Sex differences in progression to mild cognitive impairment and dementia in Parkinson's disease

被引:90
|
作者
Cholerton, Brenna [1 ]
Johnson, Catherine O. [2 ]
Fish, Brian [2 ]
Quinn, Joseph F. [3 ,4 ]
Chung, Kathryn A. [3 ,4 ]
Peterson-Hiller, Amie L. [3 ,4 ]
Rosenthal, Liana S. [5 ,6 ]
Dawson, Ted M. [5 ,6 ,7 ,8 ]
Albert, Marilyn S. [6 ]
Hu, Shu-Ching [2 ,9 ]
Mata, Ignacio F. [2 ,9 ]
Leverenz, James B. [10 ]
Poston, Kathleen L. [11 ]
Montine, Thomas J. [1 ]
Zabetian, Cyrus P. [2 ,9 ]
Edwards, Karen L. [12 ]
机构
[1] Stanford Univ, Sch Med, Dept Pathol, Palo Alto, CA 94304 USA
[2] Univ Washington, Sch Med, Dept Neurol, Seattle, WA USA
[3] Portland Vet Affairs Hlth Care Syst, Portland, OR USA
[4] Oregon Hlth & Sci Univ, Dept Neurol, Portland, OR 97201 USA
[5] Johns Hopkins Univ, Sch Med, Inst Cell Engn, Neurodegenerat & Stem Cell Programs, Baltimore, MD USA
[6] Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD 21205 USA
[7] Johns Hopkins Univ, Sch Med, Solomon H Snyder Dept Neurosci, Baltimore, MD USA
[8] Johns Hopkins Univ, Sch Med, Dept Pharmacol & Mol Sci, Baltimore, MD 21205 USA
[9] Vet Affairs Puget Sound Hlth Care Syst, Seattle, WA USA
[10] Cleveland Clin, Neurol Inst, Lou Ruvo Ctr Brain Hlth, Cleveland, OH 44106 USA
[11] Stanford Sch Med, Dept Neurol & Neurol Sci, Palo Alto, CA USA
[12] Univ Calif Irvine, Sch Med, Dept Epidemiol, Irvine, CA 92717 USA
关键词
Parkinson's disease; Cognition; Dementia; Mild cognitive impairment; Sex differences; VASCULAR RISK-FACTORS; 5-YEAR FOLLOW-UP; COHORT; MOTOR; DYSFUNCTION; STEROIDS; DECLINE; GENDER;
D O I
10.1016/j.parkreldis.2018.02.007
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: Identification of factors associated with progression of cognitive symptoms in Parkinson's disease (PD) is important for treatment planning, clinical care, and design of future clinical trials. The current study sought to identify whether prediction of cognitive progression is aided by examining baseline cognitive features, and whether this differs according to stage of cognitive disease. Methods: Participants with PD in the Pacific Udall Center Clinical Consortium who had longitudinal data available and were nondemented at baseline were included in the study (n = 418). Logistic and Cox regression models were utilized to examine the relationship between cognitive, demographic, and clinical variables with risk and time to progression from no cognitive impairment to mild cognitive impairment (PD-MCI) or dementia (PDD), and from PD-MCI to PDD. Results: Processing speed (OR = 1.05, p = 0.009) and working memory (OR = 1.01, p = 0.03) were associated with conversion to PDD among those with PD-MCI at baseline, over and above demographic variables. Conversely, the primary predictive factor in the transition from no cognitive impairment to PD-MCI or PDD was male sex (OR = 4.47, p = 0.004), and males progressed more rapidly than females (p = 0.01). Further, among females with shorter disease duration, progression was slower than for their male counterparts, and poor baseline performance on semantic verbal fluency was associated with shorter time to cognitive impairment in females but not in males. Conclusions: This study provides evidence for sex differences in the progression to cognitive impairment in PD, while specific cognitive features become more important indicators of progression with impending conversion to PDD. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:29 / 36
页数:8
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