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Hepatic fibrosis is associated with total proteinuria in Korean patients with type 2 diabetes

The association between non-alcoholic fatty liver disease (NAFLD) and diabetic kidney disease assessed using either albuminuria or proteinuria remains controversial. This study aimed to investigate the association between hepatic steatosis or fibrosis and albuminuria or proteinuria in Korean patient...

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Autores principales: Han, Eugene, Cho, Yongin, Kim, Kyung-won, Lee, Yong-ho, Kang, Eun Seok, Cha, Bong-Soo, Lee, Byung-wan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7437801/
https://www.ncbi.nlm.nih.gov/pubmed/32871978
http://dx.doi.org/10.1097/MD.0000000000021038
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author Han, Eugene
Cho, Yongin
Kim, Kyung-won
Lee, Yong-ho
Kang, Eun Seok
Cha, Bong-Soo
Lee, Byung-wan
author_facet Han, Eugene
Cho, Yongin
Kim, Kyung-won
Lee, Yong-ho
Kang, Eun Seok
Cha, Bong-Soo
Lee, Byung-wan
author_sort Han, Eugene
collection PubMed
description The association between non-alcoholic fatty liver disease (NAFLD) and diabetic kidney disease assessed using either albuminuria or proteinuria remains controversial. This study aimed to investigate the association between hepatic steatosis or fibrosis and albuminuria or proteinuria in Korean patients with type 2 diabetes mellitus (T2D). We enrolled 1108 patients with T2D and categorized as 3 groups; non-proteinuria (NP), isolated non-albumin proteinuria (iNAP), and albuminuria. Urinary albumin and protein levels were assessed as urinary albumin-to-creatinine ratio (uACR) and urinary protein-to-creatinine ratio (uPCR), respectively. Hepatic steatosis and fibrotic burden were assessed using the NAFLD liver fat score, Fibrosis-4 calculator (FIB-4) index, and NAFLD fibrosis score (NFS). The prevalence of significant steatosis was similar among groups (NP: 74.6% vs iNAP: 70.3% vs albuminuria: 79.9%, P = .085). The prevalence of significant fibrosis was significantly higher in the iNAP (18.7%) and albuminuria (16.5%) groups than in the NP group (9.5%, P = .001). Both uPCR and uACR showed a correlation with NFS (uPCR: r = 0.123, P < .001; uACR: r = 0.064, P = .033). In multivariate logistic regression analysis, uPCR ≥150 mg/g was found to have a stronger association with hepatic fibrosis than uACR ≥30 mg/g (adjusted odds ratio 1.55 [95% CI 1.03–2.33] vs adjusted odds ratio 1.16 [95% CI, 0.72–1.87]). In conclusion, patients with iNAP and albuminuria had a higher prevalence of hepatic fibrosis than those without proteinuria. Total proteinuria was associated with advanced liver fibrosis, whereas albuminuria was related to hepatic steatosis.
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spelling pubmed-74378012020-09-02 Hepatic fibrosis is associated with total proteinuria in Korean patients with type 2 diabetes Han, Eugene Cho, Yongin Kim, Kyung-won Lee, Yong-ho Kang, Eun Seok Cha, Bong-Soo Lee, Byung-wan Medicine (Baltimore) 4300 The association between non-alcoholic fatty liver disease (NAFLD) and diabetic kidney disease assessed using either albuminuria or proteinuria remains controversial. This study aimed to investigate the association between hepatic steatosis or fibrosis and albuminuria or proteinuria in Korean patients with type 2 diabetes mellitus (T2D). We enrolled 1108 patients with T2D and categorized as 3 groups; non-proteinuria (NP), isolated non-albumin proteinuria (iNAP), and albuminuria. Urinary albumin and protein levels were assessed as urinary albumin-to-creatinine ratio (uACR) and urinary protein-to-creatinine ratio (uPCR), respectively. Hepatic steatosis and fibrotic burden were assessed using the NAFLD liver fat score, Fibrosis-4 calculator (FIB-4) index, and NAFLD fibrosis score (NFS). The prevalence of significant steatosis was similar among groups (NP: 74.6% vs iNAP: 70.3% vs albuminuria: 79.9%, P = .085). The prevalence of significant fibrosis was significantly higher in the iNAP (18.7%) and albuminuria (16.5%) groups than in the NP group (9.5%, P = .001). Both uPCR and uACR showed a correlation with NFS (uPCR: r = 0.123, P < .001; uACR: r = 0.064, P = .033). In multivariate logistic regression analysis, uPCR ≥150 mg/g was found to have a stronger association with hepatic fibrosis than uACR ≥30 mg/g (adjusted odds ratio 1.55 [95% CI 1.03–2.33] vs adjusted odds ratio 1.16 [95% CI, 0.72–1.87]). In conclusion, patients with iNAP and albuminuria had a higher prevalence of hepatic fibrosis than those without proteinuria. Total proteinuria was associated with advanced liver fibrosis, whereas albuminuria was related to hepatic steatosis. Lippincott Williams & Wilkins 2020-08-14 /pmc/articles/PMC7437801/ /pubmed/32871978 http://dx.doi.org/10.1097/MD.0000000000021038 Text en Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0
spellingShingle 4300
Han, Eugene
Cho, Yongin
Kim, Kyung-won
Lee, Yong-ho
Kang, Eun Seok
Cha, Bong-Soo
Lee, Byung-wan
Hepatic fibrosis is associated with total proteinuria in Korean patients with type 2 diabetes
title Hepatic fibrosis is associated with total proteinuria in Korean patients with type 2 diabetes
title_full Hepatic fibrosis is associated with total proteinuria in Korean patients with type 2 diabetes
title_fullStr Hepatic fibrosis is associated with total proteinuria in Korean patients with type 2 diabetes
title_full_unstemmed Hepatic fibrosis is associated with total proteinuria in Korean patients with type 2 diabetes
title_short Hepatic fibrosis is associated with total proteinuria in Korean patients with type 2 diabetes
title_sort hepatic fibrosis is associated with total proteinuria in korean patients with type 2 diabetes
topic 4300
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7437801/
https://www.ncbi.nlm.nih.gov/pubmed/32871978
http://dx.doi.org/10.1097/MD.0000000000021038
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