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辅酶Q10减量用于帕金森病的随机、双盲、安慰剂对照试验性研究

Randomized, double-blind, placebo-controlled pilot trial of reduced coenzyme Q10 for Parkinson's disease.

作者信息

Yoritaka Asako, Kawajiri Sumihiro, Yamamoto Yorihiro, Nakahara Toshiki, Ando Maya, Hashimoto Kazuhiko, Nagase Midori, Saito Yufuko, Hattori Nobutaka

机构信息

Department of Neurology, Juntendo University School of Medicine, Japan; Department of Neurology, Juntendo University Koshigaya Hospital, Japan.

Department of Neurology, Juntendo University School of Medicine, Japan.

出版信息

Parkinsonism Relat Disord. 2015 Aug;21(8):911-6. doi: 10.1016/j.parkreldis.2015.05.022. Epub 2015 May 29.

Abstract

INTRODUCTION

Mitochondrial complex I deficiencies have been found in post-mortem brains of patients with Parkinson's disease (PD). Coenzyme Q10 (CoQ10) is the electron acceptor found in complexes I and II, and is a potent antioxidant. A recent trial of the oxidized form of CoQ10 for PD failed to show benefits; however, the reduced form of CoQ10 (ubiquinol-10) has shown better neuroprotective effects in animal models.

METHODS

Randomized, double-blind, placebo-controlled, parallel-group pilot trials were conducted to assess the efficacy of ubiquinol-10 in Japanese patients with PD. Participants were divided into two groups: PD experiencing wearing off (Group A), and early PD, without levodopa (with or without a dopamine agonist) (Group B). Participants took 300 mg of ubiquinol-10 or placebo per day for 48 weeks (Group A) or 96 weeks (Group B).

RESULTS

In Group A, total Unified Parkinson's Disease Rating Scale (UPDRS) scores decreased in the ubiquinol-10 group (n = 14; mean ± SD [-4.2 ± 8.2]), indicating improvement in symptoms. There was a statistically significant difference (p < 0.05) compared with the placebo group (n = 12; 2.9 ± 8.9). In Group B, UPDRS increased in the ubiquinol-10 group (n = 14; 3.9 ± 8.0), as well as in the placebo group (n = 8; 5.1 ± 10.3).

CONCLUSIONS

This is the first report showing that ubiquinol-10 may significantly improve PD with wearing off, as judged by total UPDRS scores, and that ubiquinol-10 is safe and well tolerated.

摘要

引言

在帕金森病(PD)患者的尸检大脑中发现了线粒体复合物I缺陷。辅酶Q10(CoQ10)是在复合物I和II中发现的电子受体,并且是一种有效的抗氧化剂。最近一项针对PD的氧化形式CoQ10的试验未显示出益处;然而,CoQ10的还原形式(泛醇-10)在动物模型中显示出更好的神经保护作用。

方法

进行了随机、双盲、安慰剂对照、平行组试点试验,以评估泛醇-10对日本PD患者的疗效。参与者分为两组:出现剂末现象的PD患者(A组)和未使用左旋多巴(使用或不使用多巴胺激动剂)的早期PD患者(B组)。参与者每天服用300毫克泛醇-10或安慰剂,持续48周(A组)或96周(B组)。

结果

在A组中,泛醇-10组(n = 14;平均值±标准差[-4.2±8.2])的帕金森病统一评分量表(UPDRS)总分下降,表明症状有所改善。与安慰剂组(n = 12;2.9±8.9)相比,存在统计学显著差异(p < 0.05)。在B组中,泛醇-10组(n = 14;3.9±8.0)以及安慰剂组(n = 8;5.1±10.3)的UPDRS均升高。

结论

这是第一份报告表明,根据UPDRS总分判断,泛醇-10可能显著改善出现剂末现象的PD,并且泛醇-10安全且耐受性良好。

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