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Misleading HbA1c Measurement in Diabetic Patients with Hemoglobin Variants

Background and Objectives: Hemoglobin A1c (HbA1c) is widely used for the monitoring and management of diabetes mellitus. The aim of this study is to investigate the influence of hemoglobin (Hb) variants on the measurement of HbA1c. Materials and Methods: HbA1c levels of 845 blood samples obtained fr...

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Autores principales: Mitchai, Manthana, Suwansaksri, Nattakarn, Seanseeha, Suphakdee, Saenboonsiri, Jindamanee, Kraitree, Putthichai, Piyapromdee, Jirasak, Silsirivanit, Atit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8293317/
https://www.ncbi.nlm.nih.gov/pubmed/34200315
http://dx.doi.org/10.3390/medsci9020043
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author Mitchai, Manthana
Suwansaksri, Nattakarn
Seanseeha, Suphakdee
Saenboonsiri, Jindamanee
Kraitree, Putthichai
Piyapromdee, Jirasak
Silsirivanit, Atit
author_facet Mitchai, Manthana
Suwansaksri, Nattakarn
Seanseeha, Suphakdee
Saenboonsiri, Jindamanee
Kraitree, Putthichai
Piyapromdee, Jirasak
Silsirivanit, Atit
author_sort Mitchai, Manthana
collection PubMed
description Background and Objectives: Hemoglobin A1c (HbA1c) is widely used for the monitoring and management of diabetes mellitus. The aim of this study is to investigate the influence of hemoglobin (Hb) variants on the measurement of HbA1c. Materials and Methods: HbA1c levels of 845 blood samples obtained from diabetic patients with various hemoglobin types were measured using a turbidimetric inhibition immunoassay and capillary electrophoresis. Results: Of 845 patients with diabetes, 65.7% (555/845) have the normal hemoglobin type (A(2)A) and 34.3% (290/845) have various abnormal hemoglobin types, including heterozygous HbE 30.2% (255/845), homozygous HbE 1.9 % (16/845), Hb Constant Spring (CS) trait 1.4% (12/845), CSEA Bart’s 0.2% (2/845), and beta-thalassemia trait 0.6% (5/845). In most of the patients with diabetes, HbA1c levels determined by two different methods, inhibition immunoassay and capillary electrophoresis, gave strong positive correlation (R = 0.901, P < 0.001), except for those with homozygous HbE (N = 16) and CSEA Bart’s (N = 2). In all 18 patients with homozygous HbE and CSEA Bart’s, the HbA1c was undetectable by capillary electrophoresis, meaning that their estimated average glucose was undeterminable, although their HbA1c levels could be measured using an inhibition immunoassay. The discrepancy of HbA1c results obtained from two different methods is noted in patients without HbA. Conclusions: We have demonstrated the erroneous nature of HbA1c measurement in patients with hemoglobin variants, especially in those without HbA expression. Therefore, in the population with a high prevalence of hemoglobinopathies, hemoglobin typing should be considered as basic information prior to HbA1c measurement.
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spelling pubmed-82933172021-07-22 Misleading HbA1c Measurement in Diabetic Patients with Hemoglobin Variants Mitchai, Manthana Suwansaksri, Nattakarn Seanseeha, Suphakdee Saenboonsiri, Jindamanee Kraitree, Putthichai Piyapromdee, Jirasak Silsirivanit, Atit Med Sci (Basel) Article Background and Objectives: Hemoglobin A1c (HbA1c) is widely used for the monitoring and management of diabetes mellitus. The aim of this study is to investigate the influence of hemoglobin (Hb) variants on the measurement of HbA1c. Materials and Methods: HbA1c levels of 845 blood samples obtained from diabetic patients with various hemoglobin types were measured using a turbidimetric inhibition immunoassay and capillary electrophoresis. Results: Of 845 patients with diabetes, 65.7% (555/845) have the normal hemoglobin type (A(2)A) and 34.3% (290/845) have various abnormal hemoglobin types, including heterozygous HbE 30.2% (255/845), homozygous HbE 1.9 % (16/845), Hb Constant Spring (CS) trait 1.4% (12/845), CSEA Bart’s 0.2% (2/845), and beta-thalassemia trait 0.6% (5/845). In most of the patients with diabetes, HbA1c levels determined by two different methods, inhibition immunoassay and capillary electrophoresis, gave strong positive correlation (R = 0.901, P < 0.001), except for those with homozygous HbE (N = 16) and CSEA Bart’s (N = 2). In all 18 patients with homozygous HbE and CSEA Bart’s, the HbA1c was undetectable by capillary electrophoresis, meaning that their estimated average glucose was undeterminable, although their HbA1c levels could be measured using an inhibition immunoassay. The discrepancy of HbA1c results obtained from two different methods is noted in patients without HbA. Conclusions: We have demonstrated the erroneous nature of HbA1c measurement in patients with hemoglobin variants, especially in those without HbA expression. Therefore, in the population with a high prevalence of hemoglobinopathies, hemoglobin typing should be considered as basic information prior to HbA1c measurement. MDPI 2021-06-07 /pmc/articles/PMC8293317/ /pubmed/34200315 http://dx.doi.org/10.3390/medsci9020043 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Mitchai, Manthana
Suwansaksri, Nattakarn
Seanseeha, Suphakdee
Saenboonsiri, Jindamanee
Kraitree, Putthichai
Piyapromdee, Jirasak
Silsirivanit, Atit
Misleading HbA1c Measurement in Diabetic Patients with Hemoglobin Variants
title Misleading HbA1c Measurement in Diabetic Patients with Hemoglobin Variants
title_full Misleading HbA1c Measurement in Diabetic Patients with Hemoglobin Variants
title_fullStr Misleading HbA1c Measurement in Diabetic Patients with Hemoglobin Variants
title_full_unstemmed Misleading HbA1c Measurement in Diabetic Patients with Hemoglobin Variants
title_short Misleading HbA1c Measurement in Diabetic Patients with Hemoglobin Variants
title_sort misleading hba1c measurement in diabetic patients with hemoglobin variants
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8293317/
https://www.ncbi.nlm.nih.gov/pubmed/34200315
http://dx.doi.org/10.3390/medsci9020043
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