MitoQ is commercially available as a dietary supplement and it has been tested as a potential drug in other diseases, but it has never been tested in patients with sickle cell disease. The goal of this research is to study if MitoQ, a molecule that works as an antioxidant by removing potentially damaging agents in a living organism, improves platelet function in patients with sickle cell disease (SCD).
Antioxidant therapies targeted to specific enzymes or compartments may be beneficial in sickle cell anemia (SCA). MitoQ, the most extensively studied mitochondrial-targeted antioxidant, has been shown to be protective against ischemia/reperfusion injury in the heart, endothelial damage due to hypertension and ROS in animal models. MitoQ is commercially available as a dietary supplement to reduce overall oxidative stress and anti-ageing. However, MitoQ has not been tested either as a platelet antagonist or as an endothelial protectant in SCA patients. Investigators propose to conduct a small clinical trial of MitoQ in subjects with SCA to test the hypothesis that MitoQ scavenges platelet mtROS to prevent platelet activation and attenuate vascular dysfunction in SCA. Investigators will test whether MitoQ decreases basal platelet activation in SCD patients and attenuates vascular dysfunction in subjects with SCA. Investigators will administer MitoQ orally to patients and healthy controls for 14 days. Investigators will obtain platelet count, hemolytic markers, platelet mtROS levels and activation markers, clinic BP measurements before and after MitoQ. Adult male and female SCA subjects in steady state (n=10) and 5 healthy African-American volunteers will be recruited after obtaining informed consent.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
OTHER
Masking
NONE
Enrollment
18
Oral; 20mg once a day for 14 days
Magee Women's Hospital
Pittsburgh, Pennsylvania, United States
UPMC Montefiore
Pittsburgh, Pennsylvania, United States
UPMC Presbyterian
Pittsburgh, Pennsylvania, United States
Children's Hospital of Pittsburgh
Pittsburgh, Pennsylvania, United States
Effect of MitoQ on platelet activation markers in subjects with SCA
Change in the percentage of platelet activation markers in blood will be measured (p-selectin, activated GpIIb/IIIa expression, platelet mtROS \[mitochondrial reactive oxygen species\], platelet bioenergetics, mitochondrial Complex V activity)
Time frame: Baseline to 14 days
Effect of MitoQ on vascular dysfunction in subjects with SCA
Changes in both systolic and diastolic blood pressure will be measured during the study period
Time frame: Baseline to 14 days
Effect of MitoQ on hemolysis in subjects with SCA
Changes in plasma free hemoglobin level (mg/dL) will be measured in blood.
Time frame: Baseline to 14 days
Effect of MitoQ on hemolysis in subjects with SCA
Changes in plasma adenosine diphosphate level (micromole/liter) will be measured in blood.
Time frame: Baseline to 14 days
Effect of MitoQ on hemolysis in subjects with SCA
Changes in serum lactate dehydrogenase level (units/L) will be measured in blood.
Time frame: Baseline to 14 days
Treatment related severe adverse events (SAE)
Overall incidence of treatment emergent severe adverse events (SAE)
Time frame: Baseline to 14 days
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Hillman Cancer Center
Pittsburgh, Pennsylvania, United States