Outcome
    Moderate Evidence

    PQQ for Antioxidant Protection

    PQQ is a redox cofactor with strong laboratory antioxidant credentials and minimal human data.

    Overview

    PQQ is a redox cofactor with strong laboratory antioxidant credentials and minimal human data.

    Verdict

    Insufficient evidence

    How It Works

    PQQ cycles through repeated redox reactions without degrading, quenching reactive oxygen species with high catalytic turnover.

    Dosing & Protocol

    Typical dose

    Recommended dose
    Studied at 20 mg/day; antioxidant outcomes in humans have not been demonstrated
    Expected timeframe
    Not established

    Protocol

    form
    Pyrroloquinoline quinone disodium salt (BioPQQ was used in most trials)
    duration
    Trials ran 8-12 weeks
    co factor
    Evidence is insufficient. PQQ is a genuinely interesting redox cofactor - it can undergo thousands of catalytic redox cycles compared with a few for ascorbate, which is the origin of claims about its antioxidant potency, and in vitro and rodent studies show it reduces oxidative stress markers and protects mitochondria. Human data are sparse: a small study by Harris and colleagues in ten subjects at 0.2 mg/kg reported changes in urinary metabolites and reduced plasma C-reactive protein and IL-6, but this was uncontrolled and tiny. No adequately powered randomised trial has shown meaningful antioxidant effects in humans at the 20 mg/day dose typically sold.
    titration
    Not applicable - no dose has been shown to produce a clinically meaningful antioxidant effect in people
    starting dose
    Not established for this outcome. Human trials used 20 mg/day of PQQ disodium salt, occasionally 40 mg/day

    Evidence

    What the studies say

    In vitro data is striking, but human trials are few and small, reporting inconsistent changes in oxidative stress markers.

    Dietary pyrroloquinoline quinone (PQQ) alters indicators of inflammation and mitochondrial-related metabolism in human subjects

    Score: 4/10
    2013
    crossover
    n=10

    Harris CB, Chowanadisai W, Mishchuk DO +3 more

    PQQ 0.3 mg/kg/day reduced plasma CRP and IL-6 and shifted urinary metabolites consistent with enhanced mitochondrial-related metabolism.

    View source

    Safety

    Caveats

    Antioxidant capacity in a test tube does not predict health benefit, and this is one of the better-established lessons in nutrition research - large trials of beta-carotene, vitamin E and vitamin C at supplemental doses found no benefit and in some cases harm, with beta-carotene increasing lung cancer in smokers. Reactive oxygen species also have necessary signalling roles, including in exercise adaptation, so blanket suppression is not desirable. Safety of PQQ: human trials are short and small, so the long-term safety profile is genuinely unknown - this is a compound with a thin safety database rather than an established one. Reported side effects at 20-40 mg/day include headache, fatigue and sleep disturbance. A rodent study found kidney effects at very high doses, and there is no established upper limit for humans, so doses above the 20 mg/day studied should be avoided. Avoid in pregnancy and breastfeeding, as no safety data exist. No significant drug interactions are documented, but the absence of data is not the same as the absence of risk, and anyone on medication should discuss it. If oxidative stress is the concern, a diet rich in vegetables, fruit, legumes and whole grains has the evidence that isolated antioxidant supplements lack.

    Less likely to help if

    Everyone - no human trial has shown a meaningful antioxidant outcome at the doses sold.

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