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The calculated versus the measured glycosylated haemoglobin (HbA(1c)) levels in patients with type 2 diabetes mellitus

BACKGROUND: Diabetes mellitus (DM) is a chronic metabolic disorder that is increasing globally. It is associated with chronic complications that are more common among patients with poor glycaemic control. Glycosylated haemoglobin (HbA(1c)) is the gold standard for monitoring glycaemic control. Measu...

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Autores principales: Musa, Imad R., Omar, Saeed M., Sharif, Manal E., Ahmed, Abdel B. A., Adam, Ishag
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8373363/
https://www.ncbi.nlm.nih.gov/pubmed/34125975
http://dx.doi.org/10.1002/jcla.23873
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author Musa, Imad R.
Omar, Saeed M.
Sharif, Manal E.
Ahmed, Abdel B. A.
Adam, Ishag
author_facet Musa, Imad R.
Omar, Saeed M.
Sharif, Manal E.
Ahmed, Abdel B. A.
Adam, Ishag
author_sort Musa, Imad R.
collection PubMed
description BACKGROUND: Diabetes mellitus (DM) is a chronic metabolic disorder that is increasing globally. It is associated with chronic complications that are more common among patients with poor glycaemic control. Glycosylated haemoglobin (HbA(1c)) is the gold standard for monitoring glycaemic control. Measurements of HbA(1c) are relatively expensive and not available in some remote areas of developing countries. METHODS: We conducted a cross‐sectional study to evaluate the agreement between the calculated and measured HbA(1c) levels. The equation to compute the calculated HbA(1c) also incorporated the fasting blood glucose (FBG) level and was as follows: HbA(1c) = 2.6 + 0.03 × FBG (mg/dl). RESULT: We enrolled 290 patients with type 2 DM in this study. Of these, 204 (70.3%) were females and the mean (SD) age was 54.9 (12.8) years. The mean (SD) diabetes duration was 6.8 (5.5) years. There were 211 (72.8%) patients using oral hypoglycaemic agents, 62 (21.4%) were using insulin and 17 (5.9%) were using both insulin and oral hypoglycaemic agents. There was a borderline difference between the mean (SD) calculated and measured HbA(1c) levels (p = 0.054). There was a significant correlation between the calculated and measured HbA(1c) (r = 0.595, p < 0.001). However, there was no agreement between the calculated and measured HbA(1c). The bias ±SD (limits of agreement) for calculated versus measured HbA(1c) was −1.008 ± 2.02% (−5.05, 2.032). CONCLUSION: Despite the presence of a significant correlation between the calculated and measured HbA(1c), the calculated level has shown an unacceptable agreement with the measured HbA(1c).
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spelling pubmed-83733632021-08-24 The calculated versus the measured glycosylated haemoglobin (HbA(1c)) levels in patients with type 2 diabetes mellitus Musa, Imad R. Omar, Saeed M. Sharif, Manal E. Ahmed, Abdel B. A. Adam, Ishag J Clin Lab Anal Research Articles BACKGROUND: Diabetes mellitus (DM) is a chronic metabolic disorder that is increasing globally. It is associated with chronic complications that are more common among patients with poor glycaemic control. Glycosylated haemoglobin (HbA(1c)) is the gold standard for monitoring glycaemic control. Measurements of HbA(1c) are relatively expensive and not available in some remote areas of developing countries. METHODS: We conducted a cross‐sectional study to evaluate the agreement between the calculated and measured HbA(1c) levels. The equation to compute the calculated HbA(1c) also incorporated the fasting blood glucose (FBG) level and was as follows: HbA(1c) = 2.6 + 0.03 × FBG (mg/dl). RESULT: We enrolled 290 patients with type 2 DM in this study. Of these, 204 (70.3%) were females and the mean (SD) age was 54.9 (12.8) years. The mean (SD) diabetes duration was 6.8 (5.5) years. There were 211 (72.8%) patients using oral hypoglycaemic agents, 62 (21.4%) were using insulin and 17 (5.9%) were using both insulin and oral hypoglycaemic agents. There was a borderline difference between the mean (SD) calculated and measured HbA(1c) levels (p = 0.054). There was a significant correlation between the calculated and measured HbA(1c) (r = 0.595, p < 0.001). However, there was no agreement between the calculated and measured HbA(1c). The bias ±SD (limits of agreement) for calculated versus measured HbA(1c) was −1.008 ± 2.02% (−5.05, 2.032). CONCLUSION: Despite the presence of a significant correlation between the calculated and measured HbA(1c), the calculated level has shown an unacceptable agreement with the measured HbA(1c). John Wiley and Sons Inc. 2021-06-14 /pmc/articles/PMC8373363/ /pubmed/34125975 http://dx.doi.org/10.1002/jcla.23873 Text en © 2021 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Musa, Imad R.
Omar, Saeed M.
Sharif, Manal E.
Ahmed, Abdel B. A.
Adam, Ishag
The calculated versus the measured glycosylated haemoglobin (HbA(1c)) levels in patients with type 2 diabetes mellitus
title The calculated versus the measured glycosylated haemoglobin (HbA(1c)) levels in patients with type 2 diabetes mellitus
title_full The calculated versus the measured glycosylated haemoglobin (HbA(1c)) levels in patients with type 2 diabetes mellitus
title_fullStr The calculated versus the measured glycosylated haemoglobin (HbA(1c)) levels in patients with type 2 diabetes mellitus
title_full_unstemmed The calculated versus the measured glycosylated haemoglobin (HbA(1c)) levels in patients with type 2 diabetes mellitus
title_short The calculated versus the measured glycosylated haemoglobin (HbA(1c)) levels in patients with type 2 diabetes mellitus
title_sort calculated versus the measured glycosylated haemoglobin (hba(1c)) levels in patients with type 2 diabetes mellitus
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8373363/
https://www.ncbi.nlm.nih.gov/pubmed/34125975
http://dx.doi.org/10.1002/jcla.23873
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