Probable rapid eye movement sleep behavior disorder increases risk for mild cognitive impairment and Parkinson disease: A population-based study

被引:153
作者
Boot, Brendon P. [1 ,6 ]
Boeve, Bradley F. [1 ,2 ,6 ,7 ]
Roberts, Rosebud O. [3 ,8 ]
Ferman, Tanis J. [4 ,9 ]
Geda, Yonas E. [3 ,4 ,8 ,9 ]
Pankratz, V. Shane [3 ,8 ]
Ivnik, Robert J. [4 ,9 ]
Smith, Glenn E. [4 ,9 ]
McDade, Eric [1 ,6 ]
Christianson, Teresa J. H. [3 ,8 ]
Knopman, David S. [1 ,6 ]
Tangalos, Eric G. [5 ,10 ]
Silber, Michael H. [1 ,2 ,6 ,7 ]
Petersen, Ronald C. [1 ,3 ,6 ,8 ]
机构
[1] Mayo Clin, Coll Med, Dept Neurol, Rochester, MN 55905 USA
[2] Mayo Clin, Coll Med, Ctr Sleep Med, Rochester, MN 55905 USA
[3] Mayo Clin, Coll Med, Dept Hlth Sci Res, Rochester, MN 55905 USA
[4] Mayo Clin, Coll Med, Dept Psychiat & Psychol, Rochester, MN 55905 USA
[5] Mayo Clin, Coll Med, Dept Internal Med, Rochester, MN 55905 USA
[6] Mayo Clin, Coll Med, Dept Neurol, Jacksonville, FL 32224 USA
[7] Mayo Clin, Coll Med, Ctr Sleep Med, Jacksonville, FL 32224 USA
[8] Mayo Clin, Coll Med, Dept Hlth Sci Res, Jacksonville, FL 32224 USA
[9] Mayo Clin, Coll Med, Dept Psychiat & Psychol, Jacksonville, FL 32224 USA
[10] Mayo Clin, Coll Med, Dept Internal Med, Jacksonville, FL 32224 USA
关键词
DELAYED EMERGENCE; EARLY MARKER; RBD; PATHOPHYSIOLOGY; DEMENTIA;
D O I
10.1002/ana.22655
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: Rapid eye movement sleep behavior disorder (RBD) is associated with neurodegenerative disease and particularly with the synucleinopathies. Convenience samples involving subjects with idiopathic RBD have suggested an increased risk of incident mild cognitive impairment (MCI), dementia (usually dementia with Lewy bodies), and Parkinson disease (PD). There are no data on such risks in a population-based sample. Methods: Cognitively normal subjects aged 70 to 89 years in a population-based study of aging who screened positive for probable RBD using the Mayo Sleep Questionnaire were followed at 15-month intervals. In a Cox proportional hazards model, we measured the risk of developing MCI, dementia, and PD among the exposed (probable RBD [ pRBD] _) and unexposed (pRBD+) cohorts. Results: Forty-four subjects with pRBD_ status at enrollment (median duration of pRBD features was 7.5 years) and 607 pRBD+ subjects were followed prospectively for a median of 3.8 years. Fourteen of the pRBD_ subjects developed MCI, and 1 developed PD (15/ 44 34% developed MCI/ PD); none developed dementia. After adjustment for age, sex, education, and medical comorbidity, pRBD_ subjects were at increased risk of MCI/ PD (hazard ratio [ HR], 2.2; 95% confidence interval [ CI], 1.3-3.9; p 0.005). Inclusion of subjects who withdrew from the study produced similar results, as did exclusion of subjects with medication-associated RBD. Duration of pRBD symptoms did not predict the development of MCI/ PD (HR, 1.05 per 10 years; 95% CI, 0.84-1.3; p 0.68). Interpretation: In this population-based cohort study, we observed that pRBD confers a 2.2-fold increased risk of developing MCI/ PD over 4 years.
引用
收藏
页码:49 / 56
页数:8
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