Metabolic Syndrome Clinical Trial
Official title:
Effect of Cocoa Polyphenols Supplementation on Cardiovascular Risk of Overweight or Obese Postmenopausal Women: Double Blind Randomized Clinical Trial
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.
Status | Not yet recruiting |
Enrollment | 30 |
Est. completion date | July 1, 2023 |
Est. primary completion date | December 31, 2022 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 50 Years to 60 Years |
Eligibility | Inclusion Criteria: - -According to the STRAW classification (+ 1A + 1B + 1C), women with an early postmenopause diagnosis attend the INPerIER Peri and Postmenopause Clinic. - Age between 50 and 60 years. - who have metabolic syndrome - Who present an altered lipid and glycemic profile that have not reached the critical point of pharmacological treatment (blood glucose between 100 and 125 mg/dl, cholesterol between 200 and 280 mg/dl, triglycerides between 150 and 300 mg/dl, lower HDL 50 mg/dl). - That they are not taking metformin - That they have not taken metformin in the three months before entering the study. - That they are not taking bezafibrate and/or statins. - That they have not taken bezafibrate and/or statins in the three months before entering the study. - No indication for hormone replacement therapy. - That they sign the informed consent. Exclusion Criteria: - Women who present pathologies such as Diabetes Mellitus, rheumatoid arthritis, lupus, neoplasms of any type, HIV, or kidney diseases during the development of the study. - Women who require hormone replacement therapy during the development of the protocol. - That the patient has any surgical intervention during the development of the study. - Women who consume or require the use of lipid-lowering drugs during the development of the protocol |
Country | Name | City | State |
---|---|---|---|
Mexico | Instituto Nacional de Perinatología Isidro Espinosa de los Reyes | Mexico City |
Lead Sponsor | Collaborator |
---|---|
Instituto Nacional de Perinatologia Isidro Espinosa de los Reyes | National Polytechnic Institute, Mexico |
Mexico,
Goya L, Martín MÁ, Sarriá 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. Review. — View Citation
Gutiérrez-Salmeán G, Meaney E, Lanaspa MA, Cicerchi C, Johnson RJ, Dugar S, Taub P, Ramírez-Sánchez 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. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | 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 | |
Secondary | 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 | |
Secondary | Malondialdehyde | Marker of oxidative stress measured by spectrophotometry expressed as pmol MDA/mg dry weight | Three months after starting the intervention in each group | |
Secondary | Superoxide Dismutase activity | Enzymatic activity measured by Colorimetric Activity Kit expressed as nmol/min/mL | Three months after starting the intervention in each group | |
Secondary | Catalase activity | Enzymatic activity measured by Colorimetric Activity Kit expressed as nmol/min/mL | Three months after starting the intervention in each group | |
Secondary | 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 | |
Secondary | 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 |
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