MedPath

Pivotal Assessment of the Effects of Bioactive on Health and Wellbeing. From Human Genome to Food Industry

Not Applicable
Terminated
Conditions
Metabolic Syndrome
Interventions
Dietary Supplement: Dairy BEF
Dietary Supplement: Bakery BEF
Dietary Supplement: Egg BEF
Dietary Supplement: Bakery placebo
Dietary Supplement: Dairy placebo
Dietary Supplement: Egg placebo
Registration Number
NCT02702713
Lead Sponsor
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Brief Summary

This is a multi-centre, randomised, double-blind, placebo-controlled, parallel-arm dietary intervention study. In total, 800 men and women at risk for Metabolic Syndrome (MS) will be recruited. Subjects will be eligible to the study if they present with two to four of the MS diagnostic criteria, at least one of them being:

* fasting triglycerides ≥150 mg/dL but ≤400 mg/dL OR

* HDL-cholesterol ≤50 mg/mL in women, ≤ 40mg/mL in men (with fasting triglycerides ≥110 mg/dL).

Each of the four recruiting centres will recruit 200 volunteers. Participants will be randomly assigned to one of four groups to receive either:

* Dairy BEF + egg placebo + bakery placebo

* Egg BEF + dairy placebo + bakery placebo

* Bakery BEF + dairy placebo + egg placebo

* Dairy, egg and bakery placebo

Participants will be required to consume all three of the allocated products each day for 12 weeks.

Eligible volunteers will be included and randomly allocated to one of the four groups. At baseline, 6 weeks and 12 weeks after inclusion, each participant will visit the recruiting centre for clinical and biochemical investigations. At 3 weeks and 9 weeks participants will complete questionnaires relating to their satisfaction with the food products, compliance to consumption of the study food products, and any gastrointestinal side effects or health-related adverse events that have occurred in the previous 3 weeks.

At each recruiting centre 40 participants will be required to take part in additional activities, these are: stool sample collection, adipose tissue aspiration, body composition analysis by dual energy x-ray absorptiometry (DEXA) and assessment of physical activity.

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
325
Inclusion Criteria
  • subjects presenting with two to four diagnostic criteria for metabolic syndrome, at least one of them being elevated fasting triglycerides OR HDL-cholesterol ≤50 mg/mL in women, ≤ 40mg/mL in men (with fasting triglycerides ≥110 mg/dL).
Exclusion Criteria
  • subjects with five clinical criteria for metabolic syndrome
  • Regular drug therapy with impact on serum lipids;
  • Diabetes (fasting glucose > 1.26 g/L, or anti-diabetic treatment);
  • Celiac disease, lactose intolerance, allergy to milk or egg proteins;
  • Antibiotic treatment within the last 3 months;
  • Recent history of cancer or cancer treatment (less than 2 years);
  • Active or recently diagnosed intestinal malabsorption;
  • Diagnosis of organ failure
  • Familial dyslipidemia (TG ≥ 4.5 mmol/l or 400 mg/dl);
  • Illegal drug use or chronic alcoholism or smoking;
  • Intensive physical exercise (≥ 5 hour/week);
  • Consumption of nutritional supplements containing DHA, BG or AC;
  • History of allergy or intolerance to any components used in BEF;
  • Women who are pregnant or lactating;

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Egg BEF + dairy placebo + bakery placeboBakery placebo200 subjects consuming every day for 12 weeks: 1 portion of Egg BEF + 1 portion of Dairy placebo + 1 portion of Bakery placebo
Dairy BEF + egg placebo + bakery placeboDairy BEF200 subjects consuming every day for 12 weeks: 1 portion of Dairy BEF + 1 portion of Egg placebo + 1 portion of Bakery placebo
Egg BEF + dairy placebo + bakery placeboDairy placebo200 subjects consuming every day for 12 weeks: 1 portion of Egg BEF + 1 portion of Dairy placebo + 1 portion of Bakery placebo
All placeboBakery placebo200 subjects consuming every day for 12 weeks: 1 portion of Egg placebo + 1 portion of Dairy placebo + 1 portion of Bakery placebo
Bakery BEF + dairy placebo + egg placeboBakery BEF200 subjects consuming every day for 12 weeks: 1 portion of Bakery BEF + 1 portion of Dairy placebo + 1 portion of Egg placebo
All placeboEgg placebo200 subjects consuming every day for 12 weeks: 1 portion of Egg placebo + 1 portion of Dairy placebo + 1 portion of Bakery placebo
Dairy BEF + egg placebo + bakery placeboBakery placebo200 subjects consuming every day for 12 weeks: 1 portion of Dairy BEF + 1 portion of Egg placebo + 1 portion of Bakery placebo
Dairy BEF + egg placebo + bakery placeboEgg placebo200 subjects consuming every day for 12 weeks: 1 portion of Dairy BEF + 1 portion of Egg placebo + 1 portion of Bakery placebo
Egg BEF + dairy placebo + bakery placeboEgg BEF200 subjects consuming every day for 12 weeks: 1 portion of Egg BEF + 1 portion of Dairy placebo + 1 portion of Bakery placebo
Bakery BEF + dairy placebo + egg placeboEgg placebo200 subjects consuming every day for 12 weeks: 1 portion of Bakery BEF + 1 portion of Dairy placebo + 1 portion of Egg placebo
All placeboDairy placebo200 subjects consuming every day for 12 weeks: 1 portion of Egg placebo + 1 portion of Dairy placebo + 1 portion of Bakery placebo
Bakery BEF + dairy placebo + egg placeboDairy placebo200 subjects consuming every day for 12 weeks: 1 portion of Bakery BEF + 1 portion of Dairy placebo + 1 portion of Egg placebo
Primary Outcome Measures
NameTimeMethod
HDL-cholesterol blood levels (mg/dl)Baseline and 12 weeks

Change from baseline in HDL-cholesterol blood levels after 12 weeks of consumption of foods

Triglycerides blood levels (mg/dl)Baseline and 12 weeks

Change from baseline in triglycerides blood levels after 12 weeks of consumption of foods enriched with DHA, alone or in combination with AC or BG, in subjects at risk for or affected by MS.

Secondary Outcome Measures
NameTimeMethod
Blood glucose (mg/dl).Baseline and 12 weeks

Change from baseline in blood glucose levels after 12 weeks of consumption of foods enriched with DHA, alone or in combination with AC or BG, in subjects at risk for or affected by MS.

Blood pressure (mmHg)Baseline and 12 weeks

Change from baseline in blood pressure after 12 weeks of consumption of foods enriched with DHA, alone or in combination with AC or BG, in subjects at risk for or affected by MS.

Homeostasis Model Assessment (HOMA) Index levels.Baseline and 12 weeks

Change from baseline in Homeostasis Model Assessment Index levels, after 12 weeks of consumption of foods enriched with DHA, alone or in combination with AC or BG, in subjects at risk for or affected by MS.

Dna methylation levels (%).Baseline and 12 weeks

To test whether lymphocytes may be useful as a surrogate for adipose tissue to detect changes in DNA methylation and gene expression, genome-wide methylation differences will be performed in parallel in lymphocytes and fat cells from baseline and after 12 weeks of consumption of foods enriched with DHA, alone or in combination with AC or BG, in subjects at risk for or affected by MS. Expression of affected genes will be evaluated by qRT-PCR.

Serum Hemoglobin A1c (HbA1c) levels (%)Baseline and 12 weeks

Change from baseline in HbA1c levels, after 12 weeks of consumption of foods enriched with DHA, alone or in combination with AC or BG, in subjects at risk for or affected by MS.

Waist circumference (cm).Baseline and 12 weeks

Change from baseline in waist circumference after 12 weeks of consumption of foods enriched with DHA, alone or in combination with AC or BG, in subjects at risk for or affected by MS.

Fecal microbiota composition (analysis of principal coordinates - PCOA)Baseline and 12 weeks

Changes in fecal bacterial composition and diversity will be determined at baseline and after 12 weeks of consumption of foods enriched with DHA, alone or in combination with AC or BG, in subjects at risk for or affected by MS. The predominant microbial community and specific functional groups will be characterized by next-generation sequencing (NGS) of the 16S rDNA gene. The interindividual differences in the composition of the intestinal microbiota (beta-diversity) will be evaluated with the analysis of principal coordinates (PCOA). Appropriate statistical analysis will be performed to evaluate significant differences in the relative abundance of the microbial groups of intestinal microbiota between different groups of subjects.

Fecal Short Chain Fatty Acids (parts per million).Baseline and 12 weeks

Change from baseline in production/uptake in the stool of Short Chain Fatty Acids, after 12 weeks of consumption of foods enriched with DHA, alone or in combination with AC or BG, in subjects at risk for or affected by MS.

Fecal metabolite levels (parts per millions).Baseline and 12 weeks

Change from baseline in food metabolite levels in the stools after 12 weeks of consumption of foods enriched with DHA, alone or in combination with AC or BG, in subjects at risk for or affected by MS.

Urinary food metabolite levels (parts per millions).Baseline and 12 weeks

Changes from baseline in urinary food metabolite levels, after 12 weeks of consumption of foods enriched with DHA, alone or in combination with AC or BG, in subjects at risk for or affected by MS.

Trial Locations

Locations (4)

Max Rubner-Institut

🇩🇪

Karlsruhe, Baden-Württemberg, Germany

Centre de Récherche en Nutrition Humaine d'Auvergne

🇫🇷

Clermont-Ferrand, Auvergne, France

University of Leeds

🇬🇧

Leeds, United Kingdom

University of Bologna, Department of Medical and Surgical Sciences and Azienda Ospedaliero Universitaria di Bologna, Policlinico S.Orsola-Malpighi

🇮🇹

Bologna, BO, Italy

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