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Independent Association Between Obstructive Sleep Apnea Severity and Glycated Hemoglobin in Adults Without Diabetes

OBJECTIVE: We tested the hypothesis of an independent cross-sectional association between obstructive sleep apnea (OSA) severity and glycated hemoglobin (HbA(1c)) in adults without known diabetes. RESEARCH DESIGN AND METHODS: HbA(1c) was measured in whole-blood samples from 2,139 patients undergoing...

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Autores principales: Priou, Pascaline, Le Vaillant, Marc, Meslier, Nicole, Chollet, Sylvaine, Masson, Philippe, Humeau, Marie P., Pigeanne, Thierry, Bizieux-Thaminy, Acya, Goupil, François, Gagnadoux, Frédéric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Diabetes Association 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3425014/
https://www.ncbi.nlm.nih.gov/pubmed/22688546
http://dx.doi.org/10.2337/dc11-2538
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author Priou, Pascaline
Le Vaillant, Marc
Meslier, Nicole
Chollet, Sylvaine
Masson, Philippe
Humeau, Marie P.
Pigeanne, Thierry
Bizieux-Thaminy, Acya
Goupil, François
Gagnadoux, Frédéric
author_facet Priou, Pascaline
Le Vaillant, Marc
Meslier, Nicole
Chollet, Sylvaine
Masson, Philippe
Humeau, Marie P.
Pigeanne, Thierry
Bizieux-Thaminy, Acya
Goupil, François
Gagnadoux, Frédéric
author_sort Priou, Pascaline
collection PubMed
description OBJECTIVE: We tested the hypothesis of an independent cross-sectional association between obstructive sleep apnea (OSA) severity and glycated hemoglobin (HbA(1c)) in adults without known diabetes. RESEARCH DESIGN AND METHODS: HbA(1c) was measured in whole-blood samples from 2,139 patients undergoing nocturnal recording for suspected OSA. Participants with self-reported diabetes, use of diabetes medication, or HbA(1c) value ≥6.5% were excluded from this study. Our final sample size comprised 1,599 patients. RESULTS: A dose-response relationship was observed between apnea-hypopnea index (AHI) and the percentage of patients with HbA(1c) >6.0%, ranging from 10.8% for AHI <5 to 34.2% for AHI ≥50. After adjustment for age, sex, smoking habits, BMI, waist circumference, cardiovascular morbidity, daytime sleepiness, depression, insomnia, sleep duration, and study site, odds ratios (95% CIs) for HbA(1c) >6.0% were 1 (reference), 1.40 (0.84–2.32), 1.80 (1.19–2.72), 2.02 (1.31–3.14), and 2.96 (1.58–5.54) for AHI values <5, 5 to <15, 15 to <30, 30 to <50, and ≥50, respectively. Increasing hypoxemia during sleep was also independently associated with the odds of HbA(1c) >6.0%. CONCLUSIONS: Among adults without known diabetes, increasing OSA severity is independently associated with impaired glucose metabolism, as assessed by higher HbA(1c) values, which may expose them to higher risks of diabetes and cardiovascular disease.
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spelling pubmed-34250142013-09-01 Independent Association Between Obstructive Sleep Apnea Severity and Glycated Hemoglobin in Adults Without Diabetes Priou, Pascaline Le Vaillant, Marc Meslier, Nicole Chollet, Sylvaine Masson, Philippe Humeau, Marie P. Pigeanne, Thierry Bizieux-Thaminy, Acya Goupil, François Gagnadoux, Frédéric Diabetes Care Original Research OBJECTIVE: We tested the hypothesis of an independent cross-sectional association between obstructive sleep apnea (OSA) severity and glycated hemoglobin (HbA(1c)) in adults without known diabetes. RESEARCH DESIGN AND METHODS: HbA(1c) was measured in whole-blood samples from 2,139 patients undergoing nocturnal recording for suspected OSA. Participants with self-reported diabetes, use of diabetes medication, or HbA(1c) value ≥6.5% were excluded from this study. Our final sample size comprised 1,599 patients. RESULTS: A dose-response relationship was observed between apnea-hypopnea index (AHI) and the percentage of patients with HbA(1c) >6.0%, ranging from 10.8% for AHI <5 to 34.2% for AHI ≥50. After adjustment for age, sex, smoking habits, BMI, waist circumference, cardiovascular morbidity, daytime sleepiness, depression, insomnia, sleep duration, and study site, odds ratios (95% CIs) for HbA(1c) >6.0% were 1 (reference), 1.40 (0.84–2.32), 1.80 (1.19–2.72), 2.02 (1.31–3.14), and 2.96 (1.58–5.54) for AHI values <5, 5 to <15, 15 to <30, 30 to <50, and ≥50, respectively. Increasing hypoxemia during sleep was also independently associated with the odds of HbA(1c) >6.0%. CONCLUSIONS: Among adults without known diabetes, increasing OSA severity is independently associated with impaired glucose metabolism, as assessed by higher HbA(1c) values, which may expose them to higher risks of diabetes and cardiovascular disease. American Diabetes Association 2012-09 2012-08-14 /pmc/articles/PMC3425014/ /pubmed/22688546 http://dx.doi.org/10.2337/dc11-2538 Text en © 2012 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
Priou, Pascaline
Le Vaillant, Marc
Meslier, Nicole
Chollet, Sylvaine
Masson, Philippe
Humeau, Marie P.
Pigeanne, Thierry
Bizieux-Thaminy, Acya
Goupil, François
Gagnadoux, Frédéric
Independent Association Between Obstructive Sleep Apnea Severity and Glycated Hemoglobin in Adults Without Diabetes
title Independent Association Between Obstructive Sleep Apnea Severity and Glycated Hemoglobin in Adults Without Diabetes
title_full Independent Association Between Obstructive Sleep Apnea Severity and Glycated Hemoglobin in Adults Without Diabetes
title_fullStr Independent Association Between Obstructive Sleep Apnea Severity and Glycated Hemoglobin in Adults Without Diabetes
title_full_unstemmed Independent Association Between Obstructive Sleep Apnea Severity and Glycated Hemoglobin in Adults Without Diabetes
title_short Independent Association Between Obstructive Sleep Apnea Severity and Glycated Hemoglobin in Adults Without Diabetes
title_sort independent association between obstructive sleep apnea severity and glycated hemoglobin in adults without diabetes
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3425014/
https://www.ncbi.nlm.nih.gov/pubmed/22688546
http://dx.doi.org/10.2337/dc11-2538
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