Glycated albumin is correlated with glycated hemoglobin in type 2 diabetes

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DOI:

https://doi.org/10.15386/mpr-1247

Keywords:

glycated serum albumin, glycated hemoglobin, type 2 diabetes mellitus

Abstract

Background and aims. Glycated hemoglobin (HbA1c) retrospectively evaluates mean glycemia in the preceding 2-3 months and is the gold standard for assessing glycemic control, while glycated albumin (GA) is currently considered a short to intermediate term integrated glycemic control marker, since it reflects glycemic status over the last 3 weeks. We aimed to investigate the levels of GA, HbA1c and fasting glycemia in a group of patients with type 2 diabetes.

Methods. The observational study included adult type 2 diabetes patients (n=135) according to inclusion and exclusion criteria, randomly selected from Clinical Centre of Diabetes, Cluj-Napoca, Romania. Fasting glycemia, GA, HbA1c and creatinine were measured using commercially available methods. 

Results. Of the whole group, 62 (45.9 %) were men. Mean age was 62.1±8.6 years old, body mass index was 31.8±6.1 kg/m2 and diabetes duration was 10.0 (4.0; 15.0) years. Fasting glycemia was 162±13.7 mg/dl, GA was 28.0 (21.0; 40.0)% and HbA1c 8.9±2.3%. We found GA was significantly correlated with HbA1c (r=0.19; p=0.029) and fasting glycemia (r=0.32; p<0.001), while HbA1c was significantly correlated with fasting glycemia (r=0.40; p<0.001).

Conclusions. GA was significantly correlated with both HbA1c and fasting glycemia in our patients with type 2 diabetes. While HbA1c is recognized as being the reference test for diabetes control monitoring, GA might a useful biomarker for assessing short to intermediate term glycemic control, particularly important in situations when HbA1c test cannot be reliable or earlier clinical decision making is mandatory.

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Published

2019-04-23

How to Cite

1.
Ciobanu DM, Bogdan F, Pătruț C-I, Roman G. Glycated albumin is correlated with glycated hemoglobin in type 2 diabetes. Med Pharm Rep [Internet]. 2019 Apr. 23 [cited 2025 Oct. 5];92(2):134-8. Available from: https://medpharmareports.com/index.php/mpr/article/view/1247

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Section

Original Research