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Evidence That Kidney Function but Not Type 2 Diabetes Determines Retinol-Binding Protein 4 Serum Levels

OBJECTIVE— It has been suggested that retinol-binding protein 4 (RBP4) links adiposity, insulin resistance, and type 2 diabetes. However, circulating RBP4 levels are also affected by kidney function. Therefore, the aim of this study was to test whether RBP4 serum levels are primarily associated with...

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Autores principales: Henze, Andrea, Frey, Simone K., Raila, Jens, Tepel, Martin, Scholze, Alexandra, Pfeiffer, Andreas F. H., Weickert, Martin O., Spranger, Joachim, Schweigert, Florian J.
Formato: Texto
Lenguaje:English
Publicado: American Diabetes Association 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2584139/
https://www.ncbi.nlm.nih.gov/pubmed/18796616
http://dx.doi.org/10.2337/db08-0866
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author Henze, Andrea
Frey, Simone K.
Raila, Jens
Tepel, Martin
Scholze, Alexandra
Pfeiffer, Andreas F. H.
Weickert, Martin O.
Spranger, Joachim
Schweigert, Florian J.
author_facet Henze, Andrea
Frey, Simone K.
Raila, Jens
Tepel, Martin
Scholze, Alexandra
Pfeiffer, Andreas F. H.
Weickert, Martin O.
Spranger, Joachim
Schweigert, Florian J.
author_sort Henze, Andrea
collection PubMed
description OBJECTIVE— It has been suggested that retinol-binding protein 4 (RBP4) links adiposity, insulin resistance, and type 2 diabetes. However, circulating RBP4 levels are also affected by kidney function. Therefore, the aim of this study was to test whether RBP4 serum levels are primarily associated with kidney function or type 2 diabetes. RESEARCH DESIGN AND METHODS— RBP4 serum concentration was determined by enzyme-linked immunosorbent assay in 126 nondiabetic and 104 type 2 diabetic subjects. The study population was divided according to estimated glomerular filtration rate (eGFR) into the following groups: eGFR >90 ml/min per 1.73 m(2) (n = 53), 60–90 ml/min per 1.73 m(2) (n = 90), 30–60 ml/min per 1.73 m(2) (n = 38), and <30 ml/min per 1.73 m(2) (n = 49). Each group was subdivided into nondiabetic and type 2 diabetic subjects. RESULTS— RBP4 serum concentration was elevated (2.65 vs. 2.01 μmol/l; P < 0.001) and eGFR was reduced (56 vs. 74 ml/min per 1.73 m(2); P < 0.001) in type 2 diabetic vs. nondiabetic subjects, respectively. By stratifying for eGFR, no more differences in RBP4 serum concentration were detectable between type 2 diabetic and nondiabetic subjects. A linear regression analysis revealed an influence of eGFR (r = −0.477; P < 0.001) but not A1C (r = 0.093; P = 0.185) on RBP4 serum concentration. CONCLUSIONS— Existing human data showing elevated RBP4 levels in type 2 diabetic patients may be the result of moderate renal insufficiency rather than support for the suggestion that RBP4 links obesity to type 2 diabetes.
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spelling pubmed-25841392009-12-01 Evidence That Kidney Function but Not Type 2 Diabetes Determines Retinol-Binding Protein 4 Serum Levels Henze, Andrea Frey, Simone K. Raila, Jens Tepel, Martin Scholze, Alexandra Pfeiffer, Andreas F. H. Weickert, Martin O. Spranger, Joachim Schweigert, Florian J. Diabetes Pathophysiology OBJECTIVE— It has been suggested that retinol-binding protein 4 (RBP4) links adiposity, insulin resistance, and type 2 diabetes. However, circulating RBP4 levels are also affected by kidney function. Therefore, the aim of this study was to test whether RBP4 serum levels are primarily associated with kidney function or type 2 diabetes. RESEARCH DESIGN AND METHODS— RBP4 serum concentration was determined by enzyme-linked immunosorbent assay in 126 nondiabetic and 104 type 2 diabetic subjects. The study population was divided according to estimated glomerular filtration rate (eGFR) into the following groups: eGFR >90 ml/min per 1.73 m(2) (n = 53), 60–90 ml/min per 1.73 m(2) (n = 90), 30–60 ml/min per 1.73 m(2) (n = 38), and <30 ml/min per 1.73 m(2) (n = 49). Each group was subdivided into nondiabetic and type 2 diabetic subjects. RESULTS— RBP4 serum concentration was elevated (2.65 vs. 2.01 μmol/l; P < 0.001) and eGFR was reduced (56 vs. 74 ml/min per 1.73 m(2); P < 0.001) in type 2 diabetic vs. nondiabetic subjects, respectively. By stratifying for eGFR, no more differences in RBP4 serum concentration were detectable between type 2 diabetic and nondiabetic subjects. A linear regression analysis revealed an influence of eGFR (r = −0.477; P < 0.001) but not A1C (r = 0.093; P = 0.185) on RBP4 serum concentration. CONCLUSIONS— Existing human data showing elevated RBP4 levels in type 2 diabetic patients may be the result of moderate renal insufficiency rather than support for the suggestion that RBP4 links obesity to type 2 diabetes. American Diabetes Association 2008-12 /pmc/articles/PMC2584139/ /pubmed/18796616 http://dx.doi.org/10.2337/db08-0866 Text en Copyright © 2008, American Diabetes Association https://creativecommons.org/licenses/by-nc-nd/3.0/Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.
spellingShingle Pathophysiology
Henze, Andrea
Frey, Simone K.
Raila, Jens
Tepel, Martin
Scholze, Alexandra
Pfeiffer, Andreas F. H.
Weickert, Martin O.
Spranger, Joachim
Schweigert, Florian J.
Evidence That Kidney Function but Not Type 2 Diabetes Determines Retinol-Binding Protein 4 Serum Levels
title Evidence That Kidney Function but Not Type 2 Diabetes Determines Retinol-Binding Protein 4 Serum Levels
title_full Evidence That Kidney Function but Not Type 2 Diabetes Determines Retinol-Binding Protein 4 Serum Levels
title_fullStr Evidence That Kidney Function but Not Type 2 Diabetes Determines Retinol-Binding Protein 4 Serum Levels
title_full_unstemmed Evidence That Kidney Function but Not Type 2 Diabetes Determines Retinol-Binding Protein 4 Serum Levels
title_short Evidence That Kidney Function but Not Type 2 Diabetes Determines Retinol-Binding Protein 4 Serum Levels
title_sort evidence that kidney function but not type 2 diabetes determines retinol-binding protein 4 serum levels
topic Pathophysiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2584139/
https://www.ncbi.nlm.nih.gov/pubmed/18796616
http://dx.doi.org/10.2337/db08-0866
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