Research output: Chapter in Book/Report/Conference proceeding › Chapter › peer-review
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 proceeding › Chapter › peer-review
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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