search
Back to results

Study of Sleeve Gastrectomy on Iron Intestinal Absorption in Morbidly Obese Patients (FORBES)

Primary Purpose

Obesity, Iron Deficiency

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Sleeve gastrectomy for morbid obesity
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obesity focused on measuring Sleeve gastrectomy, Obesity surgery, Iron deficiency, HEPCIDINE

Eligibility Criteria

18 Years - 60 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • morbid obese women selected for bariatric surgery

Exclusion Criteria:

  • non obese patients, less than 18 years old, haematological disease with need of blood transfusions

Sites / Locations

  • Hôpital Louis Mourier

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Arm A:

Arm Description

Sleeve gastrectomy for morbid obesity

Outcomes

Primary Outcome Measures

The intestinal absorption of iron
The intestinal absorption of iron will be assessed by the level of expression of iron transporters (DMT1 and ferroportin) mRNA level by RT-qPCR and at the protein level by Western blot.

Secondary Outcome Measures

Full Information

First Posted
November 30, 2011
Last Updated
October 10, 2018
Sponsor
Assistance Publique - Hôpitaux de Paris
search

1. Study Identification

Unique Protocol Identification Number
NCT01483768
Brief Title
Study of Sleeve Gastrectomy on Iron Intestinal Absorption in Morbidly Obese Patients
Acronym
FORBES
Official Title
Evaluation of the Impact of Bariatric Surgery by Sleeve Gastrectomy on Iron Intestinal Absorption in Morbidly Obese Patients
Study Type
Interventional

2. Study Status

Record Verification Date
October 2018
Overall Recruitment Status
Completed
Study Start Date
September 25, 2012 (Actual)
Primary Completion Date
December 2016 (Actual)
Study Completion Date
December 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Subject: Evaluation of the impact of obesity surgery by sleeve gastrectomy on intestinal iron absorption of morbid obese subjects. Control of intestinal absorption of iron is mediated by hepcidin, which is expressed in adipose tissue and that its expression is increased in morbidly obese subjects. The working hypothesis is that this increase could explain the high prevalence of systemic iron depletion observed in obese patients. Main objective: Assess the impact of the decrease in fat mass induced by surgery in obese patients on the intestinal absorption of iron (evaluated by measuring the expression of iron transporters in the duodenum)
Detailed Description
Study Rationale a high prevalence of iron deficiency and anemia has recently been characterized in obese patients and may be related to the stage of low-grade systemic inflammation associated with obesity Control of intestinal absorption of iron is mediated by hepcidin, a small circulating peptide synthesized primarily by the liver. the synthesis of hepcidin is increased in inflammatory condition and very recently it was shown that hepcidin is expressed in adipose tissue and that its expression is increased in morbidly obese subjects The working hypothesis is that this increase could explain the high prevalence of systemic iron depletion observed in these patients. the use of bariatric surgery is becoming more common to treat severe obesity (BMI above 35 kg / m2) The sleeve gastrectomy, recently introduced, involves a very significant weight loss. however, its impact on iron deficiency and anemia are not known main objective Assess the impact of the decrease in fat mass induced by surgery in obese patients on the intestinal absorption of iron (evaluated by measuring the expression of iron transporters in the duodenum Secondary objectives: Assess the impact of the decrease in fat mass induced by surgery in obese patients on the concentration of circulating hepcidin. To study the correlation between the level of expression of iron transporters in the duodenum and the plasma concentration of circulating hepcidin Search for a correlation between the level of hepcidin expression in subcutaneous adipose tissue and visceral and concentration of plasma hepcidin before surgery. Evaluate the effects of sleeve gastrectomy surgery on haematological and iron status of obese patients. Selection criteria for patients: Inclusion criteria: female subjects, having a body mass index > 40 kg/m2 (or > 35 kg/m2 with comorbidity) justifies a obesity surgery, For whom the indication of obesity surgery has been laid, the collective decision is taken in consultation, as part of care between different specialty (physicians, surgeons, psychiatrists ...) Non-inclusion criteria strictly less than age 18 years or strictly greater than 60 years, history of bariatric surgery or stomach, hepatic cytolysis (transaminases > 3n) during cancer treatment (radio or chemotherapy treatments) coefficient of transferrin saturation > 45%; known history of any of the following: hematologic disease requiring transfusions, hemochromatosis, Wilson's disease (because of known interference between metabolism of iron and copper), Chronic inflammation; Patient did not receive a medical examination; Patient did not give informed consent in writing, not affiliated with Patient Social Security or CMU ( universal health coverage) (recipient or beneficiary), known pregnancy Number needed: 88 patients enrolled Total duration of the study: 54 months Duration of participation for each patient: 24 months Duration of inclusion: 30 months Methods: Prospective open multicenter study cognitive. 4 visits are planned as part of this research with some specificity for the different centers. Visit 1: Presentation of the study and obtaining consent. Visit 2: consultation with implementation of a multidisciplinary assessment of duodenal biopsies by gastroscopy, additional laboratory tests and a pregnancy test if necessary. Visit 3: surgery (sleeve gastrectomy) with adipose tissue biopsies. Visit 4: creation of a consultation with multidisciplinary assessment of duodenal biopsies by gastroscopy and additional laboratory tests. Examinations required specifically for research: duodenal biopsies, additional laboratory tests, biopsies of adipose tissue and pregnancy test (dipstick) for all premenopausal women (contraceptives or not). Primary assessment criteria: The intestinal absorption of iron will be assessed by the level of expression of iron transporters (DMT1 and ferroportin) mRNA (messenger ribonucleic acid) level by RT-qPCR (reverse transcription quantification polymerase chain reaction) and at the protein level by Western blot. secondary assessment (s) criteria (s) The concentration of hepcidin plasma will be measured by ELISA in adipose tissue, the level of hepcidin expression is quantified by RT-qPCR . The haematological will assess the presence of anemia (hemoglobin less than 12g/dl) its micro or macrocytic hemolytic and / or regenerative

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Iron Deficiency
Keywords
Sleeve gastrectomy, Obesity surgery, Iron deficiency, HEPCIDINE

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
88 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Arm A:
Arm Type
Experimental
Arm Description
Sleeve gastrectomy for morbid obesity
Intervention Type
Procedure
Intervention Name(s)
Sleeve gastrectomy for morbid obesity
Other Intervention Name(s)
Longitudinal gastrectomy
Intervention Description
Sleeve gastrectomy or longitudinal gastrectomy for morbid obesity: is a partial gastrectomy without interruption of the gastric continuity. This procedure includes the resection of the great curvature of the stomach, the fundus , except the lesser curvature and the antrum.
Primary Outcome Measure Information:
Title
The intestinal absorption of iron
Description
The intestinal absorption of iron will be assessed by the level of expression of iron transporters (DMT1 and ferroportin) mRNA level by RT-qPCR and at the protein level by Western blot.
Time Frame
Time Frame 1 year (Time point(s) at which outcome measure is assessed):

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: morbid obese women selected for bariatric surgery Exclusion Criteria: non obese patients, less than 18 years old, haematological disease with need of blood transfusions
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Simon MSIKA, MD, Ph D
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hôpital Louis Mourier
City
Colombes
State/Province
Ile De France
ZIP/Postal Code
92701
Country
France

12. IPD Sharing Statement

Plan to Share IPD
Undecided

Learn more about this trial

Study of Sleeve Gastrectomy on Iron Intestinal Absorption in Morbidly Obese Patients

We'll reach out to this number within 24 hrs