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Effects of a Metabolic Mixture on Gut Inflammation and Permeability in Elderly Patients with Chronic Kidney Disease: A Proof-of-Concept Study

Intestinal barrier dysfunction is a risk factor for the progression of Chronic Kidney Disease (CKD). In this proof-of-concept study, we tested the effects of a mixture of Essential Amino Acids (EAAs) and mitochondrial substrates on intestinal inflammation and permeability of CKD patients. Eight pati...

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Autores principales: Aquilani, Roberto, Bolasco, Piergiorgio, Murtas, Stefano, Maestri, Roberto, Iadarola, Paolo, Testa, Cristian, Deiana, Maria Luisa, Esposito, Maria Paola, Contu, Rita, Cadeddu, Mariella, Secci, Romina, Boschi, Federica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9611170/
https://www.ncbi.nlm.nih.gov/pubmed/36295889
http://dx.doi.org/10.3390/metabo12100987
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author Aquilani, Roberto
Bolasco, Piergiorgio
Murtas, Stefano
Maestri, Roberto
Iadarola, Paolo
Testa, Cristian
Deiana, Maria Luisa
Esposito, Maria Paola
Contu, Rita
Cadeddu, Mariella
Secci, Romina
Boschi, Federica
author_facet Aquilani, Roberto
Bolasco, Piergiorgio
Murtas, Stefano
Maestri, Roberto
Iadarola, Paolo
Testa, Cristian
Deiana, Maria Luisa
Esposito, Maria Paola
Contu, Rita
Cadeddu, Mariella
Secci, Romina
Boschi, Federica
author_sort Aquilani, Roberto
collection PubMed
description Intestinal barrier dysfunction is a risk factor for the progression of Chronic Kidney Disease (CKD). In this proof-of-concept study, we tested the effects of a mixture of Essential Amino Acids (EAAs) and mitochondrial substrates on intestinal inflammation and permeability of CKD patients. Eight patients with stage 3b-4 CKD and 11 healthy controls after overnight fasting underwent fecal measures of calprotectin and zonulin levels (indicators of gut inflammation and permeability, respectively) and determinations of plasma amino acids. Only CKD patients were supplemented with the mixture (8 g/d diluted in water). Compared to controls, baseline fecal calprotectin, zonulin and plasma levels of some AA in CKD patients were significantly higher (p = 0.005; p = 0.001 and p = 0.02 to 0.003, respectively). After six months of supplementation, CKD baseline fecal levels of calprotectin and zonulin significantly (borderline for zonulin) decreased (p = 0.008 and p = 0.05, respectively). Plasma AA concentrations, including glutamine and alanine, were higher than at the baseline (p: 0.05 to 0.008). The supplementation of this mixture was associated with improved intestinal barrier dysfunction. Increased plasma AA levels might contribute to the improvement of gut barrier dysfunction.
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spelling pubmed-96111702022-10-28 Effects of a Metabolic Mixture on Gut Inflammation and Permeability in Elderly Patients with Chronic Kidney Disease: A Proof-of-Concept Study Aquilani, Roberto Bolasco, Piergiorgio Murtas, Stefano Maestri, Roberto Iadarola, Paolo Testa, Cristian Deiana, Maria Luisa Esposito, Maria Paola Contu, Rita Cadeddu, Mariella Secci, Romina Boschi, Federica Metabolites Article Intestinal barrier dysfunction is a risk factor for the progression of Chronic Kidney Disease (CKD). In this proof-of-concept study, we tested the effects of a mixture of Essential Amino Acids (EAAs) and mitochondrial substrates on intestinal inflammation and permeability of CKD patients. Eight patients with stage 3b-4 CKD and 11 healthy controls after overnight fasting underwent fecal measures of calprotectin and zonulin levels (indicators of gut inflammation and permeability, respectively) and determinations of plasma amino acids. Only CKD patients were supplemented with the mixture (8 g/d diluted in water). Compared to controls, baseline fecal calprotectin, zonulin and plasma levels of some AA in CKD patients were significantly higher (p = 0.005; p = 0.001 and p = 0.02 to 0.003, respectively). After six months of supplementation, CKD baseline fecal levels of calprotectin and zonulin significantly (borderline for zonulin) decreased (p = 0.008 and p = 0.05, respectively). Plasma AA concentrations, including glutamine and alanine, were higher than at the baseline (p: 0.05 to 0.008). The supplementation of this mixture was associated with improved intestinal barrier dysfunction. Increased plasma AA levels might contribute to the improvement of gut barrier dysfunction. MDPI 2022-10-18 /pmc/articles/PMC9611170/ /pubmed/36295889 http://dx.doi.org/10.3390/metabo12100987 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Aquilani, Roberto
Bolasco, Piergiorgio
Murtas, Stefano
Maestri, Roberto
Iadarola, Paolo
Testa, Cristian
Deiana, Maria Luisa
Esposito, Maria Paola
Contu, Rita
Cadeddu, Mariella
Secci, Romina
Boschi, Federica
Effects of a Metabolic Mixture on Gut Inflammation and Permeability in Elderly Patients with Chronic Kidney Disease: A Proof-of-Concept Study
title Effects of a Metabolic Mixture on Gut Inflammation and Permeability in Elderly Patients with Chronic Kidney Disease: A Proof-of-Concept Study
title_full Effects of a Metabolic Mixture on Gut Inflammation and Permeability in Elderly Patients with Chronic Kidney Disease: A Proof-of-Concept Study
title_fullStr Effects of a Metabolic Mixture on Gut Inflammation and Permeability in Elderly Patients with Chronic Kidney Disease: A Proof-of-Concept Study
title_full_unstemmed Effects of a Metabolic Mixture on Gut Inflammation and Permeability in Elderly Patients with Chronic Kidney Disease: A Proof-of-Concept Study
title_short Effects of a Metabolic Mixture on Gut Inflammation and Permeability in Elderly Patients with Chronic Kidney Disease: A Proof-of-Concept Study
title_sort effects of a metabolic mixture on gut inflammation and permeability in elderly patients with chronic kidney disease: a proof-of-concept study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9611170/
https://www.ncbi.nlm.nih.gov/pubmed/36295889
http://dx.doi.org/10.3390/metabo12100987
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