CFS patients compared to healthy age- and gender-matched control individuals. Treatment with Acclydine did not result in significant differences compared with the placebo group on any of the outcome measures: CIS-fatigue +1.1 (95% CI -4.4 to +6.5, p = 0.70), SIP-8 +59.1 (95% CI -201.7 to +319.8, p = 0.65), and IGFBP3/IGF1 ratio -0.5 (95% CI -2.8 to +1.7, p = 0.63).

Conclusion: We found no differences in IGF1 status in CFS patients compared to healthy matched neighborhood controls. In addition, the results of this clinical trial do not demonstrate any benefit of Acclydine over placebo in the treatment of CFS.

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丙炔在慢性疲劳综合征中的作用:一项随机对照试验。
目的:目前尚不清楚胰岛素样生长因子(IGF)功能是否参与慢性疲劳综合征(CFS)的病理生理过程。未发表的数据和患者组织通讯中的报告表明,Acclydine(一种食品补充剂)可能通过增加生物活性IGF1水平而有效治疗CFS。在这里,我们旨在测量与年龄和性别匹配的社区对照组相比,CFS患者的IGF1和IGF结合蛋白(IGFBP) 3状态,并评估Acclydine对疲劳严重程度、功能损害和生物活性IGF1水平(IGFBP3/IGF1比值)的影响。设计:随机、安慰剂对照、双盲临床试验。地点:荷兰内梅亨大学奈梅亨医学中心。参与者:57名符合美国疾病控制和预防中心CFS标准的成年患者。将22名慢性疲劳综合症患者的IGF状态与22名年龄和性别匹配的健康社区对照个体进行比较。干预:阿克莱因或安慰剂14周。结果测量:结果是疲劳严重程度(检查表个人力量,亚量表疲劳严重程度[cis -疲劳]),功能损害(疾病影响概况-8 [SIP-8])和生物活性IGF1血清浓度。分析以意向治疗为基础。结果:22名CFS患者的IGF状态与年龄和性别匹配的健康对照个体没有差异。与安慰剂组相比,Acclydine治疗在任何结果测量上都没有显著差异:cis -疲劳+1.1 (95% CI -4.4至+6.5,p = 0.70), cip -8 +59.1 (95% CI -201.7至+319.8,p = 0.65), IGFBP3/IGF1比值-0.5 (95% CI -2.8至+1.7,p = 0.63)。结论:我们发现与健康匹配的社区对照相比,CFS患者的IGF1状态没有差异。此外,本临床试验的结果并没有显示阿克莱丁在治疗慢性疲劳综合症方面比安慰剂有任何益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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