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Effect of Eriocitrin Supplementation in Subjects With Intermediate Hyperglycemia

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Mots clés

Abstrait

First, it will be evaluated whether supplementation of eriocitrin reduces hyperglycemia and insulin resistance, significantly reducing the risk of diabetes. The effects of eriocitrin on the lipid profile, inflammatory, endothelial, hepatic and renal biomarkers will also be evaluated. It is expected that metabolic parameters that constitute risk factors for diabetes and associated chronic diseases are expected to be improved by supplementation with eriocitrin

La description

Volunteers will be invited to appear in a 12-hour fast to measure glucose levels, glycated hemoglobin and to perform the glucose tolerance test, in addition to an individual interview to confirm eligibility according to the inclusion and exclusion criteria. The collection of blood and the glycemic curves will be carried out next to a Laboratory of Clinical Analyzes, commercial, based in the city of Araraquara.

The sample number took into account variances on glycated hemoglobin with a type I error α = 0.05 and a type II error β = 0.2 (80% power) (Mohammad, 2015). The minimum sample size considering an approximately 20% dropout rate, should have 20 individuals per group.

In order to ensure adequate nutrition for the nutritional and energetic needs of volunteers, an individual food plan shall be prescribed, calculated according to the DRI equations. The volunteer will be asked to complete the Food Record for three days at the 3rd, 5th, 7th, 9th and 11th week. Data analysis of energy intake, macronutrients and micronutrients will be performed through the DietBox® . The anthropometric measurements will be performed before the intervention and in the 3rd, 5th, 7th, 9th and 11th week by Nutritionist. Four samples of 30mL of fasting blood each will be obtained before the intervention, in the 4th, 8th and 12th week in the Laboratory of Clinical Analyzes. The blood will be centrifuged to obtain the serum, which will be frozen at -80 ° C until subsequent biochemical analyzes.

Normality and homogeneity will be evaluated by Shapiro-Wilk test and Levine tests, respectively. The T test will be used to compare baseline time between groups. The two-way repeated-measures ANOVA will be used to compare changes within and between the eriocitrin and control groups over the 12-week period. P significant at ≤ 0.05.

Rendez-vous

Dernière vérification: 12/31/2018
Première soumission: 07/10/2017
Inscription estimée soumise: 07/10/2017
Première publication: 07/11/2017
Dernière mise à jour soumise: 01/13/2019
Dernière mise à jour publiée: 01/14/2019
Date de début réelle de l'étude: 07/01/2017
Date d'achèvement primaire estimée: 02/27/2018
Date estimée d'achèvement de l'étude: 02/27/2018

Condition ou maladie

Pre Diabetes

Intervention / traitement

Dietary Supplement: Eriocitrin

Other: Group D

Phase

-

Groupes d'armes

BrasIntervention / traitement
Experimental: Group A
Individuals will receive a dose of 140 mg / d eriocitrin for 12 weeks
Experimental: Group B
Individuals will receive a dose of 280 mg / d eriocitrin for 12 weeks
Experimental: Group C
Individuals will receive a dose of 560 mg / d eriocitrin for 12 weeks
Placebo Comparator: Group D
Individuals will receive the placebo with corn starch excipient for 12 weeks
Other: Group D
The selected individuals will be randomly distributed in 4 groups through random number generator program. Group A (n = 20) will receive a dose of 140 mg / d eriocitrin; Group B (n = 20) eriocitrin 280 mg / d; The C group (n = 20) 560 mg / d eriocitrin; And group D (n = 20) will receive the placebo with corn starch excipient. All doses will be packaged in Manipulation Pharmacy, and should be of the same type, color and size. Individuals will be instructed to regularly ingest a pre-dinner capsule for 12 weeks.

Critère d'éligibilité

Âges éligibles aux études 30 Years À 30 Years
Sexes éligibles à l'étudeAll
Accepte les bénévoles en santéOui
Critères

Inclusion Criteria:

- Glycemia of 6.1 to 7.0 mmol / L

- Glycated hemoglobin with values between 5.7 and 6.4%

Exclusion Criteria:

- use of drugs, vitamins and dietary supplements, alcohol consumption (> 20 g alcohol/d), and intense physical activity (> 5 hours/week).

- History of cardiovascular disease, diabetes mellitus, liver or kidney disease

Résultat

Mesures des résultats primaires

1. Glucose [12 Weeks]

mg/dL

Mesures des résultats secondaires

1. glycated hemoglobin [12 Weeks]

percentage

2. insulin [12 Weeks]

µU/mL

3. Cholesterol [12 Weeks]

mg/dL

4. triglycerides [12 Weeks]

mg/dL

5. HDL-C [12 Weeks]

mg/dL

6. LDL-C [12 Weeks]

mg/dL

7. TNF-alpha [12 Weeks]

pg.mL

8. Interleucina 6 [12 Weeks]

pg.mL

9. c-reactive protein [12 Weeks]

mg/dL

10. aspartate aminotransferase [12 Weeks]

U/L

11. alkaline phosphatase [12 Weeks]

U/L

12. Gamma-Glutamyl Transferase [12 Weeks]

U/L

13. alanine aminotransferase [12 Weeks]

U/L

Autres mesures des résultats

1. Body mass [12 Weeks]

Kg

2. fat mass [12 Weeks]

kg

3. percentage of total body fat [12 Weeks]

Percentage

4. visceral fat area [12 Weeks]

cm2

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