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Implication of Nonalcoholic Fatty Liver Disease, Metabolic Syndrome, and Subclinical Inflammation on Mild Renal Insufficiency

BACKGROUND: Limited information exists about the impact of nonalcoholic fatty liver disease (NAFLD) on mild renal insufficiency. We compared the relative influence of NAFLD, metabolic syndrome (MetS), and subclinical inflammation, alone or in combination, on mild renal insufficiency. METHODS: This s...

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Autores principales: Nam, Ga Eun, Hwang, Soon Young, Chung, Hye Soo, Choi, Ju Hee, Lee, Hyun Jung, Kim, Nam Hoon, Yoo, Hye Jin, Seo, Ji-A, Kim, Sin Gon, Kim, Nan Hee, Baik, Sei Hyun, Choi, Kyung Mook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5902012/
https://www.ncbi.nlm.nih.gov/pubmed/29808087
http://dx.doi.org/10.1155/2018/1835486
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author Nam, Ga Eun
Hwang, Soon Young
Chung, Hye Soo
Choi, Ju Hee
Lee, Hyun Jung
Kim, Nam Hoon
Yoo, Hye Jin
Seo, Ji-A
Kim, Sin Gon
Kim, Nan Hee
Baik, Sei Hyun
Choi, Kyung Mook
author_facet Nam, Ga Eun
Hwang, Soon Young
Chung, Hye Soo
Choi, Ju Hee
Lee, Hyun Jung
Kim, Nam Hoon
Yoo, Hye Jin
Seo, Ji-A
Kim, Sin Gon
Kim, Nan Hee
Baik, Sei Hyun
Choi, Kyung Mook
author_sort Nam, Ga Eun
collection PubMed
description BACKGROUND: Limited information exists about the impact of nonalcoholic fatty liver disease (NAFLD) on mild renal insufficiency. We compared the relative influence of NAFLD, metabolic syndrome (MetS), and subclinical inflammation, alone or in combination, on mild renal insufficiency. METHODS: This study included 1174 Korean adults. NAFLD was diagnosed using ultrasonography. Mild renal insufficiency was defined as an estimated glomerular filtration rate (eGFR) ≥ 60 and <90 mL/min/1.73 m(2). RESULTS: In partial correlation analysis, several components of MetS and liver aminotransferase levels, but not high-sensitivity C-reactive protein (hsCRP), were associated with eGFR. Multivariate logistic regression analysis demonstrated the independent association of NAFLD (P = 0.034) and MetS (P = 0.018) with mild renal insufficiency, but not elevated hsCRP (P = 0.885). Furthermore, NAFLD without the MetS group (odds ratio (95% confidence interval) = 1.56 (1.05–2.34)) or MetS without the NAFLD group (1.82 (1.11–3.00)) was associated with mild renal insufficiency after adjusting for confounding variables. However, individuals with high hsCRP showed no relationship with mild renal insufficiency, irrespective of the existence of NAFLD. CONCLUSIONS: This study demonstrated that NAFLD and MetS are independently associated with mild renal insufficiency, whereas subclinical inflammation did not affect the risk for mild renal insufficiency in Korean adults.
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spelling pubmed-59020122018-05-28 Implication of Nonalcoholic Fatty Liver Disease, Metabolic Syndrome, and Subclinical Inflammation on Mild Renal Insufficiency Nam, Ga Eun Hwang, Soon Young Chung, Hye Soo Choi, Ju Hee Lee, Hyun Jung Kim, Nam Hoon Yoo, Hye Jin Seo, Ji-A Kim, Sin Gon Kim, Nan Hee Baik, Sei Hyun Choi, Kyung Mook Int J Endocrinol Research Article BACKGROUND: Limited information exists about the impact of nonalcoholic fatty liver disease (NAFLD) on mild renal insufficiency. We compared the relative influence of NAFLD, metabolic syndrome (MetS), and subclinical inflammation, alone or in combination, on mild renal insufficiency. METHODS: This study included 1174 Korean adults. NAFLD was diagnosed using ultrasonography. Mild renal insufficiency was defined as an estimated glomerular filtration rate (eGFR) ≥ 60 and <90 mL/min/1.73 m(2). RESULTS: In partial correlation analysis, several components of MetS and liver aminotransferase levels, but not high-sensitivity C-reactive protein (hsCRP), were associated with eGFR. Multivariate logistic regression analysis demonstrated the independent association of NAFLD (P = 0.034) and MetS (P = 0.018) with mild renal insufficiency, but not elevated hsCRP (P = 0.885). Furthermore, NAFLD without the MetS group (odds ratio (95% confidence interval) = 1.56 (1.05–2.34)) or MetS without the NAFLD group (1.82 (1.11–3.00)) was associated with mild renal insufficiency after adjusting for confounding variables. However, individuals with high hsCRP showed no relationship with mild renal insufficiency, irrespective of the existence of NAFLD. CONCLUSIONS: This study demonstrated that NAFLD and MetS are independently associated with mild renal insufficiency, whereas subclinical inflammation did not affect the risk for mild renal insufficiency in Korean adults. Hindawi 2018-04-02 /pmc/articles/PMC5902012/ /pubmed/29808087 http://dx.doi.org/10.1155/2018/1835486 Text en Copyright © 2018 Ga Eun Nam et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Nam, Ga Eun
Hwang, Soon Young
Chung, Hye Soo
Choi, Ju Hee
Lee, Hyun Jung
Kim, Nam Hoon
Yoo, Hye Jin
Seo, Ji-A
Kim, Sin Gon
Kim, Nan Hee
Baik, Sei Hyun
Choi, Kyung Mook
Implication of Nonalcoholic Fatty Liver Disease, Metabolic Syndrome, and Subclinical Inflammation on Mild Renal Insufficiency
title Implication of Nonalcoholic Fatty Liver Disease, Metabolic Syndrome, and Subclinical Inflammation on Mild Renal Insufficiency
title_full Implication of Nonalcoholic Fatty Liver Disease, Metabolic Syndrome, and Subclinical Inflammation on Mild Renal Insufficiency
title_fullStr Implication of Nonalcoholic Fatty Liver Disease, Metabolic Syndrome, and Subclinical Inflammation on Mild Renal Insufficiency
title_full_unstemmed Implication of Nonalcoholic Fatty Liver Disease, Metabolic Syndrome, and Subclinical Inflammation on Mild Renal Insufficiency
title_short Implication of Nonalcoholic Fatty Liver Disease, Metabolic Syndrome, and Subclinical Inflammation on Mild Renal Insufficiency
title_sort implication of nonalcoholic fatty liver disease, metabolic syndrome, and subclinical inflammation on mild renal insufficiency
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5902012/
https://www.ncbi.nlm.nih.gov/pubmed/29808087
http://dx.doi.org/10.1155/2018/1835486
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