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| Name | Class |
|---|---|
| National Polytechnic Institute, Mexico | OTHER |
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Several epidemiological studies have shown that premenopausal women are protected from cardiovascular diseases compared to men of the same age; however, after menopause (postmenopause), the cardiovascular risk increases progressively to equal the cardiovascular risk of men of the same age group. In addition, in Mexico, the incidence of women entering the postmenopausal stage with overweight or obesity increases each year. Therefore, it is essential to generate public initiatives to reduce the metabolic and physiological alterations caused by overweight/obesity and improve postmenopausal women's health and quality of life. Flavonoids are bioactive compounds that have been shown to reduce the cardiovascular risk associated with obesity since they participate in the regulation of lipid metabolism, improve body composition, reduce oxidative stress and inflammation; Therefore, our objective is to reduce the cardiovascular risk of postmenopausal women and improve the oxidative and inflammatory state, through oral supplementation with cocoa flavonoids. To do this, an innovative method will be used to assess cardiovascular risk based on knowledge of the type, number, and size of lipoprotein particles and knowing the oxidative and inflammatory state before and after supplementation with cocoa flavonoids.
Some interventions have been carried out to reduce obesity and the incidence of cardio-metabolic pathologies since the foods consumed in the daily diet, directly and indirectly, influence the modulation of metabolic signaling pathways. Flavonoids, nutrients of plant origin, have beneficial effects on health since they can prevent and reduce the impact of overweight/obesity. Significant benefits have also been shown in blood pressure, platelet reactivity, HDL cholesterol, LDL cholesterol, insulin sensitivity, and prostaglandin metabolism, improving health in patients with chronic diseases related to metabolic disorders and OS.
Food rich in flavonoids is cocoa; the plant contains many polyphenols (anthocyanidins, proanthocyanidins, and catechins), concentrated mainly in the pods and seeds, which provides a highly bitter taste. The polyphenols that can be identified in cocoa beans are (-) - epicatechin and, to a lesser extent (+) - catechin, (+) - gallocatechin, and (-) - epigallocatechin.
Polyphenols derived from cocoa are characterized by being powerful antioxidants, by having effects on muscle and fat tissue: inducing the darkening of adipocytes (change from white adipocytes (fat deposit) to beige adipocytes; promoting mitochondrial biogenesis; increasing the expression of vital thermogenic genes and upstream regulators of fatty acid oxidation; reducing serum TG concentrations; phosphorylating metabolism regulators and acetylating (activating) proteins involved in mitochondrial structure and function. Actions culminate in regulating the metabolic profile, decreasing adipose tissue, increasing muscle mass, and, therefore, decreasing BMI.
There is evidence of the beneficial effects of cocoa polyphenols as antioxidants, improving the lipid profile levels and pro and anti-inflammatory markers. Cocoa is one of the foods of natural origin with high antioxidant capacity due to the tricyclic structure of flavonoids. The compounds act as electron donors and stabilize free radicals through their aromatic rings with hydroxyl substituents. Cocoa polyphenols have been shown to protect cells from oxidative stress at the membrane level by reducing lipoperoxidation and DNA damage through the chelating action of the catechol group and hydroxyl substituents. Furthermore, cocoa flavonoids inhibit xanthine oxidase, NADPH-oxidase, tyrosine kinases, and protein kinases.
Cocoa polyphenols have been shown to have antioxidant activity that helps counteract the atherosclerotic process by reducing the activation of NADPH oxidase. In addition, to improve the dilation of the arteries in smoking patients with atherosclerosis. The antioxidants in cocoa inhibit LDL oxidation, which is related to delaying atherosclerotic progression by reducing ox-LDL and increasing HDL-c.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Group A (Placebo) | Placebo Comparator | The administration of two capsules of 500 mg orally of placebo (excipient q.s. starch capsule) 1 every 12 hours, for 12 weeks. |
|
| Group B (Flavonoid) | Active Comparator | Two capsules of 500 mg of the flavonoid supplement (whose total flavonoid content is 15 mg/capsule) orally every 12 hours for 12 weeks. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Placebo of Cocoa flavonoids | Dietary Supplement | Dietary supplement: The administration of two capsules of 500 mg orally of placebo (excipient q.s. starch capsule) 1 every 12 hours, for 12 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Number of participants with Metabolic Syndrome | Metabolic syndrome according to International Diabetes Federation Criteria | Metabolic Syndrome at three months after starting the intervention in each group |
| Measure | Description | Time Frame |
|---|---|---|
| Carbonylation of proteins | Marker of oxidative stress measured by spectrophotometry expressed as pmol PC/mg protein | Three months after starting the intervention in each group |
| Malondialdehyde |
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Inclusion Criteria:
Exclusion Criteria:
Women with an early postmenopause diagnosis
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Araceli Montoya-Estrada, PhD | Contact | 525555209900 | 307 | ara_mones@hotmail.com |
| Nayelli Najéra, PhD | Contact | 525557296000 | 62820 | nnajerag@ipn.mx |
| Name | Affiliation | Role |
|---|---|---|
| Araceli Montoya-Estrada, PhD | Instituto Nacional de PerinatologĂa Isidro Espinosa de los Reyes | Principal Investigator |
| Nayelli Najera, PhD | Instituto Politecnico Nacional | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Instituto Nacional de PerinatologĂa Isidro Espinosa de los Reyes | Mexico City | 11000 | Mexico |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 27070643 | Background | Goya L, Martin MA, Sarria B, Ramos S, Mateos R, Bravo L. Effect of Cocoa and Its Flavonoids on Biomarkers of Inflammation: Studies of Cell Culture, Animals and Humans. Nutrients. 2016 Apr 9;8(4):212. doi: 10.3390/nu8040212. | |
| 27552564 | Background | Gutierrez-Salmean G, Meaney E, Lanaspa MA, Cicerchi C, Johnson RJ, Dugar S, Taub P, Ramirez-Sanchez I, Villarreal F, Schreiner G, Ceballos G. A randomized, placebo-controlled, double-blind study on the effects of (-)-epicatechin on the triglyceride/HDLc ratio and cardiometabolic profile of subjects with hypertriglyceridemia: Unique in vitro effects. Int J Cardiol. 2016 Nov 15;223:500-506. doi: 10.1016/j.ijcard.2016.08.158. Epub 2016 Aug 8. |
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| ID | Term |
|---|---|
| D024821 | Metabolic Syndrome |
| ID | Term |
|---|---|
| D007333 | Insulin Resistance |
| D006946 | Hyperinsulinism |
| D044882 | Glucose Metabolism Disorders |
| D008659 | Metabolic Diseases |
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Randomized Clinical Trial
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Randomized Clinical Trial only the principal investigator is not blinded
| Cocoa flavonoids | Dietary Supplement | Dietary supplement: Two 500 mg capsules of the flavonoid supplement (whose total flavonoid content is 15 mg/capsule) orally every 12 hours (one in the morning and one at night) for 12 weeks |
|
Marker of oxidative stress measured by spectrophotometry expressed as pmol MDA/mg dry weight
| Three months after starting the intervention in each group |
| Superoxide Dismutase activity | Enzymatic activity measured by Colorimetric Activity Kit expressed as nmol/min/mL | Three months after starting the intervention in each group |
| Catalase activity | Enzymatic activity measured by Colorimetric Activity Kit expressed as nmol/min/mL | Three months after starting the intervention in each group |
| Lipid profile quantification | size of cholesterol (main classes and subclasses of lipoproteins) expressed in large, medium and small) | Three months after starting the intervention in each group |
| IL-4, IL-6, IL10 and TNFa | They will be quantified by ELISA technique expressed in pg/ul | Three months after starting the intervention in each group |
| D009750 |
| Nutritional and Metabolic Diseases |