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Genetic Susceptibility to Predict Weight Loss After Bariatric Surgery

Genetic Susceptibility to Predict Weight Loss After Bariatric Surgery

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06226194
Acronym
GENBASU
Enrollment
6966
Registered
2024-01-26
Start date
2024-03-15
Completion date
2028-11-29
Last updated
2024-03-06

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

Conditions

Bariatric Surgery Candidate, Genetic Predisposition, Metabolic Syndrome, Obesity, Morbid, Weight Loss

Brief summary

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.

Interventions

None listed

Sponsors

ISCIII
CollaboratorUNKNOWN
Institut de Recerca Biomèdica de Lleida
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* 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. * With available baseline data (anthropometric, analytical, surgical procedure, pharmacological therapies, and obesity-related comorbidities).

Exclusion criteria

* 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) * Known type 1 diabetes or LADA diabetes * Women who become pregnant during the follow-up period * Current drug or alcohol abuse * Uncontrolled psychiatric illness or eating disorders developed during the follow-up period.

Design outcomes

Primary

MeasureTime frameDescription
Genomic markers that can predict the weight change response to bariatric surgery3 yearsPercentage of initial weight change

Secondary

MeasureTime frameDescription
Genomic markers that can predict comorbidities response to bariatric surgery3 yearsType 2 diabetes mellitus, sleep apnea, fatty liver

Countries

Spain

Contacts

Primary ContactAlbert Lecube Torelló, PhD
alecube@gmail.com0034973705183
Backup ContactEva López
elopez@irblleida.cat0034973706636

Outcome results

None listed

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