Evidence map›Paper›PMID 23806384›Full record

Trial reportFree radical biology & medicine2013

Antiplatelet effects of dietary nitrate in healthy volunteers: involvement of cGMP and influence of sex.

Shanti Velmurugan, Vikas Kapil, Suborno M Ghosh, Sheridan Davies, Andrew McKnight, Zainab Aboud, Rayomand S Khambata, Andrew J Webb, Alastair Poole, Amrita Ahluwalia

Erratum issued Registry-linked trialOpen access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Free radical biology & medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT06375694 (Oral Probiotic Effect on Dietary Nitrate to Plasma Nitrite Production), which is not on this map. Cited by 57 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 3 pooled it
7.9field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT06375694 naunknown statusnot on this mapstarted 2024, after this paper: background citation

Oral Probiotic Effect on Dietary Nitrate to Plasma Nitrite Production

TypeinterventionalSponsorWake Forest UniversityRan2024 to 2025Enrolled20ConditionsHypertension, Cardiovascular Diseases, DiabetesArmsHerbiotics Oral + Ent Probiotic, Placebo
3 · Its place in the literature

Who cites it

57 citing papers in PubMed, 3 syntheses or guidelines pooled it, 113 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 1 country.

Shanti VelmuruganCentre of Clinical Pharmacology, William Harvey Research Institute, Barts NIHR Cardiovascular Biomedical Research Unit, Queen Mary University of London, Charterhouse Square, London EC1M 6BQ.
Vikas KapilCentre of Clinical Pharmacology, William Harvey Research Institute, Barts NIHR Cardiovascular Biomedical Research Unit, Queen Mary University of London, Charterhouse Square, London EC1M 6BQ.
Suborno M GhoshCentre of Clinical Pharmacology, William Harvey Research Institute, Barts NIHR Cardiovascular Biomedical Research Unit, Queen Mary University of London, Charterhouse Square, London EC1M 6BQ.
Sheridan DaviesCentre of Clinical Pharmacology, William Harvey Research Institute, Barts NIHR Cardiovascular Biomedical Research Unit, Queen Mary University of London, Charterhouse Square, London EC1M 6BQ.
Andrew McKnightCentre of Clinical Pharmacology, William Harvey Research Institute, Barts NIHR Cardiovascular Biomedical Research Unit, Queen Mary University of London, Charterhouse Square, London EC1M 6BQ.
Zainab AboudCentre of Clinical Pharmacology, William Harvey Research Institute, Barts NIHR Cardiovascular Biomedical Research Unit, Queen Mary University of London, Charterhouse Square, London EC1M 6BQ.
Rayomand S KhambataCentre of Clinical Pharmacology, William Harvey Research Institute, Barts NIHR Cardiovascular Biomedical Research Unit, Queen Mary University of London, Charterhouse Square, London EC1M 6BQ.
Andrew J WebbCentre of Clinical Pharmacology, William Harvey Research Institute, Barts NIHR Cardiovascular Biomedical Research Unit, Queen Mary University of London, Charterhouse Square, London EC1M 6BQ.
Alastair PooleSchool of Physiology and Pharmacology, University of Bristol, Medical Sciences Building, University Walk, Bristol BS8 1TD, UK.
Amrita AhluwaliaCentre of Clinical Pharmacology, William Harvey Research Institute, Barts NIHR Cardiovascular Biomedical Research Unit, Queen Mary University of London, Charterhouse Square, London EC1M 6BQ. Electronic address: a.ahluwalia@qmul.ac.uk.
Queen Mary University of London · GBWilliam Harvey Research Institute · GBUniversity of Bristol · GB

Funding

British Heart Foundation FS/11/41/28749Medical Research Council
6 · The paper itself

Abstract

Ingestion of vegetables rich in inorganic nitrate has emerged as an effective method, via the formation of a nitrite intermediate, for acutely elevating vascular NO levels. As such a number of beneficial effects of dietary nitrate ingestion have been demonstrated including the suggestion that platelet reactivity is reduced. In this study we investigated whether inorganic nitrate supplementation might also reduce platelet reactivity in healthy volunteers and have determined the mechanisms involved in the effects seen. We conducted two randomised crossover studies each in 24 (12 of each sex) healthy subjects assessing the acute effects of dietary nitrate (250 ml beetroot juice) or potassium nitrate capsules (KNO3, 8 mmol) vs placebo control on platelet reactivity. Inorganic nitrate ingested either from a dietary source or via supplementation raised circulating nitrate and nitrite levels in both sexes and attenuated ex vivo platelet aggregation responses to ADP and, albeit to a lesser extent, collagen but not epinephrine in male but not female volunteers. These inhibitory effects were associated with a reduced platelet P-selectin expression and elevated platelet cGMP levels. In addition, we show that nitrite reduction to NO occurs at the level of the erythrocyte and not the platelet. In summary, our results demonstrate that inorganic nitrate ingestion, whether via the diet or through supplementation, causes a modest decrease in platelet reactivity in healthy males but not females. Our studies provide strong support for further clinical trials investigating the potential of dietary nitrate as an adjunct to current antiplatelet therapies to prevent atherothrombotic complications. Moreover, our observations highlight a previously unknown sexual dimorphism in platelet reactivity to NO and intimate a greater dependence of males on the NO-soluble guanylate cyclase pathway in limiting thrombotic potential.

Indexed as

AdolescentAdultBeta vulgarisBlood PlateletsCardiovascular DiseasesCollagenCross-Over StudiesCyclic GMPDietDietary SupplementsEpinephrineErythrocytesFemaleGuanylate CyclaseHumansMaleCollagenCyclic GMPEpinephrineGuanylate CyclaseNitratesNitric OxidePlatelet Aggregation InhibitorsPotassium Compoundspotassium nitrateP-Selectin3-isobutyl-1-methylxanthineblood pressureBPcGMPIBMXInorganic nitratelight transmission aggregometryLTANitritePBSphosphate-buffered salinePlateletplatelet-poor plasmaplatelet-rich plasmaPPPPRPspermine-NONOate.Sper-NO

Identifiers

PMID23806384
PMCPMC3878381
OpenAlexW2028916136

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.