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| ID | Type | Description | Link |
|---|---|---|---|
| R01AG066730 | U.S. NIH Grant/Contract | View source |
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| Name | Class |
|---|---|
| National Institute on Aging (NIA) | NIH |
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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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| MitoQ, 20 mg/day | Experimental | Each MitoQ capsule contains 20 mg of mitoquinol mesylate. Dosage: 20 mg orally per day for 3 months. |
|
| Placebo | Placebo Comparator | Matched placebo capsules. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| MitoQ | Dietary Supplement | MitoQ is a biochemically modified form of ubiquinol |
|
| Measure | Description | Time Frame |
|---|---|---|
| Change from baseline in endothelial function at 3 months | Brachial artery flow-mediated dilation | 3 months |
| Measure | Description | Time Frame |
|---|---|---|
| Change from baseline in suppression of endothelial function by mitochondrial oxidative stress at 3 months | Change in brachial artery flow-mediated dilation with acute, supratherapeutic MitoQ (160mg) | 3 months |
| Change from baseline in aortic stiffness at 3 months |
| Measure | Description | Time Frame |
|---|---|---|
| Change from baseline in serum exposure-induced endothelial cell reactive oxygen species production at 3 months | Endothelial cell whole-cell (CellROX) and mitochondria-specific (MitoSOX) reactive oxygen species levels after treatment with serum from subjects | 3 months |
| Change from baseline in endothelial cell markers of oxidative stress and mitochondrial health from baseline at 3 months |
Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Douglas R Seals | University of Colorado, Boulder | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Colorado Boulder | Boulder | Colorado | 80309 | United States |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 41264372 | Derived | Oh ES, Opoku G, Darvish S, Craighead DH, Ostrow A, Rossman MJ, Steele CN, Struemph T, You Z, Seals DR, Chonchol M, Nowak KL. Sex Differences in Dementia and Mild Cognitive Impairment in Nondialysis CKD. Clin J Am Soc Nephrol. 2026 Mar 1;21(3):389-400. doi: 10.2215/CJN.0000000922. Epub 2025 Nov 20. | |
| 36187760 | Derived | Murray KO, Berryman-Maciel M, Darvish S, Coppock ME, You Z, Chonchol M, Seals DR, Rossman MJ. Mitochondrial-targeted antioxidant supplementation for improving age-related vascular dysfunction in humans: A study protocol. Front Physiol. 2022 Sep 15;13:980783. doi: 10.3389/fphys.2022.980783. eCollection 2022. |
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| ID | Term |
|---|---|
| C429014 | mitoquinone |
| C429015 | mitoquinol |
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| Placebo | Dietary Supplement | Each placebo capsule contains inert excipient and is identical in appearance |
|
Carotid-femoral pulse wave velocity |
| 3 months |
Endothelial cell protein expression of nitrotyrosine and Fis1 |
| 3 months |
| Change from baseline in carotid artery stiffness at 3 months | Carotid artery beta-stiffness index | 3 months |
| Change from baseline in circulating marker of oxidative stress at 3 months | Oxidized LDL levels in blood | 3 months |
| Change from baseline in cerebrovascular reactivity at 3 months | Change in middle cerebral artery blood velocity in response to hypercapnia | 3 months |
| Change from baseline in mitochondrial oxidative stress-mediated suppression of cerebrovascular reactivity at 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 | 3 months |
| Change from baseline in internal carotid artery dilation at 3 months | Dilation of the internal carotid artery in response to hypercapnia | 3 months |
| Change from baseline in mitochondrial oxidative stress-mediated suppression of internal carotid artery dilation at 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 | 3 months |
| Change from baseline in total cerebral blood flow at 3 months | Total cerebral blood flow | 3 months |
| Change from baseline in serum exposure-induced brain endothelial cell nitric oxide and mitochondrial reactive oxygen species production at 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 | 3 months |