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Cardiac autonomic function in REM-related obstructive sleep apnoea: insights from nocturnal heart rate variability profiles.
Ucak, Seren; Dissanayake, Hasthi U; Sutherland, Kate; Yee, Brendon J; Kairaitis, Kristina; Wheatley, John R; Piper, Amanda J; de Chazal, Philip; Cistulli, Peter A.
Afiliação
  • Ucak S; Charles Perkins Centre and Northern Clinical School, Faculty of Medicine and Health, University of Sydney, Sydney, Australia. seren.ucak@sydney.edu.au.
  • Dissanayake HU; Charles Perkins Centre and Northern Clinical School, Faculty of Medicine and Health, University of Sydney, Sydney, Australia.
  • Sutherland K; Department of Respiratory and Sleep Medicine, Royal North Shore Hospital, Sydney, Australia.
  • Yee BJ; Charles Perkins Centre and Northern Clinical School, Faculty of Medicine and Health, University of Sydney, Sydney, Australia.
  • Kairaitis K; Department of Respiratory and Sleep Medicine, Royal North Shore Hospital, Sydney, Australia.
  • Wheatley JR; Sydney Medical School, Faculty of Medicine and Health, University of Sydney, Sydney, Australia.
  • Piper AJ; Woolcock Institute of Medical Research, Royal Prince Alfred Hospital, Sydney, Australia.
  • de Chazal P; Sydney Medical School, Faculty of Medicine and Health, University of Sydney, Sydney, Australia.
  • Cistulli PA; Ludwig Engel Centre for Respiratory Research, Westmead Institute for Medical Research, Sydney, Australia.
Sleep Breath ; 2024 Jul 01.
Article em En | MEDLINE | ID: mdl-38951383
ABSTRACT

PURPOSE:

In light of the reported association between REM-related obstructive sleep apnoea (OSA) and heightened cardiovascular risk, this study aims to compare cardiac autonomic function in patients with REM-OSA and OSA independent of sleep stage. We hypothesized that REM-OSA patients would exhibit higher sympathetic cardiac modulation based on heart rate variability (HRV) profiles.

METHODS:

HRV was compared between the OSA group (AHI ≥ 5 events/h, n = 252) and the REM-OSA group (AHI ≥ 5 events/h, AHIREMAHINREM ≥ 2, n = 137). Time- and frequency-domain measures of HRV were analysed during N2 and REM sleep.

RESULTS:

Clinical characteristics between the two test groups differed significantly, 45% of REM-OSA patients were female, with mild OSA (median, interquartile range (IQR)) AHI of 10 (7) events/h. Only 26% of the OSA cohort were female with moderate OSA (AHI = 17 (20) events/h, p < 0.001). Compared with the OSA group, the low frequency to high frequency ratio (LFHF) and LF power were lower and HF power was higher in the REM-OSA group during N2 (LFHF, p = 0.012; LF; p = 0.013; HF, p = 0.007) and in REM sleep (LFHF, p = 0.002; LF, p = 0.004; HF, p < 0.001). Patient sex and OSA severity had a significant combined effect on average N to N interval, LF power, and LFHF ratio during N2 and REM sleep (all p < 0.001).

CONCLUSION:

Contrary to our hypothesis, REM-OSA patients demonstrated consistently higher cardiac vagal modulation, reflecting better cardiac autonomic adaptation. These results were attributed to differences in OSA severity and sex in these two groups, both independently affecting HRV. This study emphasises the need for future research into the underlying pathophysiology of REM-OSA and the potential implications of sex and OSA severity on cardiovascular risk.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Sleep Breath Assunto da revista: NEUROLOGIA / OTORRINOLARINGOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Austrália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Sleep Breath Assunto da revista: NEUROLOGIA / OTORRINOLARINGOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Austrália