Lipophilic Organic Polluants and Morbid Obesity (POLOB)
Primary Purpose
Obesity
Status
Unknown status
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Lipophilic Organic Polluants dosage
Sponsored by
About this trial
This is an interventional basic science trial for Obesity
Eligibility Criteria
Inclusion Criteria:
- age 18 to 65 years
- health coverage
- mentally competent
- signed consent form
- stable weight over the last three months
Non inclusion criteria :
- pregnancy
- insulin treated diabetes
- significant weight change over the last three months
Sites / Locations
- Nice University Hospital
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Other
Other
Other
Arm Label
sleeve bariatric surgery
morbidly obese adults with by pass surgery
non obese
Arm Description
morbidly obese adults, with or without metabolic syndrome eligible for bariatric surgery undergoing sleeve gastrectomy
morbidly obese adults, with or without metabolic syndrome eligible for bariatric surgery undergoing gastric bypass
non obese patients
Outcomes
Primary Outcome Measures
measurement of POPs
Urinary and blood POPs dosage 18 months after bariatric surgery
clinical and biological assessment of metabolic syndrome
blood dosage for clinical and biological assessment of metabolic syndrome including glucose tolerance test 18 months after bariatric surgery
Secondary Outcome Measures
Kinetic profiles of POP release within 18 months following bariatric surgery
blood and urinary dosage
Total body burden of selected POPs before and after surgery
Total body burden of selected POPs before and after surgery
Full Information
NCT ID
NCT01969968
First Posted
October 22, 2013
Last Updated
February 15, 2018
Sponsor
Centre Hospitalier Universitaire de Nice
1. Study Identification
Unique Protocol Identification Number
NCT01969968
Brief Title
Lipophilic Organic Polluants and Morbid Obesity
Acronym
POLOB
Official Title
Lipophilic Organic Polluants and Morbid Obesity: Kinetic of the Release and Impact on the Metabolic Syndrome Before and After Bariatric Surgery
Study Type
Interventional
2. Study Status
Record Verification Date
February 2018
Overall Recruitment Status
Unknown status
Study Start Date
December 18, 2013 (Actual)
Primary Completion Date
December 2018 (Anticipated)
Study Completion Date
December 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier Universitaire de Nice
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
To study the kinetics of release after bariatric surgery of selected polluants stored in adipose tissue, looking for clinical and/or predictive factors
To test the hypothesis of a deleterious effect of this release on the expected improvement of insulin-resistance and on the liver inflammation.
To determine the level of contamination of morbidly obese patients, with or without metabolic syndrome, compared to a control, non obese population, with special attention to clinical (age, gender, reproductive history, pregnancy, nursing) and biological parameters (insulin-resistance, inflammation).
Detailed Description
I- Goals Because of its exponential prevalence and its co-morbidities, obesity, particularly in its most massive forms, has become a public health problem. It is likely that this epidemic be secondary to both genetic and behavioural factors, and also to environmental factors. Specifically, the "obesogen" and "diabetogen" role of several persistant organic polluants (POP) known as endocrine disruptors used in farming or industry has recently been suggested by experimental animal studies and by human epidemiologic studies. Those chemicals are usually lipophilic, are stored in adipose tissue where they bio-accumulate, and are released in the blood stream during the lipolysis that occurs in any weight loss. This weight loss is particularly rapid and important after bariatric surgery, that is proposed as a treatment for morbid obesity usually leading to an improvement of insulin resistance, metabolic syndrome, and diabetes. However, this improvement is not constant, or is less important than would be anticipated for the massive weight loss observed. This raises the question of the importance and of deleterious impact of the blood release of lipophilic POPs on the evolution of metabolic syndrome and the low grade associated inflammation.
In a prospective, multicentric study, we propose to analyse the kinetic of the release of several POPs during rapid and massive weight loss obtained after bariatric surgery. Those POPs have been chosen for their obesogen or diabetogen properties, reported in vitro or in vivo, for their lipophilic nature, and their ubiquitous presence in the home environment and/or into the food chain: bisphenol A (plastics); tributyltin (fungicide, anti-fouling agent or thermic stabilizant); polybrominated diphenyl ethers (PBDE, fire retardants); perchlorated octanoïd acid and its sulphated compounds (PFOA and PFOS, perfluoroalkyls used as surfactant, lubrifiants, and usted in wrappings); and organochorinated compounds such as: PCB153, representing the polychlorinated bisphenyls (electric isolation); hexachlorobenzene (HBC), and several pesticides: DDE, metabolite of DDT, now banned but with a very long half life, hexachlorocyclohexane (HCH), heptachlor, nanochlor and chlordane used in agriculture.
II- Originality and /or new aspect of the project Though suggested by several experimental studies, the role of POP in human obesity remains largely unknown.
There are no or very few papers on the role in humans of the POPs we have selected, but they are supported by animal experimental studies.
The concept of release in the blood stream after weight loss is recent and deserves to be studied.
III- Reasons for the choice of questions (3 maximum) Interest of the results/method to improve knowledge on those questions
To study the kinetics of release after bariatric surgery of selected polluants stored in adipose tissue, looking for clinical and/or predictive factors
To test the hypothesis of a deleterious effect of this release on the expected improvement of insulin-resistance and on the liver inflammation.
To determine the level of contamination of morbidly obese patients, with or without metabolic syndrome, compared to a control, non obese population, with special attention to clinical (age, gender, reproductive history, pregnancy, nursing) and biological parameters (insulin-resistance, inflammation).
IV- Description of the methods/ Calendar The POPs will be measured in serum, urine (for BPA) and in adipose tissue (subcutaneous and visceral) by gas chromatography coupled to mass spectrometry.
Fat mass will be estimated when possible by DEXA (if weight<150 kg), or by impedancemetry, allowing the calculation of an estimated total body burden for each POP (since they are lipophilic, we will multiply the concentration of each chemical in adipose tissue expressed in ng/g of fat by the total estimated body mass of fat).
The number of patients included will be 250 morbidly obese adults, with or without metabolic syndrome (3 out of 5 classical criteria), eligible for bariatric surgery (125 from Nice undergoing gastric bypass, and 125 from Montpellier undergoing sleeve gastrectomy).
Concentrations of polluants will be measured at baseline and 3, 6 and 12 month after bariatric surgery, and at 18 months as well for patients who will undergo abdominoplasty required by their massive weight loss. Baseline concentrations in obese patients will be compared to those measured in 100 controls, matched for age and gender, with a BMI<25.
Insulin resistance will be assessed by HOMA-IR, adiponectine and SHBG, inflammation by us CRP, leptin, interleukin 6, TNF alpha, transaminases, gammaGT, alkalin phosphatase.
The redistribution of POPs in serum and adipose tissue, and the estimation of total body burden will be assessed before and after surgery.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
236 (Actual)
8. Arms, Groups, and Interventions
Arm Title
sleeve bariatric surgery
Arm Type
Other
Arm Description
morbidly obese adults, with or without metabolic syndrome eligible for bariatric surgery undergoing sleeve gastrectomy
Arm Title
morbidly obese adults with by pass surgery
Arm Type
Other
Arm Description
morbidly obese adults, with or without metabolic syndrome eligible for bariatric surgery undergoing gastric bypass
Arm Title
non obese
Arm Type
Other
Arm Description
non obese patients
Intervention Type
Other
Intervention Name(s)
Lipophilic Organic Polluants dosage
Intervention Description
Urinary, blood and fat dosage of Lipophilic Organic Polluants
Primary Outcome Measure Information:
Title
measurement of POPs
Description
Urinary and blood POPs dosage 18 months after bariatric surgery
Time Frame
18 months
Title
clinical and biological assessment of metabolic syndrome
Description
blood dosage for clinical and biological assessment of metabolic syndrome including glucose tolerance test 18 months after bariatric surgery
Time Frame
18 months after bariatric surgery
Secondary Outcome Measure Information:
Title
Kinetic profiles of POP release within 18 months following bariatric surgery
Description
blood and urinary dosage
Time Frame
18 months following bariatric surgery
Title
Total body burden of selected POPs before and after surgery
Description
Total body burden of selected POPs before and after surgery
Time Frame
before surgery and 18 months after surgery
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:
age 18 to 65 years
health coverage
mentally competent
signed consent form
stable weight over the last three months
Non inclusion criteria :
pregnancy
insulin treated diabetes
significant weight change over the last three months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Patrick FENICHEL, PhD
Organizational Affiliation
Nice University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Nice University Hospital
City
Nice
ZIP/Postal Code
06000
Country
France
12. IPD Sharing Statement
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Lipophilic Organic Polluants and Morbid Obesity
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