Bidirectional association between Parkinson's disease and obstructive sleep apnea: a cohort study

被引:9
作者
Jeon, Seung-Ho [1 ,2 ,3 ]
Hwang, Yun Su [1 ,2 ,3 ]
Oh, Sun-Young [1 ,2 ,3 ]
Shin, Byoung-Soo [1 ,2 ,3 ]
Kang, Min Gu [5 ]
Lee, Min Gyu [5 ]
Yeom, Sang Woo [5 ]
Lee, Jong Hwan [3 ,4 ]
Kang, Hyun Goo [1 ,2 ,3 ,6 ,7 ]
Kim, Jong Seung [1 ,3 ,4 ,5 ,8 ,9 ]
机构
[1] Jeonbuk Natl Univ, Med Sch & Hosp, Biomed Res Inst, Jeonju 54907, South Korea
[2] Jeonbuk Natl Univ, Dept Neurol, Jeonju, South Korea
[3] Jeonbuk Natl Univ, Res Inst Clin Med, Jeonju, South Korea
[4] Jeonbuk Natl Univ, Dept Otorhinolaryngol, Jeonju, South Korea
[5] Jeonbuk Natl Univ, Dept Med Informat, Jeonju, South Korea
[6] Jeonbuk Natl Univ Hosp, Dept Neurol, 20 Geonji Ro, Jeonju Si 54907, Jeonbuk Do, South Korea
[7] Jeonbuk Natl Univ, Jeonbuk Natl Univ Hosp, Biomed Res Inst, Res Inst Clin Med, 20 Geonji Ro, Jeonju Si 54907, Jeonbuk Do, South Korea
[8] Jeonbuk Natl Univ, Eonbuk Natl Univ Hosp, Dept Otorhinolaryngol, Biomed Res Inst, 20 Geonji Ro, Jeonju Si 54907, Jeonbuk Do, South Korea
[9] Jeonbuk Natl Univ, Eonbuk Natl Univ Hosp, Biomed Res Inst, Res Inst Clin Med, 20 Geonji Ro, Jeonju Si 54907, Jeonbuk Do, South Korea
来源
JOURNAL OF CLINICAL SLEEP MEDICINE | 2023年 / 19卷 / 09期
关键词
obstructive sleep apnea; Parkinson's disease; risk factor; EXCESSIVE DAYTIME SLEEPINESS; OXIDATIVE STRESS; RISK; INFLAMMATION; DYSFUNCTION;
D O I
10.5664/jcsm.10596
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Study Objectives: Chronic intermittent hypoxia due to obstructive sleep apnea (OSA) causes oxidative stress, which may contribute to the pathophysiology of Parkinson's disease (PD). However, the bidirectional relationship between PD and OSA has not been satisfactorily established. The objective of this study was to try to estimate whether there is a bidirectional relationship between PD and OSA through a retrospective cohort study in the South Korean population.Methods: This study used data from the Korean National Health Information Database of the National Health Insurance Service, which contains data from 3.5 million individuals evenly distributed. In study 1, patients with OSA were matched in a 1:2 ratio with non-OSA controls. In study 2, patients with PD were matched in a 1:2 ratio with non-PD controls. A stratified Cox proportional hazards model was used to calculate hazard ratios.Results: In study 1, which included 6,396 patients with OSA and 12,792 non-OSA controls, the incidence of PD per 10,000 person-years was 11.59 in the OSA group and 8.46 in the non-OSA group. The OSA group demonstrated a 1.54-fold higher incidence of PD than the non-OSA group (95% confidence interval, 1.14-2.07; P < .05). In study 2, which included 3,427 patients with PD and 6,854 non-PD controls, the incidence of OSA per 10,000 person-years was 14.97 in the PD group and 7.72 in the non-PD group. The PD group demonstrated a 1.92-fold higher incidence of OSA than the non-PD group (95% confidence interval, 1.32-2.78; P < .05).Conclusions: This study supports a possible bidirectional relationship between PD and OSA.
引用
收藏
页码:1615 / 1623
页数:9
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