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临床试验/NCT04851288
NCT04851288已完成2 期

Mitochondrial-targeted Antioxidant Supplementation for Improving Age-related Vascular Dysfunction in Humans

University of Colorado, Boulder1 个研究点 分布在 1 个国家目标入组 112 人开始时间: 2021年4月2日最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
已完成
入组人数
112
试验地点
1
主要终点
Change from baseline in endothelial function at 3 months

研究概览

简要总结

The majority of cardiovascular diseases (CVD) occur in men and women ≥60 years of age. Vascular dysfunction, including endothelial dysfunction, as assessed by reduced endothelium-dependent dilation (EDD), and stiffening of the large elastic arteries (i.e., aortic and carotid artery stiffening), is a major mechanism of increased risk of CVD in older adults. Excess production of ROS (reactive oxygen species) by mitochondria (mtROS) has emerged as a central feature of vascular oxidative stress with aging and driver of age-related vascular dysfunction. As such, identifying novel strategies to decrease mtROS and improve vascular function, to ultimately reduce the risk of age-related CVD, is an important biomedical objective.

MitoQ is a mitochondria-targeted antioxidant that accumulates at the inner mitochondrial membrane where it is optimally positioned to reduce mtROS. Preclinical findings showed that 4 weeks of oral MitoQ supplementation completely restored EDD in old mice, ameliorated mtROS-associated suppression of EDD, and was associated with reduced arterial mtROS, oxidative stress, and improved mitochondrial health. MitoQ therapy also reduced aortic stiffness in old mice. A recent small pilot study of older adults (n=20) found that supplementation with MitoQ was well-tolerated, improved endothelial function, and reduced plasma levels of oxidized low-density lipoprotein, a circulating biomarker of oxidative stress. Consistent with the preclinical findings, preliminary mechanistic assessments in subsets of subjects from the pilot study suggested that improved endothelial function with MitoQ was mediated by reduced endothelial cell mtROS production, associated reductions in tonic mtROS-related suppression of EDD, and improved mitochondrial health, linked in part to changes in circulating factors in the serum induced by chronic MitoQ supplementation. Lastly, MitoQ reduced aortic stiffness in older adults who exhibited age-related aortic stiffening at baseline.

The investigators are conducting a randomized, placebo-controlled, double-blind clinical trial to establish oral MitoQ (20 mg/day; MitoQ, Ltd.) for 3 months vs. placebo (n=56/group) for improving endothelial function in older men and women (≥60 years), and determine the mechanisms by which MitoQ improves endothelial function. The investigators will also assess the effect of MitoQ on aortic stiffness.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
60 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Age 60 years and over
  • •Ability to provide informed consent
  • •Willing to accept random assignment to condition
  • •Body mass index <40 kg/m2
  • •Weight stable in the prior 3 months (<2 kg weight change) and willing to remain weight stable throughout the study
  • •Free from alcohol dependence or abuse,
  • •Mini-mental stage examination score ≥21

排除标准

  • •Uncontrolled thyroid disease
  • •Regular vigorous aerobic (>6 bouts/week, >60 min/bout at a workload >6 METS)
  • •Blood donation within 8 weeks prior to enrolling in the study

研究组 & 干预措施

MitoQ, 20 mg/day

Experimental

Each MitoQ capsule contains 20 mg of mitoquinol mesylate. Dosage: 20 mg orally per day for 3 months.

干预措施: MitoQ (Dietary Supplement)

Placebo

Placebo Comparator

Matched placebo capsules.

干预措施: Placebo (Dietary Supplement)

结局指标

主要结局

Change from baseline in endothelial function at 3 months

时间窗: 3 months

Brachial artery flow-mediated dilation

次要结局

  • Change from baseline in suppression of endothelial function by mitochondrial oxidative stress at 3 months(3 months)
  • Change from baseline in aortic stiffness at 3 months(3 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Douglas Seals

PI

University of Colorado, Boulder

研究点 (1)

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