Obesity and Type 2 diabetes mellitus (DMT2) are two of the most common chronic diseases of the Western society. Obesity is one critical factor in DMT2 development, with weight loss having profound beneficial effects on DMT2 and improving the metabolic pathophysiology leading to hyperglycemia. Observational studies reported that surgical intervention of morbid obesity achieved significant improvement of resolution of DMT2, both in short and long-term. Bariatric surgery has been considered the best option for treatment of diabetic obese patients, with the laparoscopic Roux-en-Y Gastric Bypass being the gold standard of the surgical treatment. Bariatric arterial embolization (BAE) technique has proved to be safe effective for weight loss in obese patients, but its metabolic effects have not been studied yet. The hypothesis of the study is that BAE is effective for the resolution of DMT2 inpatients with BMI between 30-43 Kg/m2. The aim is to assess DMT2 remission after BAE and bariatric surgery, to analyze potential conditioning factors, and to compare remission criteria between bariatric surgery and BAE.
The present project is a prospective, randomized, no-blinded, controlled and interventional clinical single- center study, which seeks to compare the impact of the following interventions: Roux-en-Y gastric By-pass (RYGB) and bariatric arterial embolization (BAE) on metabolic control in patients with DMT2 and BMI between 30-43 Kg/m2 over 2 years. Study initial recruitment will be achieved by an awareness campaign, which will emphasize a study of methods of diabetes management and include identification of patients into treatment at Cruz Vermelha Hospital. The investigator will initially pre-screen patients for the inclusion and exclusion criteria. Detailed information regarding of Diabetes, Obesity and randomization arms of the study would be provided in service meeting. Evaluation of the inclusion and exclusion criteria will occur both at the initial screening visit and the baseline visit prior to randomization. Patients who fail to be include during initial screening may be considered for re-consenting when clinically appropriate, and will have screening/baseline procedures repeated at the discretion of the Investigator. Patients who fail to be include during initial screening based on glycated hemoglobin (HbA1c) and or BMI and are re/screened within 6 months, will only have the baseline HbA1c and BMI repeated. On visit 2 (after 30 days) the 60 patients randomized per study arm for embolization or surgery procedures will be evaluated by the anaesthetist. RYGB or BAE will be scheduled as soon as possible after randomization. After BAE or surgery, patients will be followed 1, 3, 6 and 12 months. At 12 months visit patients will be evaluated for primary endpoint of percent of treatment group achieving HbA1c ≤ 6%. Pre-specified secondary outcomes include measures of glycaemic control, weight loss, mean blood pressure, lipid levels, renal function, assessment of diabetes quality of life (DQoL) and biomarkers in blood. Also, metabolic parameters and other markers will be evaluated from liver and adipose tissue biopsies collected at the beginning of the RYGB surgery to correlate with biochemical evaluations. During the follow-up visits primary and secondary outcomes will be evaluated by different techniques and approaches: body weight loss will be evaluated by bioimpedance analysis; blood will be collected for HbAlc, fasting glucose, lipids, comprehensive Metabolic Panel, Urinalysis (microalbumin and creatinine) and hepatogram by common clinical analysis; the diabetes quality of life (DQoL) question; liver and adipose tissues will be collected during the surgical procedure to asses by western blot the levels of each adenosine receptors, adipokynes, cytokines and inflammatory markers receptors.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
30
RYGB procedure requires 1-2 hours of operating time and two to three days length of hospital stay. Use the Kit-RYGB by J\& company.
use of Embosphere Microspheres (EM) that are designed to offer controlled, target embolization.
Cruz Vermelha Hospital
Lisbon, Portugal
RECRUITINGNumber of participants with glycated haemoglobin < 6%
The primary outcome of the study will be a level of glycated haemoglobin of 6.0% or less without the use of diabetes medications.
Time frame: 12 months
Determination of glycemic level (mg/dL)
Measures of glycemic control by evaluating glycemic level at fast in the blood in mg/dL. less than 126mg/dL will represent a good glycemic control
Time frame: up to 48 months
Weight evaluation in Kg
Evaluation of weight loss in Kg from the first appointment and during the different admissions time-points of each patient
Time frame: up to 48 months
Blood pressure measurement
Evaluation of mean blood pressure in mmHg in the first appointment and during the entire trial
Time frame: up to 48 months
Determination of lipid levels
Evaluation of lipid levels in the first appointment and during the entire trial
Time frame: up to 48 months
Determination of renal function
Evaluation of renal function by measuring creatinine levels in the blood in the first appointment and during the entire trial
Time frame: up to 48 months
Assess diabetes quality of life (DQoL) questionnaire
Evaluation of diabetes quality of life (DQoL) questionnaire in the first appointment and during the entire trial. it will measure reliability and validity of a diabetes quality-of-life and will measure the diabetes control and complications. The instrument provides an overall scale score ranging from 0 (lowest DQoL score) to 100 (highest DQoL score), as well as four subscale scores for: 1- satisfaction with treatment, 2- impact of treatment, 3- worry about the future effects of diabetes, and 4- worry about social/vocational issues.
Time frame: up to 48 months
Evaluation of adenosine metabolism in liver and adipose tissue biopsies
evaluation of adenosine receptors protein levels (A1R, A2aR, A2bR) (given in % of protein levels from control) on liver and adipose tissue collected at the beginning of RYGB surgery. the evaluation of the 3 receptors levels will allow to evaluate adenosine metabolism in a whole.
Time frame: At the beginning of the RYGB surgery
Evaluation of adipokines in adipose tissue biopsies
Evaluation of adipokines protein levels (leptin, adiponectin and resistin; given in % of protein levels from control) on adipose tissue collected at the beginning of RYGB surgery. the evaluation of the adipokines levels will allow to evaluate overall adipose tissue function.
Time frame: At the beginning of the RYGB surgery
Evaluation of cytokines in liver and adipose tissue biopsies
evaluation of cytokines protein levels \[interleukin 10 (IL10), tumor necrosis factor alpha (TNFalpha), interleukin 6 (IL6); given in % protein levels from the control) on liver and adipose tissue collected at the beginning of RYGB surgery. the evaluation of cytokines on both tissues will allow to determine the overall inflammatory status of the tissues.
Time frame: At the beginning of the RYGB surgery
Evaluation of inflammatory receptors levels in liver and adipose tissue biopsies
evaluation of inflammatory receptors protein levels (IL10 receptor, TNFalpha receptor, IL6 receptor; given in % protein levels from the control) on liver and adipose tissue collected at the beginning of RYGB surgery. the evaluation of cytokines on both tissues will allow to determine the overall inflammatory status of the tissues.
Time frame: At the beginning of the RYGB surgery
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