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Sarcopenic Obesity in Individuals With Neurodisabilities: The SarcObeNDS Study

INTRODUCTION: Patients with neurodisabilities (NDS) are prone to alterations in body composition. Sarcopenic obesity (SO) is a condition characterized by increased adipose tissue accompanied by sarcopenia. The aim of this study was to investigate the prevalence of SO in patients with NDS, including...

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Detalles Bibliográficos
Autores principales: Dionyssiotis, Yannis, Prokopidis, Konstantinos, Trovas, George, Papadatou, Maria-Christina, Ananidis, Nikolaos, Tragoulias, Vasileios, Lazarou, Eleni, Christaki, Evangelia, Domazou, Marilena, Galanos, Antonios, Tyllianakis, Minos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9343584/
https://www.ncbi.nlm.nih.gov/pubmed/35928890
http://dx.doi.org/10.3389/fendo.2022.868298
Descripción
Sumario:INTRODUCTION: Patients with neurodisabilities (NDS) are prone to alterations in body composition. Sarcopenic obesity (SO) is a condition characterized by increased adipose tissue accompanied by sarcopenia. The aim of this study was to investigate the prevalence of SO in patients with NDS, including stroke, spinal cord, and traumatic brain injuries. METHODS: The study Sarcopenic Obesity in NeuroDisabled Subjects (acronym: SarcObeNDS) was a cross-sectional study of hospitalized patients (n = 82) and healthy controls (n = 32) with a mean age of 60.00 ± 14.22 years old. SO and sarcopenia were assessed through total body fat % (TBF %), fat mass index (fat mass to height(2): FMI = FM/h(2); kg/m(2)), and skeletal muscle index (appendicular skeletal muscle to height(2): SMI = ASM/h(2); kg/m(2)) via full-body dual-energy X-ray absorptiometry (DXA). This study was registered in the international database ClinicalTrials.gov with the unique identification number NCT03863379. RESULTS: A statistically significant difference was found in SMI (7.18 ± 0.95 vs. 6.00 ± 1.13 kg/m(2), p < 0.001) between controls and patients with NDS. No statistical significance was found for TBF (p = 0.783) and FMI (p = 0.143) between groups. The results remained the same after controlling the results for gender and BMI. A strong positive correlation was demonstrated between BMI and TBF for the total population (r = 0.616, p < 0.001), the control group (r = 0.616, p < 0.001), and patients with NDS (r = 0.728, p < 0.001). CONCLUSION: In summary, we observed significantly lower BMI and SMI scores in both genders compared to healthy controls. At the clinical level, a timely diagnosis and rapid treatment of sarcopenia and/or obesity in this population may prevent further metabolic repercussions accompanied by higher functional decline and lower quality of life.