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Association between serum Cystatin C and renal injury in patients with chronic hepatitis B
To explore the association between serum cystatin C (Cys-C) and renal damage in patients with chronic hepatitis B. We retrospectively analyzed the clinical data of 425 patients with chronic hepatitis B virus (HBV) infection. Liver stiffness measured by FibroScan was used to diagnosis liver fibrosis....
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7593051/ https://www.ncbi.nlm.nih.gov/pubmed/32769895 http://dx.doi.org/10.1097/MD.0000000000021551 |
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author | Zheng, Hui Liu, Haidong Hao, Anhua Zhang, Min Wang, Dexin |
author_facet | Zheng, Hui Liu, Haidong Hao, Anhua Zhang, Min Wang, Dexin |
author_sort | Zheng, Hui |
collection | PubMed |
description | To explore the association between serum cystatin C (Cys-C) and renal damage in patients with chronic hepatitis B. We retrospectively analyzed the clinical data of 425 patients with chronic hepatitis B virus (HBV) infection. Liver stiffness measured by FibroScan was used to diagnosis liver fibrosis. Cys-C levels were detected via latex-enhanced immunoturbidimetric assay. A total of 425 patients were enrolled. Among them, 217 were patients with CHB with an eGFR > 90 mL/min/1.73 m(2) and 208 with an eGFR ≤90 mL/min/1.73 m(2). Cys-C levels significantly differed in patients with eGFR > 90 mL/min/1.73 m(2) compared with patients with eGFR ≤90 mL/min/1.73 m(2) (0.81 ± 0.05 vs 1.05 ± 0.06 mg/L, P < .001). Moreover, the Cys-C levels were 0.82 ± 0.04 mg/L in patients without liver fibrosis, 0.98 ± 0.05 mg/L in patients with mild liver fibrosis, 1.05 ± 0.08 mg/L in patients with advanced liver fibrosis, and 1.12 ± 0.07 mg/L in patients with liver cirrhosis (P < .001). Multivariate analyses were conducted to explore the independent factors associated with a decreased eGFR. Multivariate analysis suggested that T2DM (P = .032), liver fibrosis (P = .013), and Cys-C level (P = .035) were the independent factors associated with the decreased eGFR in patients with CHB. While age (P = .020) and Cys-C level (P = .001) were the independent factors associated with the decreased eGFR in patients with CHB-related fibrosis. The fibrosis group had significantly higher Cys-C levels than those without fibrosis. Routine monitoring of Cys-C levels is of positive significance in preventing the development of renal impairment of CHB patients. |
format | Online Article Text |
id | pubmed-7593051 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-75930512020-10-29 Association between serum Cystatin C and renal injury in patients with chronic hepatitis B Zheng, Hui Liu, Haidong Hao, Anhua Zhang, Min Wang, Dexin Medicine (Baltimore) 4900 To explore the association between serum cystatin C (Cys-C) and renal damage in patients with chronic hepatitis B. We retrospectively analyzed the clinical data of 425 patients with chronic hepatitis B virus (HBV) infection. Liver stiffness measured by FibroScan was used to diagnosis liver fibrosis. Cys-C levels were detected via latex-enhanced immunoturbidimetric assay. A total of 425 patients were enrolled. Among them, 217 were patients with CHB with an eGFR > 90 mL/min/1.73 m(2) and 208 with an eGFR ≤90 mL/min/1.73 m(2). Cys-C levels significantly differed in patients with eGFR > 90 mL/min/1.73 m(2) compared with patients with eGFR ≤90 mL/min/1.73 m(2) (0.81 ± 0.05 vs 1.05 ± 0.06 mg/L, P < .001). Moreover, the Cys-C levels were 0.82 ± 0.04 mg/L in patients without liver fibrosis, 0.98 ± 0.05 mg/L in patients with mild liver fibrosis, 1.05 ± 0.08 mg/L in patients with advanced liver fibrosis, and 1.12 ± 0.07 mg/L in patients with liver cirrhosis (P < .001). Multivariate analyses were conducted to explore the independent factors associated with a decreased eGFR. Multivariate analysis suggested that T2DM (P = .032), liver fibrosis (P = .013), and Cys-C level (P = .035) were the independent factors associated with the decreased eGFR in patients with CHB. While age (P = .020) and Cys-C level (P = .001) were the independent factors associated with the decreased eGFR in patients with CHB-related fibrosis. The fibrosis group had significantly higher Cys-C levels than those without fibrosis. Routine monitoring of Cys-C levels is of positive significance in preventing the development of renal impairment of CHB patients. Wolters Kluwer Health 2020-08-07 /pmc/articles/PMC7593051/ /pubmed/32769895 http://dx.doi.org/10.1097/MD.0000000000021551 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 | 4900 Zheng, Hui Liu, Haidong Hao, Anhua Zhang, Min Wang, Dexin Association between serum Cystatin C and renal injury in patients with chronic hepatitis B |
title | Association between serum Cystatin C and renal injury in patients with chronic hepatitis B |
title_full | Association between serum Cystatin C and renal injury in patients with chronic hepatitis B |
title_fullStr | Association between serum Cystatin C and renal injury in patients with chronic hepatitis B |
title_full_unstemmed | Association between serum Cystatin C and renal injury in patients with chronic hepatitis B |
title_short | Association between serum Cystatin C and renal injury in patients with chronic hepatitis B |
title_sort | association between serum cystatin c and renal injury in patients with chronic hepatitis b |
topic | 4900 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7593051/ https://www.ncbi.nlm.nih.gov/pubmed/32769895 http://dx.doi.org/10.1097/MD.0000000000021551 |
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