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α(1)-Acid Glycoprotein and Dietary Intake in End-Stage Renal Disease Patients

Management of end-stage renal disease (ESRD) patients requires monitoring each of the components of malnutrition–inflammation–atherosclerosis (MIA) syndrome. Restrictive diet can negatively affect nutritional status and inflammation. An acute-phase protein—α(1)-acid glycoprotein (AGP), has been asso...

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Autores principales: Maraj, Małgorzata, Hetwer, Paulina, Kuśnierz-Cabala, Beata, Maziarz, Barbara, Dumnicka, Paulina, Kuźniewski, Marek, Ceranowicz, Piotr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8621909/
https://www.ncbi.nlm.nih.gov/pubmed/34835927
http://dx.doi.org/10.3390/nu13113671
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author Maraj, Małgorzata
Hetwer, Paulina
Kuśnierz-Cabala, Beata
Maziarz, Barbara
Dumnicka, Paulina
Kuźniewski, Marek
Ceranowicz, Piotr
author_facet Maraj, Małgorzata
Hetwer, Paulina
Kuśnierz-Cabala, Beata
Maziarz, Barbara
Dumnicka, Paulina
Kuźniewski, Marek
Ceranowicz, Piotr
author_sort Maraj, Małgorzata
collection PubMed
description Management of end-stage renal disease (ESRD) patients requires monitoring each of the components of malnutrition–inflammation–atherosclerosis (MIA) syndrome. Restrictive diet can negatively affect nutritional status and inflammation. An acute-phase protein—α(1)-acid glycoprotein (AGP), has been associated with energy metabolism in animal and human studies. The aim of our study was to look for a relationship between serum AGP concentrations, laboratory parameters, and nutrient intake in ESRD patients. The study included 59 patients treated with maintenance hemodialysis. A 24 h recall assessed dietary intake during four non-consecutive days—two days in the post-summer period, and two post-winter. Selected laboratory tests were performed: complete blood count, serum iron, total iron biding capacity (TIBC) and unsaturated iron biding capacity (UIBC), vitamin D, AGP, C-reactive protein (CRP), albumin, prealbumin, and phosphate–calcium metabolism markers (intact parathyroid hormone, calcium, phosphate). Recorded dietary intake was highly deficient. A majority of patients did not meet recommended daily requirements for energy, protein, fiber, iron, magnesium, folate, and vitamin D. AGP correlated positively with CRP (R = 0.66), platelets (R = 0.29), and negatively with iron (R = −0.27) and TIBC (R = −0.30). AGP correlated negatively with the dietary intake of plant protein (R = −0.40), potassium (R = −0.27), copper (R = −0.30), vitamin B(6) (R = −0.27), and folates (R = −0.27), p < 0.05. However, in multiple regression adjusted for confounders, only CRP was significantly associated with AGP. Our results indicate that in hemodialyzed patients, serum AGP is weakly associated with dietary intake of several nutrients, including plant protein.
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spelling pubmed-86219092021-11-27 α(1)-Acid Glycoprotein and Dietary Intake in End-Stage Renal Disease Patients Maraj, Małgorzata Hetwer, Paulina Kuśnierz-Cabala, Beata Maziarz, Barbara Dumnicka, Paulina Kuźniewski, Marek Ceranowicz, Piotr Nutrients Article Management of end-stage renal disease (ESRD) patients requires monitoring each of the components of malnutrition–inflammation–atherosclerosis (MIA) syndrome. Restrictive diet can negatively affect nutritional status and inflammation. An acute-phase protein—α(1)-acid glycoprotein (AGP), has been associated with energy metabolism in animal and human studies. The aim of our study was to look for a relationship between serum AGP concentrations, laboratory parameters, and nutrient intake in ESRD patients. The study included 59 patients treated with maintenance hemodialysis. A 24 h recall assessed dietary intake during four non-consecutive days—two days in the post-summer period, and two post-winter. Selected laboratory tests were performed: complete blood count, serum iron, total iron biding capacity (TIBC) and unsaturated iron biding capacity (UIBC), vitamin D, AGP, C-reactive protein (CRP), albumin, prealbumin, and phosphate–calcium metabolism markers (intact parathyroid hormone, calcium, phosphate). Recorded dietary intake was highly deficient. A majority of patients did not meet recommended daily requirements for energy, protein, fiber, iron, magnesium, folate, and vitamin D. AGP correlated positively with CRP (R = 0.66), platelets (R = 0.29), and negatively with iron (R = −0.27) and TIBC (R = −0.30). AGP correlated negatively with the dietary intake of plant protein (R = −0.40), potassium (R = −0.27), copper (R = −0.30), vitamin B(6) (R = −0.27), and folates (R = −0.27), p < 0.05. However, in multiple regression adjusted for confounders, only CRP was significantly associated with AGP. Our results indicate that in hemodialyzed patients, serum AGP is weakly associated with dietary intake of several nutrients, including plant protein. MDPI 2021-10-20 /pmc/articles/PMC8621909/ /pubmed/34835927 http://dx.doi.org/10.3390/nu13113671 Text en © 2021 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
Maraj, Małgorzata
Hetwer, Paulina
Kuśnierz-Cabala, Beata
Maziarz, Barbara
Dumnicka, Paulina
Kuźniewski, Marek
Ceranowicz, Piotr
α(1)-Acid Glycoprotein and Dietary Intake in End-Stage Renal Disease Patients
title α(1)-Acid Glycoprotein and Dietary Intake in End-Stage Renal Disease Patients
title_full α(1)-Acid Glycoprotein and Dietary Intake in End-Stage Renal Disease Patients
title_fullStr α(1)-Acid Glycoprotein and Dietary Intake in End-Stage Renal Disease Patients
title_full_unstemmed α(1)-Acid Glycoprotein and Dietary Intake in End-Stage Renal Disease Patients
title_short α(1)-Acid Glycoprotein and Dietary Intake in End-Stage Renal Disease Patients
title_sort α(1)-acid glycoprotein and dietary intake in end-stage renal disease patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8621909/
https://www.ncbi.nlm.nih.gov/pubmed/34835927
http://dx.doi.org/10.3390/nu13113671
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