Insomnia in adults with cystic fibrosis: strong association with anxiety/depression and impaired quality of life
Abstract Background While sleep disruption is a common complaint among children with cystic fibrosis (CF), only a few studies have investigated insomnia in adults. The aim of this study was to identify factors associated with insomnia in clinically stable adult CF patients. Methods Twenty-eight CF p...
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doaj-8eada16303314746916cbbd5ad7aa3c02021-04-04T11:26:39ZengBMCBMC Pulmonary Medicine1471-24662021-04-0121111010.1186/s12890-021-01473-yInsomnia in adults with cystic fibrosis: strong association with anxiety/depression and impaired quality of lifePauline Mulette0Bruno Ravoninjatovo1Camille Guguen2Coralie Barbe3Julien Ancel4Sandra Dury5Antoine Dumazet6Dominique Perdu7Jeanne-Marie Perotin8Thomas Guillard9François Lebargy10Gaëtan Deslee11Claire Launois12Service Des Maladies Respiratoires, CHU ReimsService Des Maladies Respiratoires, CHU ReimsService Des Maladies Respiratoires, CHU ReimsDépartement de Méthodologie, CHU ReimsService Des Maladies Respiratoires, CHU ReimsService Des Maladies Respiratoires, CHU ReimsService Des Maladies Respiratoires, CHU ReimsService Des Maladies Respiratoires, CHU ReimsService Des Maladies Respiratoires, CHU ReimsInserm UMR-S 1250 “Pathologies Pulmonaires et Plasticité Cellulaire”Service Des Maladies Respiratoires, CHU ReimsService Des Maladies Respiratoires, CHU ReimsService Des Maladies Respiratoires, CHU ReimsAbstract Background While sleep disruption is a common complaint among children with cystic fibrosis (CF), only a few studies have investigated insomnia in adults. The aim of this study was to identify factors associated with insomnia in clinically stable adult CF patients. Methods Twenty-eight CF patients (18M/10F), with a median age of 27 (22–34) (median (interquartile range) years and a median of forced expiratory volume in one second of 72 (39–93) % predicted completed questionnaires on insomnia (Insomnia Severity Index, ISI), sleep quality (PSQI), daytime sleepiness (Epworth), restless legs syndrome (IRLS), pain (NRS), anxiety/depression (HAD) and quality of life (CFQ-R 14+). Respiratory assessment data, including symptoms, sputum analysis, arterial blood gases, 6-min walking test, pulmonary function tests and polysomnographic variables, were also analyzed. Results Forty-three percent of patients were insomniac (ISI > 7). Compared with non-insomniac patients (ISI ≤ 7), insomniac patients had more severely impaired quality of life and a higher HAD score: median anxiety score of 9 (8–11) vs 4 (3–6) (p < 0.0001), median depression score of 7 (5–10) vs 1 (1–4) (p < 0.001), with a positive correlation between ISI and HAD anxiety/depression scores (r = 0.702/r = 0.701, respectively, p < 0.0001). Insomnia was also associated with mMRC dyspnea scale ≥ 2, restless legs syndrome, pain and lower SpO2 during sleep. Conclusions The strong association between insomnia, impaired quality of life and increased HAD score should prompt physicians to be particularly attentive to the management of anxiety and depression in adult CF patients with insomnia. Trial registration: On clinicaltrials.gov (NCT02924818, date of registration: October 5, 2016).https://doi.org/10.1186/s12890-021-01473-yCystic fibrosisInsomniaSleepAnxiety-depressionQuality of life |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Pauline Mulette Bruno Ravoninjatovo Camille Guguen Coralie Barbe Julien Ancel Sandra Dury Antoine Dumazet Dominique Perdu Jeanne-Marie Perotin Thomas Guillard François Lebargy Gaëtan Deslee Claire Launois |
spellingShingle |
Pauline Mulette Bruno Ravoninjatovo Camille Guguen Coralie Barbe Julien Ancel Sandra Dury Antoine Dumazet Dominique Perdu Jeanne-Marie Perotin Thomas Guillard François Lebargy Gaëtan Deslee Claire Launois Insomnia in adults with cystic fibrosis: strong association with anxiety/depression and impaired quality of life BMC Pulmonary Medicine Cystic fibrosis Insomnia Sleep Anxiety-depression Quality of life |
author_facet |
Pauline Mulette Bruno Ravoninjatovo Camille Guguen Coralie Barbe Julien Ancel Sandra Dury Antoine Dumazet Dominique Perdu Jeanne-Marie Perotin Thomas Guillard François Lebargy Gaëtan Deslee Claire Launois |
author_sort |
Pauline Mulette |
title |
Insomnia in adults with cystic fibrosis: strong association with anxiety/depression and impaired quality of life |
title_short |
Insomnia in adults with cystic fibrosis: strong association with anxiety/depression and impaired quality of life |
title_full |
Insomnia in adults with cystic fibrosis: strong association with anxiety/depression and impaired quality of life |
title_fullStr |
Insomnia in adults with cystic fibrosis: strong association with anxiety/depression and impaired quality of life |
title_full_unstemmed |
Insomnia in adults with cystic fibrosis: strong association with anxiety/depression and impaired quality of life |
title_sort |
insomnia in adults with cystic fibrosis: strong association with anxiety/depression and impaired quality of life |
publisher |
BMC |
series |
BMC Pulmonary Medicine |
issn |
1471-2466 |
publishDate |
2021-04-01 |
description |
Abstract Background While sleep disruption is a common complaint among children with cystic fibrosis (CF), only a few studies have investigated insomnia in adults. The aim of this study was to identify factors associated with insomnia in clinically stable adult CF patients. Methods Twenty-eight CF patients (18M/10F), with a median age of 27 (22–34) (median (interquartile range) years and a median of forced expiratory volume in one second of 72 (39–93) % predicted completed questionnaires on insomnia (Insomnia Severity Index, ISI), sleep quality (PSQI), daytime sleepiness (Epworth), restless legs syndrome (IRLS), pain (NRS), anxiety/depression (HAD) and quality of life (CFQ-R 14+). Respiratory assessment data, including symptoms, sputum analysis, arterial blood gases, 6-min walking test, pulmonary function tests and polysomnographic variables, were also analyzed. Results Forty-three percent of patients were insomniac (ISI > 7). Compared with non-insomniac patients (ISI ≤ 7), insomniac patients had more severely impaired quality of life and a higher HAD score: median anxiety score of 9 (8–11) vs 4 (3–6) (p < 0.0001), median depression score of 7 (5–10) vs 1 (1–4) (p < 0.001), with a positive correlation between ISI and HAD anxiety/depression scores (r = 0.702/r = 0.701, respectively, p < 0.0001). Insomnia was also associated with mMRC dyspnea scale ≥ 2, restless legs syndrome, pain and lower SpO2 during sleep. Conclusions The strong association between insomnia, impaired quality of life and increased HAD score should prompt physicians to be particularly attentive to the management of anxiety and depression in adult CF patients with insomnia. Trial registration: On clinicaltrials.gov (NCT02924818, date of registration: October 5, 2016). |
topic |
Cystic fibrosis Insomnia Sleep Anxiety-depression Quality of life |
url |
https://doi.org/10.1186/s12890-021-01473-y |
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