A randomized, double-blind, placebo-controlled study of oral coenzyme Q10 to relieve self-reported treatment-related fatigue in newly diagnosed patients with breast cancer.

Glenn J Lesser, Doug Case, Nancy Stark, Susan Williford, Jeff Giguere, L Astrid Garino, Michelle J Naughton, Mara Z Vitolins, Mark O Lively, Edward G Shaw
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Abstract

Background: Coenzyme Q10 (CoQ10) is a common antioxidant supplement with known cardioprotective effects and potential anticancer benefits.

Objectives: We performed a randomized, double-blind, placebo-controlled study of oral CoQ10 in female breast cancer patients with the primary objective of determining CoQ10's effects on self-reported fatigue, depression, and quality of life (QOL). Methods Eligible women with newly diagnosed breast cancer and planned adjuvant chemotherapy were randomized to oral supplements of 300 mg CoQ10 or placebo, each combined with 300 IU vitamin E, divided into 3 daily doses. Treatment was continued for 24 weeks. Blood tests, QOL measures, and levels of plasma CoQ10 and vitamin E were obtained at baseline and at 8, 16, and 24 weeks. Mixed-effects models were used to assess treatment differences in outcomes over time.

Results: Between September 2004 and March 2009, 236 women were enrolled. Treatment arms were well balanced with respect to age (range, 28-85 years), pathologic stage (stage 0, 91%; stage 1, 8%; stage II, 1%), ethnicity (white, 87%; black, 11%; Hispanic, 2%), and planned therapy. Baseline CoQ10 levels in the CoQ10 and placebo arms were 0.70 and 0.73 microg/mL, respectively; the 24-week CoQ10 levels were 1.83 and 0.79 microg/mL, respectively. There were no significant differences between the CoQ10 and placebo arms at 24 weeks for scores on the Profile of Mood States-Fatigue questionnaire (least squares means, 7.08 vs 8.24, P = .257), the Functional Assessment of Chronic Illness Therapy-Fatigue tool (37.6 vs 37.6, P = .965), the Functional Assessment of Cancer Therapy-Breast Cancer instrument (111.9 vs 110.4, P = .577), or the Center for Epidemiologic Studies-Depression scale (11.6 vs 12.3, P = .632).

Conclusions: Supplementation with conventional doses of CoQ10 led to sustained increases in plasma CoQ10 levels but did not result in improved self-reported fatigue or QOL after 24 weeks of treatment.

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一项随机、双盲、安慰剂对照研究,通过口服辅酶Q10缓解新确诊乳腺癌患者自我报告的与治疗相关的疲劳。
背景:辅酶Q10(CoQ10)是一种常见的抗氧化补充剂,具有已知的心脏保护作用和潜在的抗癌功效:我们对女性乳腺癌患者进行了一项口服辅酶Q10的随机、双盲、安慰剂对照研究,主要目的是确定辅酶Q10对自我报告的疲劳、抑郁和生活质量(QOL)的影响。方法 将符合条件的新诊断为乳腺癌并计划接受辅助化疗的女性患者随机分配到 300 毫克 CoQ10 或安慰剂口服补充剂中,每种补充剂均与 300 IU 维生素 E 混合服用,每天分 3 次服用。治疗持续 24 周。在基线、8周、16周和24周时进行血液检测、QOL测量以及血浆CoQ10和维生素E水平的测定。采用混合效应模型评估治疗效果随时间变化的差异:2004年9月至2009年3月期间,236名妇女参加了研究。各治疗组在年龄(28-85 岁)、病理分期(0 期,91%;1 期,8%;II 期,1%)、种族(白人,87%;黑人,11%;西班牙裔,2%)和计划治疗方面非常均衡。辅酶Q10治疗组和安慰剂治疗组的基线辅酶Q10水平分别为0.70和0.73微克/毫升;24周的辅酶Q10水平分别为1.83和0.79微克/毫升。24周时,辅酶Q10治疗组和安慰剂治疗组在情绪状态概况-疲劳问卷(Profile of Mood States-Fatigue questionnaire)评分(最小二乘法均值,7.08 vs 8.24,P = .257)、慢性疾病治疗功能评估-疲劳工具(Functional Assessment of Chronic Illness Therapy-Fatigue tool)评分(37.6 vs 37.6,P = .257)方面无明显差异。6 vs 37.6,P = .965)、癌症治疗功能评估-乳腺癌工具(111.9 vs 110.4,P = .577)或流行病学研究中心-抑郁量表(11.6 vs 12.3,P = .632):结论:补充常规剂量的辅酶Q10可使血浆中的辅酶Q10水平持续上升,但在治疗24周后,自我报告的疲劳程度或QOL并未得到改善。
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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