NCT07731438Recruiting
Bone Marrow Adipose Tissue in Relation to Bone and Energy Metabolism in Obesity and Type 2 Diabetes Mellitus
Bone Marrow Adipose Tissue as a New Parameter in Relation to Bone and Energy Metabolism in Obesity and Type 2 Diabetes Mellitus
Source: ClinicalTrials.gov · Last updated 28 Jul 2026
Brief summary (registry, in English)
This interventional study is part of a broader research project entitled "Bone Marrow Adipose Tissue in Relation to Bone and Energy Metabolism in Obesity and Type 2 Diabetes Mellitus." The broader project includes both a cross-sectional study evaluating bone marrow adipose tissue and bone marrow mesenchymal stem cells in people with different metabolic and bone disorders and the present dietary intervention study. The interventional study investigates whether caloric restriction changes bone marrow adipose tissue, bone health, whole-body metabolism, and the molecular and cellular characteristics of bone marrow mesenchymal stem cells in obese non-diabetic premenopausal women. A group of lean healthy premenopausal women will serve as a comparison group. Participants in the intervention group will undergo an eight-week formula-based very-low-calorie diet using Cambridge Weight Plan products, providing approximately 2.5-3.35 MJ (600-800 kcal) per day, followed by a dietary weight-maintenance phase. Participants will receive nutritional counselling, and dietary adherence, body weight, physical activity, and clinical status will be monitored during scheduled study visits. Clinical and laboratory assessments will be conducted at baseline and after 2, 6, and 12 months. Assessments will include magnetic resonance imaging and proton magnetic resonance spectroscopy of the lumbar spine to measure the amount and lipid composition of vertebral bone marrow adipose tissue. Bone mineral density and body composition will be measured using dual-energy X-ray absorptiometry, with particular attention to bone mineral density at the total hip and femoral neck. Additional measurements will include body weight, waist and hip circumference, body composition, physical activity, and fasting blood tests evaluating bone turnover, glucose and lipid metabolism, inflammatory markers, hormones, and adipokines. Bone marrow aspirates and abdominal subcutaneous adipose tissue biopsies will be obtained at baseline and after six months. Bone marrow-derived and adipose tissue-derived mesenchymal stem cells will be examined for changes in cellular composition, gene-expression profiles, metabolic activity, oxidative stress, differentiation capacity, and senescence-related characteristics. Single-cell RNA sequencing will be used to characterize specific bone marrow mesenchymal stem cell subpopulations. Bone marrow plasma and other biological samples will also undergo metabolomic, lipidomic, and proteomic profiling using high-resolution mass spectrometry. These analyses will be used to identify extracellular molecules and molecular patterns associated with glucose and lipid metabolism, inflammation, cellular senescence, and the response to caloric restriction. The study aims to determine whether diet-induced weight loss can improve the bone marrow microenvironment and modify vertebral bone marrow fat, bone parameters, and the metabolic and senescent phenotype of mesenchymal stem cells. The findings may help identify imaging, cellular, and molecular markers of obesity-related bone fragility.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 45 (estimated)
- First submitted
- 16 Jul 2026
- Start date
- 1 May 2023
- Primary completion date
- 1 Nov 2026
- Lead sponsor
- General University Hospital, Prague
- Diseases
- Obesity, Type 2 diabetes
- NCT number
- NCT07731438
What you commit to
- Study type: Interventional
- Planned participants: 45
- From 1 May 2023 to the primary completion date, 1 Nov 2026
- 3 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Current or recent use of any of the following medications:
- Adrenal or anabolic steroids
- Metallic implants incompatible with MRI
Other illness
- Diabetes mellitus
- History of severe neuropathic disease
- Chronic gastrointestinal disease
- Significant chronic renal impairment, including any of the following:
- Chronic kidney disease
- Chronic hepatic impairment
- Unstable cardiovascular disease
- Uncontrolled hypertension
Lab values
- Serum creatinine greater than 110 µmol/L
- Estimated glomerular filtration rate (eGFR) less than 1 mL/s/1.73 m²
Other
- Secondary osteoporosis
- Hyperparathyroidism
- Hyperthyroidism
- Immobilization
- Alcoholism
- Proteinuria
- Diabetic nephropathy
- Bisphosphonates
- Estrogen
- Denosumab
- Gonadotropin-releasing hormone (GnRH) analogs
- Glucocorticoids at a dose equivalent to at least 5 mg of prednisone daily for at least 1 month
- Phenytoin
- Thiazolidinediones
- Insulin
- Anticonvulsants
- Anticoagulants
- Pharmacological doses of vitamin D or vitamin A supplements
- Contraindications to magnetic resonance imaging (MRI), including:
- Pacemaker
- Claustrophobia
Who the study is looking for
- Premenopausal women and age-eligible men assigned to either the obese intervention group or the lean control group
- Obese intervention group:
- Body mass index (BMI) of 30-42 kg/m²
- Fasting plasma glucose less than 6.4 mmol/L
- Age 25-55 years
- Lean control group:
- BMI of 19-25 kg/m²
- Fasting plasma glucose less than 6.4 mmol/L
- Age 25-50 years
Criteria the registry did not label
- Interventional Study: Effect of Caloric Restriction on BMAT/BM-MSCs Phenotype
Age in the registry: 21 years to 55 years · Sex: All · Accepts healthy volunteers
Sites (3)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Institute of Endocrinology, Prague, a state-funded organization established by the Ministry of Health of the Czech Republic. Coordinator of this site? Confirm its status | Prague | Czechia | Recruiting |
| Institute of Physiology of the Czech Academy of Sciences Coordinator of this site? Confirm its status | Prague | Czechia | Recruiting |
| General University Hospital in Prague Coordinator of this site? Confirm its status | Prague | Czechia | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.