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Clinical-functional Effects of Bariatric Surgery on the Musculoskeletal System in Relation to Bone Turnover.

Not Applicable
Not yet recruiting
Conditions
Bariatric Surgery Candidate
Interventions
Other: 50 adult patients suffering from severe or morbid obesity, male and female, candidates for bariatric surgery.
Registration Number
NCT06299085
Lead Sponsor
I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio
Brief Summary

By studying "in vivo" new possible predictive factors of increased bone turnover and risk of fractures after bariatric surgery, our study aims to improve health not only musculoskeletal but general of patients with severe obesity, a pathology which represents one of the main causes of disability and mortality.

Detailed Description

To date, there are no studies in scientific literature aimed at identifying the hormonal mechanisms that could contribute to increased bone turnover in patients undergoing bariatric surgery. All randomized controlled trials conducted to date have focused on nutritional factor deficiency (vitamin D3, calcium and protein), mechanical unloading and reduction of adiposity at the bone marrow level.

By studying "in vivo" new possible predictive factors of increased bone turnover and risk of fractures after bariatric surgery, our study aims to improve health not only musculoskeletal but general of patients with severe obesity, a pathology which represents one of the main causes of disability and mortality.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
50
Inclusion Criteria
  • Age ≥ 18 and ≤ 60 years.
  • BMI (Body Mass Index: expressed as weight ratio in kg/height in m2) ≥ 35 kg/m2 with comorbidities or BMI ≥ 40 Kg/m2 without comorbidities.
  • Absence of diagnosis of primary obesity.
  • Absence of medical-psychiatric contraindications.
  • Previous diet therapy and/or pharmacological history verified.
  • Signing of the informed consent for the study.
  • Patients who are clinical candidates for bariatric surgery (Sleeve Gastrectomy and Roux-en-Y Gastric Bypass).
Exclusion Criteria
  • Presence of chronic diseases of the digestive system, such as chronic intestinal diseases, malabsorption syndrome, diverticulosis of the colon.
  • Current pregnancy and/or breastfeeding via self-declaration.
  • Subjects suffering from endocrine pathologies (e.g. Cushing's disease, uncontrolled thyroid disease).
  • Presence of known renal insufficiency or creatinine levels above 1.8 mg/dl and eGFR < 60 ml/min.
  • Presence of chronic liver disease or ALT and AST levels above two standard deviations from normal levels.
  • Presence of malignant pathology.
  • Alcohol or drug abuse.
  • Previous bariatric surgery.
  • Severe psychological-psychiatric disorders.
  • Difficulty adhering to the protocol due to language barriers or other reasons.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
50 adult patients suffering from severe or morbid obesity50 adult patients suffering from severe or morbid obesity, male and female, candidates for bariatric surgery.50 adult patients suffering from severe or morbid obesity (BMI ≥ 35 kg/m2 in the presence of comorbidities and BMI ≥ 40 kg/m2, respectively), male and female, candidates for bariatric surgery (Sleeve Gastrectomy and Roux-en-Y Gastric Bypass). Two timepoints: T0 (pre-hospitalization) and T1 (follow-up 12 months +/- 1 month). Expected assessments at T0 and T1: * Blood chemistry tests to monitor metabolic markers involved in dietary and metabolic changes. * Bone densitometry for body composition analysis (DEXA). * Analysis of pre-intervention walking and the ability to recover motor activity after bariatric surgery using gait analysis.
Primary Outcome Measures
NameTimeMethod
Study of new predictive markers of possible bone remodeling through specific blood tests before (pre-admission) and 12 months after bariatric surgery.Two timepoints: pre-admission before bariatric surgery and 12 months after.

Study of new predictive markers of possible bone remodeling through specific blood tests before (pre-admission) and 12 months after bariatric surgery by evaluating the circulating levels of gastro-entero hormones, adipokines and hormones associated with anabolism of muscle and bone tissue.

Secondary Outcome Measures
NameTimeMethod
Evaluation of the bone health status of patients pre- and post-bariatric surgery using different methods.Two timepoints: pre-admission before bariatric surgery and 12 months after.

Analysis of circulating levels of hormones linked to the anabolism of muscle and bone tissue such as estrogens, androgens and insulin.

Evaluation of the bone health status of patients pre- and post-bariatric surgery through:

1. Dual-Energy x-Ray (DEXA) for body composition analysis;

2. measurement of biomarkers of bone turnover and parathyroid hormone levels;

3. evaluation of the nutritional status of patients.

Analysis of pre-intervention walking and the ability to recover motor activity after bariatric surgery using gait analysis. Through Gait Analysis it is possible to analyze body movement and muscle activity.

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