Storch Alexander, Jost Wolfgang H, Vieregge Peter, Spiegel Jörg, Greulich Wolfgang, Durner Joachim, Müller Thomas, Kupsch Andreas, Henningsen Henning, Oertel Wolfgang H, Fuchs Gerd, Kuhn Wilfried, Niklowitz Petra, Koch Rainer, Herting Birgit, Reichmann Heinz
Department of Neurology, Technical University of Dresden, Fetscherstrasse 74, 01307 Dresden, Germany.
Arch Neurol. 2007 Jul;64(7):938-44. doi: 10.1001/archneur.64.7.nct60005. Epub 2007 May 14.
Major hallmarks in the pathophysiology of Parkinson disease are cellular energy depletion and oxidative stress leading to cellular dysfunction and death. Coenzyme Q(10) (CoQ(10)) is an electron acceptor bridging mitochondrial complexes I and II/III and a potent antioxidant that consistently partially recovers the function of dopaminergic neurons.
To determine whether nanoparticular CoQ(10) is safe and displays symptomatic effects in patients with midstage Parkinson disease without motor fluctuations.
Multicenter, randomized, double-blind, placebo-controlled, stratified, parallel-group, single-dose trial.
Academic and nonacademic movement disorder clinics.
One hundred thirty-one patients with Parkinson disease without motor fluctuations and a stable antiparkinsonian treatment. Intervention Random assignment to placebo or nanoparticular CoQ(10) (100 mg 3 times a day) for a treatment period of 3 months. Stratification criterion was levodopa treatment.
The subjects underwent evaluation with the Unified Parkinson's Disease Rating Scale (UPDRS) at each visit on a monthly basis. The primary outcome variable was the change of the sum score of the UPDRS parts II and III between the baseline and 3-month visits.
One hundred thirty-one subjects were randomized according to the protocol. The mean changes of the sum UPDRS parts II/III score were -3.69 for the placebo group and -3.33 for the CoQ(10) group (P = .82). Statistical analysis according to the stratification did not result in significant changes of the primary outcome variable. No secondary outcome measure showed a significant change between the placebo group and the CoQ(10) group. The frequency and quality of adverse events were similar in both treatment groups.
Nanoparticular CoQ(10) at a dosage of 300 mg/d is safe and well tolerated and leads to plasma levels similar to 1200 mg/d of standard formulations. Add-on CoQ(10) does not display symptomatic effects in midstage Parkinson disease.
帕金森病病理生理学的主要特征是细胞能量耗竭和氧化应激,导致细胞功能障碍和死亡。辅酶Q(10)(CoQ(10))是连接线粒体复合体I和II/III的电子受体,也是一种有效的抗氧化剂,能持续部分恢复多巴胺能神经元的功能。
确定纳米颗粒CoQ(10)对无运动波动的中期帕金森病患者是否安全并具有症状改善作用。
多中心、随机、双盲、安慰剂对照、分层、平行组单剂量试验。
学术和非学术性运动障碍诊所。
131例无运动波动且帕金森病治疗稳定的患者。干预措施:随机分为安慰剂组或纳米颗粒CoQ(10)组(每日3次,每次100mg),治疗期为3个月。分层标准为左旋多巴治疗情况。
受试者每月就诊时均接受统一帕金森病评定量表(UPDRS)评估。主要结局变量是基线访视和3个月访视之间UPDRS第II部分和第III部分总分的变化。
131名受试者按方案随机分组。安慰剂组UPDRS第II/III部分总分的平均变化为-3.69,CoQ(10)组为-3.33(P = 0.82)。根据分层进行的统计分析未导致主要结局变量有显著变化。安慰剂组和CoQ(10)组之间的次要观察指标均未显示出显著变化。两个治疗组不良事件的频率和性质相似。
剂量为300mg/d的纳米颗粒CoQ(10)安全且耐受性良好,血浆水平与标准制剂1200mg/d相似。添加CoQ(10)对中期帕金森病无症状改善作用。