Cerebrospinal Fluid α-Synuclein Predicts Cognitive Decline in Parkinson Disease Progression in the DATATOP Cohort

被引:123
|
作者
Stewart, Tessandra [1 ]
Liu, Changqin [1 ,3 ,4 ]
Ginghina, Carmen [1 ]
Cain, Kevin C. [5 ]
Auinger, Peggy [6 ]
Cholerton, Brenna [2 ,7 ]
Shi, Min [1 ]
Zhang, Jing [1 ]
机构
[1] Univ Washington, Sch Med, Dept Pathol, Seattle, WA 98104 USA
[2] Univ Washington, Sch Med, Dept Psychiat & Behav Sci, Seattle, WA 98104 USA
[3] Xiamen Univ, Affiliated Hosp 1, Dept Endocrinol & Metab, Xiamen, Peoples R China
[4] Xiamen Univ, Affiliated Hosp 1, Xiamen Diabet Inst, Xiamen, Peoples R China
[5] Univ Washington, Sch Publ Hlth, Dept Biostat, Seattle, WA 98104 USA
[6] Univ Rochester, Sch Med & Dent, Dept Neurol, Ctr Human Expt Therapeut, Rochester, NY 14642 USA
[7] Vet Affairs Puget Sound Hlth Care Syst, Geriatr Res Educ & Clin Ctr, Seattle, WA USA
来源
AMERICAN JOURNAL OF PATHOLOGY | 2014年 / 184卷 / 04期
关键词
CORTICAL LEWY BODIES; DEMENTIA; CSF; LEVODOPA; ASSOCIATION; IMPAIRMENT; DEFICITS; MODEL; RISK; TAU;
D O I
10.1016/j.ajpath.2013.12.007
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Most patients with Parkinson disease (PD) develop both cognitive and motor impairment, and biomarkers for progression are urgently needed. Although alpha-synuclein is altered in cerebrospinal fluid of patients with PD, it is not known whether it predicts motor or cognitive deterioration. We examined clinical data and alpha-synuclein in >300 unmedicated patients with PD who participated in the deprenyl and tocopherol antioxidative therapy of parkinsonism (DATATOP) study, with up to 8 years of follow-up. Longitudinal measures of motor and cognitive function were studied before (phase 1) and during (phase 2) levodopa therapy; cerebrospinal fluid was collected at the beginning of each phase. Correlations and linear mixed models were used to assess alpha-synuclein association with disease severity and prediction of progression in the subsequent follow-up period. Despite decreasing cc-synuclein (phase 1 to phase 2 change of -0.05 +/- 0.21 log-transformed values, P < 0.001), no correlations were observed between alpha-synuclein and motor symptoms. Longitudinally, lower alpha-synuclein predicted better preservation of cognitive function by several measures [Selective Reminding Test total recall alpha-synuclein x time interaction effect coefficient, -0.12 (P = 0.037); delayed recall, -0.05 (P = 0.002); New Dot Test, -0.03 (P = 0.002)]. Thus, alpha-synuclein, although not clinically useful for motor progression, might predict cognitive decline, and future longitudinal studies should include this outcome for further validation.
引用
收藏
页码:966 / 975
页数:10
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