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Hemoglobin A(1c) as a Diagnostic Tool for Diabetes Screening and New-Onset Diabetes Prediction: A 6-year community-based prospective study

OBJECTIVE: Various cutoff levels of hemoglobin A(1c) (A1C) have been suggested to screen for diabetes, although more consensus about the best level, especially for different ethnicities, is required. We evaluated the usefulness of A1C levels when screening for undiagnosed diabetes and as a predictor...

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Autores principales: Choi, Sung Hee, Kim, Tae Hyuk, Lim, Soo, Park, Kyong Soo, Jang, Hak C., Cho, Nam H.
Formato: Texto
Lenguaje:English
Publicado: American Diabetes Association 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3064055/
https://www.ncbi.nlm.nih.gov/pubmed/21335372
http://dx.doi.org/10.2337/dc10-0644
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author Choi, Sung Hee
Kim, Tae Hyuk
Lim, Soo
Park, Kyong Soo
Jang, Hak C.
Cho, Nam H.
author_facet Choi, Sung Hee
Kim, Tae Hyuk
Lim, Soo
Park, Kyong Soo
Jang, Hak C.
Cho, Nam H.
author_sort Choi, Sung Hee
collection PubMed
description OBJECTIVE: Various cutoff levels of hemoglobin A(1c) (A1C) have been suggested to screen for diabetes, although more consensus about the best level, especially for different ethnicities, is required. We evaluated the usefulness of A1C levels when screening for undiagnosed diabetes and as a predictor of 6-year incident diabetes in a prospective, population-based cohort study. RESEARCH DESIGN AND METHODS: A total 10,038 participants were recruited from the Ansung-Ansan cohort study. All subjects underwent a 75-g oral glucose tolerance test at baseline and at each biennial follow-up. Excluding subjects with a previous history of diabetes (n = 572), the receiver operating characteristic curve was used to evaluate the diagnostic accuracy of the A1C cutoff. The Cox proportional hazards model was used to predict diabetes at 6 years. RESULTS: At baseline, 635 participants (6.8%) had previously undiagnosed diabetes. An A1C cutoff of 5.9% produced the highest sum of sensitivity (68%) and specificity (91%). At 6 years, 895 (10.2%) subjects had developed incident diabetes. An A1C cutoff of 5.6% had the highest sum of sensitivity (59%) and specificity (77%) for the identification of subsequent 6-year incident diabetes. After multivariate adjustment, men with baseline A1C ≥5.6% had a 2.4-fold increased risk and women had a 3.1-fold increased risk of new-onset diabetes. CONCLUSIONS: A1C is an effective and convenient method for diabetes screening. An A1C cutoff of 5.9% may identify subjects with undiagnosed diabetes. Individuals with A1C ≥5.6% have an increased risk for future diabetes.
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spelling pubmed-30640552012-04-01 Hemoglobin A(1c) as a Diagnostic Tool for Diabetes Screening and New-Onset Diabetes Prediction: A 6-year community-based prospective study Choi, Sung Hee Kim, Tae Hyuk Lim, Soo Park, Kyong Soo Jang, Hak C. Cho, Nam H. Diabetes Care Original Research OBJECTIVE: Various cutoff levels of hemoglobin A(1c) (A1C) have been suggested to screen for diabetes, although more consensus about the best level, especially for different ethnicities, is required. We evaluated the usefulness of A1C levels when screening for undiagnosed diabetes and as a predictor of 6-year incident diabetes in a prospective, population-based cohort study. RESEARCH DESIGN AND METHODS: A total 10,038 participants were recruited from the Ansung-Ansan cohort study. All subjects underwent a 75-g oral glucose tolerance test at baseline and at each biennial follow-up. Excluding subjects with a previous history of diabetes (n = 572), the receiver operating characteristic curve was used to evaluate the diagnostic accuracy of the A1C cutoff. The Cox proportional hazards model was used to predict diabetes at 6 years. RESULTS: At baseline, 635 participants (6.8%) had previously undiagnosed diabetes. An A1C cutoff of 5.9% produced the highest sum of sensitivity (68%) and specificity (91%). At 6 years, 895 (10.2%) subjects had developed incident diabetes. An A1C cutoff of 5.6% had the highest sum of sensitivity (59%) and specificity (77%) for the identification of subsequent 6-year incident diabetes. After multivariate adjustment, men with baseline A1C ≥5.6% had a 2.4-fold increased risk and women had a 3.1-fold increased risk of new-onset diabetes. CONCLUSIONS: A1C is an effective and convenient method for diabetes screening. An A1C cutoff of 5.9% may identify subjects with undiagnosed diabetes. Individuals with A1C ≥5.6% have an increased risk for future diabetes. American Diabetes Association 2011-04 2011-03-21 /pmc/articles/PMC3064055/ /pubmed/21335372 http://dx.doi.org/10.2337/dc10-0644 Text en © 2011 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.
spellingShingle Original Research
Choi, Sung Hee
Kim, Tae Hyuk
Lim, Soo
Park, Kyong Soo
Jang, Hak C.
Cho, Nam H.
Hemoglobin A(1c) as a Diagnostic Tool for Diabetes Screening and New-Onset Diabetes Prediction: A 6-year community-based prospective study
title Hemoglobin A(1c) as a Diagnostic Tool for Diabetes Screening and New-Onset Diabetes Prediction: A 6-year community-based prospective study
title_full Hemoglobin A(1c) as a Diagnostic Tool for Diabetes Screening and New-Onset Diabetes Prediction: A 6-year community-based prospective study
title_fullStr Hemoglobin A(1c) as a Diagnostic Tool for Diabetes Screening and New-Onset Diabetes Prediction: A 6-year community-based prospective study
title_full_unstemmed Hemoglobin A(1c) as a Diagnostic Tool for Diabetes Screening and New-Onset Diabetes Prediction: A 6-year community-based prospective study
title_short Hemoglobin A(1c) as a Diagnostic Tool for Diabetes Screening and New-Onset Diabetes Prediction: A 6-year community-based prospective study
title_sort hemoglobin a(1c) as a diagnostic tool for diabetes screening and new-onset diabetes prediction: a 6-year community-based prospective study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3064055/
https://www.ncbi.nlm.nih.gov/pubmed/21335372
http://dx.doi.org/10.2337/dc10-0644
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