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Phellodendron and Citrus extracts benefit cardiovascular health in osteoarthritis patients: a double-blind, placebo-controlled pilot study.

Identifieur interne : 000990 ( PubMed/Checkpoint ); précédent : 000989; suivant : 000991

Phellodendron and Citrus extracts benefit cardiovascular health in osteoarthritis patients: a double-blind, placebo-controlled pilot study.

Auteurs : Julius Oben [Cameroun] ; Ebangha Enonchong ; Shil Kothari ; Walter Chambliss ; Robert Garrison ; Deanne Dolnick

Source :

RBID : pubmed:18492265

English descriptors

Abstract

The objective of this clinical study was to assess the potential benefit of a dietary supplement, NP 06-1, on cardiovascular protective properties in overweight and normal weight adults diagnosed with osteoarthritis of the knee.

DOI: 10.1186/1475-2891-7-16
PubMed: 18492265


Affiliations:


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pubmed:18492265

Le document en format XML

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<title xml:lang="en">Phellodendron and Citrus extracts benefit cardiovascular health in osteoarthritis patients: a double-blind, placebo-controlled pilot study.</title>
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<name sortKey="Oben, Julius" sort="Oben, Julius" uniqKey="Oben J" first="Julius" last="Oben">Julius Oben</name>
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<term>Blood Pressure (drug effects)</term>
<term>Body Mass Index</term>
<term>Cardiovascular Diseases (blood)</term>
<term>Cardiovascular Diseases (prevention & control)</term>
<term>Citrus (chemistry)</term>
<term>Dietary Supplements</term>
<term>Double-Blind Method</term>
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<term>Humans</term>
<term>Lipid Metabolism (drug effects)</term>
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<term>Osteoarthritis (blood)</term>
<term>Overweight</term>
<term>Phellodendron (chemistry)</term>
<term>Pilot Projects</term>
<term>Plant Extracts (pharmacology)</term>
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<term>Cardiovascular Diseases</term>
<term>Osteoarthritis</term>
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<term>Phellodendron</term>
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<div type="abstract" xml:lang="en">The objective of this clinical study was to assess the potential benefit of a dietary supplement, NP 06-1, on cardiovascular protective properties in overweight and normal weight adults diagnosed with osteoarthritis of the knee.</div>
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<Day>4</Day>
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<Day>10</Day>
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<Volume>7</Volume>
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<Month>May</Month>
<Day>20</Day>
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<Title>Nutrition journal</Title>
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<ArticleTitle>Phellodendron and Citrus extracts benefit cardiovascular health in osteoarthritis patients: a double-blind, placebo-controlled pilot study.</ArticleTitle>
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<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">The objective of this clinical study was to assess the potential benefit of a dietary supplement, NP 06-1, on cardiovascular protective properties in overweight and normal weight adults diagnosed with osteoarthritis of the knee.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">An 8-week, placebo-controlled, randomized, double-blind study was conducted with four groups, comparing the effects of NP 06-1 to placebo in overweight and normal weight subjects diagnosed with primary osteoarthritis of the knee. NP 06-1 (a combination of two botanical extracts; Phellodendron amurense bark and Citrus sinensis peel) or matching placebo was given in a dose of two capsules (370 mg each) twice daily. The outcome measures reported are lipid levels, weight, BMI, blood pressure and fasting glucose. Analyses of variance were used to compare changes of physiological measures over the trial period and between groups.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Eighty (80) subjects were enrolled and 45 subjects completed the study. No serious adverse events were reported. NP 06-1 administration was associated with a general improvement in lipid levels. Both the overweight and normal weight treatment groups had significant reductions in triglycerides and LDL-cholesterol, as well as a significant increase in HDL-cholesterol compared to their respective control groups. Overall there were decreases in blood pressure in both overweight and normal weight treatment groups compared to respective placebo groups. There was also a significant decrease in fasting glucose levels in the overweight treatment group compared to the start of the study and to the overweight placebo group. There was no change in fasting blood sugar for the normal weight groups. Both overweight and normal weight treatment groups lost a significant amount of weight compared to their respective placebo groups. The overweight treatment group lost an average of 5% body weight after 8 weeks, which was associated with a significant loss in BMI over time.</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">In this pilot study NP 06-1 had a beneficial effect on cardiovascular risk factors; namely lipid levels, blood pressure and fasting glucose levels. Administration of NP 06-1 was also associated with weight loss.</AbstractText>
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<RefSource>J Am Acad Nurse Pract. 2004 Aug;16(8):335-42</RefSource>
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<RefSource>J Agric Food Chem. 2004 May 19;52(10):2879-86</RefSource>
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<CommentsCorrections RefType="Cites">
<RefSource>Atherosclerosis. 2005 Jan;178(1):25-32</RefSource>
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<CommentsCorrections RefType="Cites">
<RefSource>Am J Cardiol. 2005 Aug 22;96(4A):53E-59E</RefSource>
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<CommentsCorrections RefType="Cites">
<RefSource>J Lipid Res. 2006 Jun;47(6):1281-8</RefSource>
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</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Life Sci. 2006 Jun 20;79(4):365-73</RefSource>
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</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Diabetes. 2006 Aug;55(8):2256-64</RefSource>
<PMID Version="1">16873688</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Arthritis Res Ther. 2006;8(4):R127</RefSource>
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</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Arzneimittelforschung. 2007;57(1):26-30</RefSource>
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<RefSource>Ann Rheum Dis. 2007 Apr;66(4):433-9</RefSource>
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<RefSource>J Clin Hypertens (Greenwich). 2008 Jan;10(1 Suppl 1):40-8</RefSource>
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</CommentsCorrections>
<CommentsCorrections RefType="Cites">
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</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Rheumatology (Oxford). 2001 Jul;40(7):779-93</RefSource>
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</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Lipids. 2004 Feb;39(2):143-51</RefSource>
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</CommentsCorrections>
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<RefSource>Nat Med. 2004 Dec;10(12):1344-51</RefSource>
<PMID Version="1">15531889</PMID>
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