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Protein glycation in diabetes mellitus. | LitMetric

Protein glycation in diabetes mellitus.

Adv Clin Chem

Department of Pathology & Anatomical Sciences, School of Medicine, University of Missouri, Columbia, MO, United States. Electronic address:

Published: March 2023

AI Article Synopsis

  • Diabetes mellitus ranks as the ninth leading cause of death globally, characterized by chronic high blood sugar levels and resulting biochemical changes, particularly through the accumulation of glycated proteins like hemoglobin A1c (HbA1c) and glycated albumin.
  • Many proteins undergo glycation, affecting various cellular functions and potentially serving as indicators for diabetic complications, thus highlighting the need for further research in this area.
  • Modern proteomics, including advanced techniques like mass spectrometry, offers powerful tools for analyzing these glycation processes, aiming to bridge the gap between clinical questions and recent scientific findings for better understanding and managing diabetes.

Article Abstract

Diabetes mellitus is the ninth leading cause of mortality worldwide. It is a complex disease that manifests as chronic hyperglycemia. Glucose exposure causes biochemical changes at the proteome level as reflected in accumulation of glycated proteins. A prominent example is hemoglobin A1c (HbA1c), a glycated protein widely accepted as a diabetic indicator. Another emerging biomarker is glycated albumin which has demonstrated utility in situations where HbA1c cannot be used. Other proteins undergo glycation as well thus impacting cellular function, transport and immune response. Accordingly, these glycated counterparts may serve as predictors for diabetic complications and thus warrant further inquiry. Fortunately, modern proteomics has provided unique analytic capability to enable improved and more comprehensive exploration of glycating agents and glycated proteins. This review broadly covers topics from epidemiology of diabetes to modern analytical tools such as mass spectrometry to facilitate a better understanding of diabetes pathophysiology. This serves as an attempt to connect clinically relevant questions with findings of recent proteomic studies to suggest future avenues of diabetes research.

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Source
http://dx.doi.org/10.1016/bs.acc.2022.11.003DOI Listing

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