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Exploring obstructive sleep apnea and sleep architecture in Parkinson's disease motor subtypes
被引:0
作者:
Scanga, Amanda
[1
,3
]
Benedetti, Andrea
[2
,3
]
Kimoff, R. John
[3
,4
]
Lafontaine, Anne-Louise
[5
]
Robinson, Ann
[4
]
Gingras, Marianne
[4
]
Kaminska, Marta
[1
,3
,4
]
机构:
[1] McGill Univ, Div Expt Med, Montreal, PQ, Canada
[2] McGill Univ, Dept Epidemiol Biostat & Occupat Hlth, Montreal, PQ, Canada
[3] McGill Univ, Resp Epidemiol & Clin Res Unit, Hlth Ctr, Montreal, PQ, Canada
[4] McGill Univ, Hlth Ctr, Resp Div, Sleep Lab, Montreal, PQ, Canada
[5] McGill Univ, Hlth Ctr, Montreal Neurol Inst Hosp, Montreal, PQ, Canada
基金:
加拿大健康研究院;
关键词:
Obstructive sleep apnea;
Parkinson's disease;
motor subtypes;
sleep;
DIAGNOSIS;
VALUES;
SCALE;
D O I:
10.1016/j.parkreldis.2024.106064
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Introduction: Parkinson's disease (PD) can be divided into motor subtypes: postural instability/gait difficulty (PIGD), tremor dominant, and indeterminate. This study aimed to assess differences in sleep structure and obstructive sleep apnea (OSA) between the PIGD and non-PIGD subtypes. Methods: PD participants with or without OSA (defined as apnea-hypopnea index (AHI) >= 15 events/hour on overnight polysomnography) were included. Patients were separated into two groups: PIGD and non-PIGD. Linear regression was used to explore differences in sleep, AHI, and other respiratory parameters between groups (adjusted for variables determined a priori). Logistic regression adjusted for the same variables was used to determine if the proportion of patients with OSA differed across groups. Subset analyses were performed: subset 1 excluding patients on psychoactive medication; subset 2 excluding patients taking levodopa or dopaminergic agonists (DAs) at nighttime and subset 3 excluding patients on either of the abovementioned drugs. Results: 146 participants were studied. The non-PIGD group had less N3 sleep compared to the PIGD group (12.4% vs 16.9% p = 0.06), reaching significance in subsets 1 and 3. The AHI was significantly lower in the PIGD group (p = 0.047), including when medication effects were removed (p < 0.05). OSA was more frequent in the non-PIGD group, but only significantly in subset 3 (adjusted OR 0.3, p = 0.04). Conclusion: OSA may be more severe in non-PIGD subtypes, and more frequent, in a subset free of psychoactive medication, and of levodopa and DAs, possibly owing to motor complications and dyskinesia. Future studies are required to confirm this.
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页数:7
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