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Bariatric surgery and calcifediol treatment, Gordian knot of severe-obesity-related comorbidities treatment

BACKGROUND: Obesity (OB) is a chronic metabolic disease with important associated comorbidities and mortality. Vitamin D supplementation is frequently administered after bariatric surgery (BS), so as to reduce OB-related complications, maybe including chronic inflammation. AIM: This study aimed to e...

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Detalles Bibliográficos
Autores principales: Herrera-Martínez, Aura D., Castillo-Peinado, Laura L. S., Molina-Puerta, María J., Calañas-Continente, Alfonso, Membrives, Antonio, Castilla, Juan, Camacho Cardenosa, Marta, Casado-Díaz, Antonio, Gálvez-Moreno, María A., Gahete, Manuel D., Quesada Gómez, José Manuel, Bouillon, Roger, Priego-Capote, Feliciano, Luque, Raúl M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10588639/
https://www.ncbi.nlm.nih.gov/pubmed/37867510
http://dx.doi.org/10.3389/fendo.2023.1243906
Descripción
Sumario:BACKGROUND: Obesity (OB) is a chronic metabolic disease with important associated comorbidities and mortality. Vitamin D supplementation is frequently administered after bariatric surgery (BS), so as to reduce OB-related complications, maybe including chronic inflammation. AIM: This study aimed to explore relations between vitamin D metabolites and components of the inflammasome machinery in OB before and after BS and their relations with the improvement of metabolic comorbidities. PATIENTS AND METHODS: Epidemiological/clinical/anthropometric/biochemical evaluation was performed in patients with OB at baseline and 6 months after BS. Evaluation of i) vitamin-D metabolites in plasma and ii) components of the inflammasome machinery and inflammatory-associated factors [NOD-like-receptors (NLRs), inflammasome-activation-components, cytokines and inflammation/apoptosis-related components, and cell-cycle and DNA-damage regulators] in peripheral blood mononuclear cells (PBMCs) was performed at baseline and 6 months after BS. Clinical and molecular correlations/associations were analyzed. RESULTS: Significant correlations between vitamin D metabolites and inflammasome-machinery components were observed at baseline, and these correlations were significantly reduced 6 months after BS in parallel to a decrease in inflammation markers, fat mass, and body weight. Treatment with calcifediol remarkably increased 25OHD levels, despite 24,25(OH)(2)D(3) remained stable after BS. Several inflammasome-machinery components were associated with improvement in metabolic comorbidities, especially hypertension and dyslipidemia. CONCLUSION: The beneficial effects of vitamin D on OB-related comorbidities after BS patients are associated with significant changes in the molecular expression of key inflammasome-machinery components. The expression profile of these inflammasome components can be dynamically modulated in PBMCs after BS and vitamin D supplementation, suggesting that this profile could likely serve as a sensor and early predictor of the reversal of OB-related complications after BS.