About this trial
Obesity is a complex chronic disease, in which both genetic and environmental factors are involved, that shows a great heterogeneity in the response to different weight loss programs. Identifying patients as responder or no responder to the different obesity treatment options is a concept of great interest, both due to the high prevalence of obesity and its high consumption of resources. More than 500,000 surgeries are performed every year around the world, of which approximately 30% will present unsatisfactory results.
The general objective is to carry out a multi-omics approach for the discovery and validation of markers of weight response to bariatric surgery (BS) in a large sample of people with severe obesity (n=6,966 men and women who underwent sleeve gastrectomy or gastric bypass, including an additional external validation set). Thus, the investigators want to know the integrated contribution of several genomic markers (Genome Wide Association study, GWAs), new clinical and analytical variables (human exposome concept) and gender perspective to the prediction of response to the intervention at 12 month and its long-term longitudinal maintenance (3 years). The investigators intend, therefore, to provide new evidence to advance towards precision medicine. The investigators will focus our attention also on identifying those patients who, after being classified at the weight loss nadir as responders experienced weight regain.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Men and women between the ages of 18 and 65 at the time of surgery
SG or RYBP as bariatric procedure.
With a BMI≥35.0 kg/m2 with one or more comorbidities or a BMI>40.0 kg/m2 at the time of surgery.
Provision of an informed consent form signed and personally dated by the patient.
Disqualifiers
Any previous gastrointestinal surgery
Treatment with any approved antiobesity drug in Spain (orlistat, liraglutide 3.0 mg and/or naltrexone/bupropion extended release) or systemic glucocorticoids for more than 4 consecutive weeks during the 3 years following BS
End stage kidney disease (eGFR <15 ml/min/1.73m2) or liver cirrhosis at baseline
Patients who developed any major medical conditions that limits the practice of a healthy life within normal limits (advanced cardiovascular disease or heart failure, stroke with neurological sequelae, chronic pulmonary obstructive disease with dyspnea at minimal exertion, severe joint pathology, end stage renal failure, or active cancer)
Trial population
This multicenter retrospective study will be aimed at 6,966 obese patients undergoing BS, whose surgical technique (sleeve gastrectomy vs gastric bypass) has been performed at least 3 years before, evaluating the best combination of genetic and exposomal characteristics (clinical and analytical) that will predict which patients will be responders and non-responders in terms of weight loss.
Trial design
Cohort
Prospective
Treatments tested in this trial
Not listed
Trial groups
11
Trial groupsSee each trial group below.
Trial outcomes
Primary outcomes
Genomic markers that can predict the weight change response to bariatric surgery
Percentage of initial weight change
Secondary outcomes
Genomic markers that can predict comorbidities response to bariatric surgery
Type 2 diabetes mellitus, sleep apnea, fatty liver
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Institut de Recerca Biomèdica de Lleida
Lead sponsor
ISCIII
Collaborator