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Variability of glycated hemoglobin levels in the first year post renal transplantation in patients without diabetes.
- Source :
-
Clinical biochemistry [Clin Biochem] 2017 Dec; Vol. 50 (18), pp. 997-1001. Date of Electronic Publication: 2017 Jul 20. - Publication Year :
- 2017
-
Abstract
- Background: Glycated hemoglobin (HbA1c) is an alternative test used for the diagnosis and monitoring of diabetes in kidney transplant recipients. Immunosuppressive drugs are the most important risk factors related with changes in the glucose metabolism after transplant. It is still unknown if they impact on the variability of HbA1c. We assessed the variability of HbA1c levels in a group of renal transplant recipients without diabetes during the first year after transplant.<br />Methods: We estimated the variability of HbA1c in a group of 95 Brazilian kidney transplant recipients. Three EDTA whole blood samples were collected from each patient, one every four months for twelve months, totalizing 285 blood specimens. HbA1c values were measured by HPLC (Bio-Rad Variantâ„¢ II Turbo analyzer). Estimations were calculated according to Fraser and Harris method.<br />Results: There was no difference in HbA1c mean levels between men and women. Within-subject and between-subject biological variations were 4.42% and 7.05%, respectively. The reference change value calculated for HbA1c was 16.15% and the index of individuality was 0.63.<br />Conclusions: Kidney transplant patients without diabetes presented higher HbA1c within-subject variation than individuals without diabetes from the general population. This should be considered when interpreting HbA1c results in the diagnosis and management of diabetes after kidney transplantation.<br /> (Copyright © 2017 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved.)
Details
- Language :
- English
- ISSN :
- 1873-2933
- Volume :
- 50
- Issue :
- 18
- Database :
- MEDLINE
- Journal :
- Clinical biochemistry
- Publication Type :
- Academic Journal
- Accession number :
- 28736056
- Full Text :
- https://doi.org/10.1016/j.clinbiochem.2017.07.009