The Safety of Flavocoxid, a Medical Food, in the Dietary Management of Knee Osteoarthritis

被引:27
作者
Morgan, Sarah L. [1 ,4 ]
Baggott, Joseph E. [1 ]
Moreland, Larry [5 ]
Desmond, Renee [2 ,4 ]
Kendrach, Angela C. [3 ,4 ]
机构
[1] Univ Alabama Birmingham, Dept Nutr Sci, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Div Prevent Med, Birmingham, AL 35294 USA
[3] Univ Alabama Birmingham, Div Rheumatol Immunol, Birmingham, AL 35294 USA
[4] Univ Alabama Birmingham, Dept Med, Birmingham, AL 35294 USA
[5] Univ Pittsburgh, Dept Med, Pittsburgh, PA USA
基金
美国国家卫生研究院;
关键词
flavocoxid; knee; medical food; osteoarthritis; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; NITRIC-OXIDE SYNTHASE; SCUTELLARIA-BAICALENSIS; INVENTORY-II; INHIBITORS; CYCLOOXYGENASE-2; DEPRESSION; BAICALIN; EXTRACT; ACACIA;
D O I
10.1089/jmf.2008.0244
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
This study was designed to determine the safety of a medical food, flavocoxid, a proprietary blend of free-B ring flavonoids and flavans from the root of Scutellaria baicalensis (Chinese skullcap) and the bark of Acacia catechu in the dietary management of knee osteoarthritis. The 12-week, randomized, double-blind, placebo-controlled trial in an academic medical center enrolled 59 patients with moderate osteoarthritis of at least one knee who were recruited who were classified as having "below average'' to "a moderately above average cardiovascular risk'' with a Framingham-based scoring tool. Subjects were randomized to flavocoxid 250 mg twice a day versus identical placebo. Safety measures, including recording of adverse events, incidence of serious adverse events, and results of routine laboratory values, were compared between the two groups. There were no major differences in the baseline demographic characteristics of the placebo and flavocoxid groups. With one exception no significant differences were found between the two groups with respect to adverse events by body system, blood pressure, or laboratory values. There was a significantly higher incidence of upper respiratory adverse events in the placebo group (35.4% vs. 5.8%, P = .0003). There were no intra- or inter-group differences in any of the laboratory parameters from study baseline to completion. Thus, flavocoxid is safe when used in a population with "below average'' to "moderately above average cardiovascular risk'' compared to placebo.
引用
收藏
页码:1143 / 1148
页数:6
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