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1.
Nutrients ; 13(6)2021 Jun 06.
Article in English | MEDLINE | ID: mdl-34204042

ABSTRACT

A randomized, double-blind, placebo-controlled study was conducted with the primary objective of assessing the effect of a natural extract of Sclerocarya birrea on glucose metabolism in subjects with prediabetes. The duration of the study was 90 days. Thirty-three subjects assigned to the experimental group (daily ingestion of 100 mg of the nutraceutical product) and 34 assigned to the placebo group completed the study. There were 36 men and 31 women with a mean age of 32.3 ± 14.1 years. In the area under the curve (AUC) of the oral glucose tolerance test (OGTT), statistically significant decreases in the experimental group at 40 and 90 days as compared with baseline were found, whereas significant changes in the placebo group were not observed. Within-group differences were statistically significant in favor of the experimental group for glucose peak at OGTT, serum insulin, insulin resistance markers, and flow-mediated dilation. Changes in lipid and anthropometric parameters were not observed, although there was a trend for lower cholesterol levels and a decrease in body weight in the experimental group. Decreases in systolic blood pressure were also higher among subjects in the experimental group. This exploratory study confirms the antidiabetic activity of Sclerocarya birrea in prediabetes. Further studies using better measurements of beta-cell function are needed to clarify the underlying mechanisms of the hypoglycemic effect of this natural compound.


Subject(s)
Anacardiaceae , Dietary Supplements , Hypoglycemic Agents/administration & dosage , Plant Extracts/administration & dosage , Prediabetic State/therapy , Adult , Area Under Curve , Biomarkers/blood , Blood Glucose/drug effects , Blood Pressure/drug effects , Body Weight/drug effects , Cholesterol/blood , Double-Blind Method , Female , Glucose Tolerance Test , Glycemic Control/methods , Humans , Insulin/blood , Insulin Resistance , Male , Middle Aged , Prediabetic State/blood
2.
Nutrients ; 12(5)2020 May 19.
Article in English | MEDLINE | ID: mdl-32438719

ABSTRACT

A single-center, randomized, double-blind controlled trial was conducted to assess the efficacy of a food supplement based on a combination of grapefruit, bitter orange, and olive extracts administered for eight weeks (n = 51) versus placebo (n = 45) on reduction of cardiovascular risk in healthy volunteers. Study variables included flow-mediated vasodilation (FMD), blood pressure (BP), lipid profile, thrombotic status, oxidative stress biomarkers, inflammation-related biomarkers, anthropometric variables, quality of life, and physical activity. The per-protocol data set was analyzed. In the active product group, there were statistically significant within-group differences at eight weeks as compared with baseline in FMD, systolic and diastolic BP, total cholesterol, LDL-C, LDL-oxidase, oxidized/reduced glutathione ratio, protein carbonyl, and IL-6. Significant between-group differences in these variables were also found. Significant changes in anthropometric variables and quality of life were not observed in the study groups. Changes in the level of physical activity were not recorded. Treatment with the active product was well tolerated. All these findings, taken together, support a beneficial effect of supplementation with a mixture of grapefruit, bitter orange fruits, and olive leaf extracts on underlying mechanisms that may interact each other to decrease the cardiovascular risk in healthy people.


Subject(s)
Cardiovascular Diseases/prevention & control , Citrus/chemistry , Dietary Supplements , Flavanones/administration & dosage , Flavones/administration & dosage , Olea/chemistry , Polyphenols/administration & dosage , Adult , Anthropometry , Blood Pressure/drug effects , Citrus paradisi , Double-Blind Method , Endothelium, Vascular/drug effects , Exercise , Female , Healthy Volunteers , Heart Disease Risk Factors , Humans , Inflammation Mediators/blood , Lipids/blood , Male , Middle Aged , Oxidative Stress/drug effects , Quality of Life , Vasodilation/drug effects
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