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Factors Influencing Renal Parenchymal Stiffiness in Patients with Diabetic Nephropathy

OBJECTIVE: Glomerulosclerosis and tubulointerstitial fibrosis are associated with lower renal parenchymal resilience. The purpose of this study is to determine the factors influencing renal resilience in patients with diabetic nephropathy (DN). METHODS: We recruited 56 healthy volunteers and 187 pat...

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Autores principales: Fang, Jian-Xiu, Chen, Xiao-Yan, Yang, Qing-Mei, Xue, Meng-Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8140885/
https://www.ncbi.nlm.nih.gov/pubmed/34040423
http://dx.doi.org/10.2147/IJGM.S311420
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author Fang, Jian-Xiu
Chen, Xiao-Yan
Yang, Qing-Mei
Xue, Meng-Hua
author_facet Fang, Jian-Xiu
Chen, Xiao-Yan
Yang, Qing-Mei
Xue, Meng-Hua
author_sort Fang, Jian-Xiu
collection PubMed
description OBJECTIVE: Glomerulosclerosis and tubulointerstitial fibrosis are associated with lower renal parenchymal resilience. The purpose of this study is to determine the factors influencing renal resilience in patients with diabetic nephropathy (DN). METHODS: We recruited 56 healthy volunteers and 187 patients with DN. All the participants were evaluated using shear-wave elastography (SWE), and the size of their kidneys and Young’s modulus values for the parenchyma were recorded. A total of 187 patients with DN are allocated to three groups according to their urinary albumin-to-creatinine ratio: normoalbuminuric (<30 mg/g creatinine), microalbuminuric (30–300 mg/g), and macroalbuminuric (≥300 mg/g) groups. Renal resilience is compared between the stages of diabetic nephropathy and the healthy control group, and the factors affecting the stiffiness of the renal parenchyma in DN are analyzed. RESULTS: The renal parenchyma is harder in participants with DN than in healthy participants (P < 0.001), and the stiffiness increases with the progression of the disease (P < 0.001). Multivariate logistic regression analysis shows that disease stage (β = 0.789, P < 0.001), duration of diabetes (β = 0.028, P < 0.001), and serum creatinine (SCr) concentration (β = 0.001, p < 0.001) influence the stiffiness of the renal parenchyma. CONCLUSION: We show that SWE can be used to measure changes in the stiffiness of the renal parenchyma in patients with DN. Furthermore, Young’s modulus of the renal parenchyma is related to the duration of diabetes, urinary albumin excretion, and SCr concentration. Thus, SWE can be used to objectively and non-invasively stage DN.
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spelling pubmed-81408852021-05-25 Factors Influencing Renal Parenchymal Stiffiness in Patients with Diabetic Nephropathy Fang, Jian-Xiu Chen, Xiao-Yan Yang, Qing-Mei Xue, Meng-Hua Int J Gen Med Original Research OBJECTIVE: Glomerulosclerosis and tubulointerstitial fibrosis are associated with lower renal parenchymal resilience. The purpose of this study is to determine the factors influencing renal resilience in patients with diabetic nephropathy (DN). METHODS: We recruited 56 healthy volunteers and 187 patients with DN. All the participants were evaluated using shear-wave elastography (SWE), and the size of their kidneys and Young’s modulus values for the parenchyma were recorded. A total of 187 patients with DN are allocated to three groups according to their urinary albumin-to-creatinine ratio: normoalbuminuric (<30 mg/g creatinine), microalbuminuric (30–300 mg/g), and macroalbuminuric (≥300 mg/g) groups. Renal resilience is compared between the stages of diabetic nephropathy and the healthy control group, and the factors affecting the stiffiness of the renal parenchyma in DN are analyzed. RESULTS: The renal parenchyma is harder in participants with DN than in healthy participants (P < 0.001), and the stiffiness increases with the progression of the disease (P < 0.001). Multivariate logistic regression analysis shows that disease stage (β = 0.789, P < 0.001), duration of diabetes (β = 0.028, P < 0.001), and serum creatinine (SCr) concentration (β = 0.001, p < 0.001) influence the stiffiness of the renal parenchyma. CONCLUSION: We show that SWE can be used to measure changes in the stiffiness of the renal parenchyma in patients with DN. Furthermore, Young’s modulus of the renal parenchyma is related to the duration of diabetes, urinary albumin excretion, and SCr concentration. Thus, SWE can be used to objectively and non-invasively stage DN. Dove 2021-05-18 /pmc/articles/PMC8140885/ /pubmed/34040423 http://dx.doi.org/10.2147/IJGM.S311420 Text en © 2021 Fang et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Fang, Jian-Xiu
Chen, Xiao-Yan
Yang, Qing-Mei
Xue, Meng-Hua
Factors Influencing Renal Parenchymal Stiffiness in Patients with Diabetic Nephropathy
title Factors Influencing Renal Parenchymal Stiffiness in Patients with Diabetic Nephropathy
title_full Factors Influencing Renal Parenchymal Stiffiness in Patients with Diabetic Nephropathy
title_fullStr Factors Influencing Renal Parenchymal Stiffiness in Patients with Diabetic Nephropathy
title_full_unstemmed Factors Influencing Renal Parenchymal Stiffiness in Patients with Diabetic Nephropathy
title_short Factors Influencing Renal Parenchymal Stiffiness in Patients with Diabetic Nephropathy
title_sort factors influencing renal parenchymal stiffiness in patients with diabetic nephropathy
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8140885/
https://www.ncbi.nlm.nih.gov/pubmed/34040423
http://dx.doi.org/10.2147/IJGM.S311420
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