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Synbiotics and Low Grade Inflammation in Obese Subjects

Impact of the Administration of a Synbiotic on Low Grade Inflammation in Obese Subjects

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01235026
Enrollment
44
Registered
2010-11-05
Start date
2010-11-30
Completion date
2011-01-31
Last updated
2010-12-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes Mellitus Type-2, Insulin Resistance, Metabolic Syndrome, Obesity

Keywords

Obesity, Type-2 Diabetes, Metabolic syndrome, Low grade inflammation, Metabolic endotoxinemia, Insulin resistance, Lipopolysaccharide, LPS-binding protein, sCD14, Synbiotic, Oligofructose, Bifidobacterium animalis subsp. lactis Bb12, probiotic, Prebiotic

Brief summary

The purpose of this study is to determine whether the daily administration of a synbiotic (oligofructose and Bifidobacterium animalis subsp. lactis Bb12) for six weeks contributes to improve the glucose tolerance and the low grade inflammation (as reflected as the plasmatic concentrations of ultrasensitive CRP, IL-6, sCD14 and LPS-binding protein) in obese subjects.

Detailed description

Obesity is associated with a spectrum of metabolic disorders including high blood pressure, dyslipidemia, insulin resistance and a state of low grade inflammation that predispose individuals to the development of type-2 diabetes mellitus and cardiovascular diseases. The intestinal microbiota has been recently proposed as a new actor in the development of obesity and its complications. In animal models, high-fat diets have been shown to affect the intestinal microbiota, increasing colonic gram-negative bacteria and lipopolysaccharide (LPS) concentrations, resulting in an impaired gastrointestinal barrier function and in subsequent endotoxinemia in the animals. This phenomenon would trigger chronic inflammatory and metabolic disorders leading to insulin resistance and other complication such as hepatic steatosis. Probiotics and prebiotics are GRAS (Generally recognized as safe) food ingredients which have been proposed to maintain the balance of the intestinal microbiota. Studies in mice fed a high fat diet have shown that the administration of oligofructose increases the counts of Bifidobacterium spp. in the colon and correlatively induced decreases of the endotoxinemia and low-grade inflammation while at the same time improving insulin sensitivity. On the basis of these antecedents, the aim of this study is to determine whether the intake of a synbiotic product (B. animalis subsp. lactis BB12+ Oligofructose) for six weeks contributes to improve the low grade inflammation and glucose tolerance of obese subjects. Obese subjects will be randomized into two groups (Synbiotic or Placebo) stratifying by sex and age. Anthropometric data (body composition by Bod-pod, weight, height, waist circumference) and systolic and diastolic blood pressure will be registered. A food survey will be carried out by a trained dietitian to quantify fat consumption. Each subject of the Synbiotic group must ingest one gram of BB12 (containing 1010 CFU) and 5 g of oligofructose twice a day for 6 weeks while those from the Control group will receive the corresponding placebo (maltodextrin). Digestive symptoms as well as stool frequency and consistency will be registered daily during the study using ad hoc forms and the Bristol Chart. Blood samples will be obtained at baseline, at the end of the six weeks period and one month after the end of the treatment, to determine lipid profiles and ultrasensitive C-reactive protein (CRP); plasmatic biomarkers of inflammation including IL-6, LPS binding protein and sCD14 will be also determined by Elisa using commercial kits. At the same times, a glycemia /insulinemia curve will be performed in the fasted subjects, as well as an intestinal permeability test (lactulose/mannitol/sucralose) to assess their gut barrier function. A fresh stool sample will be also obtained to characterize some bacterial population of their IM (Bifidobacterium, Lactobacillus, F. prausnitzii, Bacteroides and Clostridium cluster) by real-time PCR.

Interventions

DIETARY_SUPPLEMENTSynbiotic

5g of the prebiotic Oligofructose + 1 g of the probiotic Bifidobacterium animalis subsp. lactis Bb12 (4x10\^10 CFU/g), twice a day, for 6 weeks.

DIETARY_SUPPLEMENTPlacebo

6g of maltodextrin, twice a day for 6 weeks.

Sponsors

University of Chile
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
20 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* BMI \> 30 * Non-smokers

Exclusion criteria

* Current digestive diseases or antecedents of chronic digestive diseases and/or malabsorption (celiac disease, Inflammatory bowel diseases, gastroduodenal ulcers, digestive malignancies, etc) * Use of drugs that could interfere with the intestinal microbiota or with the integrity of the gut barrier function (antibiotics, anti-inflammatory drugs, laxatives, prokinetics, etc.) during the three weeks preceding the start the study * Treatments (medication or nutritional program) affecting body weight or glucose control * Basal glycemia\>130mg/dl (evaluated with glucose-meter) * Immunodeficiencies (HIV, chemotherapy, radiotherapy, organ transplant). * Current participation or recent previous having participation in another clinical trial. * Pregnant or breastfeeding women. * Consumption of probiotic products * Drug or alcohol abuse

Design outcomes

Primary

MeasureTime frameDescription
Plasmatic Interleukin-6 (IL-6)6 weeksPlasmatic IL-6 will be determined after 6 weeks of administration of the synbiotic and compared with the IL-6 values at baseline.

Secondary

MeasureTime frameDescription
Plasmatic sCD146 weeksPlasmatic sCD14 will be determined after 6 weeks of administration of the synbiotic and compared with the sCD14 values at baseline.
glucose tolerance curve6 weeksGlucose tolerance will be determined after 6 weeks of administration of the synbiotic and compared with glucose tolerance at baseline.
Lipid profile6 weeksLipid profile will be determined after 6 weeks of administration of the synbiotic and compared with the lipid profile at baseline.
plasmatic ultrasensitive C-Reactive Protein6 weeksPlasmatic ultrasensitive CRP will be determined after 6 weeks of administration of the synbiotic and compared with the usCRP values at baseline.
Plasmatic LPS-binding protein6 weeksPlasmatic LPS-binding protein (LBP) will be determined after 6 weeks of administration of the synbiotic and compared with the LBP values at baseline.
Plasmatic LBP10 weeksPlasmatic LBP will be determined after a 1-month washout period without synbiotic administration (week 10)and compared with the baseline and post-treatment (6 weeks) values.
Glucose tolerance curve10 weeksGlucose tolerance curves will be determined after a 1-month washout period without synbiotic administration (week 10)and compared with the baseline and post-treatment (6 weeks) values.
Plasmatic usCRP10 weeksPlasmatic usCRP will be determined after a 1-month washout period without synbiotic administration (week 10)and compared with the baseline and post-treatment (6 weeks) values.
Plasmatic IL-610 weeksPlasmatic IL-6 will be determined after a 1-month washout period without synbiotic administration (week 10)and compared with the baseline and post-treatment (6 weeks) values.

Countries

Chile

Contacts

Primary ContactMartin Gotteland, PhD
mgottela@inta.cl56-2-9781471

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026