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Nocturic obstructive sleep apnea as a clinical phenotype of severe disease

STUDY OBJECTIVES: This study was done to find whether a history of nocturia is associated with severity of obstructive sleep apnea (OSA) and also whether patients with nocturia constitute a separate phenotype of OSA. MATERIALS AND METHODS: Retrospective chart review was done in consecutive OSA patie...

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Autores principales: Goyal, Abhishek, Pakhare, Abhijit, Chaudhary, Poonam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330796/
https://www.ncbi.nlm.nih.gov/pubmed/30604701
http://dx.doi.org/10.4103/lungindia.lungindia_153_18
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author Goyal, Abhishek
Pakhare, Abhijit
Chaudhary, Poonam
author_facet Goyal, Abhishek
Pakhare, Abhijit
Chaudhary, Poonam
author_sort Goyal, Abhishek
collection PubMed
description STUDY OBJECTIVES: This study was done to find whether a history of nocturia is associated with severity of obstructive sleep apnea (OSA) and also whether patients with nocturia constitute a separate phenotype of OSA. MATERIALS AND METHODS: Retrospective chart review was done in consecutive OSA patients who were diagnosed in sleep laboratory of our institute. Detailed sleep history, examination, biochemical investigations, and polysomnography reports were taken for the analysis. Nocturia was defined as urine frequency ≥2/night. RESULTS: Of 172 OSA patients, 87 (50.5%) patients had nocturia. On multivariate analysis, a history of nocturia had 2.429 times (confidence interval 1.086–5.434) more chances of having very severe OSA (P = 0.031). Time between bedtime and first time for urination was significantly less in very severe OSA compared to severe OSA and mild-to-moderate OSA (2.4 ± 0.9, 3.1 ± 1.3, and 3.0 ± 1.1 h, respectively) (P = 0.021). Patients with nocturia were older (52.3 ± 11.9 vs. 47.6 ± 12.1 years; P = 0.012), had higher STOP BANG scores (P = 0.002), higher apnea–hypopnea index (AHI) (64.8 ± 35.9 vs. 43.9 ± 29.1; P < 0.001), and higher Epworth sleepiness scale (ESS) (9.2 ± 5.3 vs. 7.7 ± 4.4; P = 0.052) and were more likely to be fatigued during day (P = 0.001). Nocturics had higher body mass index (BMI) (P = 0.030), higher waist, and hip circumference (P = 0.001and 0.023, respectively). Nocturic patients had lower awake SpO(2) (P = 0.032) and lower nadir SpO(2) during sleep (P = 0.002). CONCLUSIONS: A history of nocturia (≥2/night) predicts very severe OSA (AHI >60). Nocturic OSA is a phenotype of OSA with more severe AHI, lower oxygen levels, higher BMI, and higher ESS. We believe nocturia can be used for screening in OSA questionnaires, which needs to be validated in further community-based studies.
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spelling pubmed-63307962019-04-17 Nocturic obstructive sleep apnea as a clinical phenotype of severe disease Goyal, Abhishek Pakhare, Abhijit Chaudhary, Poonam Lung India Original Article STUDY OBJECTIVES: This study was done to find whether a history of nocturia is associated with severity of obstructive sleep apnea (OSA) and also whether patients with nocturia constitute a separate phenotype of OSA. MATERIALS AND METHODS: Retrospective chart review was done in consecutive OSA patients who were diagnosed in sleep laboratory of our institute. Detailed sleep history, examination, biochemical investigations, and polysomnography reports were taken for the analysis. Nocturia was defined as urine frequency ≥2/night. RESULTS: Of 172 OSA patients, 87 (50.5%) patients had nocturia. On multivariate analysis, a history of nocturia had 2.429 times (confidence interval 1.086–5.434) more chances of having very severe OSA (P = 0.031). Time between bedtime and first time for urination was significantly less in very severe OSA compared to severe OSA and mild-to-moderate OSA (2.4 ± 0.9, 3.1 ± 1.3, and 3.0 ± 1.1 h, respectively) (P = 0.021). Patients with nocturia were older (52.3 ± 11.9 vs. 47.6 ± 12.1 years; P = 0.012), had higher STOP BANG scores (P = 0.002), higher apnea–hypopnea index (AHI) (64.8 ± 35.9 vs. 43.9 ± 29.1; P < 0.001), and higher Epworth sleepiness scale (ESS) (9.2 ± 5.3 vs. 7.7 ± 4.4; P = 0.052) and were more likely to be fatigued during day (P = 0.001). Nocturics had higher body mass index (BMI) (P = 0.030), higher waist, and hip circumference (P = 0.001and 0.023, respectively). Nocturic patients had lower awake SpO(2) (P = 0.032) and lower nadir SpO(2) during sleep (P = 0.002). CONCLUSIONS: A history of nocturia (≥2/night) predicts very severe OSA (AHI >60). Nocturic OSA is a phenotype of OSA with more severe AHI, lower oxygen levels, higher BMI, and higher ESS. We believe nocturia can be used for screening in OSA questionnaires, which needs to be validated in further community-based studies. Medknow Publications & Media Pvt Ltd 2019 /pmc/articles/PMC6330796/ /pubmed/30604701 http://dx.doi.org/10.4103/lungindia.lungindia_153_18 Text en Copyright: © 2018 Indian Chest Society http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Goyal, Abhishek
Pakhare, Abhijit
Chaudhary, Poonam
Nocturic obstructive sleep apnea as a clinical phenotype of severe disease
title Nocturic obstructive sleep apnea as a clinical phenotype of severe disease
title_full Nocturic obstructive sleep apnea as a clinical phenotype of severe disease
title_fullStr Nocturic obstructive sleep apnea as a clinical phenotype of severe disease
title_full_unstemmed Nocturic obstructive sleep apnea as a clinical phenotype of severe disease
title_short Nocturic obstructive sleep apnea as a clinical phenotype of severe disease
title_sort nocturic obstructive sleep apnea as a clinical phenotype of severe disease
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330796/
https://www.ncbi.nlm.nih.gov/pubmed/30604701
http://dx.doi.org/10.4103/lungindia.lungindia_153_18
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