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Bone Marrow Adiposity and Fragility Fractures in Postmenopausal Women

Bone Marrow Adiposity and Fragility Fractures in Postmenopausal Women: a Case-control Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03219125
Acronym
ADIMOS
Enrollment
203
Registered
2017-07-17
Start date
2018-10-16
Completion date
2021-06-25
Last updated
2022-11-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fractures, Bone, Bone Marrow Disease, Fat Disorder, Adiposity

Keywords

marrow adipose tissue, bone marrow adiposity

Brief summary

The purpose is to determine in a case-control study if an association exist between bone marrow adiposity and fragility fractures in post-menopausal women.

Interventions

DEVICEDixon Magnetic Resonance Imaging

MRI of the lumbar spine (L1 to L4) and hip (non-dominant) for the measurement of Ad Med. (In%) by the DIXON sequence.

Subjects will undergo DXA scan to assess total body (less head) and lumbar spine bone mineral density.

Sponsors

University Hospital, Lille
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
50 Years to 90 Years
Healthy volunteers
Yes

Inclusion criteria

* post-menopausal women : 50-90 years old * Group 1 (cases) : occurence of incident major osteoporotic fracture less than 12 months * Group 2 (controls) : no history of fragility fracture

Exclusion criteria

* Implants that are contraindicated for the magnetic resonance (MR) examination. * Implants that might create a health risk or other problem during an MR exam include: 1) cardiac pacemaker or implantable defibrillator, 2) catheter that has metal components that may pose a risk of a burn injury, 3) a ferromagnetic metal clip placed to prevent bleeding from an intracranial aneurysm, 4) an implanted medication pump (such as that used to deliver insulin or a pain-relieving drug), and 5) a cochlear implant. * body mass index \[BMI\] \>38 kg/m2, weight \>140 kg * Disease or current use of medications known to affect bone density, including oral glucocorticoids, treatments for osteoporosis (bisphosphonates, raloxifene, calcitonin, or PTH), hormone therapy. * Chronic kidney disease with DFG \<30 ml/mn

Design outcomes

Primary

MeasureTime frameDescription
Bone marrow fat content at lumbar spine24 monthsTotal bone marrow fat content (percentage) at lumbar spine (L1-L4) measured with magnetic resonance imaging

Secondary

MeasureTime frameDescription
Bone marrow fat content at total hip24 monthsTotal bone marrow fat content (percentage) at total hip measured with magnetic resonance imaging
Bone mineral density at lumbar spine24 monthsBone mineral density (g/cm2) at lumbar spine (L1-L4) measured by DXA
Bone mineral density at total hip24 monthsBone mineral density (g/cm2) at total hip measured by DXA

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026