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Long-term study of the association of adipokines and glucose variability with diabetic complications

BACKGROUND/AIMS: Recent studies have suggested an important role of adipokines in the development of insulin resistance and diabetes mellitus. The clinical relevance of adipokines on long-term outcomes in patients with diabetes and chronic kidney disease is uncertain. The purpose of this study was t...

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Autores principales: Cha, Jin Joo, Min, Hye Sook, Kim, Kitae, Lee, Mi Jin, Lee, Mi Hwa, Kim, Jung Eun, Song, Hye Kyoung, Cha, Dae Ryong, Kang, Young Sun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Association of Internal Medicine 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5840591/
https://www.ncbi.nlm.nih.gov/pubmed/27809453
http://dx.doi.org/10.3904/kjim.2016.114
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author Cha, Jin Joo
Min, Hye Sook
Kim, Kitae
Lee, Mi Jin
Lee, Mi Hwa
Kim, Jung Eun
Song, Hye Kyoung
Cha, Dae Ryong
Kang, Young Sun
author_facet Cha, Jin Joo
Min, Hye Sook
Kim, Kitae
Lee, Mi Jin
Lee, Mi Hwa
Kim, Jung Eun
Song, Hye Kyoung
Cha, Dae Ryong
Kang, Young Sun
author_sort Cha, Jin Joo
collection PubMed
description BACKGROUND/AIMS: Recent studies have suggested an important role of adipokines in the development of insulin resistance and diabetes mellitus. The clinical relevance of adipokines on long-term outcomes in patients with diabetes and chronic kidney disease is uncertain. The purpose of this study was to identify a predictable factor in patients with long-term diabetic complications. METHODS: A total of 161 diabetic individuals were followed-up from 2002 to 2013. Circulating plasma levels of adiponectin, glypican-4, irisin, visfatin, and visit-to-visit glucose variability were measured in diabetic patients. Associations among adipokines and variable metabolic parameters and microvascular, and macrovascular complications were evaluated. RESULTS: Plasma adiponectin and glypican-4 levels were significantly increased in patients with renal insufficiency. These adipokines were negatively associated with estimated glomerular filtration rate and positively associated with urinary albumin excretion. The relative risk of renal progression to dialysis increased independently with increasing level of adiponectin. Glypican-4 and visfatin were not predictive of any microvascular or macrovascular complications. Glucose variability increased the risk of diabetic nephropathy and cerebrovascular complications. CONCLUSIONS: Adiponectin and glypican-4 were associated with renal function and might be able to predict renal progression. Glucose variability was a predictable factor for diabetic nephropathy and cerebrovascular complications.
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spelling pubmed-58405912018-03-08 Long-term study of the association of adipokines and glucose variability with diabetic complications Cha, Jin Joo Min, Hye Sook Kim, Kitae Lee, Mi Jin Lee, Mi Hwa Kim, Jung Eun Song, Hye Kyoung Cha, Dae Ryong Kang, Young Sun Korean J Intern Med Original Article BACKGROUND/AIMS: Recent studies have suggested an important role of adipokines in the development of insulin resistance and diabetes mellitus. The clinical relevance of adipokines on long-term outcomes in patients with diabetes and chronic kidney disease is uncertain. The purpose of this study was to identify a predictable factor in patients with long-term diabetic complications. METHODS: A total of 161 diabetic individuals were followed-up from 2002 to 2013. Circulating plasma levels of adiponectin, glypican-4, irisin, visfatin, and visit-to-visit glucose variability were measured in diabetic patients. Associations among adipokines and variable metabolic parameters and microvascular, and macrovascular complications were evaluated. RESULTS: Plasma adiponectin and glypican-4 levels were significantly increased in patients with renal insufficiency. These adipokines were negatively associated with estimated glomerular filtration rate and positively associated with urinary albumin excretion. The relative risk of renal progression to dialysis increased independently with increasing level of adiponectin. Glypican-4 and visfatin were not predictive of any microvascular or macrovascular complications. Glucose variability increased the risk of diabetic nephropathy and cerebrovascular complications. CONCLUSIONS: Adiponectin and glypican-4 were associated with renal function and might be able to predict renal progression. Glucose variability was a predictable factor for diabetic nephropathy and cerebrovascular complications. The Korean Association of Internal Medicine 2018-03 2016-11-04 /pmc/articles/PMC5840591/ /pubmed/27809453 http://dx.doi.org/10.3904/kjim.2016.114 Text en Copyright © 2018 The Korean Association of Internal Medicine This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Cha, Jin Joo
Min, Hye Sook
Kim, Kitae
Lee, Mi Jin
Lee, Mi Hwa
Kim, Jung Eun
Song, Hye Kyoung
Cha, Dae Ryong
Kang, Young Sun
Long-term study of the association of adipokines and glucose variability with diabetic complications
title Long-term study of the association of adipokines and glucose variability with diabetic complications
title_full Long-term study of the association of adipokines and glucose variability with diabetic complications
title_fullStr Long-term study of the association of adipokines and glucose variability with diabetic complications
title_full_unstemmed Long-term study of the association of adipokines and glucose variability with diabetic complications
title_short Long-term study of the association of adipokines and glucose variability with diabetic complications
title_sort long-term study of the association of adipokines and glucose variability with diabetic complications
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5840591/
https://www.ncbi.nlm.nih.gov/pubmed/27809453
http://dx.doi.org/10.3904/kjim.2016.114
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