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Glycated Albumin Correlates With Time-in-Range Better Than HbA(1c) or Fructosamine

CONTEXT: Intermediate-term glycemic control metrics may represent a viable alternative to continuous glucose monitoring (CGM) in patients without access to CGM. OBJECTIVE: This work aimed to compare the relationship between CGM parameters and glycated albumin (GA), glycated hemoglobin A(1c) (HbA(1c)...

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Autores principales: Desouza, Cyrus V, Rosenstock, Julio, Kohzuma, Takuji, Fonseca, Vivian A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10583977/
https://www.ncbi.nlm.nih.gov/pubmed/37259605
http://dx.doi.org/10.1210/clinem/dgad298
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author Desouza, Cyrus V
Rosenstock, Julio
Kohzuma, Takuji
Fonseca, Vivian A
author_facet Desouza, Cyrus V
Rosenstock, Julio
Kohzuma, Takuji
Fonseca, Vivian A
author_sort Desouza, Cyrus V
collection PubMed
description CONTEXT: Intermediate-term glycemic control metrics may represent a viable alternative to continuous glucose monitoring (CGM) in patients without access to CGM. OBJECTIVE: This work aimed to compare the relationship between CGM parameters and glycated albumin (GA), glycated hemoglobin A(1c) (HbA(1c)), and fructosamine for 24 weeks. METHODS: We conducted exploratory comparative analyses of CGM subgroup data from a previously published 24-week prospective study of assay performance in 8 US clinics. Participants included 34 individuals with type 1 (n = 18) and type 2 diabetes (n = 16) undergoing changes to improve glycemic control (n = 22; group 1) or with stable diabetes therapy (n = 12; group 2). Main outcome measures included Pearson correlations between CGM and glycemic indices and receiver operating characteristic (ROC) analysis of glycemic index values predictive of time in range (TIR) greater than 70%. RESULTS: At weeks 4 and 8, GA correlations with TIR were higher than HbA(1c) correlations in group 1. In group 2, GA correlations with TIR were statistically significant, whereas HbA(1c) correlations were not. In both groups over the first 12 weeks, GA correlations with TIR were higher than fructosamine-TIR correlations. In the ROC analysis, GA predicted a TIR greater than 70% during weeks 2 to 24 (area under the curve >0.80); HbA(1c) was predictive during weeks 12 to 24. Cutoff values for TIR greater than 70% were 17.5% (sensitivity and specificity, 0.88) for GA and 7.3% (0.86) for HbA(1c). CONCLUSION: GA is the most accurate predictor of TIR over 8 weeks compared with other glycemic indices, which may assist in clinical evaluation of changes in treatment where CGM is not possible and it is too early to use HbA(1c) (NCT02489773).
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spelling pubmed-105839772023-10-19 Glycated Albumin Correlates With Time-in-Range Better Than HbA(1c) or Fructosamine Desouza, Cyrus V Rosenstock, Julio Kohzuma, Takuji Fonseca, Vivian A J Clin Endocrinol Metab Clinical Research Article CONTEXT: Intermediate-term glycemic control metrics may represent a viable alternative to continuous glucose monitoring (CGM) in patients without access to CGM. OBJECTIVE: This work aimed to compare the relationship between CGM parameters and glycated albumin (GA), glycated hemoglobin A(1c) (HbA(1c)), and fructosamine for 24 weeks. METHODS: We conducted exploratory comparative analyses of CGM subgroup data from a previously published 24-week prospective study of assay performance in 8 US clinics. Participants included 34 individuals with type 1 (n = 18) and type 2 diabetes (n = 16) undergoing changes to improve glycemic control (n = 22; group 1) or with stable diabetes therapy (n = 12; group 2). Main outcome measures included Pearson correlations between CGM and glycemic indices and receiver operating characteristic (ROC) analysis of glycemic index values predictive of time in range (TIR) greater than 70%. RESULTS: At weeks 4 and 8, GA correlations with TIR were higher than HbA(1c) correlations in group 1. In group 2, GA correlations with TIR were statistically significant, whereas HbA(1c) correlations were not. In both groups over the first 12 weeks, GA correlations with TIR were higher than fructosamine-TIR correlations. In the ROC analysis, GA predicted a TIR greater than 70% during weeks 2 to 24 (area under the curve >0.80); HbA(1c) was predictive during weeks 12 to 24. Cutoff values for TIR greater than 70% were 17.5% (sensitivity and specificity, 0.88) for GA and 7.3% (0.86) for HbA(1c). CONCLUSION: GA is the most accurate predictor of TIR over 8 weeks compared with other glycemic indices, which may assist in clinical evaluation of changes in treatment where CGM is not possible and it is too early to use HbA(1c) (NCT02489773). Oxford University Press 2023-06-01 /pmc/articles/PMC10583977/ /pubmed/37259605 http://dx.doi.org/10.1210/clinem/dgad298 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the Endocrine Society. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Clinical Research Article
Desouza, Cyrus V
Rosenstock, Julio
Kohzuma, Takuji
Fonseca, Vivian A
Glycated Albumin Correlates With Time-in-Range Better Than HbA(1c) or Fructosamine
title Glycated Albumin Correlates With Time-in-Range Better Than HbA(1c) or Fructosamine
title_full Glycated Albumin Correlates With Time-in-Range Better Than HbA(1c) or Fructosamine
title_fullStr Glycated Albumin Correlates With Time-in-Range Better Than HbA(1c) or Fructosamine
title_full_unstemmed Glycated Albumin Correlates With Time-in-Range Better Than HbA(1c) or Fructosamine
title_short Glycated Albumin Correlates With Time-in-Range Better Than HbA(1c) or Fructosamine
title_sort glycated albumin correlates with time-in-range better than hba(1c) or fructosamine
topic Clinical Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10583977/
https://www.ncbi.nlm.nih.gov/pubmed/37259605
http://dx.doi.org/10.1210/clinem/dgad298
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