Cargando…

Salivary Metabolomics of Well and Poorly Controlled Type 1 and Type 2 Diabetes

OBJECTIVE: The concentrations of endogenous metabolites in saliva can be altered based on the systemic condition of the hosts and may, in theory, serve as a reflection of systemic disease progression. Hemoglobin A1C is used clinically to measure long-term average glycemic control. The aim of the stu...

Descripción completa

Detalles Bibliográficos
Autores principales: Bencharit, Sompop, Carlson, James, Byrd, Warren C., Howard-Williams, Escher L., Seagroves, Jackson T., McRitchie, Susan, Buse, John B., Sumner, Susan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9433218/
https://www.ncbi.nlm.nih.gov/pubmed/36059915
http://dx.doi.org/10.1155/2022/7544864
_version_ 1784780574130438144
author Bencharit, Sompop
Carlson, James
Byrd, Warren C.
Howard-Williams, Escher L.
Seagroves, Jackson T.
McRitchie, Susan
Buse, John B.
Sumner, Susan
author_facet Bencharit, Sompop
Carlson, James
Byrd, Warren C.
Howard-Williams, Escher L.
Seagroves, Jackson T.
McRitchie, Susan
Buse, John B.
Sumner, Susan
author_sort Bencharit, Sompop
collection PubMed
description OBJECTIVE: The concentrations of endogenous metabolites in saliva can be altered based on the systemic condition of the hosts and may, in theory, serve as a reflection of systemic disease progression. Hemoglobin A1C is used clinically to measure long-term average glycemic control. The aim of the study was to demonstrate if there were differences in the salivary metabolic profiles between well and poorly controlled type 1 and type 2 subjects with diabetes. Subjects and Methods. Subjects with type 1 and type 2 diabetes were enrolled (n = 40). The subjects were assigned to phenotypic groups based on their current level of A1C: <7 = well-controlled and >7 = poorly controlled. Demographic data, age, gender, and ethnicity, were used to match the two phenotypic groups. Whole saliva samples were collected and immediately stored at −80°C. Samples were spiked using an isotopically labeled internal standard and analyzed by UPLC-TOF-MS using a Waters SYNAPT G2-Si mass spectrometer. RESULTS: Unsupervised principal components analysis (PCA) and orthogonal partial least squares regression discrimination analysis (OPLS-DA) were used to define unique metabolomic profiles associated with well and poorly controlled diabetes based on A1C levels. CONCLUSION: OPLS-DA demonstrates good separation of well and poorly controlled in both type 1 and type 2 diabetes. This provides evidence for developing saliva-based monitoring tools for diabetes.
format Online
Article
Text
id pubmed-9433218
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Hindawi
record_format MEDLINE/PubMed
spelling pubmed-94332182022-09-01 Salivary Metabolomics of Well and Poorly Controlled Type 1 and Type 2 Diabetes Bencharit, Sompop Carlson, James Byrd, Warren C. Howard-Williams, Escher L. Seagroves, Jackson T. McRitchie, Susan Buse, John B. Sumner, Susan Int J Dent Research Article OBJECTIVE: The concentrations of endogenous metabolites in saliva can be altered based on the systemic condition of the hosts and may, in theory, serve as a reflection of systemic disease progression. Hemoglobin A1C is used clinically to measure long-term average glycemic control. The aim of the study was to demonstrate if there were differences in the salivary metabolic profiles between well and poorly controlled type 1 and type 2 subjects with diabetes. Subjects and Methods. Subjects with type 1 and type 2 diabetes were enrolled (n = 40). The subjects were assigned to phenotypic groups based on their current level of A1C: <7 = well-controlled and >7 = poorly controlled. Demographic data, age, gender, and ethnicity, were used to match the two phenotypic groups. Whole saliva samples were collected and immediately stored at −80°C. Samples were spiked using an isotopically labeled internal standard and analyzed by UPLC-TOF-MS using a Waters SYNAPT G2-Si mass spectrometer. RESULTS: Unsupervised principal components analysis (PCA) and orthogonal partial least squares regression discrimination analysis (OPLS-DA) were used to define unique metabolomic profiles associated with well and poorly controlled diabetes based on A1C levels. CONCLUSION: OPLS-DA demonstrates good separation of well and poorly controlled in both type 1 and type 2 diabetes. This provides evidence for developing saliva-based monitoring tools for diabetes. Hindawi 2022-08-24 /pmc/articles/PMC9433218/ /pubmed/36059915 http://dx.doi.org/10.1155/2022/7544864 Text en Copyright © 2022 Sompop Bencharit et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Bencharit, Sompop
Carlson, James
Byrd, Warren C.
Howard-Williams, Escher L.
Seagroves, Jackson T.
McRitchie, Susan
Buse, John B.
Sumner, Susan
Salivary Metabolomics of Well and Poorly Controlled Type 1 and Type 2 Diabetes
title Salivary Metabolomics of Well and Poorly Controlled Type 1 and Type 2 Diabetes
title_full Salivary Metabolomics of Well and Poorly Controlled Type 1 and Type 2 Diabetes
title_fullStr Salivary Metabolomics of Well and Poorly Controlled Type 1 and Type 2 Diabetes
title_full_unstemmed Salivary Metabolomics of Well and Poorly Controlled Type 1 and Type 2 Diabetes
title_short Salivary Metabolomics of Well and Poorly Controlled Type 1 and Type 2 Diabetes
title_sort salivary metabolomics of well and poorly controlled type 1 and type 2 diabetes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9433218/
https://www.ncbi.nlm.nih.gov/pubmed/36059915
http://dx.doi.org/10.1155/2022/7544864
work_keys_str_mv AT bencharitsompop salivarymetabolomicsofwellandpoorlycontrolledtype1andtype2diabetes
AT carlsonjames salivarymetabolomicsofwellandpoorlycontrolledtype1andtype2diabetes
AT byrdwarrenc salivarymetabolomicsofwellandpoorlycontrolledtype1andtype2diabetes
AT howardwilliamsescherl salivarymetabolomicsofwellandpoorlycontrolledtype1andtype2diabetes
AT seagrovesjacksont salivarymetabolomicsofwellandpoorlycontrolledtype1andtype2diabetes
AT mcritchiesusan salivarymetabolomicsofwellandpoorlycontrolledtype1andtype2diabetes
AT busejohnb salivarymetabolomicsofwellandpoorlycontrolledtype1andtype2diabetes
AT sumnersusan salivarymetabolomicsofwellandpoorlycontrolledtype1andtype2diabetes