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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....

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Detalles Bibliográficos
Autores principales: Wang, Zijie, Yang, Haiwei, Zhao, Chunchun, Wei, Jifu, Wang, Junsong, Han, Zhijian, Tao, Jun, Xu, Zhen, Ju, Xiaobin, Tan, Ruoyun, Gu, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2017
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
Descripción
Sumario: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.