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Evaluation of urinary biomarkers for prediction of diabetic kidney disease: a propensity score matching analysis

BACKGROUND: The aim of this study was to evaluate the diagnostic value of six urinary biomarkers for prediction of diabetic kidney disease (DKD). METHODS: The cross-sectional study recruited 1053 hospitalized patients with type 2 diabetes mellitus (T2DM), who were categorized into the diabetes melli...

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Autores principales: Qin, Yongzhang, Zhang, Shuang, Shen, Xiaofang, Zhang, Shunming, Wang, Jingyu, Zuo, Minxia, Cui, Xiao, Gao, Zhongai, Yang, Juhong, Zhu, Hong, Chang, Baocheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6887810/
https://www.ncbi.nlm.nih.gov/pubmed/31832131
http://dx.doi.org/10.1177/2042018819891110
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author Qin, Yongzhang
Zhang, Shuang
Shen, Xiaofang
Zhang, Shunming
Wang, Jingyu
Zuo, Minxia
Cui, Xiao
Gao, Zhongai
Yang, Juhong
Zhu, Hong
Chang, Baocheng
author_facet Qin, Yongzhang
Zhang, Shuang
Shen, Xiaofang
Zhang, Shunming
Wang, Jingyu
Zuo, Minxia
Cui, Xiao
Gao, Zhongai
Yang, Juhong
Zhu, Hong
Chang, Baocheng
author_sort Qin, Yongzhang
collection PubMed
description BACKGROUND: The aim of this study was to evaluate the diagnostic value of six urinary biomarkers for prediction of diabetic kidney disease (DKD). METHODS: The cross-sectional study recruited 1053 hospitalized patients with type 2 diabetes mellitus (T2DM), who were categorized into the diabetes mellitus (DM) with normoalbuminuria (NA) group (n = 753) and DKD group (n = 300) according to 24-h urinary albumin excretion rate (24-h UAE). Data on the levels of six studied urinary biomarkers [transferrin (TF), immunoglobulin G (IgG), retinol-binding protein (RBP), β-galactosidase (GAL), N-acetyl-beta-glucosaminidase (NAG), and β2-microglobulin (β2MG)] were obtained. The propensity score matching (PSM) method was applied to eliminate the influences of confounding variables. RESULTS: Patients with DKD had higher levels of all six urinary biomarkers. All indicators demonstrated significantly increased risk of DKD, except for GAL and β2MG. Single RBP yielded the greatest area under the curve (AUC) value of 0.920 compared with the other five markers, followed by TF (0.867) and IgG (0.867). However, GAL, NAG, and β2MG were shown to have a weak prognostic ability. The diagnostic values of the different combinations were not superior to the single RBP. CONCLUSIONS: RBP, TF, and IgG could be used as reliable or good predictors of DKD. The combined use of these biomarkers did not improve DKD detection.
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spelling pubmed-68878102019-12-12 Evaluation of urinary biomarkers for prediction of diabetic kidney disease: a propensity score matching analysis Qin, Yongzhang Zhang, Shuang Shen, Xiaofang Zhang, Shunming Wang, Jingyu Zuo, Minxia Cui, Xiao Gao, Zhongai Yang, Juhong Zhu, Hong Chang, Baocheng Ther Adv Endocrinol Metab Original Research BACKGROUND: The aim of this study was to evaluate the diagnostic value of six urinary biomarkers for prediction of diabetic kidney disease (DKD). METHODS: The cross-sectional study recruited 1053 hospitalized patients with type 2 diabetes mellitus (T2DM), who were categorized into the diabetes mellitus (DM) with normoalbuminuria (NA) group (n = 753) and DKD group (n = 300) according to 24-h urinary albumin excretion rate (24-h UAE). Data on the levels of six studied urinary biomarkers [transferrin (TF), immunoglobulin G (IgG), retinol-binding protein (RBP), β-galactosidase (GAL), N-acetyl-beta-glucosaminidase (NAG), and β2-microglobulin (β2MG)] were obtained. The propensity score matching (PSM) method was applied to eliminate the influences of confounding variables. RESULTS: Patients with DKD had higher levels of all six urinary biomarkers. All indicators demonstrated significantly increased risk of DKD, except for GAL and β2MG. Single RBP yielded the greatest area under the curve (AUC) value of 0.920 compared with the other five markers, followed by TF (0.867) and IgG (0.867). However, GAL, NAG, and β2MG were shown to have a weak prognostic ability. The diagnostic values of the different combinations were not superior to the single RBP. CONCLUSIONS: RBP, TF, and IgG could be used as reliable or good predictors of DKD. The combined use of these biomarkers did not improve DKD detection. SAGE Publications 2019-12-02 /pmc/articles/PMC6887810/ /pubmed/31832131 http://dx.doi.org/10.1177/2042018819891110 Text en © The Author(s), 2019 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research
Qin, Yongzhang
Zhang, Shuang
Shen, Xiaofang
Zhang, Shunming
Wang, Jingyu
Zuo, Minxia
Cui, Xiao
Gao, Zhongai
Yang, Juhong
Zhu, Hong
Chang, Baocheng
Evaluation of urinary biomarkers for prediction of diabetic kidney disease: a propensity score matching analysis
title Evaluation of urinary biomarkers for prediction of diabetic kidney disease: a propensity score matching analysis
title_full Evaluation of urinary biomarkers for prediction of diabetic kidney disease: a propensity score matching analysis
title_fullStr Evaluation of urinary biomarkers for prediction of diabetic kidney disease: a propensity score matching analysis
title_full_unstemmed Evaluation of urinary biomarkers for prediction of diabetic kidney disease: a propensity score matching analysis
title_short Evaluation of urinary biomarkers for prediction of diabetic kidney disease: a propensity score matching analysis
title_sort evaluation of urinary biomarkers for prediction of diabetic kidney disease: a propensity score matching analysis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6887810/
https://www.ncbi.nlm.nih.gov/pubmed/31832131
http://dx.doi.org/10.1177/2042018819891110
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