Cargando…

Plasma and Vitreous Metabolomics Profiling of Proliferative Diabetic Retinopathy

PURPOSE: To determine the differences of metabolites and metabolic pathways between patients with proliferative diabetic retinopathy (PDR) and without diabetes (nondiabetic controls) in plasma and vitreous, respectively, and to characterize the relationship between plasma and vitreous metabolic prof...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Hanying, Li, Shu, Wang, Chingyi, Wang, Yihan, Fang, Junwei, Liu, Kun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8842420/
https://www.ncbi.nlm.nih.gov/pubmed/35133401
http://dx.doi.org/10.1167/iovs.63.2.17
_version_ 1784651045609144320
author Wang, Hanying
Li, Shu
Wang, Chingyi
Wang, Yihan
Fang, Junwei
Liu, Kun
author_facet Wang, Hanying
Li, Shu
Wang, Chingyi
Wang, Yihan
Fang, Junwei
Liu, Kun
author_sort Wang, Hanying
collection PubMed
description PURPOSE: To determine the differences of metabolites and metabolic pathways between patients with proliferative diabetic retinopathy (PDR) and without diabetes (nondiabetic controls) in plasma and vitreous, respectively, and to characterize the relationship between plasma and vitreous metabolic profiles. METHODS: Liquid chromatography/tandem mass spectrometry technology was performed to distinct metabolite profiles of plasma and vitreous. A total of 139 plasma samples from 88 patients with PDR and 51 nondiabetic controls, as well as 74 vitreous samples from 51 patients with PDR and 23 nondiabetic controls, were screened. Pathway analysis was performed using MetaboAnalyst 5.0. Pearson correlation analysis was used to investigate the correlation of metabolites in vitreous and plasma. RESULTS: After adjusting for age, fasting blood glucose, and urea, in vitreous metabolomes, a total of 76 features distinguished patients with PDR from controls. Fifteen differential metabolites were found in plasma metabolites. Pantothenate and CoA biosynthesis was the common metabolic pathway altered in both plasma and vitreous. Aromatic amino acid metabolism pathways were dysregulated in vitreous of PDR. For four metabolic features, there were positive correlations between vitreous and plasma. CONCLUSIONS: Despite great differences between the metabolic profiles of plasma and vitreous in PDR cases, there are also similarities in the change of metabolites and metabolic pathways. Exploring the relationship of metabolomics between vitreous and plasma may help provide new understanding of the mechanism of PDR.
format Online
Article
Text
id pubmed-8842420
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher The Association for Research in Vision and Ophthalmology
record_format MEDLINE/PubMed
spelling pubmed-88424202022-02-18 Plasma and Vitreous Metabolomics Profiling of Proliferative Diabetic Retinopathy Wang, Hanying Li, Shu Wang, Chingyi Wang, Yihan Fang, Junwei Liu, Kun Invest Ophthalmol Vis Sci Retina PURPOSE: To determine the differences of metabolites and metabolic pathways between patients with proliferative diabetic retinopathy (PDR) and without diabetes (nondiabetic controls) in plasma and vitreous, respectively, and to characterize the relationship between plasma and vitreous metabolic profiles. METHODS: Liquid chromatography/tandem mass spectrometry technology was performed to distinct metabolite profiles of plasma and vitreous. A total of 139 plasma samples from 88 patients with PDR and 51 nondiabetic controls, as well as 74 vitreous samples from 51 patients with PDR and 23 nondiabetic controls, were screened. Pathway analysis was performed using MetaboAnalyst 5.0. Pearson correlation analysis was used to investigate the correlation of metabolites in vitreous and plasma. RESULTS: After adjusting for age, fasting blood glucose, and urea, in vitreous metabolomes, a total of 76 features distinguished patients with PDR from controls. Fifteen differential metabolites were found in plasma metabolites. Pantothenate and CoA biosynthesis was the common metabolic pathway altered in both plasma and vitreous. Aromatic amino acid metabolism pathways were dysregulated in vitreous of PDR. For four metabolic features, there were positive correlations between vitreous and plasma. CONCLUSIONS: Despite great differences between the metabolic profiles of plasma and vitreous in PDR cases, there are also similarities in the change of metabolites and metabolic pathways. Exploring the relationship of metabolomics between vitreous and plasma may help provide new understanding of the mechanism of PDR. The Association for Research in Vision and Ophthalmology 2022-02-08 /pmc/articles/PMC8842420/ /pubmed/35133401 http://dx.doi.org/10.1167/iovs.63.2.17 Text en Copyright 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
spellingShingle Retina
Wang, Hanying
Li, Shu
Wang, Chingyi
Wang, Yihan
Fang, Junwei
Liu, Kun
Plasma and Vitreous Metabolomics Profiling of Proliferative Diabetic Retinopathy
title Plasma and Vitreous Metabolomics Profiling of Proliferative Diabetic Retinopathy
title_full Plasma and Vitreous Metabolomics Profiling of Proliferative Diabetic Retinopathy
title_fullStr Plasma and Vitreous Metabolomics Profiling of Proliferative Diabetic Retinopathy
title_full_unstemmed Plasma and Vitreous Metabolomics Profiling of Proliferative Diabetic Retinopathy
title_short Plasma and Vitreous Metabolomics Profiling of Proliferative Diabetic Retinopathy
title_sort plasma and vitreous metabolomics profiling of proliferative diabetic retinopathy
topic Retina
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8842420/
https://www.ncbi.nlm.nih.gov/pubmed/35133401
http://dx.doi.org/10.1167/iovs.63.2.17
work_keys_str_mv AT wanghanying plasmaandvitreousmetabolomicsprofilingofproliferativediabeticretinopathy
AT lishu plasmaandvitreousmetabolomicsprofilingofproliferativediabeticretinopathy
AT wangchingyi plasmaandvitreousmetabolomicsprofilingofproliferativediabeticretinopathy
AT wangyihan plasmaandvitreousmetabolomicsprofilingofproliferativediabeticretinopathy
AT fangjunwei plasmaandvitreousmetabolomicsprofilingofproliferativediabeticretinopathy
AT liukun plasmaandvitreousmetabolomicsprofilingofproliferativediabeticretinopathy