Oxidized proportion of muscle coenzyme Q10 increases with age in healthy children
Petra Niklowitz1, Jürgen Scherer1, Frank Döring2
1Children's Hospital Datteln, Witten-Herdecke University, Datteln, Germany.
Insights
Plasma Coenzyme Q10 (CoQ10) levels do not reflect muscle CoQ10 status in children. Muscle CoQ10 shows an age-related shift towards oxidation, establishing new reference values for diagnosing deficiency.
Area of Science:
- Biochemistry
- Pediatric Medicine
- Nutritional Science
Background:
- Coenzyme Q10 (CoQ10) is vital for mitochondrial energy production and acts as an antioxidant.
- CoQ10 deficiency can impair ATP synthesis and increase oxidative stress.
- Plasma CoQ10 levels may not accurately indicate deficiency, especially in children.
Purpose of the Study:
- To investigate the relationship between plasma and muscle CoQ10 concentration and redox status in healthy children.
- To establish reference values for muscle CoQ10 in pediatric populations.
- To explore age-related changes in CoQ10 status during childhood.
Main Methods:
- High-performance liquid chromatography (HPLC) with electrochemical detection was used.
- CoQ10 concentration and redox status were analyzed in plasma and muscle tissue.
- 140 healthy children aged 0.8-15.3 years were included.
Main Results:
- No correlation was found between plasma and muscle CoQ10 concentration or redox status.
- Muscle CoQ10 exhibited a significant age-related increase in oxidation.
- Reference values for muscle CoQ10 concentration and redox status were established for children.
Conclusions:
- Plasma CoQ10 is not a reliable biomarker for muscle CoQ10 status in children.
- The observed age-related redox shift in muscle indicates evolving antioxidant defenses.
- Established reference values are crucial for diagnosing pediatric CoQ10 deficiency.
Background:
Coenzyme Q10 (CoQ10) is synthesized in most human tissues, with high concentration in the skeletal muscle. CoQ10 functions in the mitochondrial respiratory chain and serves as a potent liphophilic antioxidant in membranes. CoQ10 deficiency impairs mitochondrial ATP synthesis and increases oxidative stress. It has been suggested that plasma CoQ10 status is not a robust proxy for the diagnosis of CoQ10 deficiency.
Methods:
We determined the concentration and redox-status of CoQ10 in plasma and muscle tissue from 140 healthy children (0.8-15.3 y) by high-performance liquid chromatography (HPLC) with electrochemical detection.
Results:
There was no correlation between CoQ10 concentration or redox status between plasma and muscle tissue. Lipid-related CoQ10 plasma concentrations showed a negative correlation with age (Spearman's, P ≤ 0.02), but there was no significant age-related correlation for muscle concentration. In muscle tissue, we found a distinct shift in the redox status in favor of the oxidized proportion with increasing age (Spearman's, P ≤ 0.00001). Reference values for muscle CoQ10 concentration (40.5 ± 12.2 pmol/mg wet tissue) and CoQ10 redox status (46.8 ± 6.8% oxidized within total) were established for healthy children.
Conclusion:
The age-related redox shift in muscle tissue suggests changes in antioxidative defense during childhood. The reference values established here provide a necessary prerequisite for diagnosing early CoQ10 deficiency.
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