In spite of the growing evidence for the beneficial effects of probiotics, their anti-obesity effects are not well examined. No previous studies were conducted in this research area in the UAE. Hence, the aims of this study are to 1) Investigate the link between metabolic derangements associated with obesity and levels of LPS and LBP; 2) Study the relatedness of low grade inflammation with the ME; 3) Investigate the food intake assessment; and 4) Investigate the effectiveness of probiotics supplement on the obesity, ME and inflammation. This project will have two phases: 1) a cross-sectional, in which 250 adults will be recruited for the collection of anthropometric measures, food intake, and fasting blood samples to measure serum LPS, LBP, Lipid profile, IR, insulin-like growth factor, hs-CRP, IL-6, and glucose. 2) Intervention phase, in which 50 overweight subjects will be randomly assigned to either receive a daily probiotic (25 subjects) or a placebo capsule (25 subjects) during the intervention period.
General Objective: To study the relatedness of obesity, with the associated metabolic endotoxemia and low-grade inflammation, and the effectiveness of probiotics intervention in adults, in UAE. Specific Aims: * Investigate the link between metabolic derangements associated with obesity and levels of LPS and LBP among the population in Sharjah, UAE. * To examine the associated factors of obesity among the same population, including socio-demographic data, anthropometric measures, body composition analysis, and food frequency assessment. * To investigate the correlation of the inflammatory marker Il-6 and hs-CRP to the levels of endotoxemia in lean, overweight and obese subjects. * To evaluate the change in endotoxemia, body mass index (BMI) and inflammatory markers, after consumption of probiotics capsules of blended strains of Lactobacillus for 8 consecutive weeks among overweight and obese individuals.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Enrollment
80
probiotics capsules of blended strains including Lactobacillus acidophilus, L. casei and L. rhamnosus
Placebo
Sondos Harfil
Sharjah city, United Arab Emirates
80 participants characterized with obesity will be assessed for endotoxemia using LAL Chromogenic Endpoint Assay
Estimate the serum levels of LPS (EU/ml) before and after intervention period.
Time frame: 8 weeks
80 participants characterized with obesity will be assessed for body mass index (BMI) before and after the intervention period
BMI ( kg/m2)
Time frame: 8 weeks
Lipopolysacharide binding protein (LBP) will be assessed in the participants before and after intervention period.
LBP plasma level (ng/ml) will be assayed using ELISA technique
Time frame: 8 weeks
IL-6 serum will be assessed in participants before and after the intervention.
IL-6 serum will be assayed using ELISA
Time frame: 8 weeks
hs-CRP serum level will be assessed in participants before and after the intervention
hs-CRP will be assayed using immunoturbidimetry (ITM)
Time frame: 8 weeke
TNF-alpha serum level will be assessed in participants before and after the intervention
TNF-alpha will be assayed using ELISA technique
Time frame: 8 weeks
Lipid profile will be assayed for all participants before and after the intervention
measurement of serum levels of TG, HDL,LDL,
Time frame: 8 weeks
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