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553 results for “postprandial”
A gene variation at the ZPR1 locus (rs964184) interacts with the type of diet to modulate postprandial triglycerides in patients with coronary artery disease: From the Cordioprev Study
<p>Background and Aims: rs964184 variant in the ZPR1 gene has been associated with blood lipids levels both in fasting and postprandial state and with the risk of myocardial<br>infarction in high-risk cardiovascular patients. However, whether this association is modulated by diet has not been studied.</p> <p>Objective: To investigate whether the type of diet (low-fat or Mediterranean diets) interacts with genetic variability at this loci to modulate fasting and postprandial lipids in<br>coronary patients.</p> <p>Materials and Methods: The genotype of the rs964184 polymorphism was determined in the Cordioprev Study population (NCT00924937). Fasting and Postprandial triglycerides were assessed before and after 3 years of dietary intervention with either a Mediterranean or a low-fat diet. Postprandial lipid assessment was done by a 4-h oral fat tolerance test (OFTT). Differences in triglycerides levels were identified using repeated-measures ANCOVA.</p> <p>Results: From 523 patients (85% males, mean age 59 years) that completed the OFTT at baseline and after 3 years of intervention and had complete genotype information, 125<br>of them were carriers of the risk allele G. At the start of the study, these patients showed a higher fasting and postprandial triglycerides (TG) plasma levels. After 3 years of dietary<br>intervention, G-carriers following a Mediterranean Diet maintained higher fasting and postprandial triglycerides, while those on the low-fat diet reduced their postprandial<br>triglycerides to similar values to the population without the G-allele.</p> <p>Conclusion: After 3 years of dietary intervention, the altered postprandial triglyceride response induced by genetic variability in the rs964184 polymorphism of the ZPR1 gene<br>can be modulated by a low-fat diet, better than by a Mediterranean diet, in patients with coronary artery disease.</p>
Effects of Nateglinide on Postprandial Glucose Excursion by Restoring Early Phase Insulin Secretion
ClinicalTrials.gov study NCT01030952. IPD Sharing: Not stated. Countries: 1. Publications: 3.
Green Tea Confections For Managing Postprandial Hyperglycemia-Induced Vascular Endothelial Dysfunction
ClinicalTrials.gov study NCT01857258. IPD Sharing: YES. Countries: 1. Publications: 1.
A Study to Determine Acute (After First Dose) and Chronic (After 28 Days) Effects of Empagliflozin (BI 10773) on Pre and Postprandial Glucose Homeostasis in Patients With Impaired Glucose Tolerance an
ClinicalTrials.gov study NCT01248364. IPD Sharing: Not stated. Countries: 3. Publications: 3.
Comparison of the Postprandial Glycemic and Insulinemic Response After a Fibersym Containing Cookie With a Control
ClinicalTrials.gov study NCT04820322. IPD Sharing: NO. Countries: 1. Publications: 1.
A Study of Postprandial Hyperglycemia in Participants With Type 2 Diabetes
ClinicalTrials.gov study NCT01159938. IPD Sharing: Not stated. Countries: 1. Publications: 3.
Optoacoustic Characterization of Postprandial Intestinal Blood Flow
ClinicalTrials.gov study NCT05160077. IPD Sharing: YES. Countries: 1. Publications: 13.
Effect of Extra Virgin Olive Oil on Postprandial Blood Glucose in Type 2 Diabetes Mellitus Patients
ClinicalTrials.gov study NCT04077216. IPD Sharing: NO. Countries: 1. Publications: 7.
Regulation of Postprandial Nitric Oxide Bioavailability and Vascular Function By Dairy Milk
ClinicalTrials.gov study NCT02482675. IPD Sharing: Not stated. Countries: 1. Publications: 5.
Effect of a Fixed Pramlintide: Insulin Dose Ratio on Postprandial Glucose in Type 1 Diabetes Mellitus
ClinicalTrials.gov study NCT02500979. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Effects of Intragastric Quinine, Alone or Combined With L-leucine, on Postprandial Glycaemic Control
ClinicalTrials.gov study NCT05720390. IPD Sharing: NO. Countries: 1. Publications: 1.
The Effect of Liraglutide Treatment on Postprandial Chylomicron and VLDL Kinetics, Liver Fat and de Novo Lipogenesis
ClinicalTrials.gov study NCT02765399. IPD Sharing: NO. Countries: 1. Publications: 6.
Exercise Intensity and Postprandial Effects of Breaking Sedentary Behavior in Overweight Adults
ClinicalTrials.gov study NCT07229963. IPD Sharing: NO. Countries: 1. Publications: 51.
Effects of Antidiabetic Medications on the Postprandial State in Prediabetes
ClinicalTrials.gov study NCT02104739. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Liquid Meal Study With Insulin Lispro With/Without Recombinant Human Hyaluronidase PH20 (rHuPH20) and Regular Human Insulin With rHuPH20 to Compare Pharmacokinetics, Postprandial Glycemic Response, an
ClinicalTrials.gov study NCT00916357. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Effects of Lixisenatide Compared to Liraglutide on the Postprandial Plasma Glucose in Patients With Type 2 Diabetes
ClinicalTrials.gov study NCT01175473. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Evaluation of The Postprandial Impact of Automated Priming Bolus for Full Closed Loop Insulin Delivery
ClinicalTrials.gov study NCT05528770. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Effects of Intragastric Quinine, Alone or Combined With L-isoleucine, on Postprandial Glycaemic Control
ClinicalTrials.gov study NCT05682339. IPD Sharing: NO. Countries: 1. Publications: 1.
The Effects of Watermelon Juice Supplementation on Postprandial Vascular Endothelial Function
ClinicalTrials.gov study NCT04092439. IPD Sharing: NO. Countries: 1. Publications: 13.
Optimization of Exercise Protocol for Prediabetic Population in Postprandial State
ClinicalTrials.gov study NCT06656377. IPD Sharing: YES. Countries: 1. Publications: 4.
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