The Administration of Resveratrol and Vitamin C Reduces Oxidative Stress in Postmenopausal Women—A Pilot Randomized Clinical Trial

In postmenopausal women, due to endocrine changes, there is an increase in oxidative stress (OS) that predisposes them to cardiovascular and metabolic alterations. Sixty-one percent of women in this stage require a primary therapeutic strategy to decrease OS. This study aimed to evaluate the effect of resveratrol and vitamin C on OS in postmenopausal women. A randomized, double-blind clinical trial was carried out. Forty-six postmenopausal women with insulin resistance (HOMA-IR > 2.5) were included and divided into three treatment groups: group A: resveratrol, <i>n</i> = 13; group B: resveratrol + vitamin C, <i>n</i> = 15; and group C: vitamin C, <i>n</i> = 14. Between before and after the antioxidants, group B showed a decrease of 33% in lipohydroperoxides (<i>p</i> = 0.02), and malondialdehyde (MDA) decreased by 26% (<i>p</i> = 0.0007), 32% (<i>p</i> = 0.0001), and 38% (<i>p</i> = 0.0001) in groups A-C, respectively. For protein damage, group B is the most representative, with a decrease of 39% (<i>p</i> = 0.0001). For total antioxidant capacity (TAC), there were significant increases of 30% and 28% in groups B and C, respectively. For HOMA-IR, there were no significant differences among the study groups. Supplementation with this combination of antioxidants significantly decreases markers of OS in postmenopausal women. In addition, it increases TAC by up to 30%.

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Publication Details

Journal
Nutrients
Published
2024-11-03
DOI
https://doi.org/10.3390/nu16213775
Citations
11
Primary Topic
Vitamin C and Antioxidants Research
Type
article
Field-Weighted Citation Impact
3.41

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article

The Administration of Resveratrol and Vitamin C Reduces Oxidative Stress in Postmenopausal Women—A Pilot Randomized Clinical Trial

Arturo Flores‐Pliego, José Romo‐Yáñez, Enrique Reyes-Muñoz, Aurora Belmont-Gómez et al.
11 citations
Nutrients
Vitamin C and Antioxidants Research
3.41
article

The Administration of Resveratrol and Vitamin C Reduces Oxidative Stress in Postmenopausal Women—A Pilot Randomized Clinical Trial

Arturo Flores‐Pliego, José Romo‐Yáñez, Enrique Reyes-Muñoz, Aurora Belmont-Gómez, Arturo Arellano‐Eguiluz, Juan Mario Solís-Paredes, Guillermo Federico Ortíz-Luna, Guadalupe León‐Reyes, Aurora Espejel-Núñez, Araceli Montoya-Estrada, Aline Yunuen García-Cortés, Vivian Lopéz-Ugalde
article en
11 citations

Abstract

In postmenopausal women, due to endocrine changes, there is an increase in oxidative stress (OS) that predisposes them to cardiovascular and metabolic alterations. Sixty-one percent of women in this stage require a primary therapeutic strategy to decrease OS. This study aimed to evaluate the effect of resveratrol and vitamin C on OS in postmenopausal women. A randomized, double-blind clinical trial was carried out. Forty-six postmenopausal women with insulin resistance (HOMA-IR > 2.5) were included and divided into three treatment groups: group A: resveratrol, <i>n</i> = 13; group B: resveratrol + vitamin C, <i>n</i> = 15; and group C: vitamin C, <i>n</i> = 14. Between before and after the antioxidants, group B showed a decrease of 33% in lipohydroperoxides (<i>p</i> = 0.02), and malondialdehyde (MDA) decreased by 26% (<i>p</i> = 0.0007), 32% (<i>p</i> = 0.0001), and 38% (<i>p</i> = 0.0001) in groups A-C, respectively. For protein damage, group B is the most representative, with a decrease of 39% (<i>p</i> = 0.0001). For total antioxidant capacity (TAC), there were significant increases of 30% and 28% in groups B and C, respectively. For HOMA-IR, there were no significant differences among the study groups. Supplementation with this combination of antioxidants significantly decreases markers of OS in postmenopausal women. In addition, it increases TAC by up to 30%.

NutrientsVol. 16(21)
Instituto Nacional de Perinatología (MX), National Institute of Genomic Medicine (MX)
Instituto Nacional de Perinatología
Good health and well-being
Openalex Percentile: Top 7%
Vitamin C and Antioxidants Research
3.41
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