University of Colorado Boulder
Boulder, Colorado, 80309, United States
NCT Number: NCT04851288
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.
This study is active but is not currently recruiting participants.
60 year and older
All sexes
Interventional
Phase 2
Boulder, Colorado, 80309, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
MitoQ is a biochemically modified form of ubiquinol
Other names: Mitoquinol
Each placebo capsule contains inert excipient and is identical in appearance
Time frame: 3 months
Brachial artery flow-mediated dilation
Time frame: 3 months
Change in brachial artery flow-mediated dilation with acute, supratherapeutic MitoQ (160mg)
Time frame: 3 months
Carotid-femoral pulse wave velocity
Time frame: 3 months
Endothelial cell whole-cell (CellROX) and mitochondria-specific (MitoSOX) reactive oxygen species levels after treatment with serum from subjects
Time frame: 3 months
Endothelial cell protein expression of nitrotyrosine and Fis1
Time frame: 3 months
Carotid artery beta-stiffness index
Time frame: 3 months
Oxidized LDL levels in blood
Time frame: 3 months
Change in middle cerebral artery blood velocity in response to hypercapnia
Time frame: 3 months
Assessed as the change in cerebrovascular reactivity to hypercapnia following administration of a supratherapeutic dose of MitoQ known to scavenge mitochondrial reactive oxygen species
Time frame: 3 months
Dilation of the internal carotid artery in response to hypercapnia
Time frame: 3 months
Assessed as the change in internal carotid artery dilation to hypercapnia following administration of a supratherapeutic dose of MitoQ known to scavenge mitochondrial reactive oxygen species
Time frame: 3 months
Total cerebral blood flow
Time frame: 3 months
Brain endothelial cell acetylcholine-induced nitric oxide production (DAR-4M-AM) and mitochondria-specific (MitoSOX) reactive oxygen species levels after treatment with serum from subjects
University of Colorado, Boulder
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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