Please use this identifier to cite or link to this item: http://hdl.handle.net/10668/10915
Title: A new fructose-free, resistant-starch type IV-enriched enteral formula improves glycaemic control and cardiovascular risk biomarkers when administered for six weeks to elderly diabetic patients.
Authors: Mesa García, María Dolores
García-Rodríguez, Cruz Erika
Rico, María de la Cruz
Aguilera, Concepción María
Pérez-Rodríguez, Milagros
Pérez-de-la-Cruz, Antonio Jesús
Gil, Ángel
Keywords: Diabetes mellitus type 2. Cardiovascular risk. Enteral nutrition. Glycaemic control. Glycated haemoglobin. Resistant-starch type IV.
metadata.dc.subject.mesh: Aged
Aged, 80 and over
Biomarkers
Blood Glucose
Cardiovascular Diseases
Diabetes Complications
Diabetes Mellitus, Type 2
Enteral Nutrition
Female
Food, Formulated
Fructose
Humans
Male
Prospective Studies
Risk Factors
Starch
Issue Date: 1-Feb-2017
Abstract: Reducing the dietary glycaemic response has been proposed as a way to reduce the risk of diabetes complications. The aim of the present study was to evaluate the glycaemic control and cardiovascular risk biomarkers in fragile, elderly type 2 diabetes patients after the intake of a new fructose-free diabetes-specific formula enriched with resistant-starch type IV and high in monounsaturated fatty acids. Forty-one type 2 diabetes patients aged 78.9 ± 2.8 years were fed exclusively with an enteral diabetes-specific formula for 6 weeks. Data were collected at baseline and after 6 weeks of feeding. Carbohydrate and lipid metabolism and inflammatory and cardiovascular risk biomarkers were measured to evaluated the course of diabetes complications. Blood glycated haemoglobin significantly decreased after the intervention (6.1 ± 0.1 vs. 5.8 ± 0.1 %; p The new product improves glycaemic control and cardiovascular risk without altering lipid metabolism, which is useful for the prevention of diabetic complications. Longer intervention studies are needed in order to validate these results in a larger population.
URI: http://hdl.handle.net/10668/10915
metadata.dc.identifier.doi: 10.20960/nh.978
Appears in Collections:Producción 2020

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