Evidence mapPaperPMID 31891746Full record

Trial reportExperimental gerontology2020

Higher dose of resveratrol elevated cardiovascular disease risk biomarker levels in overweight older adults - A pilot study.

R T Mankowski, L You, T W Buford, C Leeuwenburgh, T M Manini, S Schneider, P Qiu, S D Anton

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Experimental gerontology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 3 pooled it
3.6field-weighted citation impact, top 7% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

38 citing papers in PubMed, 3 syntheses or guidelines pooled it, 60 citations in OpenAlex.

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  19. Expected and Unexpected Effects of Pharmacological Antioxidants.International journal of molecular sciences · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

R T MankowskiDepartment of Aging and Geriatric Research, University of Florida, Gainesville, FL, USA. Electronic address: r.mankowski@ufl.edu.
L YouDepartment of Biostatistics, University of Florida, Gainesville, FL, USA.
T W BufordDepartment of Medicine, UAB School of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA.
C LeeuwenburghDepartment of Aging and Geriatric Research, University of Florida, Gainesville, FL, USA.
T M ManiniDepartment of Aging and Geriatric Research, University of Florida, Gainesville, FL, USA.
S SchneiderDepartment of Aging and Geriatric Research, University of Florida, Gainesville, FL, USA.
P QiuDepartment of Biostatistics, University of Florida, Gainesville, FL, USA.
S D AntonDepartment of Aging and Geriatric Research, University of Florida, Gainesville, FL, USA.
University of Florida · USUniversity of Alabama at Birmingham · US

Funding

University of Florida Older Americans Independence Center (OAIC)P30AG028740 · NIA · UNIVERSITY OF FLORIDA · 2022 to 2025
$4.3M
NCATS NIH HHS UL1 TR000064NIA NIH HHS P30 AG028740
6 · The paper itself

Abstract

Older adults are at high risk of developing cardiovascular disease (CVD). Pre-clinical studies indicate that resveratrol (RSV), a polyphenol commonly found in grapes and red wine, may help prevent development of CVD. Based on our previous reports where the 300 mg and 1000 mg doses appeared safe and improved psychomotor function in a dose-dependent manner, our hypothesis was that RSV would reduce biomarkers of CVD risk in overweight, but otherwise healthy older adults and that 1000 mg would lower CVD biomarkers >300 mg. This analysis was performed on samples from older participants (65 years and older) who were randomized to a 90 day RSV treatment with 300 mg (n = 10), 1000 mg (n = 9) or placebo (n = 10). We measured levels of CVD risk biomarkers i.e. oxidized low-density lipoprotein (oxLDL), soluble E-selectin-1 (sE-selectin), soluble Intercellular Adhesion Molecule-1 (sICAM-1), Soluble Vascular Cell Adhesion Molecule-1 (sVCAM-1), total plasminogen activator inhibitor (tPAI-1). Statistical significance was set at p < 0.05. Both sVCAM-1 and tPAI increased significantly more in the 1000 mg vs. 300 mg and placebo groups. Other biomarkers (300 mg vs. 1000 mg vs. placebo: oxLDL, sEselectin-1 and sICAM-1) followed the same trend toward higher levels in the 1000 mg group compared to the 300 mg and placebo groups, without reaching statistical significance. This pilot project suggests that a higher dose of RSV may increase the levels of CVD risk biomarkers in overweight older adults. Given no change in the CVD risk biomarkers in response to a lower dose, future studies should test the effects of different doses of RSV to evaluate potential detrimental effects of higher doses on CVD biomarkers and measures of cardiovascular function in older adults at risk for CVD.

Indexed as

AgedAged, 80 and overBiomarkersCardiovascular DiseasesFemaleHumansIntercellular Adhesion Molecule-1Lipoproteins, LDLMaleOverweightPilot ProjectsResveratrolRisk FactorsVascular Cell Adhesion Molecule-1BiomarkersICAM1 protein, humanIntercellular Adhesion Molecule-1Lipoproteins, LDLoxidized low density lipoproteinResveratrolVascular Cell Adhesion Molecule-1Cardiovascular diseaseClinical trialOlder adultsOverweightPilot studyResveratrol

Identifiers

PMID31891746
PMCPMC8168448
OpenAlexW2998660863

What Socratic holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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 Socratic graph.