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Association of metabolic syndrome with serum fibroblast growth factor 21 in kidney transplanted patients

Introduction: Fibroblast growth factor 21 (FGF21) is a metabolic regulator with multiple beneficial effects on glucose and lipid homeostasis and insulin sensitivity. Objectives: The aim of this study was to investigate the relation between the serum level of FGF21 with and metabolic syndrome (MS) in...

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Autores principales: Bagheri, Leila, Hami, Maryam, Mojahedi, Mohammad-Javad, Ghorban Sabbagh, Mahin, Ayatollahi, Hosein
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nickan Research Institute 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4962674/
https://www.ncbi.nlm.nih.gov/pubmed/27471739
http://dx.doi.org/10.15171/jrip.2016.17
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author Bagheri, Leila
Hami, Maryam
Mojahedi, Mohammad-Javad
Ghorban Sabbagh, Mahin
Ayatollahi, Hosein
author_facet Bagheri, Leila
Hami, Maryam
Mojahedi, Mohammad-Javad
Ghorban Sabbagh, Mahin
Ayatollahi, Hosein
author_sort Bagheri, Leila
collection PubMed
description Introduction: Fibroblast growth factor 21 (FGF21) is a metabolic regulator with multiple beneficial effects on glucose and lipid homeostasis and insulin sensitivity. Objectives: The aim of this study was to investigate the relation between the serum level of FGF21 with and metabolic syndrome (MS) in kidney transplant recipients. Patients and Methods: We performed a cross-sectional study on 86 stable renal transplant recipients to detect possible relation between serum FGF21 level and MS during October 2014 and Mach 2015. Patients with past history of diabetes mellitus were excluded. Results: There were 43 patients in each group with and without MS. Totally, they were 52 (60.5%) male and 34 (39.5%) female. The mean age of the MS group was significantly higher than that of non-MS group. There was not significant difference between mean serum creatinine level and glomerular filtration rate (GFR) between two groups (P > 0.05). The MS patients had higher weight and body mass index (BMI) (P < 0.05). The prevalence of BMI >25 kg/m(2) in MS group was 25 (58.8%) versus non-MS group that only 10 (23.3%) had this condition (P < 0.05). The mean of FGF21 level in MS and non-MS groups was 1.23 ± 0.67 ng/l and 1.18 ± 0.71 ng/l, respectively (P > 0.05). There was not significant difference of serum FGF21 level between MS and non-MS patients (P > 0.05). Conclusion: While the elevated serum FGF21 level was found in subjects with insulin resistant states, however, this study revealed that serum FGF21 levels were not significantly increased in renal transplanted recipients with MS as compared with non-MS group.
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spelling pubmed-49626742016-07-28 Association of metabolic syndrome with serum fibroblast growth factor 21 in kidney transplanted patients Bagheri, Leila Hami, Maryam Mojahedi, Mohammad-Javad Ghorban Sabbagh, Mahin Ayatollahi, Hosein J Renal Inj Prev Original Article Introduction: Fibroblast growth factor 21 (FGF21) is a metabolic regulator with multiple beneficial effects on glucose and lipid homeostasis and insulin sensitivity. Objectives: The aim of this study was to investigate the relation between the serum level of FGF21 with and metabolic syndrome (MS) in kidney transplant recipients. Patients and Methods: We performed a cross-sectional study on 86 stable renal transplant recipients to detect possible relation between serum FGF21 level and MS during October 2014 and Mach 2015. Patients with past history of diabetes mellitus were excluded. Results: There were 43 patients in each group with and without MS. Totally, they were 52 (60.5%) male and 34 (39.5%) female. The mean age of the MS group was significantly higher than that of non-MS group. There was not significant difference between mean serum creatinine level and glomerular filtration rate (GFR) between two groups (P > 0.05). The MS patients had higher weight and body mass index (BMI) (P < 0.05). The prevalence of BMI >25 kg/m(2) in MS group was 25 (58.8%) versus non-MS group that only 10 (23.3%) had this condition (P < 0.05). The mean of FGF21 level in MS and non-MS groups was 1.23 ± 0.67 ng/l and 1.18 ± 0.71 ng/l, respectively (P > 0.05). There was not significant difference of serum FGF21 level between MS and non-MS patients (P > 0.05). Conclusion: While the elevated serum FGF21 level was found in subjects with insulin resistant states, however, this study revealed that serum FGF21 levels were not significantly increased in renal transplanted recipients with MS as compared with non-MS group. Nickan Research Institute 2016-04-24 /pmc/articles/PMC4962674/ /pubmed/27471739 http://dx.doi.org/10.15171/jrip.2016.17 Text en Copyright © 2016 The Author(s); Published by Nickan Research Institute http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Bagheri, Leila
Hami, Maryam
Mojahedi, Mohammad-Javad
Ghorban Sabbagh, Mahin
Ayatollahi, Hosein
Association of metabolic syndrome with serum fibroblast growth factor 21 in kidney transplanted patients
title Association of metabolic syndrome with serum fibroblast growth factor 21 in kidney transplanted patients
title_full Association of metabolic syndrome with serum fibroblast growth factor 21 in kidney transplanted patients
title_fullStr Association of metabolic syndrome with serum fibroblast growth factor 21 in kidney transplanted patients
title_full_unstemmed Association of metabolic syndrome with serum fibroblast growth factor 21 in kidney transplanted patients
title_short Association of metabolic syndrome with serum fibroblast growth factor 21 in kidney transplanted patients
title_sort association of metabolic syndrome with serum fibroblast growth factor 21 in kidney transplanted patients
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4962674/
https://www.ncbi.nlm.nih.gov/pubmed/27471739
http://dx.doi.org/10.15171/jrip.2016.17
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