RE-AGES: The Effects of Resveratrol on Sirtuins and Apoptosis Biomarkers

Sponsor
InCor Heart Institute (Other)
Overall Status
Recruiting
CT.gov ID
NCT05808387
Collaborator
(none)
80
1
2
39
2.1

Study Details

Study Description

Brief Summary

Cardiovascular diseases (CVD) and neoplasms are the main causes of death in Brazilian women. Coronary artery disease (CAD) and stroke were responsible for approximately 54% of deaths from CVD in this population. In Brazil, cancers were the second cause of death and in 2017 were responsible for 58% of deaths in women. CVD and cancer share some risk factors, and control of these factors is associated with a significant reduction in cancer incidence. These two causes of death, although apparently disparate, share similar lifestyles and health risk factors, suggesting some common pathways and basic molecular networks. In women, the presence of estrogen has protective effects against atherosclerosis and, with the decline in hormone production at menopause, the incidence and prevalence of CAD increase substantially. Although the estrogen pathway is supposed to have a central effect on this increased risk, it is still debated whether other non-estrogenic mechanisms are related, since hormone replacement alone does not reduce cardiovascular events. Sirtuins and soluble advanced glycation product receptors (sRAGE) are associated with increased vascular protection, while the role of apoptosis inhibiting proteins, a pathway linked to increased cancer incidence, is still unclear in the context of atherosclerosis. Resveratrol is a key activator of sirtuins and potentially modulates these metabolic pathways, reducing cardiovascular risk. This randomized, double-blind, parallel, placebo-controlled clinical trial will be carried out in 80 postmenopausal women with CAD to analyze the effect of treatment with resveratrol on serum concentration and gene expression of sirtuins-1 -3, in the serum sRAGE concentration and in the gene expression of apoptosis inhibitory proteins.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Resveratrol
  • Dietary Supplement: Placebo
N/A

Detailed Description

The objective of the study is to evaluate the influence of sirtuins stimulation by resveratrol on inhibitors of apoptosis proteins gene expression of circulation angiogenic cells of postmenopausal women with stable coronary artery disease.

A randomized, double-blind, parallel, placebo-controlled clinical trial in postmenopausal women with CAD submitted to 90 days of daily resveratrol supplementation days of daily supplementation with 1000 mg of resveratrol. Eighty women aged ≥55 years, with overweight or obesity grade 1 (BMI between 25 and 35 kg/m2) will be selected. The participants will be randomized into two groups, control (CON) and resveratrol (RES). After the screening, the participants will undergo the first clinical and laboratory evaluation including lipid and glucose metabolism, inflammatory biomarkers, serum concentrations and gene expression of sirtuin-1 and sirtuin-3 and soluble receptor of advanced glycation end products, and the gene expression of inhibitors of apoptosis proteins.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
80 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Double blind randomized controlled trial, parallel and placebo-controlled.Double blind randomized controlled trial, parallel and placebo-controlled.
Masking:
Double (Participant, Care Provider)
Masking Description:
Participants in the control group will receive capsules identical to those in the intervention group, but with cornstarch. The care provider and the participants do not have the information about which capsules the participant is taking, and do not have access to which groups the patients belong. Statistical analyses will be performed on a blinded database, i.e. without information of which groups the participants belong to. Only the principal investigator of the study has this information.
Primary Purpose:
Treatment
Official Title:
The Effects of Resveratrol on Inhibitors of Apoptosis Proteins, on Soluble Receptors of Advanced Glycation End Products and on Sirtuins-1 and -3 in Postmenopausal Women With Coronary Artery Disease
Actual Study Start Date :
Mar 6, 2023
Anticipated Primary Completion Date :
Jun 5, 2025
Anticipated Study Completion Date :
Jun 5, 2026

Arms and Interventions

Arm Intervention/Treatment
Experimental: Resveratrol

Trans-resveratrol, 1000mg daily for 90 days.

Dietary Supplement: Resveratrol
Trans-resveratrol, 1000 mg daily for 90 days

Placebo Comparator: Control

Starch, 1000mg daily for 90 days.

Dietary Supplement: Placebo
Starch, 1000 mg daily for 90 days

Outcome Measures

Primary Outcome Measures

  1. Sirtuin-1 and sirtuin-3 [90 days]

    Serum concentrations and gene expression

  2. Inhibitors of apoptosis proteins [90 days]

    Gene expression of Bcl-2, XIAP, c-IAP1, and survivin

  3. sRAGE [90 days]

    Serum concentrations and gene expression

Secondary Outcome Measures

  1. Inflammation [90 days]

    Serum concentrations of proinflammatory cytokines

  2. Cardiometabolic risk factors [90 days]

    Lipid and glucometabolic profiles

  3. Anthropometric measures [90 days]

    BMI, skinfold thickness, and body composition

Eligibility Criteria

Criteria

Ages Eligible for Study:
55 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Postmenopausal women;

  • Diagnosed coronary artery disease;

  • Stable coronary disease;

Exclusion Criteria:
  • hypo or hyperthyroidism,

  • rheumatic disease,

  • use of alcohol,

  • hepatic failure,

  • renal failure

  • hormone replacement therapy

  • use of insulin

Contacts and Locations

Locations

Site City State Country Postal Code
1 INCOR- Heart Institute Sao Paulo São Paulo Brazil 05403900

Sponsors and Collaborators

  • InCor Heart Institute

Investigators

  • Principal Investigator: Antonio P Mansur, PhD, InCor Heart Institute

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
ANTONIO DE PADUA MANSUR, Associate Professor, InCor Heart Institute
ClinicalTrials.gov Identifier:
NCT05808387
Other Study ID Numbers:
  • 61901722.6.0000.0068
First Posted:
Apr 11, 2023
Last Update Posted:
Apr 11, 2023
Last Verified:
Mar 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by ANTONIO DE PADUA MANSUR, Associate Professor, InCor Heart Institute
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 11, 2023