Standard

Individual Glycation Sites as Biomarkers of Type 2 Diabetes Mellitus. / Soboleva, Alena; Vashurina, Natalia; Frolov, Andrej.

Type 2 Diabetes - From Pathophysiology to Cyber Systems. ed. / Anca Pantea Stoian. InTech, 2021. p. 1-29.

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

Harvard

Soboleva, A, Vashurina, N & Frolov, A 2021, Individual Glycation Sites as Biomarkers of Type 2 Diabetes Mellitus. in A Pantea Stoian (ed.), Type 2 Diabetes - From Pathophysiology to Cyber Systems. InTech, pp. 1-29. https://doi.org/10.5772/intechopen.95532

APA

Soboleva, A., Vashurina, N., & Frolov, A. (2021). Individual Glycation Sites as Biomarkers of Type 2 Diabetes Mellitus. In A. Pantea Stoian (Ed.), Type 2 Diabetes - From Pathophysiology to Cyber Systems (pp. 1-29). InTech. https://doi.org/10.5772/intechopen.95532

Vancouver

Soboleva A, Vashurina N, Frolov A. Individual Glycation Sites as Biomarkers of Type 2 Diabetes Mellitus. In Pantea Stoian A, editor, Type 2 Diabetes - From Pathophysiology to Cyber Systems. InTech. 2021. p. 1-29 https://doi.org/10.5772/intechopen.95532

Author

Soboleva, Alena ; Vashurina, Natalia ; Frolov, Andrej. / Individual Glycation Sites as Biomarkers of Type 2 Diabetes Mellitus. Type 2 Diabetes - From Pathophysiology to Cyber Systems. editor / Anca Pantea Stoian. InTech, 2021. pp. 1-29

BibTeX

@inbook{afd1d8d22170438a84d885712d2d3411,
title = "Individual Glycation Sites as Biomarkers of Type 2 Diabetes Mellitus",
abstract = "Type 2 diabetes mellitus (T2DM) is a widely spread metabolic disease, the initialstages of which are asymptomatic and have no clinically recognizable manifestation. At the molecular level, T2DM is manifested with essential non-enzymatic structural changes of intra- and extracellular proteins, mostly represented with oxidation and glycation of multiple residues. Protein glycation is one of the most universal markers of T2DM, and is recognized as an indirect, but adequate indicator of plasma glucose levels over prolonged periods of time. Unfortunately, glycated hemoglobin (HbA1c) – the universally accepted T2DM marker, is insensitive for short-term excursions of blood glucose, which are known to precede the onset of disease. Therefore, new generation biomarkers, giving access to the time dimension of Maillard reaction in blood, are desired. In this context, establishment of individual glycation sites of plasma proteins as new T2DM biomarkers might be a promising approach. Indeed, involvement of proteins with different half-life times in such analysis will make the time dimension of protein glycation in blood available and will allow early recognition of blood sugar fluctuations, occurring within few weeks or even days.",
keywords = "Amadori compounds, biomarkers, glycation, glycation sites, label-free quantification, mass spectrometry, plasma proteins, stable isotope-labeled peptide standards, type 2 diabetes mellitus (T2DM)",
author = "Alena Soboleva and Natalia Vashurina and Andrej Frolov",
year = "2021",
month = feb,
day = "10",
doi = "10.5772/intechopen.95532",
language = "English",
isbn = "978-1-83881-904-0",
pages = "1--29",
editor = "{Pantea Stoian}, {Anca }",
booktitle = "Type 2 Diabetes - From Pathophysiology to Cyber Systems",
publisher = "InTech",
address = "United Kingdom",

}

RIS

TY - CHAP

T1 - Individual Glycation Sites as Biomarkers of Type 2 Diabetes Mellitus

AU - Soboleva, Alena

AU - Vashurina, Natalia

AU - Frolov, Andrej

PY - 2021/2/10

Y1 - 2021/2/10

N2 - Type 2 diabetes mellitus (T2DM) is a widely spread metabolic disease, the initialstages of which are asymptomatic and have no clinically recognizable manifestation. At the molecular level, T2DM is manifested with essential non-enzymatic structural changes of intra- and extracellular proteins, mostly represented with oxidation and glycation of multiple residues. Protein glycation is one of the most universal markers of T2DM, and is recognized as an indirect, but adequate indicator of plasma glucose levels over prolonged periods of time. Unfortunately, glycated hemoglobin (HbA1c) – the universally accepted T2DM marker, is insensitive for short-term excursions of blood glucose, which are known to precede the onset of disease. Therefore, new generation biomarkers, giving access to the time dimension of Maillard reaction in blood, are desired. In this context, establishment of individual glycation sites of plasma proteins as new T2DM biomarkers might be a promising approach. Indeed, involvement of proteins with different half-life times in such analysis will make the time dimension of protein glycation in blood available and will allow early recognition of blood sugar fluctuations, occurring within few weeks or even days.

AB - Type 2 diabetes mellitus (T2DM) is a widely spread metabolic disease, the initialstages of which are asymptomatic and have no clinically recognizable manifestation. At the molecular level, T2DM is manifested with essential non-enzymatic structural changes of intra- and extracellular proteins, mostly represented with oxidation and glycation of multiple residues. Protein glycation is one of the most universal markers of T2DM, and is recognized as an indirect, but adequate indicator of plasma glucose levels over prolonged periods of time. Unfortunately, glycated hemoglobin (HbA1c) – the universally accepted T2DM marker, is insensitive for short-term excursions of blood glucose, which are known to precede the onset of disease. Therefore, new generation biomarkers, giving access to the time dimension of Maillard reaction in blood, are desired. In this context, establishment of individual glycation sites of plasma proteins as new T2DM biomarkers might be a promising approach. Indeed, involvement of proteins with different half-life times in such analysis will make the time dimension of protein glycation in blood available and will allow early recognition of blood sugar fluctuations, occurring within few weeks or even days.

KW - Amadori compounds

KW - biomarkers

KW - glycation

KW - glycation sites

KW - label-free quantification

KW - mass spectrometry

KW - plasma proteins

KW - stable isotope-labeled peptide standards

KW - type 2 diabetes mellitus (T2DM)

UR - https://www.mendeley.com/catalogue/1a901858-4569-389f-a1b0-eaeef75070fa/

U2 - 10.5772/intechopen.95532

DO - 10.5772/intechopen.95532

M3 - Chapter

SN - 978-1-83881-904-0

SP - 1

EP - 29

BT - Type 2 Diabetes - From Pathophysiology to Cyber Systems

A2 - Pantea Stoian, Anca

PB - InTech

ER -

ID: 73950591