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SARCOBEAGING: Sarcopenic Obesity as a Risk of Premature Aging
Authors not listed
Hospital de Leon · 2022
Abstract
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).
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Cite this
APA
Anonymous. (2022). SARCOBEAGING: Sarcopenic Obesity as a Risk of Premature Aging. <em>Hospital de Leon</em>. https://clinicaltrials.gov/study/NCT05443711
Vancouver
Anonymous. SARCOBEAGING: Sarcopenic Obesity as a Risk of Premature Aging. Hospital de Leon. 2022.
BibTeX
@misc{anon2022SARCOB,
title = {SARCOBEAGING: Sarcopenic Obesity as a Risk of Premature Aging},
author = {Anonymous},
journal = {Hospital de Leon},
year = {2022},
}
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