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Albumin Abundance and Its Glycation Status Determine Hemoglobin Glycation
[Image: see text] Diabetes diagnosis and management majorly depend upon the measurement of glycated hemoglobin (HbA1c) levels. Various factors influence HbA1c levels such as the use of various analytical methods and the presence of various clinical conditions. Plasma albumin levels were known to be...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6217588/ https://www.ncbi.nlm.nih.gov/pubmed/30411025 http://dx.doi.org/10.1021/acsomega.8b01702 |
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author | Jagadeeshaprasad, Mashanipalya G. Venkatasubramani, Vinashya Unnikrishnan, Ambika G. Kulkarni, Mahesh J. |
author_facet | Jagadeeshaprasad, Mashanipalya G. Venkatasubramani, Vinashya Unnikrishnan, Ambika G. Kulkarni, Mahesh J. |
author_sort | Jagadeeshaprasad, Mashanipalya G. |
collection | PubMed |
description | [Image: see text] Diabetes diagnosis and management majorly depend upon the measurement of glycated hemoglobin (HbA1c) levels. Various factors influence HbA1c levels such as the use of various analytical methods and the presence of various clinical conditions. Plasma albumin levels were known to be negatively associated with HbA1c. However, the precise mechanism by which they affect HbA1c is not well understood. Therefore, we have studied the influence of albumin levels and its glycation status on hemoglobin glycation using erythrocyte culture experiments. Erythrocytes maintained at low albumin concentration exhibited relatively increased albumin and hemoglobin glycation as compared to that in those maintained at higher albumin concentration. Increase in albumin glycation may decrease its ability to protect hemoglobin glycation. This was demonstrated by treatment of erythrocytes with N(ε)-(carboxymethyl)lysine-modified serum albumin (CMSA), which failed to protect hemoglobin glycation; instead, it increased hemoglobin glycation. The inability of CMSA to reduce hemoglobin glycation was due to the lack of free lysine residues of albumin, which was corroborated by using N(ε)-(acetyl)lysine serum albumin (AcSA) and clinical diabetic plasma. This is the first study which demonstrates that the modification of lysine residues of albumin impairs its ability to inhibit hemoglobin glycation. Furthermore, correlation studies between HbA1c and albumin levels or relative albumin fructosamine from clinical subjects supported our experimental finding that albumin abundance and its glycation status influence hemoglobin glycation. Therefore, we propose albumin level and its glycation status to be quantified in conjunction with HbA1c for better management of diabetes. |
format | Online Article Text |
id | pubmed-6217588 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-62175882018-11-06 Albumin Abundance and Its Glycation Status Determine Hemoglobin Glycation Jagadeeshaprasad, Mashanipalya G. Venkatasubramani, Vinashya Unnikrishnan, Ambika G. Kulkarni, Mahesh J. ACS Omega [Image: see text] Diabetes diagnosis and management majorly depend upon the measurement of glycated hemoglobin (HbA1c) levels. Various factors influence HbA1c levels such as the use of various analytical methods and the presence of various clinical conditions. Plasma albumin levels were known to be negatively associated with HbA1c. However, the precise mechanism by which they affect HbA1c is not well understood. Therefore, we have studied the influence of albumin levels and its glycation status on hemoglobin glycation using erythrocyte culture experiments. Erythrocytes maintained at low albumin concentration exhibited relatively increased albumin and hemoglobin glycation as compared to that in those maintained at higher albumin concentration. Increase in albumin glycation may decrease its ability to protect hemoglobin glycation. This was demonstrated by treatment of erythrocytes with N(ε)-(carboxymethyl)lysine-modified serum albumin (CMSA), which failed to protect hemoglobin glycation; instead, it increased hemoglobin glycation. The inability of CMSA to reduce hemoglobin glycation was due to the lack of free lysine residues of albumin, which was corroborated by using N(ε)-(acetyl)lysine serum albumin (AcSA) and clinical diabetic plasma. This is the first study which demonstrates that the modification of lysine residues of albumin impairs its ability to inhibit hemoglobin glycation. Furthermore, correlation studies between HbA1c and albumin levels or relative albumin fructosamine from clinical subjects supported our experimental finding that albumin abundance and its glycation status influence hemoglobin glycation. Therefore, we propose albumin level and its glycation status to be quantified in conjunction with HbA1c for better management of diabetes. American Chemical Society 2018-10-10 /pmc/articles/PMC6217588/ /pubmed/30411025 http://dx.doi.org/10.1021/acsomega.8b01702 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Jagadeeshaprasad, Mashanipalya G. Venkatasubramani, Vinashya Unnikrishnan, Ambika G. Kulkarni, Mahesh J. Albumin Abundance and Its Glycation Status Determine Hemoglobin Glycation |
title | Albumin Abundance and Its Glycation Status Determine
Hemoglobin Glycation |
title_full | Albumin Abundance and Its Glycation Status Determine
Hemoglobin Glycation |
title_fullStr | Albumin Abundance and Its Glycation Status Determine
Hemoglobin Glycation |
title_full_unstemmed | Albumin Abundance and Its Glycation Status Determine
Hemoglobin Glycation |
title_short | Albumin Abundance and Its Glycation Status Determine
Hemoglobin Glycation |
title_sort | albumin abundance and its glycation status determine
hemoglobin glycation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6217588/ https://www.ncbi.nlm.nih.gov/pubmed/30411025 http://dx.doi.org/10.1021/acsomega.8b01702 |
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