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Untargeted Metabolomic Plasma Profiling of Emirati Dialysis Patients with Diabetes versus Non-Diabetic: A Pilot Study

Diabetic kidney disease (DKD) is a severe irreversible complication of diabetes mellitus that further disturbs glucose metabolism. Identifying metabolic changes in the blood may provide early insight into DKD pathogenesis. This study aims to determine blood biomarkers differentiating DKD from non-di...

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Autores principales: Banimfreg, Bayan Hassan, Alshraideh, Hussam, Shamayleh, Abdulrahim, Guella, Adnane, Semreen, Mohammad Harb, Al Bataineh, Mohammad Tahseen, Soares, Nelson C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9313445/
https://www.ncbi.nlm.nih.gov/pubmed/35883517
http://dx.doi.org/10.3390/biom12070962
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author Banimfreg, Bayan Hassan
Alshraideh, Hussam
Shamayleh, Abdulrahim
Guella, Adnane
Semreen, Mohammad Harb
Al Bataineh, Mohammad Tahseen
Soares, Nelson C.
author_facet Banimfreg, Bayan Hassan
Alshraideh, Hussam
Shamayleh, Abdulrahim
Guella, Adnane
Semreen, Mohammad Harb
Al Bataineh, Mohammad Tahseen
Soares, Nelson C.
author_sort Banimfreg, Bayan Hassan
collection PubMed
description Diabetic kidney disease (DKD) is a severe irreversible complication of diabetes mellitus that further disturbs glucose metabolism. Identifying metabolic changes in the blood may provide early insight into DKD pathogenesis. This study aims to determine blood biomarkers differentiating DKD from non-diabetic kidney disease in the Emirati population utilizing the LC-MS/MS platform. Blood samples were collected from hemodialysis subjects with and without diabetes to detect indicators of pathological changes using an untargeted metabolomics approach. Metabolic profiles were analyzed based on clinically confirmed diabetic status and current HbA1c values. Five differentially significant metabolites were identified based on the clinically confirmed diabetic status, including hydroxyprogesterone and 3,4-Dihydroxymandelic acid. Similarly, we identified seven metabolites with apparent differences between Dialysis Diabetic (DD) and Dialysis non-Diabetic (DND) groups, including isovalerylglycine based on HbA1c values. Likewise, the top three metabolic pathways, including Tyrosine metabolism, were identified following the clinically confirmed diabetic status. As a result, nine different metabolites were enriched in the identified metabolic pathways, such as 3,4-Dihydroxymandelic acid. As a result, eleven different metabolites were enriched, including Glycerol. This study provides an insight into blood metabolic changes related to DKD that may lead to more effective management strategies.
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spelling pubmed-93134452022-07-26 Untargeted Metabolomic Plasma Profiling of Emirati Dialysis Patients with Diabetes versus Non-Diabetic: A Pilot Study Banimfreg, Bayan Hassan Alshraideh, Hussam Shamayleh, Abdulrahim Guella, Adnane Semreen, Mohammad Harb Al Bataineh, Mohammad Tahseen Soares, Nelson C. Biomolecules Article Diabetic kidney disease (DKD) is a severe irreversible complication of diabetes mellitus that further disturbs glucose metabolism. Identifying metabolic changes in the blood may provide early insight into DKD pathogenesis. This study aims to determine blood biomarkers differentiating DKD from non-diabetic kidney disease in the Emirati population utilizing the LC-MS/MS platform. Blood samples were collected from hemodialysis subjects with and without diabetes to detect indicators of pathological changes using an untargeted metabolomics approach. Metabolic profiles were analyzed based on clinically confirmed diabetic status and current HbA1c values. Five differentially significant metabolites were identified based on the clinically confirmed diabetic status, including hydroxyprogesterone and 3,4-Dihydroxymandelic acid. Similarly, we identified seven metabolites with apparent differences between Dialysis Diabetic (DD) and Dialysis non-Diabetic (DND) groups, including isovalerylglycine based on HbA1c values. Likewise, the top three metabolic pathways, including Tyrosine metabolism, were identified following the clinically confirmed diabetic status. As a result, nine different metabolites were enriched in the identified metabolic pathways, such as 3,4-Dihydroxymandelic acid. As a result, eleven different metabolites were enriched, including Glycerol. This study provides an insight into blood metabolic changes related to DKD that may lead to more effective management strategies. MDPI 2022-07-08 /pmc/articles/PMC9313445/ /pubmed/35883517 http://dx.doi.org/10.3390/biom12070962 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Banimfreg, Bayan Hassan
Alshraideh, Hussam
Shamayleh, Abdulrahim
Guella, Adnane
Semreen, Mohammad Harb
Al Bataineh, Mohammad Tahseen
Soares, Nelson C.
Untargeted Metabolomic Plasma Profiling of Emirati Dialysis Patients with Diabetes versus Non-Diabetic: A Pilot Study
title Untargeted Metabolomic Plasma Profiling of Emirati Dialysis Patients with Diabetes versus Non-Diabetic: A Pilot Study
title_full Untargeted Metabolomic Plasma Profiling of Emirati Dialysis Patients with Diabetes versus Non-Diabetic: A Pilot Study
title_fullStr Untargeted Metabolomic Plasma Profiling of Emirati Dialysis Patients with Diabetes versus Non-Diabetic: A Pilot Study
title_full_unstemmed Untargeted Metabolomic Plasma Profiling of Emirati Dialysis Patients with Diabetes versus Non-Diabetic: A Pilot Study
title_short Untargeted Metabolomic Plasma Profiling of Emirati Dialysis Patients with Diabetes versus Non-Diabetic: A Pilot Study
title_sort untargeted metabolomic plasma profiling of emirati dialysis patients with diabetes versus non-diabetic: a pilot study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9313445/
https://www.ncbi.nlm.nih.gov/pubmed/35883517
http://dx.doi.org/10.3390/biom12070962
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