Sarcopenic Obesity as a Risk of Premature Aging
NCT05443711 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 75
Last updated 2024-02-29
Summary
Recently, numerous signaling proteins derived from adipose tissue and/or skeletal muscle have been described and are involved in the pathogenesis of obesity and the pathophysiology of aging. Current evidence suggests a role for the FGF-Klotho system, circulating cell-free DNA (cfDNA), miR-499, and exosomes not only in the pathophysiology of obesity, but also in the association with sarcopenic obesity (OS) and in a accelerated aging.
The investigator´s hypothesis is that obesity, especially OS, might be the cause of advanced aging, reflected in lower levels of the FGF-Klotho system, higher concentrations of cfDNA and a change in the profiles of miRNAs and exosomes, which could have an impact on risk. cardiovascular and metabolic.
For this, a descriptive cross-sectional study is proposed in 50 patients with obesity, who will be classified as OS or not, and 25 healthy controls, between 50-60 years old. The determinations are made by the IBIOMED of the University of León.
To study the evolution of aging markers over a year of follow-up, a second part of the study will analyze the possible differences according to the treatments assigned to each patient in the context of real life (lifestyle changes, drugs, bariatric surgery).
Conditions
- Obesity
- Sarcopenic Obesity
- Aging
Interventions
- OTHER
-
No intervention, observational study
No intervention, observational study
Sponsors & Collaborators
-
Universidad de León
collaborator OTHER -
Hospital de Leon
lead OTHER_GOV
Principal Investigators
-
Maria D Ballesteros Pomar, PhD · Complejo Asistencial Universitario de León
Eligibility
- Min Age
- 50 Years
- Max Age
- 60 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2022-01-19
- Primary Completion
- 2024-12-05
- Completion
- 2024-12-31
Countries
- Spain
Study Locations
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