Bioavailability of Ubiquinone and Ubiquinol in Older Adults

Completed · Phase 1

Conditions studied: Absorption

In brief

Coenzyme Q10 (or CoQ10) is a marketed supplement in US even though it can be synthesized in the body via complicated biochemical pathways. It exists in both reduced and oxidized states, namely ubiquinol and ubiquinone, respectively. It is commonly present in all cell membranes. The main function of CoQ10 is to participate in energy production. Further, the reduced form of CoQ10, ubiquinol, is appreciated as an important lipophilic antioxidant to protect free radical induced damages to DNA, lipid, and proteins. Given that older adults have increased production of free radicals, suboptimal antioxidant defenses toward free radicals, and a decreased capability to replenish utilized CoQ10, CoQ10 supplementation can be one of feasible ways to increase CoQ10 status in order adults. Most supplements available for consumers are in the oxidized form. While the ubiquinol form is also available, whether the reduced form will be more effective to replenish CoQ10 status in older subjects remains to be explored. Thus, investigators aimed to examine whether ubiquinol will be more effectively absorbed in older adults with a low antioxidant defense status. To pursue this aim, investigators will conduct a double blind, randomized, crossover design trail with 5 study visits (1 screening visit and 4 study visits). Ten older men (\>55 y, BMI: 25-5 kg/m2) with a compromised antioxidant defenses will be recruited and complete the trial. Eligible subjects will be randomized to receive 200 mg/d ubiquinol or ubiquinone for 2 weeks with 2-week washout between crossover. Ubiquinol and ubiquinone in plasma and immune cells in blood will be assessed to reveal whether the reduced form, ubiquinol, is more absorbable than the oxidized form, ubiquinone in older adults.

Key facts

Study ID

NCT03020680

Run by

Tufts University

People needed

12

Starts

2016-04-01

Expected to finish

2018-05-17

Last updated by the study team

2019-04-23

Who can join

Age: 56 and older, up to 75. Sex: male. Healthy volunteers: accepted.

You may qualify if…

• Males
• Age: >55 and <76 y
• BMI: ≥25 and <35 kg/m2
• Willing to take the assigned supplement for 4 weeks
• Willing to maintain dietary habit for 6 week
• <1000 µmol/L Fe2+ plasma total antioxidant capacity determined by Ferric Reducing Antioxidant Power and <400 µmol/L total thiol content in plasma

You may not qualify if…

• Regular use of any dietary supplements containing vitamins and minerals; however, subjects who are willing to refrain from the use of these supplements for 1 mo prior to their enrollment and throughout the entire study may be considered eligible; subjects will be excluded if they are taking physician prescribed vitamin and/or mineral supplements
• Use of medications known to affect lipid metabolism
• Gain or loss of ≥5% of body weight in the last 6 mo
• Impaired gastrointestinal, renal, and endocrine functions, diseases, conditions or medications influencing gastrointestinal absorption
• Unusual dietary pattern, including vegan/vegetarian
• Active treatment for cancer of any type longer than 1 year.
• Daily alcoholic intake of more than 14 drinks/week (168 oz. beer, 56 oz. wine, 14 oz. hard liquor)
• Values of standard blood biochemistries are critically abnormal based on study physician's

Where it is running

• Oliver Chen — Boston, Massachusetts, United States

Full record on ClinicalTrials.gov

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