Summary
Summary. Mitochondrial dysfunction contributes to the neurodegenerative process in Huntington’s disease (HO). Coenzyme Q10 (CoQ10) enhances mitochondrial complex I activity and may therefore provide a therapeutic benefit in HD. We compared serum CoQ10 levels of previously untreated — and treated HO patients with those of healthy controls. CoQ10 did not significantly (ANCOVA F(dF2,dF55)= 2.57; p = 0.086) differ between all three groups . However, the post hoc analysis showed no significant (p = 0.4) difference between treated HD patients ([CoQ10]: 88.12 [mean] ± 24.44 [SD], [range] 48.75−146.32 [pg/million platelets]) and controls (93.71 ± 20.72, 65.31−157.94), however previously untreated HD patients (70.10 ± 21.12, 38.67−106.14) had marked (p = 0.051) lower CoQ10 results than treated HO patients and controls (p = 0.017). Our results support that CoQ10 supplementation in HO patients may reduce impaired mitochondrial function in HD.
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Andrich, J. et al. (2004). Coenzyme Q10 serum levels in Huntington’s disease. In: Müller, T., Riederer, P. (eds) Focus on Extrapyramidal Dysfunction. Journal of Neural Transmission. Supplementa, vol 68. Springer, Vienna. https://doi.org/10.1007/978-3-7091-0579-5_13
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DOI: https://doi.org/10.1007/978-3-7091-0579-5_13
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