Acute and Short-term Chronic Effects of Galvus (Vildagliptin) in Diabetes Type 2 Obese Women
Study Details
Study Description
Brief Summary
The prevalence of obesity and type 2 diabetes mellitus (T2DM) has increased progressively in the past decades, and consequently, a higher incidence of cardiovascular diseases is observed. As this process develops, the endothelial dysfunction is present at early stages of the atherosclerotic disease. Studies conducted at BioVasc/UERJ show the occurrence of endothelial and microvascular dysfunction in obese carriers, even in the absence of dysglycemia. New concepts indicate the endothelium as a possible therapeutic target, and drugs which act not only on diabetes mellitus pathophysiology but also acting as direct cardiovascular protectors bring new therapeutic possibilities. The dipeptidyl-peptidase-4 inhibitors (DPP4), such as vildagliptin, are drugs used on the T2DM treatment. Its incretin mimetic and insulinotropic effects are already well established and several other studies show its effectiveness in reducing glycated hemoglobin, even in monotherapy.
Currently, fat rich foods are being increasingly introduced in the western way of life and recent evidence suggests that the postprandial lipemia (LPP) is related to cardiovascular risk. A better glucose control using vildagliptin can reduce the oxidative stress, and consequently promote a better microvascular and endothelial reactivity. However, vildagliptin can have an additional cardiovascular protective action, not only because of its effect on glycemia and oxidative stress reduction, but maybe because of its direct effect on intestinal peptides with postprandial lipemia reduction. To test this hypothesis, we will proceed the following exams: venous occlusion pletysmography, nailfold videocapilaroscopy and laser-Doppler flowmetry aiming to evaluate vascular reactivity on muscle and at cutaneous site. Anoter group of patients with the same clinical charactherisitics will use metformin, in order to compare its effects with those obtained from the use of Vildaglitpin. Our purpose is to determine whether vildagliptin, evaluated in obese and diabetic women, has vascular protective effects, and whether the regulatory mechanisms of these actions correlate with oxidative stress, inflammatory markers and intestinal peptides in baseline state and after a lipid overload.
Condition or Disease | Intervention/Treatment | Phase |
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Phase 4 |
Study Design
Arms and Interventions
Arm | Intervention/Treatment |
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Experimental: Metformin Metformin 850mg/pill will be administered at lunch time and dinner time for 30 days |
Drug: Vildagliptin
Vildagliptin 50mg/pill will be administered at 10 AM and at 6 PM also for 30 days.
Other Names:
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Experimental: Vildagliptina Vildagliptin 50mg/pill will be administered at 10 AM and at 6 PM also for 30 days. |
Drug: Vildagliptin
Vildagliptin 50mg/pill will be administered at 10 AM and at 6 PM also for 30 days.
Other Names:
|
Outcome Measures
Primary Outcome Measures
- Change from Baseline in microcirculation function at 30 days [Before and after 30 days]
For this study, there will be used two methods, the traditional one, which consists in assessing the microcirculation parameters by dynamic nailfold videocapillaroscopy technique carried out in the nailfold pleat of the fourth finger on the left hand.
Secondary Outcome Measures
- Change from Baseline in endothelial function at 30 days [before and after 30 days (intervention)]
LDF is a method for continuous non invasive determination of the microvascular perfusion, where the study of cutaneous vasomotion by spectral analysis of Laser Doppler signal allows the exploration of five frequency components: endothelial, myogenic, sympathetic, respiratory and cardiac, involved in answers to the stimuli. Therewith vasomotion during the whole study period will be assessed, to find differences in baseline, 30, 60, 120 and 180 min after the meal rich in lipids.
Other Outcome Measures
- Change from Baseline in incretins and inflammation markers at 30 days [basal and after 30 days (intervention)]
Through kits read by Multiplex® appliance, inflammatory markers will be evaluated, all simultaneously, with small sample quantity (from 10 to 50µL).
Eligibility Criteria
Criteria
Inclusion Criteria:
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All patients should have BMI > 30kg/m²
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Present untreated diabetes mellitus type 2
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Age between 19 and 50 years
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Waist Circumference > 80 cm
Exclusion Criteria:
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Renal, coronary vascular or peripheral, hematologic or hepatic disease
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Presence of severe hypertriglyceridemia (> 400mg/dl)
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Smokers
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Significant body mass loss (> 5%) within the six months prior to the study
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
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1 | Laboratory for Clinical and Experimental Research on Vascular Biology | Rio de Janeiro | Brazil | 20550-900 |
Sponsors and Collaborators
- Rio de Janeiro State University
- Laboratory for Clinical and Experimental Research on Vascular Biology
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- Galvus_2013
- BioVasc_2013