Literature DB >> 25149705

Coenzyme Q10 benefits symptoms in Gulf War veterans: results of a randomized double-blind study.

Beatrice A Golomb1, Matthew Allison, Sabrina Koperski, Hayley J Koslik, Sridevi Devaraj, Janis B Ritchie.   

Abstract

We sought to assess whether coenzyme Q10 (CoQ10) benefits the chronic multisymptom problems that affect one-quarter to one-third of 1990-1 Gulf War veterans, using a randomized, double-blind, placebo-controlled study. Participants were 46 veterans meeting Kansas and Centers for Disease Control criteria for Gulf War illness. Intervention was PharmaNord (Denmark) CoQ10 100 mg per day (Q100), 300 mg per day (Q300), or an identical-appearing placebo for 3.5 ± 0.5 months. General self-rated health (GSRH), the primary outcome, differed across randomization arms at baseline, and sex significantly predicted GSRH change, compelling adjustment for baseline GSRH and prompting sex-stratified analysis. GSRH showed no significant benefit in the combined-sex sample. Among males (85% of participants), Q100 significantly benefited GSRH versus placebo and versus Q300, providing emphasis on Q100. Physical function (summary performance score, SPS) improved on Q100 versus placebo. A rise in CoQ10 approached significance as a predictor of improvement in GSRH and significantly predicted SPS improvement. Among 20 symptoms each present in half or more of the enrolled veterans, direction-of-difference on Q100 versus placebo was favorable for all except sleep problems; sign test 19:1, p=0.00004) with several symptoms individually significant. Significance for these symptoms despite the small sample underscores large effect sizes, and an apparent relation of key outcomes to CoQ10 change increases prospects for causality. In conclusion, Q100 conferred benefit to physical function and symptoms in veterans with Gulf War illness. Examination in a larger sample is warranted, and findings from this study can inform the conduct of a larger trial.

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Year:  2014        PMID: 25149705     DOI: 10.1162/NECO_a_00659

Source DB:  PubMed          Journal:  Neural Comput        ISSN: 0899-7667            Impact factor:   2.026


  22 in total

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3.  Neurochemical and neuroinflammatory perturbations in two Gulf War Illness models: Modulation by the immunotherapeutic LNFPIII.

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Review 4.  Gulf War Illness: Mechanisms Underlying Brain Dysfunction and Promising Therapeutic Strategies.

Authors:  Brandon Dickey; Leelavathi N Madhu; Ashok K Shetty
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5.  Mitochondrial dysfunction in Gulf War illness revealed by 31Phosphorus Magnetic Resonance Spectroscopy: a case-control study.

Authors:  Hayley J Koslik; Gavin Hamilton; Beatrice A Golomb
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9.  Neuroimmune mechanisms of cognitive impairment in a mouse model of Gulf War illness.

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10.  Epigenetic impacts of stress priming of the neuroinflammatory response to sarin surrogate in mice: a model of Gulf War illness.

Authors:  David G Ashbrook; Benjamin Hing; Lindsay T Michalovicz; Kimberly A Kelly; Julie V Miller; Wilfred C de Vega; Diane B Miller; Gordon Broderick; James P O'Callaghan; Patrick O McGowan
Journal:  J Neuroinflammation       Date:  2018-03-17       Impact factor: 8.322

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