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Noninvasive assessment of renal function and fibrosis in CKD patients using histogram analysis based on diffusion kurtosis imaging

PURPOSE: To investigate the potential of histogram analysis based on diffusion kurtosis imaging (DKI) in evaluating renal function and fibrosis associated with chronic kidney disease (CKD). MATERIALS AND METHODS: Thirty-six CKD patients were enrolled, and DKI was performed in all patients before the...

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Autores principales: Yuan, Guanjie, Qu, Weinuo, Li, Shichao, Liang, Ping, He, Kangwen, Li, Anqin, Li, Jiali, Hu, Daoyu, Xu, Chuou, Li, Zhen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Nature Singapore 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9889447/
https://www.ncbi.nlm.nih.gov/pubmed/36255600
http://dx.doi.org/10.1007/s11604-022-01346-2
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author Yuan, Guanjie
Qu, Weinuo
Li, Shichao
Liang, Ping
He, Kangwen
Li, Anqin
Li, Jiali
Hu, Daoyu
Xu, Chuou
Li, Zhen
author_facet Yuan, Guanjie
Qu, Weinuo
Li, Shichao
Liang, Ping
He, Kangwen
Li, Anqin
Li, Jiali
Hu, Daoyu
Xu, Chuou
Li, Zhen
author_sort Yuan, Guanjie
collection PubMed
description PURPOSE: To investigate the potential of histogram analysis based on diffusion kurtosis imaging (DKI) in evaluating renal function and fibrosis associated with chronic kidney disease (CKD). MATERIALS AND METHODS: Thirty-six CKD patients were enrolled, and DKI was performed in all patients before the renal biopsy. The histogram parameters of diffusivity (D) and kurtosis (K) were obtained using FireVoxel. The histogram parameters between the stable [estimated glomerular filtration rate (eGFR) ≥ 60 ml/min/1.73 m(2)] and impaired (eGFR < 60 ml/min/1.73 m(2)) eGFR group were compared. Besides, patients were classified into mild, moderate, and severe fibrosis group using a semi-quantitative standard. The correlations of histogram parameters with eGFR and fibrosis scores were investigated and the diagnostic performances of histogram parameters in assessing renal dysfunction and fibrosis were analyzed. The added value of combination of most significant parameter with 24 h urinary protein (24 h-UPRO) in evaluating fibrosis was also explored. RESULTS: Seven D histogram parameters in cortex (mean, median, 10th, 25th, 75th, 90th percentiles and entropy), two D histogram parameters in medulla (75th, 90th percentiles), seven K histogram parameters in cortex (mean, min, median, 10th, 25th, 75th, 90th percentiles) and three K histogram parameters in medulla (mean, median, 25th percentile) were significantly different between the two groups. The D(mean) of cortex was the most relevant parameter to eGFR (r = 0.648, P < 0.001) and had the largest area under the curve (AUC) for differentiating the stable from impaired eGFR group [AUC = 0.889; 95% confidence interval (CI) 0.728–0.970]. The K(90th) of cortex presented the strongest correlation with fibrosis scores (r = 0.575, P < 0.001) and achieved the largest AUC for distinguishing the mild from moderate to severe fibrosis group (AUC = 0.849, 95% CI 0.706–0.993). Combining the K(90th) in cortex with 24 h-UPRO gained statistically higher AUC value (AUC = 0.880, 95% CI 0.763–0.996). CONCLUSION: Histogram analysis based on DKI is practicable for the noninvasive assessment of renal function and fibrosis in CKD patients.
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spelling pubmed-98894472023-02-02 Noninvasive assessment of renal function and fibrosis in CKD patients using histogram analysis based on diffusion kurtosis imaging Yuan, Guanjie Qu, Weinuo Li, Shichao Liang, Ping He, Kangwen Li, Anqin Li, Jiali Hu, Daoyu Xu, Chuou Li, Zhen Jpn J Radiol Original Article PURPOSE: To investigate the potential of histogram analysis based on diffusion kurtosis imaging (DKI) in evaluating renal function and fibrosis associated with chronic kidney disease (CKD). MATERIALS AND METHODS: Thirty-six CKD patients were enrolled, and DKI was performed in all patients before the renal biopsy. The histogram parameters of diffusivity (D) and kurtosis (K) were obtained using FireVoxel. The histogram parameters between the stable [estimated glomerular filtration rate (eGFR) ≥ 60 ml/min/1.73 m(2)] and impaired (eGFR < 60 ml/min/1.73 m(2)) eGFR group were compared. Besides, patients were classified into mild, moderate, and severe fibrosis group using a semi-quantitative standard. The correlations of histogram parameters with eGFR and fibrosis scores were investigated and the diagnostic performances of histogram parameters in assessing renal dysfunction and fibrosis were analyzed. The added value of combination of most significant parameter with 24 h urinary protein (24 h-UPRO) in evaluating fibrosis was also explored. RESULTS: Seven D histogram parameters in cortex (mean, median, 10th, 25th, 75th, 90th percentiles and entropy), two D histogram parameters in medulla (75th, 90th percentiles), seven K histogram parameters in cortex (mean, min, median, 10th, 25th, 75th, 90th percentiles) and three K histogram parameters in medulla (mean, median, 25th percentile) were significantly different between the two groups. The D(mean) of cortex was the most relevant parameter to eGFR (r = 0.648, P < 0.001) and had the largest area under the curve (AUC) for differentiating the stable from impaired eGFR group [AUC = 0.889; 95% confidence interval (CI) 0.728–0.970]. The K(90th) of cortex presented the strongest correlation with fibrosis scores (r = 0.575, P < 0.001) and achieved the largest AUC for distinguishing the mild from moderate to severe fibrosis group (AUC = 0.849, 95% CI 0.706–0.993). Combining the K(90th) in cortex with 24 h-UPRO gained statistically higher AUC value (AUC = 0.880, 95% CI 0.763–0.996). CONCLUSION: Histogram analysis based on DKI is practicable for the noninvasive assessment of renal function and fibrosis in CKD patients. Springer Nature Singapore 2022-10-18 2023 /pmc/articles/PMC9889447/ /pubmed/36255600 http://dx.doi.org/10.1007/s11604-022-01346-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Yuan, Guanjie
Qu, Weinuo
Li, Shichao
Liang, Ping
He, Kangwen
Li, Anqin
Li, Jiali
Hu, Daoyu
Xu, Chuou
Li, Zhen
Noninvasive assessment of renal function and fibrosis in CKD patients using histogram analysis based on diffusion kurtosis imaging
title Noninvasive assessment of renal function and fibrosis in CKD patients using histogram analysis based on diffusion kurtosis imaging
title_full Noninvasive assessment of renal function and fibrosis in CKD patients using histogram analysis based on diffusion kurtosis imaging
title_fullStr Noninvasive assessment of renal function and fibrosis in CKD patients using histogram analysis based on diffusion kurtosis imaging
title_full_unstemmed Noninvasive assessment of renal function and fibrosis in CKD patients using histogram analysis based on diffusion kurtosis imaging
title_short Noninvasive assessment of renal function and fibrosis in CKD patients using histogram analysis based on diffusion kurtosis imaging
title_sort noninvasive assessment of renal function and fibrosis in ckd patients using histogram analysis based on diffusion kurtosis imaging
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9889447/
https://www.ncbi.nlm.nih.gov/pubmed/36255600
http://dx.doi.org/10.1007/s11604-022-01346-2
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