Sleep Bruxism and Sleep Structure in Comorbid Insomnia and Obstructive Sleep Apnea (COMISA) Syndrome: A Polysomnographic Study

Author:

Blaszczyk Bartlomiej1,Meira e Cruz Miguel2,Waliszewska-Prosol Marta3ORCID,Wieckiewicz Mieszko4ORCID,Nowacki Dorian5ORCID,Kanclerska Justyna6,Lachowicz Gabriella6,Wojakowska Anna6,Michalek-Zrabkowska Monika6,Przegralek Jakub1,Smardz Joanna4,Antosz Katarzyna1ORCID,Mazur Grzegorz6ORCID,Martynowicz Helena6ORCID

Affiliation:

1. Student Research Club No K133, Faculty of Medicine, Wroclaw Medical University, 213 Borowska St., 50-556 Wroclaw, Poland

2. Sleep Unit, Centro Cardiovascular da Universidade de Lisboa, Department of Cardiology, Lisbon School of Medicine, 1649-028 Lisbon, Portugal

3. Department of Neurology, Wroclaw Medical University, 213 Borowska St., 50-556 Wroclaw, Poland

4. Department of Experimental Dentistry, Wroclaw Medical University, 26 Krakowska St., 50-425 Wroclaw, Poland

5. Department of Human Nutrition, Wroclaw University of Environmental and Life Sciences, 37 Chelmonskiego St., 51-630 Wroclaw, Poland

6. Department and Clinic of Internal Medicine, Occupational Diseases, Hypertension and Clinical Oncology, Wroclaw Medical University, 213 Borowska St., 50-556 Wroclaw, Poland

Abstract

Introduction: Comorbid insomnia and obstructive sleep apnea (COMISA) is not a well-identified sleep disorder, despite having a significant impact on health. This study investigates the relationship between sleep bruxism (SB) and sleep architecture in patients with COMISA, obstructive sleep apnea (OSA), and in those without any sleep disorders. Methods: 119 patients were included in the study and divided into three groups: OSA, COMISA, and a control group. Polysomnographic (PSG) examination provided parameters related to sleep architecture, OSA, and characteristics of SB. Results: The bruxism episode index (BEI) and other SB parameters were not found to be statistically different between the three groups (p > 0.05). There was no statistical difference in measured sleep architecture between the COMISA and OSA groups (p > 0.05). In comparison to the control group, participants in the COMISA group were found to have an increased apnea–hypopnea index (AHI), oxygen desaturation index (ODI), respiratory disturbance index (RDI), all arousals (AA), and respiratory arousals (RA) (p < 0.05). Among COMISA patients, AA and RA were shown to have a positive linear correlation with the number of bradycardia events per hour (r = 0.49, r = 0.48, p < 0.05). Conclusions: SB does not occur in patients with COMISA more frequently than in patients with OSA or those without any sleep disorders. PSG parameters are not specific for COMISA; therefore, in order to differentiate this disorder from OSA alone, a comprehensive patient assessment has to be performed.

Publisher

MDPI AG

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