References
- 1Elborn, JS. Cystic fibrosis. Lancet. 2016; 388(10059): 2519–2531. DOI: 10.1016/S0140-6736(16)00576-6
- 2Bouka, A, et al. Quality of life in clinically stable adult cystic fibrosis out-patients: Associations with daytime sleepiness and sleep quality. Respir Med. 2012; 106(9): 1244–9. DOI: 10.1016/j.rmed.2012.06.010
- 3Katz, ES. Cystic fibrosis and sleep. Clin Chest Med. 2014; 35(3): 495–504. DOI: 10.1016/j.ccm.2014.06.005
- 4Dancey, DR, et al. Sleep quality and daytime function in adults with cystic fibrosis and severe lung disease. Eur Respir J. 2002; 19(3): 504–10. DOI: 10.1183/09031936.02.00088702
- 5Jankelowitz, L, et al. Cystic fibrosis patients have poor sleep quality despite normal sleep latency and efficiency. Chest. 2005; 127(5): 1593–9. DOI: 10.1378/chest.127.5.1593
- 6Milross, MA, et al. Subjective sleep quality in cystic fibrosis. Sleep Med. 2002; 3(3): 205–12. DOI: 10.1016/S1389-9457(01)00157-5
- 7Owens, JG. Adolescent Sleep Working, and A. Committee on, Insufficient sleep in adolescents and young adults: An update on causes and consequences. Pediatrics. 2014; 134(3): e921–32. DOI: 10.1542/peds.2014-1696
- 8Irwin, MR. Why sleep is important for health: A psychoneuroimmunology perspective. Annu Rev Psychol. 2015; 66: 143–72. DOI: 10.1146/annurev-psych-010213-115205
- 9Zhai, L, Zhang, H and Zhang, D. Sleep Duration and Depression among Adults: A Meta-Analysis of Prospective Studies. Depress Anxiety. 2015; 32(9): 664–70. DOI: 10.1002/da.22386
- 10Wickens, CD, et al. The Impact of Sleep Disruption on Complex Cognitive Tasks: A Meta-Analysis. Hum Factors. 2015; 57(6): 930–46. DOI: 10.1177/0018720815571935
- 11Milross, MA, et al. Sleep disordered breathing in cystic fibrosis. Sleep Med Rev. 2004; 8(4): 295–308. DOI: 10.1016/j.smrv.2004.03.004
- 12Spicuzza, L, et al. Early occurrence of obstructive sleep apnea in infants and children with cystic fibrosis. Arch Pediatr Adolesc Med. 2012; 166(12): 1165–9. DOI: 10.1001/archpediatrics.2012.1177
- 13Jensen, JL, et al. Sleep Phase Delay in Cystic Fibrosis: A Potential New Manifestation of Cystic Fibrosis Transmembrane Regulator Dysfunction. Chest; 2017. DOI: 10.1016/j.chest.2017.03.057
- 14Kim, YS, et al. Histamine 1 receptor-Gbetagamma-cAMP/PKA-CFTR pathway mediates the histamine-induced resetting of the suprachiasmatic circadian clock. Mol Brain. 2016; 9(1): 49. DOI: 10.1186/s13041-016-0227-1
- 15Takahashi, JS, et al. The genetics of mammalian circadian order and disorder: Implications for physiology and disease. Nat Rev Genet. 2008; 9(10): 764–75. DOI: 10.1038/nrg2430
- 16Arble, DM, et al. Circadian disruption and metabolic disease: Findings from animal models. Best Pract Res Clin Endocrinol Metab. 2010; 24(5): 785–800. DOI: 10.1016/j.beem.2010.08.003
- 17King, DP and Takahashi, JS. Molecular genetics of circadian rhythms in mammals. Annu Rev Neurosci. 2000; 23: 713–42. DOI: 10.1146/annurev.neuro.23.1.713
- 18Zeiher, BG, et al. A mouse model for the delta F508 allele of cystic fibrosis. J Clin Invest. 1995; 96(4): 2051–64. DOI: 10.1172/JCI118253
- 19Revel, FG, et al. Rodent models of insomnia: A review of experimental procedures that induce sleep disturbances. Neurosci Biobehav Rev. 2009; 33(6): 874–99. DOI: 10.1016/j.neubiorev.2009.03.002
- 20Wisor, JP, et al. Sleep deprivation effects on circadian clock gene expression in the cerebral cortex parallel electroencephalographic differences among mouse strains. J Neurosci. 2008; 28(28): 7193–201. DOI: 10.1523/JNEUROSCI.1150-08.2008
- 21Colavito, V, et al. Experimental sleep deprivation as a tool to test memory deficits in rodents. Front Syst Neurosci. 2013; 7: 106. DOI: 10.3389/fnsys.2013.00106
- 22Darrah, RJ, et al. Ventilatory pattern and energy expenditure are altered in cystic fibrosis mice. J Cyst Fibros. 2013; 12(4): 345–51. DOI: 10.1016/j.jcf.2012.11.008
- 23Zaslavskaia, RM, Veklenko, GV and Teiblium, MM. Temporal organization of external respiratory function in elderly patients with chronic obstructive lung disease. Klin Med (Mosk). 2004; 82(7): 36–40.
- 24Hadden, H, Soldin, SJ and Massaro, D. Circadian disruption alters mouse lung clock gene expression and lung mechanics. J Appl Physiol (1985). 2012; 113(3): 385–92. DOI: 10.1152/japplphysiol.00244.2012
- 25Sukumaran, S, et al. Light-dark oscillations in the lung transcriptome: Implications for lung homeostasis, repair, metabolism, disease, and drug action. J Appl Physiol (1985). 2011; 110(6): 1732–47. DOI: 10.1152/japplphysiol.00079.2011
- 26Gibbs, JE, et al. Circadian timing in the lung; a specific role for bronchiolar epithelial cells. Endocrinology. 2009; 150(1): 268–76. DOI: 10.1210/en.2008-0638
- 27Darrah, RJ, et al. Early pulmonary disease manifestations in cystic fibrosis mice. J Cyst Fibros. 2016; 15(6): 736–744. DOI: 10.1016/j.jcf.2016.05.002
- 28Sato, S, et al. A circadian clock gene, Rev-erbα, modulates the inflammatory function of macrophages through the negative regulation of Ccl2 expression. J Immunol. 2014; 192(1): 407–17. DOI: 10.4049/jimmunol.1301982
- 29Gibbs, JE, et al. The nuclear receptor REV-ERBalpha mediates circadian regulation of innate immunity through selective regulation of inflammatory cytokines. Proc Natl Acad Sci U S A. 2012; 109(2): 582–7. DOI: 10.1073/pnas.1106750109
- 30Nguyen, KD, et al. Circadian gene Bmal1 regulates diurnal oscillations of Ly6C(hi) inflammatory monocytes. Science. 2013; 341(6153): 1483–8. DOI: 10.1126/science.1240636
- 31Bonfield, T and Chmiel, JF. Impaired innate immune cells in cystic fibrosis: Is it really a surprise? J Cyst Fibros. 2017; 16(4): 433–435. DOI: 10.1016/j.jcf.2017.06.001
- 32Bonfield, TL, et al. Absence of the cystic fibrosis transmembrane regulator (Cftr) from myeloid-derived cells slows resolution of inflammation and infection. J Leukoc Biol. 2012; 92(5): 1111–22. DOI: 10.1189/jlb.0412188