Safety, Tolerability and Efficacy of Dietary Supplementation with Concord Grape Juice in Gulf War Veterans with Gulf War Illness: A Phase I/IIA, Randomized, Double-Blind, Placebo-Controlled Trial

被引:12
作者
Helmer, Drew A. [1 ,2 ]
Van Doren, William W. [1 ]
Litke, David R. [1 ,3 ]
Tseng, Chin-Lin [1 ]
Ho, Lap [4 ]
Osinubi, Omowunmi [1 ,5 ]
Pasinetti, Giulio Maria [4 ,6 ]
机构
[1] Vet Affairs New Jersey Healthcare Syst, War Related Illness & Injury Study Ctr, 385 Tremont Ave, E Orange, NJ 07018 USA
[2] Michael E DeBakey VA Med Ctr, Ctr Innovat Qual Effectiveness & Safety, 2002 Holcombe Blvd, Houston, TX 77030 USA
[3] NYU, Sch Med, Dept Rehabil Med, 550 1st Ave, New York, NY 10016 USA
[4] Icahn Sch Med Mt Sinai, 1 Gustave L Levy Pl, New York, NY 10029 USA
[5] Rutgers State Univ, Sch Publ Hlth, Dept Environm & Occupat Hlth, 683 Hoes Lane West, Piscataway, NJ 08854 USA
[6] James J Peters VA Med Ctr, 130 W Kingsbridge Rd, Bronx, NY 10468 USA
关键词
Gulf War veterans; Gulf War illness; dietary polyphenols; concord grape juice; safety; tolerability; cognitive functioning; fatigue; veteran; SYMPTOMS; IDENTIFICATION; INFLAMMATION; RELIABILITY; REVISION; TRAIL;
D O I
10.3390/ijerph17103546
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Approximately 30 percent of U.S. veterans deployed during the Gulf War (1990-1991) have been diagnosed with Gulf War Illness (GWI), a chronic multi-symptom disorder without widely available specific treatments. We investigated whether the consumption of Concord grape juice (CGJ), rich in anti-inflammatory flavonoids, would be tolerated and safe in individuals with GWI and explored improvement in cognitive function and fatigue. Thirty-six veterans with GWI enrolled in a 24-week randomized, double-blind, Phase I/IIA clinical trial to explore safety, tolerability, and feasibility of 16 ounces daily of commercially available CGJ compared to placebo. Participants completed neurocognitive tests and self-reported surveys at baseline, 12 and 24 weeks. Thirty-one participants (86%) completed the study; no dropouts were related to side effects. Thirty participants (83%) documented >= 80% adherence. There were no statistically significant unadjusted differences between CGJ and placebo groups in change in efficacy measures from baseline to endpoint. We employed general linear regression models controlling for baseline differences between groups which indicated statistically significant improvement in the Halstead Category Test-Russell Revised Version (RCAT) at endpoint in the CGJ group compared to placebo (8.4 points, p = 0.04). Other measures of cognitive functioning did not indicate significant improvements in the adjusted analyses (p-values: 0.09-0.32), nor did the fatigue variable (p = 0.67). CGJ was safe and well-tolerated by veterans with GWI. Our data suggest high tolerability and potential benefit from CGJ in veterans with GWI and can be used to inform future studies of efficacy.
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页数:12
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