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Long-term HbA1c variability and the development and progression of diabetic retinopathy in subjects with type 2 diabetes
This study aimed to investigate whether long-term HbA1c variability is associated with the development and progression of diabetic retinopathy (DR) in subjects with type 2 diabetes. We retrospectively reviewed 434 type 2 diabetes subjects without DR who underwent regular DR screening. We reviewed fu...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7910456/ https://www.ncbi.nlm.nih.gov/pubmed/33637847 http://dx.doi.org/10.1038/s41598-021-84150-8 |
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author | Kim, Han Ul Park, Sung Pyo Kim, Yong-Kyu |
author_facet | Kim, Han Ul Park, Sung Pyo Kim, Yong-Kyu |
author_sort | Kim, Han Ul |
collection | PubMed |
description | This study aimed to investigate whether long-term HbA1c variability is associated with the development and progression of diabetic retinopathy (DR) in subjects with type 2 diabetes. We retrospectively reviewed 434 type 2 diabetes subjects without DR who underwent regular DR screening. We reviewed fundus findings, collected HbA1c levels, and calculated the coefficient of variation (CV) and average real variability (ARV) of each subject’s HbA1c level. DR was developed in 55 subjects and progressed to moderate nonproliferative DR or worse DR in 23 subjects. On Cox proportional hazards regression analysis, HbA1c ARV, but not HbA1c CV, was significantly associated with DR development. However, the association between HbA1c variability and the DR progression rate to moderate nonproliferative DR or worse DR was not significant. The inter-visit HbA1c difference value on consecutive examination predicted DR development well and more careful screening for DR is needed for those with an absolute value change of 2.05%, an absolute increase of 1.75%, and an absolute decrease of 1.45% in HbA1c levels on consecutive examination. These results indicate that long-term glucose variability measured by HbA1c ARV might be an independent risk factor for DR development in addition to the mean HbA1c level in early diabetic subjects. |
format | Online Article Text |
id | pubmed-7910456 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79104562021-03-02 Long-term HbA1c variability and the development and progression of diabetic retinopathy in subjects with type 2 diabetes Kim, Han Ul Park, Sung Pyo Kim, Yong-Kyu Sci Rep Article This study aimed to investigate whether long-term HbA1c variability is associated with the development and progression of diabetic retinopathy (DR) in subjects with type 2 diabetes. We retrospectively reviewed 434 type 2 diabetes subjects without DR who underwent regular DR screening. We reviewed fundus findings, collected HbA1c levels, and calculated the coefficient of variation (CV) and average real variability (ARV) of each subject’s HbA1c level. DR was developed in 55 subjects and progressed to moderate nonproliferative DR or worse DR in 23 subjects. On Cox proportional hazards regression analysis, HbA1c ARV, but not HbA1c CV, was significantly associated with DR development. However, the association between HbA1c variability and the DR progression rate to moderate nonproliferative DR or worse DR was not significant. The inter-visit HbA1c difference value on consecutive examination predicted DR development well and more careful screening for DR is needed for those with an absolute value change of 2.05%, an absolute increase of 1.75%, and an absolute decrease of 1.45% in HbA1c levels on consecutive examination. These results indicate that long-term glucose variability measured by HbA1c ARV might be an independent risk factor for DR development in addition to the mean HbA1c level in early diabetic subjects. Nature Publishing Group UK 2021-02-26 /pmc/articles/PMC7910456/ /pubmed/33637847 http://dx.doi.org/10.1038/s41598-021-84150-8 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Kim, Han Ul Park, Sung Pyo Kim, Yong-Kyu Long-term HbA1c variability and the development and progression of diabetic retinopathy in subjects with type 2 diabetes |
title | Long-term HbA1c variability and the development and progression of diabetic retinopathy in subjects with type 2 diabetes |
title_full | Long-term HbA1c variability and the development and progression of diabetic retinopathy in subjects with type 2 diabetes |
title_fullStr | Long-term HbA1c variability and the development and progression of diabetic retinopathy in subjects with type 2 diabetes |
title_full_unstemmed | Long-term HbA1c variability and the development and progression of diabetic retinopathy in subjects with type 2 diabetes |
title_short | Long-term HbA1c variability and the development and progression of diabetic retinopathy in subjects with type 2 diabetes |
title_sort | long-term hba1c variability and the development and progression of diabetic retinopathy in subjects with type 2 diabetes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7910456/ https://www.ncbi.nlm.nih.gov/pubmed/33637847 http://dx.doi.org/10.1038/s41598-021-84150-8 |
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