Natural Antioxidant Improves Heart Function in FA, Small Study Shows

Natural Antioxidant Improves Heart Function in FA, Small Study Shows
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The natural antioxidant epicatechin significantly improves heart structure and function in young people with Friedreich’s ataxia (FA) over nearly six months of treatment, a small Phase 2 study has shown. 

The findings support the need for larger trials that include control groups to establish whether epicatechin can maintain these benefits, scientists said.

The study, “Safety and Efficacy of (+)‐Epicatechin in Subjects with Friedreich’s Ataxia: A Phase II, Open‐Label, Prospective Study,” was published in the Journal of Inherited Metabolic Disease.  

FA is caused by mutations in the FXN gene, which carries instructions for producing a protein called frataxin. This protein is essential for the normal functioning of small energy-producing structures in the cells known as mitochondria. A lack of frataxin leads to mitochondrial malfunction and to oxidative stress — when the body’s antioxidant defenses are not able to protect against oxidative damage — inducing FA’s clinical symptoms.

Epicatechin is an antioxidant compound found in wine, dark chocolate, and green tea. The Mayo Clinic and Epirium Bio are developing epicatechin as a potential treatment for FA. 

This compound exists in two identical but mirror-image forms: (+)-epicatechin and (-)-epicatechin. 

In animal models, (-)-epicatechin improved cardiac structure and function, eased oxidative stress, and induced regeneration of nerve cells. In clinical trials, (-)-epicatechin promoted mitochondrial growth and function, and improved skeletal muscle regeneration.

Recent research has suggested that the other form, (+)-epicatechin, may be more potent and longer-lasting than (-)-epicatechin. A Phase 1 pilot study (NCT02330276) in 12 healthy individuals and people with prediabetes suggested that (+)-epicatechin is safe. 

Based on these results, a Phase 2 study (NCT02660112) was conducted to test the safety and effectiveness of (+)-epicatechin in young people with FA. 

Ten patients were selected, ages 10 to 22. Mean disease duration was 4.5 years.

Participants received one 25 mg capsule of (+)-epicatechin, taken orally three times per day (75 mg daily) for 12 weeks. Five patients without improvements had doses increased to two 25 mg capsules three times per day (150 mg daily). All patients were treated for 24 weeks in total, or almost six months.

Primary neurological goals were changes from baseline (study start) to 12 and 24 weeks in the Friedreich’s Ataxia Rating Scale (FARS), which is a measure of disease progression. An eight-meter timed walk measured neuromuscular ability.

After 12 and 24 weeks, overall FARS score improved, but did not reach statistical significance compared to baseline. A measure of spinal cord integrity did not show improvements either.

Still, five participants showed score improvements, three experienced benefits assessed with the eight-meter walk, and six had improvements in the nine-hole peg test of finger dexterity

Cardiac goals included changes in the structure and function of the heart, as measured by cardiac MRI and echocardiogram

At 12 weeks, no differences emerged in blood pressure or heart rate compared to baseline. At 24 weeks, treatment led to a significant reduction in diastolic blood pressure (when the heart is relaxed), but not in systolic blood pressure, when the heart is pumping. 

Cardiac MRI showed a significant reduction (improvement) in the mass of the left ventricle at 12 weeks, but not at the end of the study. Mean ejection fraction of the left ventricle, which refers to the amount of blood pumped out with each heartbeat, was unchanged at 12 weeks but increased significantly at 24 weeks. 

Echocardiograms showed no changes except for the thickness of the wall dividing the right and left side of the heart, which increased (worsened) by 1.3 millimeters at 24 weeks. 

No serious adverse events (side effects) or hospitalizations were reported. Three patients experienced nausea and dizziness, which did not affect daily activities. Compounds such as (+)-epicatechin are known to affect blood clotting; however, no impact on blood platelets was found. 

“[(+)-epicatechin] is safe and well tolerated over 24 weeks of treatment in [FA] subjects and resulted in notable improvements in cardiac structure and function in subset of patients,” the scientists wrote. 

“This study may serve as a milestone for large controlled trials of longer duration to establish whether [(+)-epicatechin] sustains positive effect on MRI derived cardiac mass and systolic function in patients with mitochondrial disease,” they added. 

Steve holds a PhD in Biochemistry from the Faculty of Medicine at the University of Toronto, Canada. He worked as a medical scientist for 18 years, within both industry and academia, where his research focused on the discovery of new medicines to treat inflammatory disorders and infectious diseases. Steve recently stepped away from the lab and into science communications, where he’s helping make medical science information more accessible for everyone.
Total Posts: 28

José holds a PhD in Neuroscience from Universidade of Porto, in Portugal. He has also studied Biochemistry at Universidade do Porto and was a postdoctoral associate at Weill Cornell Medicine, in New York, and at The University of Western Ontario in London, Ontario, Canada. His work has ranged from the association of central cardiovascular and pain control to the neurobiological basis of hypertension, and the molecular pathways driving Alzheimer’s disease.

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Steve holds a PhD in Biochemistry from the Faculty of Medicine at the University of Toronto, Canada. He worked as a medical scientist for 18 years, within both industry and academia, where his research focused on the discovery of new medicines to treat inflammatory disorders and infectious diseases. Steve recently stepped away from the lab and into science communications, where he’s helping make medical science information more accessible for everyone.
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