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No Ethnic Differences in the Association of Glycated Hemoglobin With Retinopathy: The National Health and Nutrition Examination Survey 2005–2008

OBJECTIVE: Current recommendations for the use of hemoglobin A(1c) (HbA(1c)) in diabetes screening and diagnosis aim to identify those at greatest risk for diabetic microvascular complications. However, there is current controversy regarding the clinical implications of ethnic differences in HbA(1c)...

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Autores principales: Bower, Julie K., Brancati, Frederick L., Selvin, Elizabeth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Diabetes Association 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3579340/
https://www.ncbi.nlm.nih.gov/pubmed/23069841
http://dx.doi.org/10.2337/dc12-0404
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author Bower, Julie K.
Brancati, Frederick L.
Selvin, Elizabeth
author_facet Bower, Julie K.
Brancati, Frederick L.
Selvin, Elizabeth
author_sort Bower, Julie K.
collection PubMed
description OBJECTIVE: Current recommendations for the use of hemoglobin A(1c) (HbA(1c)) in diabetes screening and diagnosis aim to identify those at greatest risk for diabetic microvascular complications. However, there is current controversy regarding the clinical implications of ethnic differences in HbA(1c) values. The objective of this study was to determine whether the association between HbA(1c) and retinopathy differs by ethnic group in a representative sample of U.S. adults. RESEARCH DESIGN AND METHODS: The study was a cross-sectional analysis of 2,945 non-Hispanic white, 1,046 non-Hispanic black, and 1,231 Hispanic American participants aged ≥40 years from the 2005–2008 National Health and Nutrition Examination Survey. RESULTS: Among nondiabetic adults, the mean HbA(1c) was 5.5% in non-Hispanic whites, 5.7% in non-Hispanic blacks, and 5.6% in Hispanic Americans. Among those with diagnosed diabetes, mean HbA(1c) was 6.9% in non-Hispanic whites, 7.5% in non-Hispanic Blacks, and 7.7% in Hispanic Americans. Overall, non-Hispanic blacks had the highest prevalence of retinopathy. In multivariable logistic models, HbA(1c) clinical categories were strongly associated with prevalent retinopathy. However, the magnitude of the association did not differ by ethnic group (all P values for interaction ≥ 0.7). Similar results were observed with HbA(1c) modeled continuously (per one percentage point) and stratified by diabetes status (all P for interactions > 0.3). CONCLUSIONS: We observed no ethnic differences in the association of HbA(1c) with retinopathy. These data do not support ethnic-specific cut points for HbA(1c) for diagnosis or screening of diabetes mellitus.
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spelling pubmed-35793402014-03-01 No Ethnic Differences in the Association of Glycated Hemoglobin With Retinopathy: The National Health and Nutrition Examination Survey 2005–2008 Bower, Julie K. Brancati, Frederick L. Selvin, Elizabeth Diabetes Care Original Research OBJECTIVE: Current recommendations for the use of hemoglobin A(1c) (HbA(1c)) in diabetes screening and diagnosis aim to identify those at greatest risk for diabetic microvascular complications. However, there is current controversy regarding the clinical implications of ethnic differences in HbA(1c) values. The objective of this study was to determine whether the association between HbA(1c) and retinopathy differs by ethnic group in a representative sample of U.S. adults. RESEARCH DESIGN AND METHODS: The study was a cross-sectional analysis of 2,945 non-Hispanic white, 1,046 non-Hispanic black, and 1,231 Hispanic American participants aged ≥40 years from the 2005–2008 National Health and Nutrition Examination Survey. RESULTS: Among nondiabetic adults, the mean HbA(1c) was 5.5% in non-Hispanic whites, 5.7% in non-Hispanic blacks, and 5.6% in Hispanic Americans. Among those with diagnosed diabetes, mean HbA(1c) was 6.9% in non-Hispanic whites, 7.5% in non-Hispanic Blacks, and 7.7% in Hispanic Americans. Overall, non-Hispanic blacks had the highest prevalence of retinopathy. In multivariable logistic models, HbA(1c) clinical categories were strongly associated with prevalent retinopathy. However, the magnitude of the association did not differ by ethnic group (all P values for interaction ≥ 0.7). Similar results were observed with HbA(1c) modeled continuously (per one percentage point) and stratified by diabetes status (all P for interactions > 0.3). CONCLUSIONS: We observed no ethnic differences in the association of HbA(1c) with retinopathy. These data do not support ethnic-specific cut points for HbA(1c) for diagnosis or screening of diabetes mellitus. American Diabetes Association 2013-03 2013-02-13 /pmc/articles/PMC3579340/ /pubmed/23069841 http://dx.doi.org/10.2337/dc12-0404 Text en © 2013 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
Bower, Julie K.
Brancati, Frederick L.
Selvin, Elizabeth
No Ethnic Differences in the Association of Glycated Hemoglobin With Retinopathy: The National Health and Nutrition Examination Survey 2005–2008
title No Ethnic Differences in the Association of Glycated Hemoglobin With Retinopathy: The National Health and Nutrition Examination Survey 2005–2008
title_full No Ethnic Differences in the Association of Glycated Hemoglobin With Retinopathy: The National Health and Nutrition Examination Survey 2005–2008
title_fullStr No Ethnic Differences in the Association of Glycated Hemoglobin With Retinopathy: The National Health and Nutrition Examination Survey 2005–2008
title_full_unstemmed No Ethnic Differences in the Association of Glycated Hemoglobin With Retinopathy: The National Health and Nutrition Examination Survey 2005–2008
title_short No Ethnic Differences in the Association of Glycated Hemoglobin With Retinopathy: The National Health and Nutrition Examination Survey 2005–2008
title_sort no ethnic differences in the association of glycated hemoglobin with retinopathy: the national health and nutrition examination survey 2005–2008
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3579340/
https://www.ncbi.nlm.nih.gov/pubmed/23069841
http://dx.doi.org/10.2337/dc12-0404
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