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Orange juice-derived flavanone and phenolic metabolites do not acutely affect cardiovascular risk biomarkers: a randomized, placebo-controlled, crossover trial in men at moderate risk of cardiovascular disease.

Identifieur interne : 000181 ( PubMed/Corpus ); précédent : 000180; suivant : 000182

Orange juice-derived flavanone and phenolic metabolites do not acutely affect cardiovascular risk biomarkers: a randomized, placebo-controlled, crossover trial in men at moderate risk of cardiovascular disease.

Auteurs : Manuel Y. Sch R ; Peter J. Curtis ; Sara Hazim ; Luisa M. Ostertag ; Colin D. Kay ; John F. Potter ; Aedín Cassidy

Source :

RBID : pubmed:25788001

English descriptors

Abstract

Epidemiologic data suggest inverse associations between citrus flavanone intake and cardiovascular disease (CVD) risk. However, insufficient randomized controlled trial data limit our understanding of the mechanisms by which flavanones and their metabolites potentially reduce cardiovascular risk factors.

DOI: 10.3945/ajcn.114.104364
PubMed: 25788001

Links to Exploration step

pubmed:25788001

Le document en format XML

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<term>Cardiovascular System (drug effects)</term>
<term>Cardiovascular System (metabolism)</term>
<term>Chromatography, High Pressure Liquid</term>
<term>Citrus sinensis (chemistry)</term>
<term>Cross-Over Studies</term>
<term>Dietary Supplements</term>
<term>Hesperidin (administration & dosage)</term>
<term>Hesperidin (blood)</term>
<term>Humans</term>
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<term>Middle Aged</term>
<term>Phenols (administration & dosage)</term>
<term>Phenols (blood)</term>
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<term>Biomarkers</term>
<term>Hesperidin</term>
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<front>
<div type="abstract" xml:lang="en">Epidemiologic data suggest inverse associations between citrus flavanone intake and cardiovascular disease (CVD) risk. However, insufficient randomized controlled trial data limit our understanding of the mechanisms by which flavanones and their metabolites potentially reduce cardiovascular risk factors.</div>
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<DateCreated>
<Year>2015</Year>
<Month>5</Month>
<Day>2</Day>
</DateCreated>
<DateCompleted>
<Year>2015</Year>
<Month>07</Month>
<Day>28</Day>
</DateCompleted>
<DateRevised>
<Year>2016</Year>
<Month>10</Month>
<Day>19</Day>
</DateRevised>
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<ISSN IssnType="Electronic">1938-3207</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>101</Volume>
<Issue>5</Issue>
<PubDate>
<Year>2015</Year>
<Month>May</Month>
</PubDate>
</JournalIssue>
<Title>The American journal of clinical nutrition</Title>
<ISOAbbreviation>Am. J. Clin. Nutr.</ISOAbbreviation>
</Journal>
<ArticleTitle>Orange juice-derived flavanone and phenolic metabolites do not acutely affect cardiovascular risk biomarkers: a randomized, placebo-controlled, crossover trial in men at moderate risk of cardiovascular disease.</ArticleTitle>
<Pagination>
<MedlinePgn>931-8</MedlinePgn>
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<ELocationID EIdType="doi" ValidYN="Y">10.3945/ajcn.114.104364</ELocationID>
<Abstract>
<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Epidemiologic data suggest inverse associations between citrus flavanone intake and cardiovascular disease (CVD) risk. However, insufficient randomized controlled trial data limit our understanding of the mechanisms by which flavanones and their metabolites potentially reduce cardiovascular risk factors.</AbstractText>
<AbstractText Label="OBJECTIVE" NlmCategory="OBJECTIVE">We examined the effects of orange juice or a dose-matched hesperidin supplement on plasma concentrations of established and novel flavanone metabolites and their effects on cardiovascular risk biomarkers in men at moderate CVD risk.</AbstractText>
<AbstractText Label="DESIGN" NlmCategory="METHODS">In an acute, randomized, placebo-controlled crossover trial, 16 fasted participants (aged 51-69 y) received orange juice or a hesperidin supplement (both providing 320 mg hesperidin) or control (all matched for sugar and vitamin C content). At baseline and 5 h postintake, endothelial function (primary outcome), blood pressure, arterial stiffness, cardiac autonomic function, platelet activation, and NADPH oxidase gene expression and plasma flavanone metabolites were assessed. Before each intervention, a diet low in flavonoids, nitrate/nitrite, alcohol, and caffeine was followed, and a standardized low-flavonoid evening meal was consumed.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Orange juice intake significantly elevated mean ± SEM plasma concentrations of 8 flavanone (1.75 ± 0.35 μmol/L, P < 0.0001) and 15 phenolic (13.27 ± 2.22 μmol/L, P < 0.0001) metabolites compared with control at 5 h postconsumption. Despite increased plasma flavanone and phenolic metabolite concentrations, cardiovascular risk biomarkers were unaltered. After hesperidin supplement intake, flavanone metabolites were not different from the control, suggesting altered absorption/metabolism compared with the orange juice matrix.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">After single-dose flavanone intake within orange juice, circulating flavanone and phenolic metabolites collectively reached a concentration of 15.20 ± 2.15 μmol/L, but no effects were observed on cardiovascular risk biomarkers. Longer-duration randomized controlled trials are required to examine previous associations between higher flavanone intakes and improved cardiovascular health and to ascertain the relative importance of food matrix and flavanone-derived phenolic metabolites. This trial was registered at clinicaltrials.gov as NCT01530893.</AbstractText>
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<LastName>Schär</LastName>
<ForeName>Manuel Y</ForeName>
<Initials>MY</Initials>
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<Affiliation>From the Department of Nutrition, Norwich Medical School, University of East Anglia, Norwich, United Kingdom.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Curtis</LastName>
<ForeName>Peter J</ForeName>
<Initials>PJ</Initials>
<AffiliationInfo>
<Affiliation>From the Department of Nutrition, Norwich Medical School, University of East Anglia, Norwich, United Kingdom.</Affiliation>
</AffiliationInfo>
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<LastName>Hazim</LastName>
<ForeName>Sara</ForeName>
<Initials>S</Initials>
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<Affiliation>From the Department of Nutrition, Norwich Medical School, University of East Anglia, Norwich, United Kingdom.</Affiliation>
</AffiliationInfo>
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<ForeName>Luisa M</ForeName>
<Initials>LM</Initials>
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<Affiliation>From the Department of Nutrition, Norwich Medical School, University of East Anglia, Norwich, United Kingdom.</Affiliation>
</AffiliationInfo>
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<LastName>Kay</LastName>
<ForeName>Colin D</ForeName>
<Initials>CD</Initials>
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<Affiliation>From the Department of Nutrition, Norwich Medical School, University of East Anglia, Norwich, United Kingdom.</Affiliation>
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<LastName>Potter</LastName>
<ForeName>John F</ForeName>
<Initials>JF</Initials>
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<Affiliation>From the Department of Nutrition, Norwich Medical School, University of East Anglia, Norwich, United Kingdom.</Affiliation>
</AffiliationInfo>
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<ForeName>Aedín</ForeName>
<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>From the Department of Nutrition, Norwich Medical School, University of East Anglia, Norwich, United Kingdom.</Affiliation>
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<Language>ENG</Language>
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<DataBankName>ClinicalTrials.gov</DataBankName>
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<AccessionNumber>NCT01530893</AccessionNumber>
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<Grant>
<GrantID>BB/I006028/1</GrantID>
<Agency>Biotechnology and Biological Sciences Research Council</Agency>
<Country>United Kingdom</Country>
</Grant>
<Grant>
<GrantID>BB/J004545/1</GrantID>
<Agency>Biotechnology and Biological Sciences Research Council</Agency>
<Country>United Kingdom</Country>
</Grant>
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<PublicationType UI="D016428">Journal Article</PublicationType>
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<ArticleDate DateType="Electronic">
<Year>2015</Year>
<Month>Mar</Month>
<Day>18</Day>
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<Keyword MajorTopicYN="N">flavanones</Keyword>
<Keyword MajorTopicYN="N">flavonoids</Keyword>
<Keyword MajorTopicYN="N">phenolic metabolites</Keyword>
<Keyword MajorTopicYN="N">randomized controlled trial</Keyword>
<Keyword MajorTopicYN="N">vascular function</Keyword>
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<Month>12</Month>
<Day>7</Day>
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<Year>2015</Year>
<Month>2</Month>
<Day>24</Day>
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<Year>2015</Year>
<Month>7</Month>
<Day>29</Day>
<Hour>6</Hour>
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<ArticleId IdType="pii">ajcn.114.104364</ArticleId>
<ArticleId IdType="doi">10.3945/ajcn.114.104364</ArticleId>
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