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Normal liver enzymes are correlated with severity of metabolic syndrome in a large population based cohort

Key features of the metabolic syndrome are insulin resistance and diabetes. The liver as central metabolic organ is not only affected by the metabolic syndrome as non-alcoholic fatty liver disease (NAFLD), but may contribute to insulin resistance and metabolic alterations. We aimed to identify poten...

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Autores principales: Kälsch, Julia, Bechmann, Lars P., Heider, Dominik, Best, Jan, Manka, Paul, Kälsch, Hagen, Sowa, Jan-Peter, Moebus, Susanne, Slomiany, Uta, Jöckel, Karl-Heinz, Erbel, Raimund, Gerken, Guido, Canbay, Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4535035/
https://www.ncbi.nlm.nih.gov/pubmed/26269425
http://dx.doi.org/10.1038/srep13058
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author Kälsch, Julia
Bechmann, Lars P.
Heider, Dominik
Best, Jan
Manka, Paul
Kälsch, Hagen
Sowa, Jan-Peter
Moebus, Susanne
Slomiany, Uta
Jöckel, Karl-Heinz
Erbel, Raimund
Gerken, Guido
Canbay, Ali
author_facet Kälsch, Julia
Bechmann, Lars P.
Heider, Dominik
Best, Jan
Manka, Paul
Kälsch, Hagen
Sowa, Jan-Peter
Moebus, Susanne
Slomiany, Uta
Jöckel, Karl-Heinz
Erbel, Raimund
Gerken, Guido
Canbay, Ali
author_sort Kälsch, Julia
collection PubMed
description Key features of the metabolic syndrome are insulin resistance and diabetes. The liver as central metabolic organ is not only affected by the metabolic syndrome as non-alcoholic fatty liver disease (NAFLD), but may contribute to insulin resistance and metabolic alterations. We aimed to identify potential associations between liver injury markers and diabetes in the population-based Heinz Nixdorf RECALL Study. Demographic and laboratory data were analyzed in participants (n = 4814, age 45 to 75y). ALT and AST values were significantly higher in males than in females. Mean BMI was 27.9 kg/m(2) and type-2-diabetes (known and unkown) was present in 656 participants (13.7%). Adiponectin and vitamin D both correlated inversely with BMI. ALT, AST, and GGT correlated with BMI, CRP and HbA1c and inversely correlated with adiponectin levels. Logistic regression models using HbA1c and adiponectin or HbA1c and BMI were able to predict diabetes with high accuracy. Transaminase levels within normal ranges were closely associated with the BMI and diabetes risk. Transaminase levels and adiponectin were inversely associated. Re-assessment of current normal range limits should be considered, to provide a more exact indicator for chronic metabolic liver injury, in particular to reflect the situation in diabetic or obese individuals.
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spelling pubmed-45350352015-08-21 Normal liver enzymes are correlated with severity of metabolic syndrome in a large population based cohort Kälsch, Julia Bechmann, Lars P. Heider, Dominik Best, Jan Manka, Paul Kälsch, Hagen Sowa, Jan-Peter Moebus, Susanne Slomiany, Uta Jöckel, Karl-Heinz Erbel, Raimund Gerken, Guido Canbay, Ali Sci Rep Article Key features of the metabolic syndrome are insulin resistance and diabetes. The liver as central metabolic organ is not only affected by the metabolic syndrome as non-alcoholic fatty liver disease (NAFLD), but may contribute to insulin resistance and metabolic alterations. We aimed to identify potential associations between liver injury markers and diabetes in the population-based Heinz Nixdorf RECALL Study. Demographic and laboratory data were analyzed in participants (n = 4814, age 45 to 75y). ALT and AST values were significantly higher in males than in females. Mean BMI was 27.9 kg/m(2) and type-2-diabetes (known and unkown) was present in 656 participants (13.7%). Adiponectin and vitamin D both correlated inversely with BMI. ALT, AST, and GGT correlated with BMI, CRP and HbA1c and inversely correlated with adiponectin levels. Logistic regression models using HbA1c and adiponectin or HbA1c and BMI were able to predict diabetes with high accuracy. Transaminase levels within normal ranges were closely associated with the BMI and diabetes risk. Transaminase levels and adiponectin were inversely associated. Re-assessment of current normal range limits should be considered, to provide a more exact indicator for chronic metabolic liver injury, in particular to reflect the situation in diabetic or obese individuals. Nature Publishing Group 2015-08-13 /pmc/articles/PMC4535035/ /pubmed/26269425 http://dx.doi.org/10.1038/srep13058 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Kälsch, Julia
Bechmann, Lars P.
Heider, Dominik
Best, Jan
Manka, Paul
Kälsch, Hagen
Sowa, Jan-Peter
Moebus, Susanne
Slomiany, Uta
Jöckel, Karl-Heinz
Erbel, Raimund
Gerken, Guido
Canbay, Ali
Normal liver enzymes are correlated with severity of metabolic syndrome in a large population based cohort
title Normal liver enzymes are correlated with severity of metabolic syndrome in a large population based cohort
title_full Normal liver enzymes are correlated with severity of metabolic syndrome in a large population based cohort
title_fullStr Normal liver enzymes are correlated with severity of metabolic syndrome in a large population based cohort
title_full_unstemmed Normal liver enzymes are correlated with severity of metabolic syndrome in a large population based cohort
title_short Normal liver enzymes are correlated with severity of metabolic syndrome in a large population based cohort
title_sort normal liver enzymes are correlated with severity of metabolic syndrome in a large population based cohort
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4535035/
https://www.ncbi.nlm.nih.gov/pubmed/26269425
http://dx.doi.org/10.1038/srep13058
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