Metabolic Syndrome Clinical Trial
Official title:
Effect of a Dietary Portfolio (PD) (Nopal, Chia, Soy, Oat and Inulin) and Physical Activity on Gut Microbiota in Patients With Metabolic Syndrome
Aim: To study the effect of a combination of functional foods on gut microbiota in subjects with metabolic syndrome. Subjects that met the metabolic syndrome criteria were enrolled in a double-blind, parallel-arm, placebo-control study. The subjects were randomized to receive a dietary portfolio (DP) or placebo (P) treatment for 2 mo. The primary endpoint was to study the effect of a DP on gut microbiota. Secondary endpoints were biochemical and anthropometric parameters, LPS, insulin, leptin, area under the curve for glucose and insulin.
This study was a single-center, randomized, controlled, double-blind, parallel versus placebo
that consisted of five visits. The first visit was a screening evaluation to determine
whether subjects met the inclusion criteria. The selected subjects were invited to a second
visit that consisted of a medical history, 2-h oral glucose tolerance test (OGTT), the
collection of stool samples for DNA isolation and collection of 5 ml blood sample. The
participants received during the first stage, a low saturated fat diet (LSFD) for 15 days. In
the third visit and second stage of dietary treatment, subjects were randomized to receive
the dietary portfolio (DP) or placebo (P) treatment + an LSFD accompanied of a reduced energy
diet for 1 mo. In the fourth visit, with a 1 mo interval, dietary assessment and compliance
to the DP or P were evaluated. During each follow-up visit, a 24-h dietary recall was
collected, a physical activity questionnaire was filled out and anthropometric and clinical
parameters were assessed. In the fifth visit, a 2 -h oral glucose tolerance test (OGTT) was
performed, and a stool sample for DNA isolation and 5 ml blood were collected.
Dietary intervention in the first stage, the participants consumed a reduced-energy diet
tailored to provide a 500-kcal/d deficit as recommended by NIH with respect to their habitual
diet for 15 days. The diet plan consisted in 50-60% carbohydrates, 15% protein, 25-35% fat,
<7% saturated fat, ≤ 200 mg, 20-35 g fiber, 2000 mg/d sodium based on total energy. In the
second stage, the participants continued to consume the reduced energy diet with the addition
of a combination of functional foods (DP). The DP provided 200 kcal that were subtracted from
the diet. The DP consisted of a mixture of 14 g de dehydrated nopal, 4 g of chia, 25 g of soy
protein, 14 g of oat, 4 g of inulin, 0.15 of flavoring. The placebo (P) consisted of 30 g of
calcium caseinate, 30 g of maltodextrin and 0.2 g of flavoring. The kcal, appearance, and
flavor were similar in DP and P. The DP and P were given in a package in the dehydrated form
ready to be dissolved in water. The DP was divided into two packages, the first package
contained 17.3 g of DP or P given in the breakfast and dissolved in 250 ml and the second
package was given at the dinner time, and contained 34.7 g of P and DP dissolved in 300 ml of
water.
Dietary compliance. Dietary compliance was assessed with a 24-h dietary recall and 3-d food
record (food lo), during each visit that was analyzed by food processor nutrition analysis
software. The compliance of the consumption of the DP or P was evaluated with the number of
empty packages returned at the following visit. Physical activity was assessed using the
International physical activity questionnaire (IPAQ)
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