Targeting Obesity With the Probiotic Lactiplantibacillus Plantarum IMC 510 (PRO-Weight-Control Study)
Primary Purpose
Obesity
Status
Active
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Probiotic
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Obesity focused on measuring obesity, probiotic, Lactiplantibacillus Plantarum, gut microbiota, clinical trial
Eligibility Criteria
Inclusion Criteria:
- Men and women 18-65 years of age
- Obesity (BMI >30 kg/m2, class I, II, III) and overweight (BMI 25-29.9 kg/m2)
- Willingness to cooperate during the study and ability to follow guidelines
- Willingness to complete questionnaires and diaries associated with the study and to complete all clinical visits
- Willingness to discontinue functional foods and dietary supplements with probiotics, laxatives and body weight control substances
- Ability to provide informed consent
Exclusion Criteria:
- Continued use of probiotics in the two months prior to treatment
- Use of other treatments (medications or nutritional programs) that affect body weight, food intake and/or energy expenditure
- Postmenopausal women
- Pregnant or lactating
- Enrolled in another obesity treatment program
Sites / Locations
- Unit of Clinical Nutrition, University Hospital of Careggi
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Probiotic
Placebo
Arm Description
Probiotic food supplement produced by SYNBIOTEC S.r.l.
Placebo food supplement.
Outcomes
Primary Outcome Measures
Body weight
Changes of body weight from baseline assessed through a balance
Secondary Outcome Measures
Fat mass
Changes of fat mass from baseline assessed through a bioelectrical impedance analysis device (BIA Akern, 101 Sport Edition).
Fat-free mass
Changes of fat-free mass from baseline assessed through a bioelectrical impedance analysis device (BIA Akern, 101 Sport Edition).
Total body water
Changes of total body water from baseline assessed through a bioelectrical impedance analysis device (BIA Akern, 101 Sport Edition).
White blood cells
Changes of white blood cells from baseline assessed to standard laboratory procedures.
Red blood cells
Changes of red blood cells from baseline assessed to standard laboratory procedures.
Hemoglobin
Changes of hemoglobin from baseline assessed to standard laboratory procedures.
Glucose
Changes of glucose from baseline assessed to standard laboratory procedures.
Urea
Changes of urea from baseline assessed to standard laboratory procedures.
Creatinine
Changes of creatinine from baseline assessed to standard laboratory procedures.
Sodium
Changes of sodium from baseline assessed to standard laboratory procedures.
Potassium
Changes of potassium from baseline assessed to standard laboratory procedures.
Calcium
Changes of calcium from baseline assessed to standard laboratory procedures.
Magnesium
Changes of magnesium from baseline assessed to standard laboratory procedures.
AST
Changes of AST from baseline assessed to standard laboratory procedures.
ALT
Changes of ALT from baseline assessed to standard laboratory procedures.
Triglycerides
Changes of triglycerides from baseline assessed to standard laboratory procedures.
Total cholesterol
Changes of total cholesterol from baseline assessed to standard laboratory procedures.
HDL-cholesterol
Changes of HDL-cholesterol from baseline assessed to standard laboratory procedures.
LDL-cholesterol
Changes of LDL-cholesterol from baseline assessed to standard laboratory procedures.
Uric Acid
Changes of uric acid from baseline assessed to standard laboratory procedures.
eGFR
Changes of eGFR from baseline assessed to standard laboratory procedures.
Gastrointestinal and systemic symptoms
Changes of gastrointestinal and systemic symptoms from baseline assessed through a modified form of the Global Assessment of Improvement Scale (GAI), with a total score ranging from 0 to 56, with higher scores meaning an improvement of the symptoms and the Symptom Severity Scale (SSS), with a total score ranging from 0 to 500, with higher scores meaning more severe symptoms.
Gut microbiota
Changes of gut microbiota from baseline assessed by Illumina MiSeq platform.
Full Information
NCT ID
NCT05358301
First Posted
March 21, 2022
Last Updated
August 5, 2022
Sponsor
Azienda Ospedaliero-Universitaria Careggi
1. Study Identification
Unique Protocol Identification Number
NCT05358301
Brief Title
Targeting Obesity With the Probiotic Lactiplantibacillus Plantarum IMC 510 (PRO-Weight-Control Study)
Official Title
Novel Strategies for Obesity Prevention and Management With the Probiotic Lactiplantibacillus Plantarum IMC 510 (PRO-Weight-Control Study)
Study Type
Interventional
2. Study Status
Record Verification Date
August 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
January 7, 2022 (Actual)
Primary Completion Date
June 30, 2022 (Actual)
Study Completion Date
October 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Azienda Ospedaliero-Universitaria Careggi
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
In recent decades, the prevalence of obesity has reached epidemic proportions, with the number of overweight or obese individuals continuing to increase worldwide. Advances in recent research have allowed a better characterization of the etiology of obesity, demonstrating the involvement of the gut microbiota. In fact, while signals from the brain influence gut function, the gut microbiota has been shown to modulate brain functions involved in the regulation of stress, depression and anxiety, which are closely linked to obesity. Oral administration of probiotics has been proposed as a valid way to modulate the gut ecosystem to promote weight reduction. Preliminary data showed that obese rats treated with probiotics containing the probiotic strain Lactiplantibacillus Plantarum IMC 510 exhibited significantly lower weight and food intake than untreated obese rats. Although exercise and diet are the first lines of intervention to be recommended, there are often failures or poor outcomes. There is currently increased interest in alternative and effective shorter-term, non-pharmacological approaches to weight control that involve the use of natural active ingredients. Thus, the aim of this intervention study is to investigate whether a probiotic supplementation with Lactiplantibacillus Plantarum IMC 510 could be beneficial for the weight reduction of people with obesity.
Detailed Description
Background
Obesity is a multifactorial disease characterized by a chronic imbalance between energy intake and energy expenditure. Risk factors for weight excess are genetic, metabolic, hormonal, psychological, and social, as well as factors related to diet, sedentary lifestyle, and medication intake. Obesity is associated with an increased risk of onset of several metabolic diseases (high blood pressure, dyslipidemia, diabetes mellitus, metabolic syndrome), cardiovascular diseases (cerebral strokes, myocardial infarction), gastrointestinal diseases (esophageal reflux, cholelithiasis, pancreatitis, hepatopathy), respiratory diseases (apnea, respiratory failure), cancer (higher incidence of cancer and worsening of prognosis), osteoarticular diseases (osteoporosis, osteoarthritis), psychological diseases (depression, low self-esteem, relationship problems).
In recent decades, the prevalence of obesity has reached epidemic proportions. In fact, current data estimate that approximately 600 million people worldwide are obese, with an additional 1.9 billion overweight. Moreover, recent trend analyses show that the number of individuals who are overweight or obese continues to increase worldwide.
Advances in recent research have allowed for better characterization of the etiology of obesity, highlighting the potential contribution of factors not traditionally considered to be involved in changes in energy balance and body composition. Experimental and clinical studies have also demonstrated the role of the gut microbiota in the regulation of energy balance and the occurrence of excess body weight. In this regard, it has been suggested that lean and obese human subjects differ in the composition of their gut microbiota, and that probiotics and prebiotics can be used to modify the microbiota to prevent body weight gain. The bidirectional gut-brain connection allows signals from the brain to influence motility, appetite sensations, secretions, and permeability of the gut. Studies have demonstrated the role and importance of the gut microbiota in modulating central nervous system activity, so some gut messages may influence brain functions involved in the regulation of stress, depression, and anxiety, which are closely related to obesity. Consequently, the gut microbiota is a potential modifiable target for the prevention and/or treatment of obesity. In fact, the gut microbiota has recently been shown to play a complex role in body weight regulation and some probiotic strains have been able to ameliorate obesity status and related metabolic disorders. Preliminary data showed that obese rats treated with probiotics containing the probiotic strain Lactiplantibacillus Plantarum IMC 510 exhibited significantly lower weight and food intake than untreated obese rats.
Oral administration of probiotics has been proposed as a viable way to modulate/modify the gut ecosystem to promote weight reduction; however, the mechanisms by which probiotic supplementation may affect the gut microbiota of obese individuals are largely unknown. In addition, byproducts of the bacterial fermentation process may also reduce appetite and increase feelings of satiety, and through modulation of bile acid metabolism, the microbiota may reduce diet-induced obesity through increased energy expenditure. In addition, gut bacteria can manipulate an individual's taste and food preferences.
Over the past 25 years, more than 120 drugs have been studied for the treatment of obesity, but only very few have been approved and maintained on the market. Although exercise and diet are the first lines of intervention in correcting overweight, obesity and related metabolic diseases, because they are measures that must be adopted and followed for a long period of time, often experience failure or poor outcomes. Currently there is an increased interest in alternative and effective short term non-pharmacological approaches to weight control that involve the use of natural active ingredients. The use of specific probiotics could represent the future weapon to fight obesity through the modulation of the intestinal microbiota, which is becoming more and more important as a critical point both for the appearance of many diseases (if altered) and for the possibility of curing them by intervening to restore the intestinal flora.
Objectives of the study
The present clinical study is directed to the evaluation of the efficacy of a probiotic formulation containing the probiotic strain Lactiplantibacillus Plantarum IMC 510 in inducing and supporting weight loss and reduction of body circumferences in overweight or obese subjects through the regularization of appetite with consequent reduction of food intake.
Primary Objectives:
1) To evaluate weight reduction in obese and/or overweight subjects after 3 months of treatment with probiotic or placebo.
Secondary Objectives:
Collection of blood and fecal samples at recruitment, after 3 months of treatment (probiotic or placebo), and after a 1-month final wash out.
Measurement of BMI, body circumferences, body composition such as fat mass, lean mass, after 3 months of probiotic or placebo treatment, and after 1 month of wash out
Evaluation of general well-being, eating habits and any gastrointestinal symptoms
Comparison of hematological and biochemical parameters related to obesity at baseline, after 3 months of probiotic or placebo intervention, and after 1 month of washout
Analysis of the composition of the intestinal microbiota and the production of short-chain fatty acids (SCFA) and bile acids (FBA).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity
Keywords
obesity, probiotic, Lactiplantibacillus Plantarum, gut microbiota, clinical trial
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomized double-blind parallel controlled trial
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
By keeping both the experimenters and the participants blind, bias is less likely to influence the results of the experiment.
Allocation
Randomized
Enrollment
40 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Probiotic
Arm Type
Experimental
Arm Description
Probiotic food supplement produced by SYNBIOTEC S.r.l.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo food supplement.
Intervention Type
Dietary Supplement
Intervention Name(s)
Probiotic
Intervention Description
Probiotic food supplement produced by SYNBIOTEC S.r.l. Each capsule of SYNBIO®slim contains the probiotic strain Lactiplantibacillus Plantarum IMC 510 at a concentration of 15 billion live cells (CFU/capsule). The assumption is of n°1 capsule/day, preferably at breakfast, for 3 months. The capsules can be opened and their content can be dispersed in a cold liquid or at intake temperature or in semi-solid food. Always store in original container or in a clean covered container, out of the reach of children. When stored in a dry, clean environment, out of direct sunlight, the product has a shelf-life of at least 24 months. Samples of probiotic supplement in closed and sealed boxes will be provided to subjects participating at the beginning of the study, in quantities sufficient for the entire duration of the study (90 capsules for 3 months).
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
N°1 capsule/day of placebo food supplement (i.e., capsules without added probiotics), with the same intake modalities as probiotic.
Primary Outcome Measure Information:
Title
Body weight
Description
Changes of body weight from baseline assessed through a balance
Time Frame
2 months
Secondary Outcome Measure Information:
Title
Fat mass
Description
Changes of fat mass from baseline assessed through a bioelectrical impedance analysis device (BIA Akern, 101 Sport Edition).
Time Frame
2 months
Title
Fat-free mass
Description
Changes of fat-free mass from baseline assessed through a bioelectrical impedance analysis device (BIA Akern, 101 Sport Edition).
Time Frame
2 months
Title
Total body water
Description
Changes of total body water from baseline assessed through a bioelectrical impedance analysis device (BIA Akern, 101 Sport Edition).
Time Frame
2 months
Title
White blood cells
Description
Changes of white blood cells from baseline assessed to standard laboratory procedures.
Time Frame
2 months
Title
Red blood cells
Description
Changes of red blood cells from baseline assessed to standard laboratory procedures.
Time Frame
2 months
Title
Hemoglobin
Description
Changes of hemoglobin from baseline assessed to standard laboratory procedures.
Time Frame
2 months
Title
Glucose
Description
Changes of glucose from baseline assessed to standard laboratory procedures.
Time Frame
2 months
Title
Urea
Description
Changes of urea from baseline assessed to standard laboratory procedures.
Time Frame
2 months
Title
Creatinine
Description
Changes of creatinine from baseline assessed to standard laboratory procedures.
Time Frame
2 months
Title
Sodium
Description
Changes of sodium from baseline assessed to standard laboratory procedures.
Time Frame
2 months
Title
Potassium
Description
Changes of potassium from baseline assessed to standard laboratory procedures.
Time Frame
2 months
Title
Calcium
Description
Changes of calcium from baseline assessed to standard laboratory procedures.
Time Frame
2 months
Title
Magnesium
Description
Changes of magnesium from baseline assessed to standard laboratory procedures.
Time Frame
2 months
Title
AST
Description
Changes of AST from baseline assessed to standard laboratory procedures.
Time Frame
2 months
Title
ALT
Description
Changes of ALT from baseline assessed to standard laboratory procedures.
Time Frame
2 months
Title
Triglycerides
Description
Changes of triglycerides from baseline assessed to standard laboratory procedures.
Time Frame
2 months
Title
Total cholesterol
Description
Changes of total cholesterol from baseline assessed to standard laboratory procedures.
Time Frame
2 months
Title
HDL-cholesterol
Description
Changes of HDL-cholesterol from baseline assessed to standard laboratory procedures.
Time Frame
2 months
Title
LDL-cholesterol
Description
Changes of LDL-cholesterol from baseline assessed to standard laboratory procedures.
Time Frame
2 months
Title
Uric Acid
Description
Changes of uric acid from baseline assessed to standard laboratory procedures.
Time Frame
2 months
Title
eGFR
Description
Changes of eGFR from baseline assessed to standard laboratory procedures.
Time Frame
2 months
Title
Gastrointestinal and systemic symptoms
Description
Changes of gastrointestinal and systemic symptoms from baseline assessed through a modified form of the Global Assessment of Improvement Scale (GAI), with a total score ranging from 0 to 56, with higher scores meaning an improvement of the symptoms and the Symptom Severity Scale (SSS), with a total score ranging from 0 to 500, with higher scores meaning more severe symptoms.
Time Frame
2 months
Title
Gut microbiota
Description
Changes of gut microbiota from baseline assessed by Illumina MiSeq platform.
Time Frame
2 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Men and women 18-65 years of age
Obesity (BMI >30 kg/m2, class I, II, III) and overweight (BMI 25-29.9 kg/m2)
Willingness to cooperate during the study and ability to follow guidelines
Willingness to complete questionnaires and diaries associated with the study and to complete all clinical visits
Willingness to discontinue functional foods and dietary supplements with probiotics, laxatives and body weight control substances
Ability to provide informed consent
Exclusion Criteria:
Continued use of probiotics in the two months prior to treatment
Use of other treatments (medications or nutritional programs) that affect body weight, food intake and/or energy expenditure
Postmenopausal women
Pregnant or lactating
Enrolled in another obesity treatment program
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Francesco Sofi, Prof.
Organizational Affiliation
Unit of Clinical Nutrition, University hospital of Careggi, Florence, italy
Official's Role
Principal Investigator
Facility Information:
Facility Name
Unit of Clinical Nutrition, University Hospital of Careggi
City
Florence
ZIP/Postal Code
50134
Country
Italy
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
25815895
Citation
Albanese D, De Filippo C, Cavalieri D, Donati C. Explaining diversity in metagenomic datasets by phylogenetic-based feature weighting. PLoS Comput Biol. 2015 Mar 27;11(3):e1004186. doi: 10.1371/journal.pcbi.1004186. eCollection 2015 Mar.
Results Reference
background
PubMed Identifier
29047207
Citation
Borgeraas H, Johnson LK, Skattebu J, Hertel JK, Hjelmesaeth J. Effects of probiotics on body weight, body mass index, fat mass and fat percentage in subjects with overweight or obesity: a systematic review and meta-analysis of randomized controlled trials. Obes Rev. 2018 Feb;19(2):219-232. doi: 10.1111/obr.12626. Epub 2017 Oct 18.
Results Reference
background
PubMed Identifier
27047743
Citation
Chung HJ, Yu JG, Lee IA, Liu MJ, Shen YF, Sharma SP, Jamal MA, Yoo JH, Kim HJ, Hong ST. Intestinal removal of free fatty acids from hosts by Lactobacilli for the treatment of obesity. FEBS Open Bio. 2016 Jan 18;6(1):64-76. doi: 10.1002/2211-5463.12024. eCollection 2016 Jan.
Results Reference
background
PubMed Identifier
23910373
Citation
Dinan TG, Cryan JF. Melancholic microbes: a link between gut microbiota and depression? Neurogastroenterol Motil. 2013 Sep;25(9):713-9. doi: 10.1111/nmo.12198.
Results Reference
background
PubMed Identifier
28008750
Citation
Gomes AC, de Sousa RG, Botelho PB, Gomes TL, Prada PO, Mota JF. The additional effects of a probiotic mix on abdominal adiposity and antioxidant Status: A double-blind, randomized trial. Obesity (Silver Spring). 2017 Jan;25(1):30-38. doi: 10.1002/oby.21671.
Results Reference
background
PubMed Identifier
21702898
Citation
Segata N, Izard J, Waldron L, Gevers D, Miropolsky L, Garrett WS, Huttenhower C. Metagenomic biomarker discovery and explanation. Genome Biol. 2011 Jun 24;12(6):R60. doi: 10.1186/gb-2011-12-6-r60.
Results Reference
background
PubMed Identifier
19365593
Citation
Verdenelli MC, Ghelfi F, Silvi S, Orpianesi C, Cecchini C, Cresci A. Probiotic properties of Lactobacillus rhamnosus and Lactobacillus paracasei isolated from human faeces. Eur J Nutr. 2009 Sep;48(6):355-63. doi: 10.1007/s00394-009-0021-2. Epub 2009 Apr 14.
Results Reference
background
PubMed Identifier
29547587
Citation
John GK, Wang L, Nanavati J, Twose C, Singh R, Mullin G. Dietary Alteration of the Gut Microbiome and Its Impact on Weight and Fat Mass: A Systematic Review and Meta-Analysis. Genes (Basel). 2018 Mar 16;9(3):167. doi: 10.3390/genes9030167.
Results Reference
background
PubMed Identifier
28294985
Citation
Sanchez M, Darimont C, Panahi S, Drapeau V, Marette A, Taylor VH, Dore J, Tremblay A. Effects of a Diet-Based Weight-Reducing Program with Probiotic Supplementation on Satiety Efficiency, Eating Behaviour Traits, and Psychosocial Behaviours in Obese Individuals. Nutrients. 2017 Mar 15;9(3):284. doi: 10.3390/nu9030284.
Results Reference
background
PubMed Identifier
27250499
Citation
Sanders ME. Probiotics and microbiota composition. BMC Med. 2016 Jun 2;14(1):82. doi: 10.1186/s12916-016-0629-z.
Results Reference
background
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Targeting Obesity With the Probiotic Lactiplantibacillus Plantarum IMC 510 (PRO-Weight-Control Study)
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