Original articleEffect of an alcohol-free beer enriched with isomaltulose and a resistant dextrin on insulin resistance in diabetic patients with overweight or obesity
Introduction
Diabetes mellitus burden is becoming a cause of concern due to its rapidly increasing global prevalence, complications and the excessive mortality rate which follows from its diagnosis [1], [2]. Lifestyle intervention is a key issue in diabetes management and includes, among other aspects, medical nutrition therapy [3]. In the presence of overweight or obesity, weight loss constitutes one of the key objectives of treatment. However, there is limited evidence on the optimal diet to control hyperglycemia and obesity in type 2 diabetes mellitus (T2DM). The amount and type of carbohydrate is one of the cornerstones in nutrition therapy of T2DM patients since they commonly comprise fifty percent or more of all calories consumed, and they have a substantial impact on glucose homeostasis [4]. The effect of low-carbohydrate diets in patients with T2DM remains unclear [3], [5], [6]. Beyond the quantity, carbohydrate composition directly impacts postprandial glucose control [7]. The metabolic effects of carbohydrate-containing foods are determined, mainly, by their content of sugars, dietary fiber, glycemic responses to digestion, processing and whole-grain content. Several clinical trials have documented the beneficial effect of low-glycemic index (GI) diets on glycemic control in T2DM [8]. More recently, several studies have demonstrated that the impact of carbohydrates on insulin secretion and postprandial glycemia can substantially change depending on the types of foods with which the carbohydrates are consumed [9].
Isomaltulose, a disaccharide composed of α-1,6–linked glucose and fructose, was recently introduced as an alternative sugar with delayed digestion and absorption resulting in a low GI of 32 [10]. A relatively high isomaltulose consumption (over 20 g per day) leads to cardiometabolic benefits including glycemic control, macronutrient oxidation and improved lipid profile, both in healthy and in diabetic patients [11]. Resistant dextrin is a glucose polymer (rich in α-1,4 and α-1,6 linkages) derived from wheat or maize [12]. It is incompletely hydrolyzed and absorbed in the small intestine, while the majority is fermented in the colon. High doses (≥10 g) of resistant dextrin induce beneficial effects on glycemic status, systemic inflammation, body weight, and body composition in humans [13], [14], [15]. To the best of our knowledge, no study has previously explored the potential synergistic beneficial effect of isomaltulose and resistant dextrin in glucose homeostasis of subjects with prediabetes or T2DM.
Beer is over 90% water while the rest of components are mainly carbohydrates (glucose polymers) and alcohol. As a product of cereals fermentation of cereals, beer has B-complex vitamins, in particular folate and choline, and trace amounts of minerals such as potassium, calcium and magnesium [16]. Beer composition also includes a range of polyphenols such as flavonoids and phenolic acids that have protective effects on cardiovascular health as measured by inflammatory biomarkers, among other biomarkers [17], [18], [19], [20]. Beer is widely consumed and it is often a preferred drink both in social events and on a daily basis. However, beer is usually restricted in T2DM patients because of its high content of carbohydrates and alcohol [3], [5]. Alcohol-free beer has the same bioactive compounds (although in lower concentrations) than regular beer, excluding the alcohol [16], [21]. GI is estimated as 119 in regular beer and 80 in alcohol-free beer, which is similar to that of potatoes, white bread or rice. In this context, we aimed to explore the effects of an alcohol-free beer with modified carbohydrates (almost completely eliminating maltose and adding isomaltulose (16.5 g/day) and a resistant maltodextrin (5.28 g/day)) on glycemic control (HOMA-IR as main outcome) in diabetic subjects who are overweight or obese, in comparison to an alcohol-free beer with regular composition to overcome the restrictions to regular beer for T2DM. A secondary and exploratory objective of the study was to address the effect of modified alcohol-free beer on satiety.
Section snippets
Study design and subjects
A randomized, controlled, double-blind design with two parallel groups was performed among volunteers of both sexes aged 18–80, with a body mass index (BMI) ranging from 25 to 40 kg/m2 and steady weight (±4 Kg) in the previous 2 months. We included those subjects with any of the following criteria: a) Diagnosis of prediabetes or T2DM according to international guidelines (fasting glucose concentration ≥100 mg/dL and/or glycated hemoglobin (HbA1c) ≥ 5.7%, and not taking antidiabetic drugs); b)
Participants and study course
A total of 57 participants were examined for eligibility of which 43 met all inclusion/exclusion criteria. Just one participant (a man beginning with alcohol-free beer with regular composition) dropped out of the study because of personal reasons and he was not included in the final analysis. As shown in Table 1, those participants assigned to one of the two study intervention sequences did not differ in terms of clinical or biochemical characteristics at baseline (P > 0.05 for all parameters).
Discussion
The main finding of this randomized, double-blind and cross-over study was that the consumption, within main meals, of 66 cL per day of alcohol-free beer including the substitution of regular carbohydrates by isomaltulose (16.5 g per day) and the addition of a resistant maltodextrine (5.28 g per day) led to an improvement in insulin resistance in subjects with T2DM and overweight or obesity. This benefit was not denoted in while consuming regular alcohol-free beer and it was observed regardless
Sources of support
This study was supported by funding from Grupo Ágora - La Zaragozana S.A. It was also partially supported by a grant from the Carlos III Research Institute: CIBERCV (co-supported by the European Regional Development Fund (ERDF) which is allocated by the European Union; IIS16/0114).
Conflict of interest
None declared.
Acknowledgments
The authors thank the participants for their enthusiastic collaboration in the study and Brandi Reed and Cecilia Bennett for their English editorial assistance. Rocío Mateo-Gallego research activity is funded by Instituto Aragonés de Ciencias de la Salud (IACS), Itziar Lamiquiz-Moneo research activity is funded by Fundación Cuenca Villoro and Martín Laclaustra research activity is funded by Fundación Aragón Investigación y Desarrollo (ARAID).
Authors would like to state that A.F. and A.P.M. work
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