Labile glycated hemoglobin: an underestimated laboratory marker of short term glycemia
Joris R Delanghe1, Stijn Lambrecht1, Tom Fiers1
1Department of Clinical Chemistry, Ghent University Hospital, Ghent, Belgium.
Insights
Labile hemoglobin A1c (l-HbA1c) offers a faster indicator for glycemic changes than standard HbA1c. This labile fraction, alongside red blood cell distribution width (RDW), aids in monitoring diabetes management.
Area of Science:
- Clinical Chemistry
- Endocrinology
- Hematology
Background:
- Diabetes mellitus poses a significant public health challenge.
- Hemoglobin A1c (HbA1c) is crucial for diabetes management but has limitations due to red blood cell (RBC) lifespan variations and slow response to glucose changes.
- A labile HbA1c (l-HbA1c) fraction exhibits faster kinetics and can be measured alongside HbA1c.
Purpose of the Study:
- To explore the utility of the l-HbA1c fraction for monitoring glycemia.
- To assess the correlation of l-HbA1c with glycemic control and HbA1c.
- To investigate the relationship between l-HbA1c, HbA1c, and red blood cell distribution width (RDW).
Main Methods:
- Simultaneous assay of l-HbA1c and HbA1c fractions using a Tosoh G8 analyzer.
- Comparison of l-HbA1c results with serum glucose and HbA1c.
- Determination of RDW using a Sysmex SN analyzer to assess erythrocyte lifespan.
Main Results:
- l-HbA1c demonstrated good measurement precision (CVs 2.2-2.3%).
- l-HbA1c showed strong correlations with glycemia (r=0.80) and HbA1c (r=0.73).
- Glycemia and HbA1c were the primary determinants of l-HbA1c in a multiple regression model (r²=0.752); RDW showed a weaker correlation.
Conclusions:
- l-HbA1c serves as an additional marker for detecting rapid glycemic fluctuations missed by standard HbA1c and blood glucose monitoring.
- RDW can indicate atypical RBC lifespan, potentially enhancing the interpretation of l-HbA1c fraction results.
Objectives:
Diabetes mellitus is a major public health problem. Hemoglobin A1c (HbA1c) is a key laboratory parameter in the management of diabetes patients. However, in diabetes monitoring, interpretation of HbA1c results is hampered by the important interindividual variation in red blood cell (RBC) life span. Furthermore, HbA1c only slowly responds to changes in glucose metabolism. Besides HbA1c, there exists a labile HbA1c fraction (l-HbA1c), exhibiting much faster kinetics. As both HbA1c and l-HbA1c are measured by modern standard chromatography, we explored the possibilities of using the l-HbA1c fraction for monitoring glycemia.
Methods:
l-HbA1c and HbA1c fractions were simultaneously assayed on a Tosoh G8 analyzer and expressed as %. l-HbA1c results were compared with serum glucose and HbA1c. Concomitantly, RBC distribution width (RDW) was determined on a Sysmex SN analyzer as a marker for erythrocyte life span.
Results:
l-HbA1c could be measured with between-run coefficient of variations (CVs) between 2.2 and 2.3%. l-HbA1c correlated with both glycemia (r=0.80) and HbA1c results (r=0.73). In a multiple regression model (r2=0.752), glycemia and HbA1c were the most determining factors. To a lesser extent, RDW correlated with l-HbA1c (r=0.158). Furthermore, the l-HbA1c/HbA1c ratio weakly positively correlated with RDW (r=0.247).
Conclusions:
L-HBA1c represents an additional marker for monitoring the rapid occurrence of glycemic disorders that escape detection when using only HbA1c and blood glucose. RDW can be used as an indicator of atypical RBCs life span, in which the l-HbA1c fraction may be helpful.
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