ADIMOS-OB: Bone Marrow Fat and Bariatric Surgery-Mediated Bone Loss

Sponsor
University Hospital, Lille (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05005039
Collaborator
(none)
40
36

Study Details

Study Description

Brief Summary

Results are inconsistent and further studies are needed to better understand the impact of bariatric surgery on the bone-BMA relationship depending on the type of bariatric surgery: RYGB vs. SG. Future studies are also needed to define the molecular mediators of bone loss and BMA changes. Several molecular mediators have been considered including gut hormones, adipokines, gonadal hormones and more recently G-CSF. However, the evidence to support any of these alone or in combination as primary mechanisms of bone loss is scant.

The study will be to explore potential changes in BMA after bariatric surgery and search for possible associated factors. Specifically, we want to investigate if such changes in BMFF differed in participants among different surgical types (RYGB vs. SG) and diabetic status. Secondly, we want to explore factors associated with BMFF changes including metabolic homeostasis (glycemic control and blood lipid levels), adipokines (leptin and adiponectin), calciotropic hormones (Ca++, PTH…), body composition parameters and bone markers (cross-laps, P1NP and sclerostin). We hypothesize that the BMFF would particularly decrease after RYGB compared to SG and that participants with T2D would have a larger decrease in BMFF than participants without T2D.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    40 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Official Title:
    Bone Marrow Fat and Bariatric Surgery-Mediated Bone Loss
    Anticipated Study Start Date :
    Aug 1, 2022
    Anticipated Primary Completion Date :
    Aug 1, 2025
    Anticipated Study Completion Date :
    Aug 1, 2025

    Arms and Interventions

    Arm Intervention/Treatment
    Obese postmenopausal women who will undergo RYGB

    Obese postmenopausal women who will undergo SG

    Outcome Measures

    Primary Outcome Measures

    1. Variation in bone marrow fat fraction (BMFF) in % [12 months]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    45 Years to 70 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:

    Postmenopausal women (defined as last menses >12 months)

    • Obesity with a BMI ≥ 35 kg/m²,

    • Patients with an indication for bariatric surgery with two surgical techniques, RYGB and SG, but who have never had a bariatric surgery procedure previously,

    • Enrollment will be stratified for each surgical techniques, RYGB and SG, by preoperative diabetes status, defined by having HbA1c >6.5% or a prior physician's diagnosis of diabetes plus use of an antidiabetic medication.

    • Patients who have signed the informed consent.

    Exclusion Criteria:
    • women who were pre- and perimenopausal and men in order to minimize sex hormone and BMA changes unrelated to the surgical procedure.

    • women who used medications known to impact bone metabolism or BMA, including bisphosphonates, teriparatide, denosumab, hormone replacement therapy (HRT) and oral glucocorticoids (>5mg prednisone equivalent daily for>10 days in the last 3 months.

    • Other exclusion criteria included prior bariatric surgery, estimated glomerular filtration rate <30 mL/min,

    • any contraindication to magnetic resonance imagery (MRI).

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • University Hospital, Lille

    Investigators

    • Principal Investigator: Julien PACCOU, MD,PhD, University Hospital, Lille

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University Hospital, Lille
    ClinicalTrials.gov Identifier:
    NCT05005039
    Other Study ID Numbers:
    • 2021_0045
    • 2021-A01440-41
    First Posted:
    Aug 13, 2021
    Last Update Posted:
    Apr 5, 2022
    Last Verified:
    Apr 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No

    Study Results

    No Results Posted as of Apr 5, 2022