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Proton Nuclear Magnetic Resonance (1H-NMR)-Based Metabolomic Evaluation of Human Renal Allografts from Donations After Circulatory Death
BACKGROUND: Delayed graft function (DGF) is a common complication that impairs allograft function after kidney transplantation. However, the mechanism of DGF remains unclear. Nuclear magnetic resonance (NMR)-based analysis has been widely used in recent times to assess changes in metabolite levels....
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5702106/ https://www.ncbi.nlm.nih.gov/pubmed/29149095 http://dx.doi.org/10.12659/MSM.905168 |
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author | Wang, Zijie Yang, Haiwei Zhao, Chunchun Wei, Jifu Wang, Junsong Han, Zhijian Tao, Jun Xu, Zhen Ju, Xiaobin Tan, Ruoyun Gu, Min |
author_facet | Wang, Zijie Yang, Haiwei Zhao, Chunchun Wei, Jifu Wang, Junsong Han, Zhijian Tao, Jun Xu, Zhen Ju, Xiaobin Tan, Ruoyun Gu, Min |
author_sort | Wang, Zijie |
collection | PubMed |
description | BACKGROUND: Delayed graft function (DGF) is a common complication that impairs allograft function after kidney transplantation. However, the mechanism of DGF remains unclear. Nuclear magnetic resonance (NMR)-based analysis has been widely used in recent times to assess changes in metabolite levels. MATERIAL/METHODS: Samples of perfusate from allografts donated after circulatory death were collected prior to transplantation, during static cold storage. (1)H-NMR-based metabolomics combined with the statistical methods, orthogonal partial least-squares discriminant analysis (OPLS-DA), and principle-component analysis (PCA), were employed to test different levels of metabolites between the allografts that exhibited DGF and those that exhibited immediate graft function (IGF). RESULTS: The study population consisted of 36 subjects, 11 with DGF and 25 with IGF. Of the 37 detected and identified metabolites, α-glucose and citrate were significantly elevated in the perfusate of DGF allografts, and taurine and betaine were significantly decreased. CONCLUSIONS: (1)H-NMR analysis of DGF and IGF perfusates revealed some significant differences in their metabolite profiles, which may help explain the mechanisms of kidney ischemia-reperfusion injury and DGF. |
format | Online Article Text |
id | pubmed-5702106 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | International Scientific Literature, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57021062017-11-29 Proton Nuclear Magnetic Resonance (1H-NMR)-Based Metabolomic Evaluation of Human Renal Allografts from Donations After Circulatory Death Wang, Zijie Yang, Haiwei Zhao, Chunchun Wei, Jifu Wang, Junsong Han, Zhijian Tao, Jun Xu, Zhen Ju, Xiaobin Tan, Ruoyun Gu, Min Med Sci Monit Clinical Research BACKGROUND: Delayed graft function (DGF) is a common complication that impairs allograft function after kidney transplantation. However, the mechanism of DGF remains unclear. Nuclear magnetic resonance (NMR)-based analysis has been widely used in recent times to assess changes in metabolite levels. MATERIAL/METHODS: Samples of perfusate from allografts donated after circulatory death were collected prior to transplantation, during static cold storage. (1)H-NMR-based metabolomics combined with the statistical methods, orthogonal partial least-squares discriminant analysis (OPLS-DA), and principle-component analysis (PCA), were employed to test different levels of metabolites between the allografts that exhibited DGF and those that exhibited immediate graft function (IGF). RESULTS: The study population consisted of 36 subjects, 11 with DGF and 25 with IGF. Of the 37 detected and identified metabolites, α-glucose and citrate were significantly elevated in the perfusate of DGF allografts, and taurine and betaine were significantly decreased. CONCLUSIONS: (1)H-NMR analysis of DGF and IGF perfusates revealed some significant differences in their metabolite profiles, which may help explain the mechanisms of kidney ischemia-reperfusion injury and DGF. International Scientific Literature, Inc. 2017-11-17 /pmc/articles/PMC5702106/ /pubmed/29149095 http://dx.doi.org/10.12659/MSM.905168 Text en © Med Sci Monit, 2017 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) ) |
spellingShingle | Clinical Research Wang, Zijie Yang, Haiwei Zhao, Chunchun Wei, Jifu Wang, Junsong Han, Zhijian Tao, Jun Xu, Zhen Ju, Xiaobin Tan, Ruoyun Gu, Min Proton Nuclear Magnetic Resonance (1H-NMR)-Based Metabolomic Evaluation of Human Renal Allografts from Donations After Circulatory Death |
title | Proton Nuclear Magnetic Resonance (1H-NMR)-Based Metabolomic Evaluation of Human Renal Allografts from Donations After Circulatory Death |
title_full | Proton Nuclear Magnetic Resonance (1H-NMR)-Based Metabolomic Evaluation of Human Renal Allografts from Donations After Circulatory Death |
title_fullStr | Proton Nuclear Magnetic Resonance (1H-NMR)-Based Metabolomic Evaluation of Human Renal Allografts from Donations After Circulatory Death |
title_full_unstemmed | Proton Nuclear Magnetic Resonance (1H-NMR)-Based Metabolomic Evaluation of Human Renal Allografts from Donations After Circulatory Death |
title_short | Proton Nuclear Magnetic Resonance (1H-NMR)-Based Metabolomic Evaluation of Human Renal Allografts from Donations After Circulatory Death |
title_sort | proton nuclear magnetic resonance (1h-nmr)-based metabolomic evaluation of human renal allografts from donations after circulatory death |
topic | Clinical Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5702106/ https://www.ncbi.nlm.nih.gov/pubmed/29149095 http://dx.doi.org/10.12659/MSM.905168 |
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