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Association Between Diabetic Retinopathy and Insomnia Risk: A Nationwide Population-Based Study
BACKGROUND: Previous studies have suggested a close link between sleep disturbances and diabetic retinopathy (DR). However, to date, no confirmatory findings have been reported. We aimed to explore the risk of insomnia in DR by considering demographic factors and diabetes mellitus (DM)-related varia...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9333090/ https://www.ncbi.nlm.nih.gov/pubmed/35909567 http://dx.doi.org/10.3389/fendo.2022.939251 |
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author | Um, Yoo Hyun Kim, Tae-Won Jeong, Jong-Hyun Hong, Seung-Chul Seo, Ho-Jun Han, Kyung-Do |
author_facet | Um, Yoo Hyun Kim, Tae-Won Jeong, Jong-Hyun Hong, Seung-Chul Seo, Ho-Jun Han, Kyung-Do |
author_sort | Um, Yoo Hyun |
collection | PubMed |
description | BACKGROUND: Previous studies have suggested a close link between sleep disturbances and diabetic retinopathy (DR). However, to date, no confirmatory findings have been reported. We aimed to explore the risk of insomnia in DR by considering demographic factors and diabetes mellitus (DM)-related variables. METHODS: A nationwide population-based cohort of 2,206,619 patients with type 2 diabetes from the Korean National Insurance Service Database was followed up for insomnia incidence. DR, non-proliferative DR (NPDR), and proliferative DR (PDR) were defined according to ICD-10 codes. The interactive effects of sex, age, and DM-related variables were analyzed to evaluate their impact on insomnia risk in DR. RESULTS: Compared with the non-DR group, insomnia risk was increased in the DR [(adjusted hazard ratio (aHR): 1.125, 95% confidence interval (CI):1.108-1.142), NPDR (aHR:1.117, 95% CI:1.099-1.134), and PDR (aHR:1.205, 95% CI: 1.156-1.256), even after controlling for comorbidities, lifestyle factors, and DM-related variables. The men and youngest age groups (<40 years) were most vulnerable to insomnia risk. Sex, age, DM duration, and chronic kidney disease (CKD) status exerted interactive effects with DR status in increasing the insomnia risk. In the PDR group, sex, age, DM duration, insulin therapy status, and CKD status exerted interactive effects that increased the risk of insomnia. CONCLUSION: Insomnia risk is significantly higher in patients with DR, and clinical attention is warranted. |
format | Online Article Text |
id | pubmed-9333090 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93330902022-07-29 Association Between Diabetic Retinopathy and Insomnia Risk: A Nationwide Population-Based Study Um, Yoo Hyun Kim, Tae-Won Jeong, Jong-Hyun Hong, Seung-Chul Seo, Ho-Jun Han, Kyung-Do Front Endocrinol (Lausanne) Endocrinology BACKGROUND: Previous studies have suggested a close link between sleep disturbances and diabetic retinopathy (DR). However, to date, no confirmatory findings have been reported. We aimed to explore the risk of insomnia in DR by considering demographic factors and diabetes mellitus (DM)-related variables. METHODS: A nationwide population-based cohort of 2,206,619 patients with type 2 diabetes from the Korean National Insurance Service Database was followed up for insomnia incidence. DR, non-proliferative DR (NPDR), and proliferative DR (PDR) were defined according to ICD-10 codes. The interactive effects of sex, age, and DM-related variables were analyzed to evaluate their impact on insomnia risk in DR. RESULTS: Compared with the non-DR group, insomnia risk was increased in the DR [(adjusted hazard ratio (aHR): 1.125, 95% confidence interval (CI):1.108-1.142), NPDR (aHR:1.117, 95% CI:1.099-1.134), and PDR (aHR:1.205, 95% CI: 1.156-1.256), even after controlling for comorbidities, lifestyle factors, and DM-related variables. The men and youngest age groups (<40 years) were most vulnerable to insomnia risk. Sex, age, DM duration, and chronic kidney disease (CKD) status exerted interactive effects with DR status in increasing the insomnia risk. In the PDR group, sex, age, DM duration, insulin therapy status, and CKD status exerted interactive effects that increased the risk of insomnia. CONCLUSION: Insomnia risk is significantly higher in patients with DR, and clinical attention is warranted. Frontiers Media S.A. 2022-07-14 /pmc/articles/PMC9333090/ /pubmed/35909567 http://dx.doi.org/10.3389/fendo.2022.939251 Text en Copyright © 2022 Um, Kim, Jeong, Hong, Seo and Han https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Endocrinology Um, Yoo Hyun Kim, Tae-Won Jeong, Jong-Hyun Hong, Seung-Chul Seo, Ho-Jun Han, Kyung-Do Association Between Diabetic Retinopathy and Insomnia Risk: A Nationwide Population-Based Study |
title | Association Between Diabetic Retinopathy and Insomnia Risk: A Nationwide Population-Based Study |
title_full | Association Between Diabetic Retinopathy and Insomnia Risk: A Nationwide Population-Based Study |
title_fullStr | Association Between Diabetic Retinopathy and Insomnia Risk: A Nationwide Population-Based Study |
title_full_unstemmed | Association Between Diabetic Retinopathy and Insomnia Risk: A Nationwide Population-Based Study |
title_short | Association Between Diabetic Retinopathy and Insomnia Risk: A Nationwide Population-Based Study |
title_sort | association between diabetic retinopathy and insomnia risk: a nationwide population-based study |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9333090/ https://www.ncbi.nlm.nih.gov/pubmed/35909567 http://dx.doi.org/10.3389/fendo.2022.939251 |
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